US20130324478A1

US20130324478A1 - Pharmacodiagnosis Test Targeting Oncology and Neurodegeneration

Info

Publication number: US20130324478A1
Application number: US13/681,164
Authority: US
Inventors: Laurence Faure
Original assignee: Individual
Current assignee: Individual
Priority date: 2008-09-08
Filing date: 2012-11-19
Publication date: 2013-12-05
Also published as: US10718029B2; US20210071260A1; US20180291462A1

Abstract

The present invention relates to the field of medicine and biology. It concerns a new test for screening and therapeutic follow-up in oncology. More particularly, it relates to diagnostic and/or therapeutic tests in oncology and on neurodegenerative diseases. Molecular targeting by peptide vectors and antibodies or by small interfering RNAs (siRNAs) opens a new concept of interdependence for diagnostic and therapeutic tools.

Description

CROSS REFERENCE TO RELATED APPLICATION

This application is a continuation in part application of U.S. patent application Ser. No. 12/282,117 filed on Sep. 8, 2008. This application is also a continuation in part application of International Patent Application Serial No. PCT/FR2011/000155 filed on Mar. 18, 2011.

FIELD OF THE INVENTION

The present invention relates to the field of medicine and biology. It concerns a new test for screening and therapeutic follow-up in oncology. More particularly, it relates to diagnostic and/or therapeutic tests in oncology and on neurodegenerative diseases. Molecular targeting by peptide vectors and antibodies or by small interfering RNAs (siRNAs) opens a new concept of interdependence for diagnostic and therapeutic tools.
The inventor highlights the mechanisms of molecular interactions and the interest of biochips dedicated according to cancers with a multi-therapy added with therapeutic additives to slow down the formation of these lesions.
The comprehension of the plays of balance between under-expression and over-expression of genes according to their localization in a cellular compartment allows to open a field of finer differential analysis and to adapt a multi-therapy with siRNA and peptides by molecular targeting.

DESCRIPTION OF THE STATE OF THE ART

Age-related neurodegenerative diseases and cancers both involve a modification of the physiological process of programmed cell death or apoptosis. Neuronal death is abnormally accelerated during neurodegenerative diseases such as Alzheimer's disease, Huntington's disease, Parkinson's disease etc. . . . On the other hand, the cancerization process corresponds to a blocking of apoptosis, which results in an uncontrolled multiplication of cells. The link between these two processes has currently become a major field of investigation in research on aging. The control of the balance between cell division (mitosis), differentiation and programmed cell death (apoptosis), is fundamental during normal physiological processes, including embryonic development, tissue regeneration and aging. An impairment of this balance can lead to major pathological situations such as the formation of tumors or some neurodegenerative diseases.
Cancer is one of the principal causes of mortality throughout the world. While, over the course of the last generation, the percentages of deaths related to cardiac and cardiovascular diseases and a large number of other diseases has decreased, the number of deaths related to the various forms of cancer has increased.
Despite the rapid advance in our understanding of the various forms of cancer, the low survival rates can generally be attributed to inadequate diagnosis and inadequate treatment. Most tumors can only be detected when they reach a size of approximately 1 cm. Since a continuously developing tumor takes a relatively short period of time to evolve to a stage which is incompatible with survival, this leaves little time for a therapeutic intervention. Early diagnosis therefore becomes the key to success for the treatment of cancer. Skin cancer for example, is the most widespread cancer in Canada. In 1992 alone, 50 300 new cases of skin cancer were reported, compared with 19 300 cases of lung cancer, 16 200 cases of colorectal cancer and 15 700 cases of breast cancer. In other words, skin cancer is as common as the three main types of cancer combined. Its incidence continues to increase, with 64 200 new cases thereof in 1997, corresponding to an increase of 14 000 cases in 5 years. In particular, the incidence of malignant melanoma is increasing at a rate of 2% per year. Early diagnosis remains the key to an effective treatment. A malignant tumor is readily accessible and can be removed with minor surgery. In fact, recovery is 100% if skin cancer is detected early enough. Early diagnosis of skin cancer remains however difficult . . . . It thus becomes important to be able to distinguish these two types of skin cancers. A final diagnosis of skin cancer requires a biopsy and a histological analysis. However, the decision to send a biopsy for analysis (or even if a patient must be referred with a dermatologist) becomes very subjective. There are several biopsies which are not taken whereas they would have being.
Colon cancer is the third most common cause of cancer-related mortality in men and women in North America (16 200 cases per year). Early detection, leading to an early intervention, has demonstrated that treatment success and survival rate can be improved. For example, the 5-year survival rate is 92% for a patient whose disease was detected at an early stage, whereas the rate drops to approximately 60% in patients with a localized cancer, and to approximately 6% in those with metastases. However, only a third of colon cancers are detected at an early stage. One of the reasons for this delay in diagnosis is the absence of a sensitive, relatively inexpensive and non-invasive screening test. Breast cancer is one of the most common cancers in women, together with colon cancer. The mortality rate is the highest among cancers affecting women. There are very few diagnostic markers allowing the detection of breast cancer and they only have a predictive value of 20%. There are no markers, either, which can detect or determine the invasiveness or the aggressiveness of metastatic cancer cells or which permit therapeutic monitoring.
For a multitude of reasons, early diagnosis remains illusory for most forms of cancer. For certain forms of cancer, disease-specific markers are not available or are only available at an advanced stage of the disease, making diagnosis difficult. In other forms of cancer, the markers are available but are not always specific for the disease or they may be associated with its benign form.
A hope this year with the marker who is the receiver with the FSH is possible. As one of our markers of the LIV21 complex (cf. figure) it is common to several cancers and allows an early diagnosis, it also appears in the vessels as ours which one can see in Alexa revealed on the level of the endothelial cells, but in more we observe a marking of the erythrocytes and also collagen. During the last years, considerable progresses were made in the comprehension of the means implemented by the oncogenes and tumor suppressor genes to control cell proliferation and the apoptosis. One of the main targets of these regulators is the family of E2F-type transcription factors in the E2F and RB protein signaling pathway.
In other cases still, the techniques exist but the prohibitory cost to in general implement them to the population makes them inappropriate.
These cancers may find it beneficial to be studied and diagnosed by biochip including the bio-markers of the major pathways of regulation to allow an adjustment of the multi-therapy according to the results of under expression and over-expression of genes of the complex Liv21. Thus the processing by standard molecular targeting siRNA or monoclonal antibodies combined or not with chemical therapeutic assets is of a greater effectiveness.
The neuroblastes are neuronal precursors resulting from the splitting of the neuro-epithelial cells. There are immature embryonic neurons which can still divide contrary to the mature neurons which cannot enter in mitosis.
The neuroblastoma, also called sympathoblastome, is a malignant tumor developed at the expense of the cells of the neural crest, which give rise to the sympathetic nervous system. It is of the solid tumor most frequent in the child (8 to 10% of cancers before 15 years) and in particular about the very young child (average age 4 years with 90% which have less than 5 years). Its incidence is from 1 to 3 cases for 100 000 older children from 0 to 14 years. There are no causes nor of recognized mailmen which support occurred of a neuroblastoma.
The neuroblastoma is discovered starting from symptoms due to the primary neoplasm (mass tumoral, in particular abdominal, or compression of a nearby part, such spinal-cord), to metastases or an endocrine secretion (deterioration of the general state, diarrhea, arterial hypertension . . . ). The neuroblastoma can develop starting from an unspecified component of the system highly-strung person sympathetic nerve, generally at the abdominal level. At the time of the diagnosis, the tumor can be localized on the level of one only part, the local or regional level, or be from the disseminated start. The metastatic sites most frequent are the bone, bone marrow, the liver and the skin. Thus, the majority of the localized tumors have an excellent forecast. It is the same for those of the children of less than one year, independently of the stage of the tumor. Some of these tumors regress even spontaneously. On the contrary, approximately 60% of the children of more than one year forward a metastatic neuroblastoma from the start of poor prognosis.
The variety of the clinical presentation is in relation to the expression of certain biochemical markers and molecular (DNA ploidy, amplification of the oncogene n-myc, Trk receptor expression, loss of the chromosome 1p, excess of the 17q . . . ). Thus, diffuse tumors occurring in the child of more than 1 year and on-expressing the oncogene myc are often chemo-resistant and have a poor prognosis (Berthold and Al, 1990; Schweigerer and Al, 1990). In the same way, the TrkB receptor expression and of BDNF allows a system of survival autocrine neuroblastic cells and induces the neuritic growth. It is also associated with the amplification of N-Myc and thus with a poor prognosis (Nakagawara and Al, 1994). On the contrary, the TrkA receptor expression, which induces the differentiation of the neuroblastoma (Borrello and Al, 1993; Eggert and Al, 2000), and TrkC (Yamashiro and Al, 1996) are rather associated with a good forecast. Thus, it is common to say that the TrkA receptor expression is conversely correlated with the amplification of the oncogene n-myc.
During the development, the gliaux precursors give rise to the astrocytes, oligodendrocytes, microglial cells, choroidal cells and ependymaires cells in the SNC, and with the Schwann cells in the peripheral nervous system. Thus, the cells gliales play a crucial role in differentiation (Lemke, 2001) and the survival of the neurons (Bar, 2000). These cells ensure the nutrition of the neurons, manage connected them inter-neuronal, control the neurotransmitters.
The glioblastomas are the malignant tumors astrocytaires (grade IV according to the classification of the World Health Organization) most undifferentiated of SNC and they are generally found on the level of the cerebral hemispheres. In the adult, they are the most frequent brain tumors (20% of all the intracranial tumors) with an angle of attack of about 3 new cases a year and for 100.000 inhabitants, that is to say approximately 2400 new cases a year in France. They occur at any age but in 70% of the cases between 45 and 70 years.
The glioblastomas form soft masses, rich in blood-vessels, from 3 to 10 cm in diameter, of vinous color, heterogeneous with active compact areas and areas of necroses wide, strewn with vessels thromboses and which infiltrate brain tissue. However, these tumors are not practically ever associated with the appearance of metastases. There are surrounded by a edema which increases the suffering of the brain. Typically, they are expressed by signs of intracranial hypertension which often joins changes of the behavior, with crises comitiales, focal neurologic deficits.
This tumor evolves quickly, in 2-3 month, and even after surgery, radiotherapy then chemotherapy, its forecast remains dark except if the glioblastoma comes from the tumor can be localized on the level of one only part, the local or regional level, or be from the disseminated start. The metastatic sites most frequent are the bone, bone marrow, the liver and the skin. Thus, the majority of the localized tumors have an excellent forecast. It is the same for those of the children of less than one year, independently of the stage of the tumor. Some of these tumors regress even spontaneously. On the contrary, approximately 60% of the children of more than one year forward a metastatic neuroblastoma from the start of poor prognosis.
The variety of the clinical presentation is in relation to the expression of certain biochemical markers and molecular (DNA ploidy, amplification of the oncogene n-myc, Trk receptor expression, loss of the chromosome 1p, excess of the 17q . . . ). Thus, diffuse tumors occurring in the child of more than 1 year and on-expressing the oncogene myc are often chemo-resistant and have a poor prognosis (Berthold and Al, 1990; Schweigerer and Al, 1990). In the same way, the TrkB receptor expression and of BDNF allows a system of survival autocrine neuroblastic cells and induces the neuritic growth. It is also associated with the amplification of N-Myc and thus with a poor prognosis (Nakagawara and Al, 1994). On the contrary, the TrkA receptor expression, which induces the differentiation of the neuroblastomata (Borrello and Al, 1993; Eggert and Al, 2000), and TrkC (Yamashiro and Al, 1996) are rather associated with a good forecast. Thus, it is common to say that the TrkA receptor expression is conversely correlated with the amplification of the oncogene n-myc.
The receivers of the superfamily of TNF-R were studied in the neuroblastic cells. Thus, the Fas receiver could be highlighted at the level of certain neuroblastic cells (Gross et al., 2001), cells which can be (Barthlen et al., 1999; Riffkin et al., 2001) or not (Bian et al., 2004) resistant to the apoptosis induced by Fas. The sensitivity of the neuroblastic cells does not depend only on the Fas receptor expression but on the presence or not of the caspase-8 in cells (Kisenge et al., 2003). The receptors of TRAIL are also expressed in the neuroblastic cells.
The neuroblastoma is one of most common in the child. Death rate is the highest of all cancers assigning the children.
There are very few diagnostic markers able to detect the neuroblastoma. There are no either markers which can detect or determine the invasivity and the aggressiveness of the metastatic cancerous cells or which allows a therapeutic follow-up.
During the last years, considerable progresses were made in the comprehension of the means implemented by the oncogenes and tumor suppressor genes to control cell proliferation and the apoptosis. One of the main targets of these regulators is the family of the mailmen of transcription of the type E2Fs (E2F1, E2F2, E2F3, E2F4 etc. . . . ) in the channel of indication of the proteins E2Fs and RB. These proteins play a central role in the control of cell division by coupling the regulation of genes necessary to the cell cycle progression with the extracellular signals (mitogenes, inhibitors of the proliferation). It behaves as an oncogene by stimulating tumor cell proliferation. Myc N and Aurora kinase are also oncogenes implied in the proliferation of the neuroblastoma. E2F3 modulates the form of the RNA m of Aurora during the cell cycle. In addition, certain data suggest that the mailmen of transcription E2F are critical for total activation and the repression of Myc N in the neuroblastoma. The combination of the dosages of genes of Myc N and the Survivin by RTPCR is correlated at the stage of the clinical change of the neuroblastoma.
Among the expressed genes are found:

- over-expression of the E2F4 transcription factor and the c-myc oncogene which induce apoptosis of post-mitotic cells by accumulation of oxygenated reactants (Tanaka, 2002) and the N Myc which is amplified in 35% of the cases of neuroblastoma, gene ALK, DDX1 and CRABP II too. HGMA1 and the Survivin also. The repression of HGMA1 by RNA interference reduces the cell proliferation of the neuroblastoma. N Myc induces the expression of FAK. N Myc down reguls the expression mRNA of many genes having a role in cellular architecture.
- the gene p53, which belongs to the tumor suppressor gene family, blocks the cell cycle in the case of DNA lesion. It has now been demonstrated that this gene is also involved in the progression of apoptosis (Oren, 1994; Yonish-Rouach, 1996);
- the cyclin D1, one of the proteins constituting the regulatory subunits of cell cycle kinases, which is essential for cell cycle progression. This protein is also expressed during apoptosis in various cell types (Han et al, 1996; Pardo et al, 1996).

A transcription factor Zinc finger can stop the activity of the D1 cyclin and lock the cycle. Data suggest that the mailmen of transcription E2F are critical for total activation and the repression of MYCN in the neuroblastomas.

- chk1 and 2, crb2, p21 and other oncogenes and cytokines such as TNF alpha etc. . . . It would be of great interest to have novel diagnostic methods detecting the presence of cancer with greater specificity and making it possible to distinguish between aggressive cancer cells with the tendency to metastasize and those which are more localized and have a lower probability of metastasizing. A marker capable of revealing cell proliferation would therefore be of great use. The works of the professor Jean Louis Mendel about the glial markers and in particular on the GFAP and the NF70 advanced the diagnosis, the expression of the synemine in the glial tumors is an important way of research like the study of the mutations of the Ras/MAPK channel. The deletion of chromosome 1 in the area 1p36 and the amplification of gene MYC N sign the state of proliferation, a forecast of neuroblastoma and an unfavourable histology. In 35% of the cases, MYC N is amplified, in 58% of the cases it is chromosome 17 in q23 and in 35% of the cases chromosome 1 in p36 is deleted.

Complex LIV21 will be studied by RT PCR and biochip and its cytoplasmic markers of interest and the membrane protein of the complex Liv 21 too.
21 additional markers and new sequences of complex LIV21 compared to the first and with the second patent deposited will allow a notable improvement and an improvement of the pharmaco diagnostic tests which we propose.
It is thanks to this improvement that the therapeutic adjustment in multi-therapy will be able to allow a greater effectiveness of processing and as it is thanks to this improvement as the diagnosis of the glial tumors will be done more precisely with a thorough knowledge on the forecast, the grade and the development of these tumors. Another improvement made it possible to have a larger precision in the study of the expression levels of various important genes for the diagnosis of glial tumor, it is the troubleshoot of a standardization of the tissue samples like punctures of the cerebrospinal fluid. Thus the comparisons of profiles of expression are more reliable and undergo less fluctuations due to skews of observation. All these new parameters which do not increase the number of variables but which decrease the background noise largely improve the diagnosis and the processing of the gliales tumors. ki 67 and Cafl are nuclear markers indicating the proliferation state of many cancers (Almouzny; Curie Institut). Liv21 complex genes will be the cytoplasmic markers at least equal and complementary to the previously identified nuclear ones.

SUMMARY OF THE INVENTION

The present invention concerns new polypeptide, ribonuclotidic and nucleotidic sequences to integrate into a novel test for screening for reinduction of the cell cycle targeting oncology and the use of some of these same functionalized sequences, like auxiliary processing by molecular targeting. It is about a major improvement without which the diagnosis and the test pharmaco diagnostic could be only partial. The consequence would be a less effective processing and of less broad implementation according to the heterogeneity of cancers. It is thus about a diagnostic test and a prognostic test for various cancers. More particularly, the invention concerns the use of the genes or proteins of the Liv21 complex and of their derivatives as therapeutic tools or as diagnostic and prognostic markers for cancers. The invention therefore concerns the detection of the LIV21 gene or LIV21 protein with a kit comprising LIV21-specific antibodies or LIV21 specific probes. The present invention also consist in using all the proliferation markers and transcription factors which play a role in the cancerization and in some cases, neurodegeneration process. The invention lies in the use of quantitative RT PCR and the PCR (QPCR) twinned at the manufacture of diagnostic DNA biochips, proteins biochips and antibody arrays including known antibodies directed against various proteins of the LIV21-associated complex according to the phases of the cell cycle, that is, without restriction thereto: peptides and antibodies specific for RBP2, E2F4, E2F1, SUMO, HDAC1, crb2, Int2, cmd2, cycE/cdk2, cdk1, CREB 1 and p300, Rb, p107 and p130 of the pocket protein family. In addition, antibodies specific for NFkB, cdc2A, mdm2, p21, p53, p65, BRCA1, TNFalpha, TGF beta. The new sequences are the poly-nucleotidic and polypeptide sequences of Liv21F, Liv21H, etc. . . . (list additional of the sequences: SEQ ID No 171 to 185) and the sequences of genes, proteins, and corresponding antibodies lately integrated in the pharmaco-diagnostic biochips are: Myc N, ALK, HMGA1, DDX1, GFAP, NF70, AD7cNTP, FAB3, Serin C2, Synemine, PDX1, HDAC6, TPX2, DKK1, DKK3, HUD, ID2, SKP2, TP531NP1, VEGF, NLRR1, PAX3-FKHR, NDP kinase A, Bora ?, Aurora A, Survivin
The protein arrays will make it possible to study the proteinic interactions and the post traductional modifications, more particularly the phosphorylations and methylations of certain proteins which sign a state characteristic of the sick cell different from the proteinic interactions and metabolism of the healthy cell. The state of expression and silencing of certain genes being different. The rate of expression of each biomolecule in front of being observed distinctly in each cellular compartment to be able in the second time controlled being (under expressed or on expressed by a standard auxiliary processing biomolecule or siRNA or vectorized peptides).
The biochips with nucleotidic sequences will make it possible to study in nuclear cellular extracts and in addition cytoplasmic or membran, under expressions or on gene expressions and the ratios between genes as between proteins of complex Liv21 and its associated partners, the analysis of the interactions within the metabolic complexes is a key of the diagnosis and also passes by the study of the functional fields.
A first objective of the present invention is to demonstrate a method for the detection and prognosis of cancer and of its metastatic potential which makes it possible to adjust a multitherapy targeted. Preferably, the cancer is selected from breast cancer on cerebral cancers and more particularly the glioblastoma, the neuroblatoma, without being limited thereto.
One aspect of the present invention consists of the use of LIV21 complex new sequences as prognostic indicator for cancer and his therapeutic monitoring.
Indeed, when Liv21 is localized in the cytoplasm, the cancer cells in tissues are aggressive. Conversely, when the product of gene expression Liv21F is preferentially localized in the cellular core, this is a prognostic indicator that the tissue cells are differentiated and quiescent and thus noninvasive. We define the Liv21 complex by the protein extract and peptides studied by mass spectrometry such as Maldi and ESIMSMS or Maldi T of T of. The said extract has been obtained by binding of the Liv21 complex to one of its polyclonal antibodies described in the patent (PCT/FR2006/000510).
The Liv21 complex is defined by its mass spectrometry global profile (FIG. 5) and the number and the molecular weight of protein extracts bands obtained on the acrylamide gels of FIGS. 1A and 1B as a function of temperature at which the sample is submitted and of described migration conditions. In fact, when for example Liv21F peptide is located in the cytoplasm and we reveal directly for example by in situ hybridization or by biochip analysis its higher expression in the cytoplasm, the cancer cells in the tissues are aggressive. Conversely, when the LIV21 gene expression product or the expression of Liv21F peptide is preferentially located in the cell nucleus, this is a prognostic indicator that the cells of the tissue are differentiated and quiescent and therefore noninvasive. This observation is associated under investigation with expression, phosphorylation and localization of the other factors of complex Liv21 and with these partners of interaction. The effectiveness of a cancer treatment can also be monitored by the traceability of new sequences and of these proteins Liv21F and Liv21K, of this Liv21 protein complex, and of its derivatives and ratios with the associated proteins but also by Diagmicroarray and sensorchip including among others this protein and its Liv21 associated complex (FIG. 12 and FIG. 14).
Moreover, detection of protein kinase C epsilon (PKCs) is also advantageous since it has been determined that PKCs phosphorylates the LIV21 protein in order to maintain it in the cytoplasm. Thus, a significant increase in PKCs is indicative of the presence of cancer cells. Moreover, the LIV21/PKCS ratio increases in the cytoplasmic fraction of cancer cells. The same is true of the detection of HDAC1, which has been shown to be involved in PML/SUMO/Rb/HDAC-1. More generally, the HDACs family plays a key role in the regulation of gene expression, when the HDACs are overexpressed, they induce tumor suppressor gene silencing, hence the advantage of using HDAC inhibitors in therapy, combined with other inhibitors which regulate the metabolic pathway involving the protein complex which contains Liv21.
In addition, the detection of the E2F1, E2F2, E2F3 and/or E2F4 proteins is advantageous. In fact, the LIV21 protein forms a complex with E2F4, which is capable of inhibiting the expression of the E2F1 gene in the nucleus, E2F1 gene expression being a sign of cell proliferation. Thus, a decrease in the association of LIV21 with the E2F4 protein is indicative of the presence of cancer cells. Similarly, the presence of the E2F1 protein in the nucleus is indicative of the presence of cancer cells.
Consequently, the present invention concerns a method for the detection of cancer cells in a biological tissue sample (for example, breast, ovary, endometrium, bladder, melanoma, prostate, glioblastoma, etc.) from patients, this method comprising the detection of the products of expression of the LIV21 complex genes in the nucleus comparatively to the same products in the cytoplasm and the membranes of the cells in the biological tissue sample from said patient, this method comprising detection of the product of expression of liv21F gene in the core and/or the cells cytoplasm in the biological tissue sample from said patient, a localization of said products of expression of the LIV21F gene in the cytoplasm is indicative of the presence of cancer cells and a localization of said products of expression of the LIV21 complex genes in the nucleus is indicative of the presence of noncancer cells. Preferably, a localization of said products of expression of the LIV21 gene in the cytoplasm is indicative of the presence of invasive and/or metastatic cancer cells, the localizations of the products of expression of the LIV21 complex genes and its associated partners described in the examples of biochips shows or not the cancer cells presence. Optionally, the method according to the present invention also comprises the detection of the product of expression of at least one gene selected from the group consisting of the protein kinase C epsilon (PKCs) gene, the E2F1 gene and the E2F4 gene. The method can in particular comprise the detection of the product of expression of two of these genes or of the three genes. Moreover, at least one of the ratios LIV21/PKCS, LIV21/E2F4 and LIV21/E2F1 can be determined in the present method. This ratio can be determined in the cytoplasm and/or in the nucleus preferably separated. Preferably, these ratios are determined in the nucleus. Preferably, these ratios are compared with those obtained in a normal cell. The level of expression of each enzyme or polypeptide of the SUMO/Rb/HDAC complex or, for certain cell types, of the PML/SUMO/Rb/HDAC complex is an additional indicator of the proliferative state of the cell.
These ratios of expression or silencing can be detected via the protein expression or inhibition level themselves in the protein arrays (biochips) fabricated according to conventional methods described (Lubman David M, QIAO TIECHENG Alex, Mathew ABY J etc.) or novel tools for the automation of hybridization and of reading, US2004152212 and Yu Xinglong US 2005019828 and novel supports which attach polypeptides (patents US 2008 213130 and US 2005/0157445 or US 2006170925 or WO 2005 016515, Klages Claus Peter and example figure).
Before describing the principle of these biochips, which are well known by man skilled in the art, we will give the following definitions: The biological sample can be in particular sample of blood, serum, saliva, tissue, tumor, bone marrow, circling cells from the patient. The biological sample can be recovered by any type of sampling know by those skilled in the art. According to the present invention, we consider a biological sample any material allowing the detection of expression of a target gene. The biological material can include in particular proteins, or nucleic acids such as desoxyribonucleoic acid (DNA) and rybonucleic acid (RNA). The nucleic acid can in particular be an RNA (rybonucleic acid). According to a preferred embodiment of the invention, the biological material comprises nucleic acids, in particular RNAs and even more specifically total RNAs. Total RNAs include transfer RNAs, messenger RNAs (mRNAs), such as mRNAs transcribed from the target gene, but also transcribed from any other gene, and ribosomal RNAs. This biological material includes specific material of the target gene, such as in particular mRNAs transcribed from the target gene or proteins issued from these RNAs, but it can also include material unspecific to the target gene, such as in particular mRNAs transcribed from a gene different from the target gene, tRNAs, rRNAs issued from other genes than the target gene. When the extracts to be studied consist of cell cultures, they will preferably be analyzed on fresh cultures (with or without previous treatment) that underwent an extraction protocol separating cellular compartments. This type of kit known by those skilled in the art allows the specific extraction of membranes or solely the cytoplasmic or nuclear or cytoskeletal content in a differential fashion by using different solutions. For instance, the kit Proteo extract (ref 539790) from Calbiochem can be used.
The other aspect of the present invention is the use of the genes and the proteins mentioned above as markers for the invasiveness and the metastatic aggressiveness of cancer cells of the prostate,—colon, bladder, melanoma, ovary, endometrium and cervix, and cancers in neurobiology or in ORL etc. . . . In fact, sequential pharmacodiagnostic tests during treatment monitoring will permit to observe, by comparing at different time points, variations of the expression level or of their silencing and therefore to better evaluate the treatment efficiency, to readjust these treatments in the case of a suitable multitherapy in such a way that the physiological equilibrium of the different products of genes involved in metabolic complexes are maintained. The plasticity of these equilibriums justifies the use of diagnostic biochips and for the therapeutic monitoring with the most pertinent genes of metabolic complexes involved in the physiology of anarchic proliferation in the case of breast cancer, which is highly heterogeneous. Therefore each individual or each phenotypic subgroup of individuals will show an under or over expression profile of genes of the metabolic complexes which is specific to him.
In one embodiment, the expression product of the genes is detected at the mRNA level. mRNA can be detected by RT-PCR analysis (i.e. following examples). It can also be detected by Northern blotting analysis or by SPR if the RNAm and DNA are functionalized at the surface of electroapplied on a support of biochip (techniques described therefore in the patents US 2008 213130 and US 2005 0157445 or US 2006 170925 or WO 2005 016515). The MICAM technique which uses the electric piezo effect in its biochips can be also used for the above mentioned invention of pharmaco diagnostic biochip dedicated to the cerebral neuroblastoma and other cerebral cancers, of biochips diagnostic dedicated to the epidermoid cancers and more specifically dedicated to the breast, ovarian and prostate cancers.
In an alternative mode of realization, the product of gene expression is detected on the level of protein or peptides characterizing complex Liv21 and its partners of interaction. Preferably, the protein and/or proteinic complex Liv21 associated, are detected using an specific antibody. For example, the protein can be detected by analysis Western Blot and SPR, a system of biochip using a wave of transverse propagation (evanescent wave) of surface plasmonic resonance (SPR). The interaction can be done with an electronic surface, conducting semi surface creates an exiton by luminescence or fluorescence. In a mode of preferred embodiment, it is detected by immuno histochimy, immuno cytochemistry, microfluidic, radiography or peroxidase labeling or any other means of optical, sonic imagery or of spectroscopy.
In one specific embodiment of the method comprising the detection of the expression product of the PKCε gene, a significant increase in PKCε is indicative of the presence of cancer cells. Moreover, the method can also comprise the determination of the LIV21/PKCε ratio in 5 the nucleus, the membranes and the cytoplasm. This ratio can be compared with the one observed in a normal cell. An increase in the LIV21/PKCε ratio in the cytoplasmic fraction is indicative of cancer cells.
In another specific embodiment of the method comprising the detection of the expression product of the E2F4 gene, the method comprises the detection of the association of LIV21 with the E2F4 protein, a decrease in this association in the cell nucleus being indicative of the presence of cancer cells. Moreover, the method can also comprise the determination of the LIV21/E2F4 ratio in the nucleus and/or the cytoplasm. This ratio can be compared with the one observed in a normal cell.
In an additional embodiment of the method comprising the detection of the expression product of the E2F1 gene, the presence of the E2F1 protein in the nucleus is indicative of the presence of cancer cells. Moreover, the method can also comprise the determination of the LIV21/E2F1 ratio in the nucleus and/or the cytoplasm. This ratio can be compared with that observed in a normal cell.
In a specific embodiment, the method comprises the detection of a labelled small interfering RNA (siRNA) in order to target its specific sequence and therefore signal the locus of messenger RNA expression of the gene of interest. In this way, the specific small interfering RNA can be used as a diagnosis marker similarly to an antibody. The specific siRNA would allow to locate in a specific case such as in extamporaneous tissues or any kind of sample from a patient, such as cancer tissues sample, the fluorescence signal or any other marker used on the siRNA is found in a cellular compartment on the sample. An siRNA targeting the E2F1, E2F4 and PKC epsilon would allow a complementary diagnosis.
The method according to the present invention allows in particular the detection of metastasized cancer, therapeutic monitoring and/or recurrences following treatment.
A second aspect of the invention concerns the human LIV21 protein and also the fragments thereof. More particularly, the present invention concerns a purified or recombinant isolated human LIV21 protein. It concerns in particular an isolated polypeptide comprising a peptide sequence selected among SEQ ID Nos 1 to 5 and more broadly selected among the peptide sequences characterizing it and obtained by MALDI (FIGS. 3, 4 and 5) and NanoLC-ESI-MS. In a preferred embodiment, the polypeptide comprises the three peptide sequences SEQ ID Nos 1 and 2 and 3. Preferably, the LIV21F protein and certain proteins of the Liv21 complex comprises a leucine zipper motif, a basic domain characteristic of DNA binding domains (FIG. 2), and a nuclearization sequence.
In an even more preferred embodiment, the present invention concerns the polypeptides with peptide sequences characterized by spectrograms of FIGS. 3, 4, 5 of gel bands 1, 2 and 3, selected among SEQ ID Nos 1 and 2 and 3 and 4 and 5 and a hundred additional non ordered sequences supplement (i.e. listing sequences in annex), the other sequences of the proteins must being checked compared with their homologies with contaminants and order during spectrometries of mass MSMS on the unmatched fragments identified in the Maldi T of analysis (i.e. FIGS. 3, 4, 5), these unmatched fragments corresponding to the masses M (H+) untagged characterized in part the Liv21 protein and some elements of the Liv21 protein complex.
A third aspect of the invention concerns an antibody, which the present invention. More particularly, the antibody can bind specifically to a polypeptide comprising a peptide sequence selected from SEQ ID Nos 1-180, preferably from SEQ ID Nos 1 and 2 or 3 and/or 5 or 51, or a sequence having more than 80% identity to said sequences. The present invention concerns in particular an anti-LIV21 serum produced by immunizing an animal or a human with a polypeptide according to the present invention, in particular a polypeptide comprising a peptide sequence selected from SEQ ID Nos 1-180, preferably from SEQ ID Nos 1-5 and 51, or a sequence having 70%, 80% or 90% identity to said sequences.
A fourth aspect of the invention concerns a kit for the detection of cancer cells in a biological sample from a patient, this kit comprising one or more elements selected from the group consisting of an antibody which binds specifically to human LIV21F according to the present invention and an anti-LIV21F serum according to the present invention, a specific oligonucleotide mRNA probe of Liv21F and a pair of primers specific of mRNA. In a specific embodiment of the invention, the kit also comprises means for detecting the product of expression of a gene or a specific oligonucleotide mRNA probe of factors selected from the group consisting of the protein kinase C epsilon (PKCc) gene, the E2F1 gene and the E2F4 gene. But also the antibodies in a specific antibodies microarray from the antibodies group consisting of RBP2, SUMO, HDAC, TNFalpha, crb2, cycE/cdk2, cdk1, CREB1, p300, Rb, p107, p130, NFkB, cdc2A, mdm2, p21, p53, p65. It also comprises Microarray with said proteins above and specific peptides known by a person skilled in the art, their antigens being referenced. The combination of these different peptides corresponding to the specific interactions of protein complexes acting in metabolic deregulation, induces anarchical proliferation, which is a specific feature of cancer or neurodegeneration. The invention concerns the use of an antibody specific for human LIV21 for the diagnosis of cancer, and antibodies specific for its protein complex, but also specific antibodies for RBP2, SUMO, HDAC, TNFalpha, crb2, cycE/cdk2, cdk1, CREB 1 and p300, Rb, p107, p130, NFKB, cdc2A, mdm2, p21, p53, p65, p73. Also, the invention concerns the used of primers pair or LIV21 specific probe for the cancer diagnosis. Preferably, the diagnosis is performed ex vivo on samples from a patient (puncture of the cerebral spinal fluid, blood test, biopsy, ground cellular material, bronchial aspirations, DNA/protein/antibodies arrays, plasmionics (SPR), hydrophobic or ion metal supports, etc). Method according to claim 15, characterized in that in addition, it implements at least any of the specific probes of the sequences of known as said complex Liv21 and these associated partners. The method is characterized in that the aforementioned biochip is: a biochip with protein, or a biochip with nucleotidic antibodies or a biochip with acids, or a biochip with mRNA, or a biochip with SiRNA.
Method is characterized in that the aforementioned biochip with protein, or the aforementioned biochip with antibody, consists of a biochip of fluidic microcomputer and for which the aforementioned stage of detection consists of a detection by SPR.
Method is characterized in that it understands a stage of amplification/retro-transcription by RT-PCR of at least a nucleotidic sequence of the known as human Liv21 complex according to claim 1 or 2 or of the known as Liv21 complex and its associated partners.
Method is characterized in that it understands a pharmaco-diagnostic test for diagnosis of the cancer or the follow-up of the development of a cellular proliferation, the aforementioned cancer being preferentially choose in the group consisted the neuroblastome, the glioblastomas and other cancers touching tissues of the nervous system.

BRIEF DESCRIPTION OF THE DRAWING FIGURES

FIG. 1A: one-dimensional gel (acrylamide gradient 12%) revealing after three hours thirty of migration 11 tapes with certain triplets and doubled tapes and a two-dimensional gel SDS Page of total cellular extracts with spots between 15 and 20 KD and to 29-32 kD and 35 KD approximately with basic pH and of the spots with 190-180 and to 100 kD with acid pH;

FIG. 1B: diagram of the interactions of the bio-markers of complex Liv21 and the surrounding metabolic pathways;

FIG. 2: scheme of nuclear and cytoplasmic protein with domain DNA binding and effects on the study of therapeutic targeting the core and the cell cytoplasm;

FIG. 3A: The listing of monoisotopic peaks of the band 1 at 50 kD and the band 2 between 49 and 50 kD;

FIG. 3B: LIV21 protein profile by mass spectrometry (Maldi) M (H⁺) for the one-dimensional gel band corresponding to the band 2 migrating at 49-50 kD wherein the peptides derived from the digestion are solubilized in a solvent: acetonitrile/water (1/1) containing 0.1% of TFA (trifluoroacetic acid);

FIG. 4A is a profile of the spectrogram of the band 6 named 6FC;

FIG. 4B: monoisotopic of certain peaks from FIG. 4A;

FIG. 5 is the third spectrogram corresponding to the one-dimensional 12% acrylamide gel band migrating at 52 kD and revealed with coomassie blue and the LIV21 antibody;

FIG. 6: analysis on the data banks the listings of monoisotopic peaks;

FIGS. 7A and 7B relate to SEQ ID NO 217;

FIG. 8: RNA pool;

FIG. 9: PCR with housekeeping genes and analysis of molecular masses;

FIG. 10: PCR with the primers showing a band of 1400 bp;

FIGS. 11A & 11B: Gel 2 with analysis of molecular masses;

FIG. 12: Gel 3 at 55° and analysis of molecular masses;

FIG. 13: Gel 4 at 45° and at 55° and analysis of molecular masses;

FIG. 14: screening ligation of 400 pb band, clones B1 to B10;

FIG. 15: screening ligation of 1400 pb band, clones CI to C10;

FIG. 16: Gel 5: ligation screening on the five new clones;

FIG. 17: Gel 6: Screening of the S55T and S55M recombinant clones and analysis of molecular masses;

FIG. 18: examples of comparison of nucleotide sequences between the sequenced clones;

FIGS. 19A & 19B: Si RNA design;

FIGS. 20A-20D: Protein biochip (array) from Yeretssian but in addition with peptides named of the proteins of the interested complex studied in the invention;

FIG. 21: Two biochips standard microfluidic of four shafts x2 with a control and three biomarkers;

FIG. 22: Example of biochip of 20 spots with 16 biomarkers of interest (and four controls) fixed on the sensorchip allowing to see by SPR on-expression and the under-expression of certain genes of complex LIV21 and its partners of interactions for example;

FIGS. 23A & 23B: Biochip with RNA allowing to explore mini RNA of complex LIV21; and

FIG. 24: Example of biochip with DNA resulting from above mentioned genes of interest targeting pathology.

DETAILED DESCRIPTION OF THE INVENTION

FIG. 1A: one-dimensional gel (acrylamide gradient 12%) revealing after three hours thirty of migration 11 tapes with certain triplets and doubled tapes and a two-dimensional gel SDS Page of total cellular extracts with spots between 15 and 20 KD and to 29-32 kD and 35 KD approximately with basic pH and of the spots with 190-180 and to 100 kD with acid pH. Spots between 49 and 51 KD and to 64 KD. Into mono-dimensional: Tapes with ISO kD approximately (TOFC), 100 KD, 64 kD, 51 à49 kD, 49 kD, 35 kD, 29 kD, 15 to 17 kD.
FIG. 1B: diagram of the interactions of the bio-markers of complex Liv21 and the surrounding metabolic pathways.
FIG. 2: scheme of nuclear and cytoplasmic protein with domain DNA binding and effects on the study of therapeutic targeting the core and the cell cytoplasm.
FIG. 3 A: The listing of monoisotopic peaks of the band 1 at 50 kD and the band 2 between 49 and 50 kD. FIG. 3B: LIV21 protein profile by mass spectrometry (Maldi) M (H⁺) for the one-dimensional gel band corresponding to the band 2 migrating at 49-50 kD. The peptides derived from the digestion are solubilized in a solvent: acetonitrile/water (1/1) containing 0.1% of TFA (trifluoroacetic acid). A saturated solution of the alpha-cyano-4-hydroxycinnamic acid matrix is prepared in the same solvent. The same volume of the two solutions is taken and mixed together, and 1 microliter is deposited onto the Maldi plate for analysis.
FIG. 4 is a profile of the spectrogram of the band 6 named 6FC.
The de novo analysis (MS MS Maldi T of T of) makes it possible to propose the sequences: RYLVTPVNA, RYVPSSNLP, RYVLSPVK, RYVPSSNPL, RYLPSANPD.
FIG. 4 bis: monoisotopic of the peak 1032.58 MSMS analyzes: YRPGTVALR, RYVPSSNPL
The peak monoisotopic 944.6 is a sequence: FAVAFPVGR
The peak monoisotopic 1603.7: KPSHPKPSTK
The peak 1328.69: AHNLFKT, TFKNLC
The common peaks monoisotopic between the first 2004 (230304 imagenium 03_H11_a _—001 and the peak 6FC from 2008 are:
Following peaks monoisotopic: 1135.563, 1151.545; 1167.604; 1206.589; 1324.634; 1336.658; 1507.735; 1604.710; 1800.940; 2087.034.
The variation of the protocol is due only to three different stages: the first is the purification of the antibody used, the second is the separation of the fractions cytoplasmic and nuclear, the third is the heating two minutes with 100° of the sample before migration on freezing of acrylamide.
FIG. 5 is the third spectrogram corresponding to the one-dimensional 12% acrylamide gel band migrating at 52 kD and revealed with coomassie blue and the LIV21 antibody.
FIG. 5 bis is a table of the monoisotopic peaks of the third spectrogram corresponding to the one-dimensional acrylamide gel band migrating at 51 kD 52 kD and revealed with coomassie blue and the LIV21 antibody.
The monoisotopic peaks with a value M H+. The masses are give with three numbers after the decimal point by the proteomic platforms since they estimate that this is the acquisition precision limit of MALDI TOF machines. The FIGS. 3-5 describe the MALDI analyses giving a set of polypeptides that can be assigned to the LIV21 protein and its complex and contaminants sometimes different according to the observers from the various platforms of proteomics under discussing.
FIG. 6: analysis on the data banks the listings of monoisotopic peaks. Example of the histatine 3. The Mascot search parameters are: trypsin enzyme, variable modifications: carbamethylation and oxidation of methionins, without molecular mass limit, without isoelectric point restriction.
FIG. 7 idem but the second example:
Type of mass: monoisotopic. Mass error (MS): according to the observer 50 ppm or 100 ppm. Non-cleavage with trypsin: 1 The masses captured are M (H⁺)/real masses. For spectrogram 1, the cysteins are blocked with iodoacetamide. The possibility of digestion with Promega bovine trypsin may be incomplete with cleavage oversight.
Sequences common with Gallus gallus (gi 50732569), the 30 Mouse Syntaxin, the histatin variant HIS3-2 (P15516-00-01-00), the ZN575-Human, the G6P translocase, the HSP60 chaperonin, the deiminase, ferrodoxin NADP(+) reductase, pseudomonas polyribonucleotide nucleotidyltransferase, the clathrin, the dehydrolipoamide dehydrogenase.
FIG. 8: RNA pool
FIG. 9: PCR with housekeeping genes and analysis of molecular masses.
FIG. 10: PCR with the primers showing a band of 1400 bp.
FIG. 11: Gel 2 with analysis of molecular masses FIG. 12: Gel 3 at 55° and analysis of molecular masses
FIG. 13: Gel 4 at 45° and at 55° and analysis of molecular masses.
FIG. 14: screening ligation of 400 pb band, clones B1 to B10.
FIG. 15: screening ligation of 1400 pb band, clones CI to C10.
FIG. 16: Gel 5: ligation screening on the five new clones. FIG. 17: Gel 6: Screening of the S55T and S55M recombinant clones and analysis of molecular masses.
FIG. 18: examples of comparison of nucleotide sequences between the sequenced clones.
FIG. 19: Si RNA design.
FIG. 20: Protein biochip (array) from Yeretssian but in addition with peptides named of the proteins of the interested complex studied in the invention.
FIG. 21: Two biochips standard microfluidic of four shafts x2 with a control and three biomarkers.
An on-expression of DDX1, MYCN and CRABPII is observed whereas one observes by testing the second sensorship an under-expression of HUD, TP53 INP1 and a major under-expression of p21.
FIG. 22: Example of biochip of 20 spots with 16 biomarkers of interest (and four controls) fixed on the sensorchip allowing to see by SPR on-expression and the under-expression of certain genes of complex LIV21 and its partners of interactions for example.
An under-expression of DKK1, SKP2, DKK3, ID2, p21, SKP2, TP531NP1, ID2, P73 is observed whereas an on-expression of MYC N, ALK, NLRR1 (the leucine rich neuronal repeat is transactivated), CRABPII, DDX1, LIV21K, AURORA kinase A is observed.
FIG. 23 Biochip with RNA allowing to explore mini RNA of complex LIV21 and more particularly those resulting from genes of the polypeptides LIV21F and LIV21K added in Mir RNA, microRNA known to be implied in pathology ((miR (=MIR) 34A. MIR9. MIR125A.125B.MIR128 MIR184 MIR221)).
We study also regulator PTEN and factors
TR AIL.
FIG. 24: Example of biochip with DNA resulting from above mentioned genes of interest targeting pathology.
The invention relates to the identification of antigens in cell lysates by immunoprecipitation. The analysis of the physical interaction of various proteins associated in the LIV21 complex as E2F4 and E2F1 has been studied by coimmunoprecipitation of protein complexes. This analysis has made it possible to demonstrate novel 10 markers, which has a diagnostic and prognostic use for cancer (i.e. PCT/FR2006/000510). Begin by using the one dimensional and two dimensional gel electrophoresis analysis (FIGS. 1 and 2), the protein samples corresponding to the putative protein and to the elements of the complex were extracted from the gels and digested with trypsin (Promega) in order to be analysed by MALDI (FIGS. 3 to 5) and ESI MS/MS mass spectrometry. The results, when put up against proteomic databanks, made it possible to reveal several peptide sequences of interest, including some given as an example (FIGS. 6 and 7), some being found in humans with very significant scores (splicing of histatin, etc., FIGS. 8 and 9), these sequences were used as primers (once reverse-transcribed to cDNA) for screening a library formed from breast cancer-specific MCF7 cells (FIGS. 10 to 17).
The cloning made it possible to bring to the fore about twenty clones out of the 150 clones obtained, of which ten clones were sequenced and characterize the new LIV21 gene LIV21F and the gene LIV21K (FIG. 1B and FIG. 2). Based on these sequences, siRNAs were determined in order to allow regulation of silencing type within this metabolic complex of interest so as to develop therapeutic applications (FIG. 18).
In post-mitotic cells, apoptosis could correspond to an aborted attempt at mitosis. It is in this context that the application of LIV21 has been developed. The inventor has identified sequences of the LIV21 gene. Using the LIV21 antibody on affinity columns he has been able to extract peptides of the LIV21 protein; it has also used a second approach by means of a coimmunoprecipitation kit (Pierce) in order to have larger amounts of proteins (Example 1). Based on peptide sequences of the LIV21 protein, obtained by mass spectrometry (Example 2), primers which make it possible to amplify a cDNA fragment were designed (Example 3). After culturing and amplification of MCF7 line cells, extraction and purification of RNAs, RT PCRs and cloning in a shuttle vector were carried out, and then screening of the resistant colonies and sequencing made it possible to reveal sequences characterizing the genes LIV21F and LIV21K (Examples 4 and 5). More than twenty characteristic clones out of 150 clones were studied. The cDNA of these clones was used to screen a library prepared from the total mRNA of MCF7 cells.
The sequence of this new products are new transcription factors, the nuclear translocation of which change their role and their function, that being correlated for some of them with the establishment of the cellular quiescence such as for example LIV21F, E2F4. In addition it is linked to the DNA role and function. Furthermore, it forms heterodimers with other transcription factors and certain bind to DNA.
Using Northern blotting, the inventor then followed the expression of this new product during development, from the embryonic stage. It was observed that the amount of the LIV21 protein increases as development progresses, i.e. as a quiescent cell state becomes established. Through the same strategy, the inventor showed that the LIV21/E2F4 complex inhibited the expression of E2F1. This complex could correspond to a new checkpoint in the arrest of cell proliferation.
LIV21 complex and associated metabolic complex:
The present invention relates to the LIV21 complex and its new nucleotide sequences SEQ ID No. 171 to SEQ ID No 217 also used for some of them in the form of siRNA for diagnostic and therapeutic applications and also LIV21F and LIV21K polypeptides and derivatives and fragments and isoforms thereof (SEQ ID No to SEQ ID No 215).
LIV21 human complex, characterized in that it comprises:
the nucleotide sequences SEQ ID No 171 to 175, and
siRNA sequence derived from one of the RNA sequences SEQ ID No 120 and SEQ ID No 121, and 171 to 175
a protein fraction comprising at least sequence SEQ ID No 1 and 181 or a sequence having 90%, and preferably 80%, and more preferably 70% identity with said SEQ ID No 1 and 181.
LIV21 human complex, characterized in that it comprises:
The nucleotide sequences SEQ-ID No 171, 172, and the protein fractions comprising at least sequence SEQ ID No 1 or a sequence having 181 or 70, 10 80 or 90% identity with said SEQ ID NO 1 or 181 and SEQ ID No 183 or a sequence having 70, 80 or 90% identity with said SEQ ID No 183.
LIV21 complex human, characterized in that it also comprises:
nucleotide sequences SEQ ID No 123, 124 and 127, and the protein fractions comprising at least sequence SEQ ID No. 1 or a sequence having 70, 80 or 90% identity with said SEQ ID NO 1 and the sequence from 181 to 185 or a sequence having 70, 80 or 90% identity with said SEQ ID NO 181 to 185.
LIV21 complex human characterized in that it further comprises:
Any of the nucleotide sequences or ribonucleic SEQ ID No 119, 120, 121, 122, 123, 124, 125, 126 or 127 or a sequence having 90%, and preferably 80%, and more preferably 70% identity with said sequence SEQ ID No 119 to 127, or

UUGGUAACGACCAUGCCAC, or UUCACUUAGAAUAAUGUCC, or UCUUUGUGAAUUUGACAAC, or UCAAGGUCCAGGCUACAAC, or

Any of the siRNA following:

	GUGGCAUGGUCGUUACCAA dTdT

	dTdT CACCGUACCAGCAAUGGUU

	GGACAUUAUUCUAAGUGAA dTdT

	dTdT CCUGUAAUAAGAUUCACUU

	GGAAGAAUCUCAUCUCAGAUUCAA )

	UUCCUUCUUAGAGUAGAGUCUAGAG-

	GCAGAUCAUGAGGUCAAGAUUCAA )

	UUCGUCUAGUACUCCAGUUCUAGAG-

	GAAGAAUCUCAUCUCAGAAUUCAA )

	UUCUUCUUAGAGUAGAGUCUUAGAG-

	GUGUGAGACUCCAUCUGAAUUCAA )

	UUCACACUCUGAGGÜAGACUÜAGAG-

	GAUCAUGAGGUCAAGAGAUUUCAA )

	UUCUAGUACUCCAGUUCUCUAAGAG-

	GAGAGUCAÜCUUACUCAGAUUCAA )

	UUCUCUCAGUAGAAUGAGUCUAGAG-

	GCUGGGUGUGGUAGUGCAUUUCAA )

	UUCGACCCACACCAUCACGUAAGAG-

	GUCAAGAGAUCGAGACCAUUUCAA )

	UUCAGUUCUCUAGCUCUGGUAAGAG-

	GUCAUCUUACUCAGAGCAUUUCAA )

	UUCAGUAGAAUGAGUCUCGUAAGAG-

	GGCUGAGGCAGGCAGAUCAUUCAA )

	UUCCGACUCCGUCCGUCUAGUAGAG-

	GGAGUAUAGGAAUCUCCUAUUCAA )

	UUCCUCAUAUCCUUAGAGGAUAGAG-

	GGUAGUGCAUGCCUGUAGUUUCAA )

	UUCCAUCACGUACGGACAUCAAGAG-

	GAGAUGGCGCCACUGUACUUUCAA )

	UUCUCUACCGCGGUGACAUGAAGAG-

	GCCUGGCGACAGUGUGAGAUÜCAA )

	UUCGGACCGCUGUCACACUCUAGAG-

	GCCUGUAGUCCCAGCUACUUUCAA )

	UUCGGACAUCAGGGUCGAUGAAGAG

LIV21 complex and associated metabolic complex:
The present invention relates to the LIV21 complex and its new nucleotide sequences SEQ ID No. 171 to SEQ ID No 217 also used for some of them in the form of siRNA for diagnostic and therapeutic applications and also LIV21F and LIV21K polypeptides and derivatives and fragments and isoforms thereof (SEQ ID No to SEQ ID No 215).
LIV21 human complex, characterized in that it comprises:
the nucleotide sequences SEQ ID No 171 to 175, and
siRNA sequence derived from one of the RNA sequences SEQ ID No 120 and SEQ ID No 121, and 171 to 175
a protein fraction comprising at least sequence SEQ ID No 1 and 181 or a sequence having 90%, and preferably 80%, and more preferably 70% identity with said SEQ ID No 1 and 181.
LIV21 human complex, characterized in that it comprises:
The nucleotide sequences SEQ-ID No 171, 172, and the protein fractions comprising at least sequence SEQ ID No 1 or a sequence having 181 or 70, 10 80 or 90% identity with said SEQ ID NO 1 or 181 and SEQ ID No 183 or a sequence having 70, 80 or 90% identity with said SEQ ID No 183.
LIV21 complex human, characterized in that it also comprises:
nucleotide sequences SEQ ID No 123, 124 and 127, and the protein fractions comprising at least sequence SEQ ID No. 1 or a sequence having 70, 80 or 90% identity with said SEQ ID NO 1 and the sequence from 181 to 185 or a sequence having 70, 80 or 90% identity with said SEQ ID NO 181 to 185.
LIV21 complex human characterized in that it further comprises:
Any of the nucleotide sequences or ribonucleic SEQ ID No 119, 120, 121, 122, 123, 124, 125, 126 or 127 or a sequence having 90%, and preferably 80%, and more preferably 70% identity with said sequence SEQ ID No 119 to 127, or

Any of the siRNA following:

	GUGGCAUGGUCGUUACCAA dTdT

	dTdT CACCGUACCAGCAAUGGUU

	GGACAUUAUUCUAAGUGAA dTdT

	dTdT CCUGUAAUAAGAUUCACUU

LIV21 complex human (figures let 2) characterized in that it further comprises at least:

- Any one of the nucleotide sequences SEQ ID No 123, SEQ ID No 124 and SEQ ID No 127 to 149, or SEQ ID No 217
- any one of amino acid sequences SEQ ID No 1 to 148 and SEQ ID No 150 to 170 and SEQ ID NO 180 to 185, or a sequence having 90%, and preferably 80%, and more preferably 70% identity with said sequence SEQ ID No 180 to 185 and SEQ ID 1,2,5 and SEQ ID No 215

LIV21 Complex human characterized in that said protein fraction further comprises any of the following proteins: E2F1, E2F4, p130, p300, p107, Liv21F, HDAC-1, PML, SUMO et PKC epsilon, Aurora A, Survivin, BCAS4, BCAS3, RFSH.
LIV21 complex human characterized in that it interacts with at least one of its associated partners, at least one of its associated partners are selected from the group consisting of: any one of the following proteins: RBP2, TNFalpha, crb2, cycE/cdk2, cdk1, CREB1, p300, p107, NFkB, cdc2A, mdm2, p21, p53, p65, p73 MYC, NMYC, TGFbéta, Chlatrin, Aurora, AKT, BRCA1, F0X04 or cyclin A et D1, CHUK, HMGA2, IKBKB

- an antibody of anyone of the following proteins: RBP2, E2F4, E2F1, SUMO, HDAC-1, crb2, Int2, cmd2, cycE/cdk2, cdk1, CREB1 et p300, Rb, p 107, p 130 of the family of pocket proteins NFkB, cdc2A, mdm2, p21, p53, p65, p73, the cyclin A and D1, CHUK, MYC, NMYC, TGF Beta, Chlatrin (2), Aurora, AKT, BRCA1, F0X04, HMGA2, BCAS3, BCAS4, solute carrier.
- in that it comprises an extract of proteins and peptides obtained by latching to a polyclonal antibody of the LIV21, and
- in that its electrophoretic profile acrylamide gel comprises at least three bands: band of 50 kD, 51 kD band, and the band of 52 kD.

Complex human LIV21 is also characterized in that, after trypsin digestion, the profile of MALDI includes at least mono isotopic peaks following:
1135.563; 1151.545; 1167.604; 1206.589; 1324.634; 1336.658; 1507.735; 1604.710; 1800.940; 2087.034.
Method of detecting the complex human LIV21, characterized in that it comprises the implementation of at least one probe specific for at least one sequence of said complex LIV21 according to claim 1 or 2.
Method of detecting the complex human LIV21, characterized in that it further comprises the implementation of at least one probe specific for at least one sequence of the LIV21 said complex and its associated partners.
Method of detection of the complex and its partners LIV21 in that it is comprises at least the steps of:

- A step of extracting biological material from a biological sample taken from a patient,
- A step of contacting said biological material with at least said probe specific for any of the sequences of said human or complex LIV21 or LIV21 said complex and its content partners, and at least one control and
- A step of detecting the expression of the expression products of the genes of said complex of said human or LIV21 LIV21 complex and its content partners, said products being comprised of expression of messenger RNA, or peptides, or proteins.

Detection method is characterized in that it also aims to screen a candidate compound, said candidate compound is capable of modulating the activity of the complex human LIV21, and that it also includes:
a step of contacting said biological material with said candidate compound, and a step of selecting said candidate compound.
Method is characterized in that said biological sample is taken from a cancer patient and in a healthy patient, and in that said biological material comprises cell nuclear extracts, and cytoplasmic cell extracts, cell membrane extracts, and in that it further comprises a step of determining of the under-expression and overexpression of the gene products of said complex of said human or LIV21 LIV21 human complex and its content partners said biological extracts.
Method is characterized in that it further comprises a step of determining the ratios of said sub-expression and overexpression of said gene products: cell nuclear extracts, and cytoplasmic cell extracts, cell extracts or membrane, and in that it further comprises a step of such analysis combined ratios of said biological material taken from a cancer patient and in a healthy patient.
Method is characterized in that said probe comprises a sequence specific siRNA labeled with rhodamine.
A method according to any one of the above approaches is, characterized in that it implements a biochip, on which is deposited at least one sequence-specific probes from said complex human LIV21.
Method is characterized in that, in addition, it implements at least one specific probe sequences LIV21 said complex human and associated partners
Method is characterized in that said biochip is a protein biochip, or a biochip antibody, or a nucleotide acid microarray, or a RNAm biochip, or a siRNA biochip.
Method is characterized in that said detecting step implements any means of optical imaging, or any means of sonic or any means of spectroscopy.
FIG. 1 characterizing the protein complex, and its PI and its PM are dependent on the temperature and conditions of migration and its observation in total extracts or in extracts of cellular compartments.
FIGS. 1, 2, 3). It gives more than 54 peptides following digestion with Promega trypsin (FIG. 7). The characteristics of the LIV21F protein are also described in FIGS. 1, 2, 3, 4. Twenty specific peptides of LIV21 have been described: LIV21a (SEQ ID No 1) and LIV21b (SEQ ID No 2) at the sequence 180.
The gene of this protein is characterized by two main sequences (i.e. patent in listing) and sequences representing an alternate splicing.
LIV21K corresponds to a sequence of strong homology (of more than 60%) with AD7cNTP, the neural thread protein in N terminal (position 193 to 299) of (060448_Human). SEQ No SVAQAGVQWRNLGSLQALPPGFMPFSCLSLLSSWDYRRLPPRPATFLYFPRQGF TVLARMVSISPRDPPASASQSVGIAYISNFFFFEMESRSVAQAGVQWHNLGSLQALPPGF MPFSCLSLLSSWDYRRLPPRPATFLYFPR
With variable ones within peptide in position (i.e. figure . . . ):
The structure of LIV21K is like that of the AD7C NTP, i.e. repeated reasons that can be also analyzed under reasons which correspond to functional fields.

SVXQAGVQWXNLGSLQXLPPGXXXFSCLSLXSSWDYXXLPPXPAXF

Or a variable one:

SVXQAGVQWXNLGSLQXLPPGFXXFSCXSLSSWDYRRXPPRXA

Between these two repeated reasons, there is a peptide of 40 amino-acids with a reason also preserved:

ISPXDXPASASQSXGIXXXSX

THE LIV21I: FLYFPRQGFTVLARMVSISPRDPPASASQSVGIAYISN

With alternatives in position:
For example for LIV21I
In position 31, an A instead of the V and in position 34 a T instead of the amino-acid A. Thus: the amendment of the end PASASQSAGIT but also an alternative where the A becomes T in position 25: . . . DPPTSASQSVGI Idem for LIV21F or K:
SEQ ID No: FSCLSL L SSWDYRR L PPRPA T FLYF where the amino-acid in position 7 here becomes a proline (P instead of L) and/or in position 15 too (with the possibility of an alternative Alanine; sometimes the position 14 changes of a R in H and/or in position 21 where an amino-acid T becomes N.
SEQ ID No: FSCLSL P SSWDYRR P PPRPA N FLYF
Moreover, two other peptides of LIV21 are also described: the peptide LIV21c (SEQ ID No 3) and the peptide LIV21d (SEQ ID No 4). The peptide LIV21e (SEQ ID No 5). KFFVFALILALMLSMCGADSHAKR with which the final section is homologous with a sequence with LIV21K.
Other specific peptides of LIV21 are described in the additional list.
A homology with a functional segment of the protein zinc finger 575 (ZN575-Human): score 13 to 48 and 91% of recovery
A homology of sequence 6 and 56 and with the field MF MR which is the bzip field of a transcription factors containing a signal of nuclear localization and a trans-regulating activity in TAF1.
For the purposes of the invention, a preferred protein comprises at least one sequence chosen from SEQ ID Nos 1-180 or a sequence having 70%, 80% or preferably 90% homology with said sequence (SEQ ID No 215).
The LIV21 complex comprises proteins including 3D helices structures, which have a major functional role for their interactions with the rest of the Liv21 complex.
The present invention concerns a purified or recombinant, isolated human polypeptide having a sequence comprising the sequence SEQ ID No 1 and/or SEQ 5 ID No 2 and/or SEQ ID No 3 and/or SEQ ID No 4 and/or SEQ ID No 5. Preferably, the polypeptide LIV21F comprises the sequences SEQ ID Nos 1, 2 and 5. In a preferred embodiment, the complex is studied based on a sequence selected among the peptide sequences obtained by MALDI (FIGS. 3, 4 and 5). The invention also concerns the three peptides LIV21a (SEQ ID No 1), LIV21b (SEQ ID No 2) and LIV21e (SEQ ID No 5). It also concerns peptides comprising at least 10 consecutive amino acids of human LIV21, preferably at least 20, 30 or 50 consecutive amino acids of LIV21 peptides (i.e. sequences list 1-215 in annexes).
The present invention also relates a polynucleotide encoding for the human protein Liv21, Liv21a and/or Liv21b, generally a polynucleotide encoding for a polypeptide according to the present invention. The polynucleotide encoding for Liv21F and this one encoding for LIV21K may be an mRNA, a cDNA or a genomic DNA. The polynucleotides according to the present invention may be isolated from cells and more particularly from human cells or from human cDNA libraries. They can also be obtained by a polymerase chain reaction (PCR) carried out on the total DNA of the cells or else by RT-PCR carried out on the total cellular RNAs or by chemical synthesis. Probes and primers described in the present invention may be used to isolate and/or prepare a polynucleotype encoding for a protein of the Liv21F. It relates also a cloning or expression vector comprising such polynucleotide.
Such vector may include the elements required for the expression (expression vector) and eventually for the secretion of the protein in a host cell (signal peptide of secretion). Preferably the said vectors comprise: a promoter, signals of initiation and termination of translation, as well as adapted regions for transcription regulation. The vector can be a plasmid, a cosmid, a BAC, a phage, a virus, or other. The invention relates to a host cell or a non-human transgenic animal including a vector or a polynucleotide according to the present invention.
The invention also concerns derivatives of interest of LIV21F or LIV21K which are for example proteins of merger in which is amalgamated with proteins markers like the GFP. In addition, the LIV21F or LIV21K protein and all described peptides (i.e. patent in listing) can be marked by any known means of those skilled in the art. The siRNA too (SEQ ID No 91 to 118).
The present invention also relates to an antibody which is linked specifically to a polypeptide according to the present invention, preferably human LIV21, a fragment or a derivative of this one. In a specific mode of realization, the antibody is linked specifically to a LIV21a or LIV21b peptide or LIV21F or LIV21K polypeptides.
The method can in particular comprise the detection of the product of expression of two of these genes or of the three genes. Moreover, at least one of the ratios LIV21/PKCS, LIV21/E2F4 and LIV21/E2F1 can be determined in the present method. This ratio can be determined in the cytoplasm and/or in the nucleus. Preferably, these ratios are determined in the nucleus. Preferably, these ratios are compared with those obtained in a normal cell.
In one embodiment, the expression product of the genes is detected at the mRNA level, it being possible for the mRNA to be detected by any means known to those skilled in the art.
Thus, the method according to the present invention also relates to the detection of a polynucleotide encoding the human LIV21 protein or a fragment thereof, for example LIV21a and/or LIV21b. The polynucleotide encoding LIV21 may be an mRNA, a cDNA or a genomic DNA. The polynucleotides may be isolated from cells of the biological sample. They may also be obtained by a polymerase chain reaction (PCR) carried out on the total DNA of the cells or else by RT PCR carried out on the total RNA of the cells or polyA RNAs.
The mRNA may be detected by an RT PCR analysis. For this, the method uses a pair of primers specific for the expression product to be detected, in particular LIV21, PKCε, E2F1 or E2F4. The term “specific pair of primers” is intended to mean that at least one of the primers is specific for the expression product to be detected, i.e. that this pair of primers makes it possible to specifically amplify a fragment of the desired mRNA. Preferably, the RT PCR analysis carried out on nuclear and/or cytoplasmic extracts of the cells contained in the sample from the patient. Optionally, the RT PCR analysis may be a quantitative analysis. A pair of primers specific for LIV21 can be prepared on the basis of the teachings of the present application. For example, the pair of primers may comprise the primers described in the sequences listing 5 SEQ ID Nos 3 and 4, and additional sequences of the list obvious thus numbered from 119 to 149 and 171 to 180 with optionally all the additional nucleotidic sequences of the additional list.
The pairs of primers specific for PKCs, E2F1 and E2F4 are well known by those skilled in the art (Caroli J S 2000; Mundle S D 2003; Stevaux 0 2002; Cheng T 2002; Opalka B 2002). The mRNA may also be detected by Northern blotting analysis. For this, the method uses a probe specific for the expression product to be detected, in particular LIV21, PKCs, E2F1 or E2F4. A probe specific for LIV21 can be prepared on the basis of the teachings of the present application. An example of a specific probe comprises the sequence SEQ ID No 5. Preferably, the Northern blotting analysis is carried out on nuclear and/or cytoplasmic extracts of the cells contained in the sample from the patient. The nucleic probe is labelled. The oligonucleotide labelling technique is well known to those skilled in the art. The labelling of the probes according to the invention can be carried out with radioactive elements or with non radioactive molecules. Among the radioactive isotopes used, mention may be made of ³²P, ³³P or ³H. The non radioactive entities are selected from ligands such as biotin, avidin, streptavidin or digoxigenin, haptens, dyes and luminescent agents such as radioluminescent, chemoluminescent, bioluminescent, fluorescent or phosphorescent agents. The probes specific for PKCs, E2F1 and E2F4 are well known to those skilled in the art. In a preferred embodiment, the expression product of the genes is detected at the protein level. Preferably, the protein is detected using a specific antibody. Thus, the method comprises a step of bringing the cells of the biological sample into contact with an anti-human LIV21 antibody. The antibodies can be monoclonal or poly-clonal. The antibody can for example be a serum anti-LIV21. When the product of expression of one of the genes PKCs, E2F1 and E2F4 must be detected, the method can use antibodies specific for the PKCs, E2F1 and E2F4 proteins, respectively. Polyclonal and monoclonal antibodies directed against PKCs, E2F1 and E2F4 are commercially available. By way of example, mention may be made of, for PKCs, a rabbit polyclonal antibody (Santa Cruz Technology, sc-214), for E2F1, a rabbit polyclonal antibody (Santa Cruz Technology, sc-860), and for E2F4, a rabbit polyclonal antibody (Santa Cruz Technology, sc-866). Preferably, the antibodies are labelled, directly or by means of a secondary antibody. The antibody labelling techniques are well known to those skilled in the art. In a specific embodiment, the protein can be detected by Western blotting analysis. The Western blotting analysis can be carried out on nuclear and/or cytoplasmic extracts of the cells contained in the sample from the patient. Briefly, the proteins are migrated in a gel and then blotted onto a membrane. This membrane is then incubated in the presence of the antibodies and the binding of the antibodies is optionally revealed using labelled secondary antibodies. In another embodiment, the protein is detected by immunohistochemistry, immunocytochemistry or immuno-radiography. These techniques are well known to those skilled in the art. The immunocytochemical analysis can be carried out on whole cells originating from the sample or which are derived there from, for example by cell culture. It can also be carried out on isolated nuclei. The immunohistochemical analysis can be carried out on mammary, nerve tissue sections etc. . . . By way of illustration, an immunocytochemical analysis can include the following steps. However, it is understood that other preparatory methods can be carried out. Cells originating from the biological 5 sample are cultured, preferably on slides (Lab Tek, Nunc, Germany), and then washed with buffer and fixed with paraformaldehyde (for example, 4%). A saturation step is preferably carried out by incubating the cells with buffer S (PBS-0.1% Triton X100-10% FCS). The cells are then incubated with a primary antibody and are then washed and incubated with a fluorescent secondary antibody, if necessary. The nuclei can be labelled with propidium iodide (Sigma). The slides are mounted in moviol for observation by fluorescence microscopy. Moreover, isolated nuclei sampled during a nuclear extraction can be fixed with paraformaldehyde (for example, 4%). The suspensions of nuclei are deposited between a slide and cover slip and the observation is carried out by fluorescence microscopy and by confocal microscopy. The primary antibodies are, for example, rabbit antibodies and the secondary antibodies are labelled antibodies directed against rabbit IgGs. The biological samples originate from a patient potentially suffering from cancer or for whom it has been established that said patient is suffering from cancer. “Biological sample” is intended in particular to mean a sample of the biological fluid, living tissue, tissue fragment, mucosity, organ or organ fragment type, or any culture supernatant obtained by means of taking a sample. The method according to the present invention can comprise a step of taking a biological sample from the patient. The detection step can be carried out directly on a tissue section of the sample, or on a culture of cells originating from the sample, or on total cell extracts, nuclear extracts and/or cytoplasmic extracts. In a specific embodiment of the method comprising the detection of the product of expression of the PKCe gene, a significant increase in PKCs is indicative of the presence of cancer cells. More specifically, the amount of PKCs in normal cells is compared with the amount of PKCs in the cells of the sample, and the significant increase is determined by means of this comparison. The method according to the present invention can optionally comprise the measurement of the LIV21/PKCS content. This LIV21/PKCS ratio increases in the cytoplasmic fraction of cancer cells compared with normal cells. In another specific embodiment of the method comprising the detection of the product of expression of the E2F4 gene, the method comprises the detection of the association of LIV21 with the E2F4 protein, and a decrease in this association is indicative of the presence of cancer cells. The detection of the association of LIV21 with the E2F4 protein can be carried out by concurrent detection of LIV21 and of F9F4. The method according to the present invention can optionally comprise the measurement of the E2F4/LIV21 content. This E2F4/LIV21 ratio decreases in the nucleus of cancer cells compared with normal cells. In an additional embodiment of the method comprising the detection of the product of expression of the E2F1 gene, the presence of the E2F1 protein in the nucleus is indicative of the presence of cancer cells. The method according to the present invention can optionally comprise the measurement of the E2F1/LIV21F content. This E2F1/LIV21F ratio increases in the nuclear fraction of cancer cells compared with normal cells. The method according to the present invention allows in particular the detection of metastasized cancer, therapeutic monitoring and/or recurrences following treatment and makes it possible to determine the degree of invasiveness of a cancer or neurodegenerative disease or Alzheimer disease. The specificity of the detection can be related to the crossing over of information obtained through the existence and the topography of LIV21 by all imaging and spectroscopy means and obtained by combination with other known cancerological indicators via protein arrays or microarrays. Thus, the detection based on LIV21 can be combined with the detection of other cancer markers, in particular breast cancer markers, known to those skilled in the art and nerve cancers. In fact, the present invention concerns a method for the therapeutic monitoring of an anticancer treatment in a patient suffering from cancer, comprising the administration of the anticancer treatment to said patient and the detection of cancer cells in a biological sample from the patient, according to the method of the present invention. A decrease in cancer cells will be indicative of the effectiveness of the treatment. The detection of cancer cells in a biological sample from the patient, according to the method of the present invention, can be carried out once or several times over the course of the anticancer treatment or after the anticancer treatment. Preferably, the biological sample originates from the tissue affected by the cancer treated.
Moreover, the present invention also concerns a method for the detection of recurrences subsequent to an anticancer treatment of a cancer in a patient, comprising the detection of cancer cells in a biological sample from the patient, according to the method of the present invention. The detection of cancer cells in a biological sample from the patient, according to the method of the present invention, can be carried out once or several times after the anticancer treatment. The detection of cancer cells is indicative of recurrences. Preferably, the biological sample originates from the tissue affected by the cancer treated. The present invention also describes a kit for carrying out a method according to the invention. More particularly, the invention concerns a kit for the detection of cancer cells in a biological sample from a patient, comprising one or more elements selected from the group consisting of an antibody which binds specifically to human LIV21 according to the present invention and an anti-LIV21 serum according to the present invention, an oligonucleotide probe specific for the LIV21 mRNA and a pair of primers specific for the LIV21 mRNA. In a preferred embodiment, the kit comprises antibodies, which bind specifically to human LIV21. In another preferred embodiment, the kit comprises an oligonucleotide probe specific for the LIV21 mRNA. It may also comprise a probe specific for a “housekeeping” gene. The kit according to the present invention can comprise reagents for the detection of an LIV21-antibody complex produced during an immunoreaction. Optionally, the kit according to the present invention also comprises means for detecting the product of expression of at least one gene selected from the group consisting of the protein kinase C epsilon (PKCs) gene, the E2F1 gene and the E2F4 gene. This detection means can be antibodies specific for the protein, oligonucleotide probes specific for the mRNA concerned and/or a pair of primers specific for the mRNA. The present invention also relates to a diagnostic composition comprising one or more elements selected from the group consisting of an antibody according to the present invention and a serum according to the present invention, an oligonucleotide probe specific for the LIV21 mRNA and a pair of primers specific for the LIV21 mRNA.

Anticancer Therapy

In the context of an anticancer therapy, it is possible to envision increasing the amount of LIV21 present in the nucleus. For this, the nuclear localization in cancer cells of LIV21 expression could be promoted. Liv21 being able to translocate in the nucleus by itself, one could envisage the construction of an expression vector including a polynucleotide coding for human Liv21 in order to over express these protein in the cell nucleus for that we wish regulate the proliferation (SEQ ID No 215). The expression vector encoding Human Liv21 can be administrate in vivo to the patient by any mean known by those skilled in the art, SEQ ID No 215 for example and inhibitor peptide of Liv 21. For example, the expression vector can be administrated as naked DNA (for example EP 465529). The microinjection, electroporation, phosphate of calcium precipitation techniques and formulations using nanocapsules or liposomes are other techniques available (SEQ ID No 217). The expression vector may also be in the form of a recombinant virus, including, a polynucleotide encoding human Liv21 inserted into its genome. The viral vector can be selected for example from an adenovirus, a retrovirus, in particular a lentivirus, and a virus adeno-associated (AAV), a herpes virus (HSV), a cytomegalovirus (CMV), a vaccine virus, etc. . . . .
So advantageous, the recombinant virus is a defective virus.
Preferably, the expression vector permits a cellular targeting. So this vector could target cancer cells or a particular cell type that is affected by cancer. Targeting of particular cellular type can be realized by placing the polynucleotide coding Liv21 under the control of a promoter tissue-specific. In another alternative the expression vector may be targeted, for example, in association with a specific molecule of a particular tissue or cancer cells, for example a specific antibody to a molecule expressed specifically by the particular tissue or the cells of cancer. Also the choice of expression vector may also influence the cellular targeting. Indeed, if the vector is a virus, the virus tropism natural or amended may also allow a certain target.
The present invention concerns a pharmaceutical composition comprising a polynucleotide encoding for Liv21 (SEQ ID No 215), more particularly an expression vector coding for Liv21. It also concerns the use of a pharmaceutical composition comprising a polynucleotide encoding for Liv21, in particular an expression vector encoding for Liv21 as medicament. Preferably, the present invention concerns the use of a pharmaceutical composition comprising a polynucleotide encoding for Liv21, in particular an expression vector encoding for Liv21, for the preparation of a medicament for use in treating cancer. Finally, it concerns a method for treating cancer in a patient, comprising the administration to the cancer cells of a polynucleotide encoding for Liv21, Liv21 expression making it possible to reduce or abolish the cancerous phenotype of the treated cells. Preferably, cancer is selected from breast cancer, bladder cancer, ovarian cancer, uterus cancer lung cancer, skin cancer, prostate cancer, colon cancer, a glioblastoma, without being limited thereto. Moreover, the nuclear localization of LIV21 could be promoted, for example by decreasing the activity of PKCs in the cancer cells and by using HDAC inhibitors.
In another specific embodiment of anticancer therapy, it is possible to envision decreasing the activity of PKCs in the cancer cells. This decrease in activity can be produced by decreasing the activity of the PKCs protein or by decreasing its expression. A decrease in the activity of the PKCs protein can be obtained by administering PKCs-protein inhibitors to the cancer cells. The PKCs-protein inhibitors are well known to those skilled in the art. A decrease in the expression of the PKCs protein can be obtained by using antisenses or siRNA specific for the PKCs gene. Kits are commercially available. Moreover, the techniques concerning inhibition by means of antisense or siRNA are well known to those skilled in the art (Arya R 2004, Lee W 2004, Sen A 2004, Platet N 1998, Hughes 1987) (SEQ ID No 215 and SEQ ID No 216).
The next siRNA can be also used:

	GCUGAGGCAGGCAGAUCAUUUCAA )

	UUCGACUCCGUCCGUCUAGUAAGAG-

	GUACCAUUUCACAACAACUUUCAA )

	UUCAUGGUAAAGUGUUGUUGAAGAG-

The present invention therefore concerns a pharmaceutical composition comprising a PKCs-protein inhibitor. It also concerns the use of a pharmaceutical composition comprising a PKCs-protein inhibitor as a medicament, in particular for the preparation of a medicament for use in treating cancer. Finally, it concerns a method for treating cancer in a patient, comprising the administration to the cancer cells of a PKCs-protein inhibitor, the pKCs-protein inhibitor making it possible to reduce or abolish the cancerous phenotype of the treated cells. In a first embodiment, the PKCs-protein inhibitor decreases the activity of the PKCs protein. In a second embodiment, the PKCs-protein inhibitor decreases the expression of the PKCs protein. Preferably, cancer is selected from breast cancer, bladder cancer, ovarian cancer, uterus cancer lung cancer, skin cancer, prostate cancer, colon cancer, liver cancer, a sarcoma, a leukaemia and glioblastoma, without being limited thereto. PKC epsilon inhibitors are published and commercially available for other applications.
In the context of a therapy for a neurodegenerative disease, it is possible to envision decreasing the amount of LIV21 present in the nucleus. For that, the Liv21 expression could be decreases or blocked in nuclear of the diseased cells of neurodegeneration. The cells affected by the neurodegenerative disease are generally neurons, motorneurons, etc.
In a preferred embodiment, the neurodegenerative disease is chosen from Alzheimer's disease, Huntington's disease, Parkinson's disease and amyotrophic lateral sclerosis (ALS). The inhibition or the blocking of LIV21 expression can be carried out by any means known to those skilled in the art. In particular, by way of illustration, mention may be made of the antisense strategy, siRNA and ribozymes. Thus, an antisense oligonucleotide or an expression vector encoding this antisense oligonucleotide could be prepared and used to block the translation of the mRNA encoding LIV21F in vivo. Moreover, a ribozyme can be prepared for cleaving and destroying, in vivo, the mRNA encoding LIV21. It is also possible to envisage a triple-helix strategy in which an oligonucleotide is designed so as to hybridize with the gene encoding LIV21 and to thus block the transcription of this gene.
Moreover, for this, the nuclear localization of LIV21 could also be hindered, for example by increasing the activity of PKCs in the cells affected by the neurodegenerative disease. In one particular therapeutic method against neurodegenerative diseases, it is possible to envision increasing PKC epsilon activity in the cells affected by the neurodegenerative disease. This increase in activity can be produced by increasing the activity of the PKCs protein or by increasing its expression. An increase in the activity of the PKCs protein can be obtained by administering PKCs-protein activators to the cells affected by the neurodegenerative disease. The PKCs-protein activators are well known to those skilled in the art (Toma 0 (2004), Activation of PKCs by DAG, AGPI: oleic acid, linoleic acid, arachidonic acid, etc. . . . Activation and proteolysis of PKCs in gonadotropic cells: Communication 2004 by Macciano H, Junoy B, Mas J L, Drouva S V, UMR6544 Marseille). An increase in the expression of the PKCs protein can be obtained by using expression vectors encoding the PKCs protein and which make it possible to overexpress it in the cells affected by the neurodegenerative disease.
Thus, the present invention concerns a pharmaceutical composition comprising a PKCs-protein activator or an expression vector encoding the PKCs protein. It also concerns the use of a PKCs-protein activator or of an expression vector encoding the PKCs protein, for the preparation of a medicament for use in the treatment of a neurodegenerative disease.

Screening Method

The invention concerns methods for the selection, identification, characterization or optimization of active compounds, which decrease cell proliferation, based on the measurement of the nuclear versus cytoplasmic localization of LIV21, or of the binding of the LIV21 protein to the E2F4 protein.
In a first embodiment, the selection, the identification, the characterization or the optimization of active compounds of therapeutic interest comprises bringing a candidate compound into contact with a cell and determining the nuclear versus cytoplasmic localization of the LIV21 expression product. An increase in the nuclear localization of LIV21 indicates that the candidate compound is active in terms of decreasing or abolishing cell proliferation. A decrease in the nuclear localization of LIV21 indicates that the candidate compound is active in terms of treating or preventing a neurodegenerative disease.
In a second embodiment, the selection, the identification, the characterization or the optimization of active compounds of therapeutic interest comprises bringing a candidate compound into contact with a cell and determining the level of expression of the gene encoding the PKCs protein. A decrease in the expression of PKCs indicates that the candidate compound is active in terms of decreasing or abolishing cell proliferation. An increase in the expression of PKCs indicates that the candidate compound is active in terms of treating or preventing a neurodegenerative disease.
In a third embodiment, the selection, the identification, the characterization or the optimization of active compounds of therapeutic interest comprises bringing a candidate compound into contact with a cell and determining the level of LIV21/E2F4 complex. An increase in the level of LIV21/E2F4 complex indicates that the candidate compound is active in terms of decreasing or abolishing cell proliferation. A decrease in the level of LIV21/E2F4 complex indicates that the candidate compound is active in terms of treating or preventing a neurodegenerative disease. In a fourth embodiment, the selection, the identification, the characterization or the optimization of active compounds of therapeutic interest comprises bringing a candidate compound into contact with a cell and determining the level of expression of the gene encoding the E2F1 protein. A decrease in the expression of E2F1 indicates that the candidate compound is active in terms of decreasing or abolishing cell proliferation. An increase in the expression of E2F1 indicates that the candidate compound is active in terms of treating or preventing a neurodegenerative disease.
The invention also relates to a method of screening for a compound capable of interacting in vitro, directly or indirectly, with LIV21, characterized in that: in a first step, the candidate compound and LIV21 are brought into contact and, in a second step, the complex formed between said candidate compound and LIV21 is detected by any appropriate means.
The present invention also relates to a method of screening for a compound capable of modulating (activating or inhibiting) the activity of the LIV21 protein, characterized in that: in a first step, cells of a biological sample expressing the LIV21 protein are brought into contact with a candidate compound, in a second step, the effect of said candidate compound on the activity of said LIV21 protein is measured by any appropriate means, and in a third step, candidate compounds capable of modulating said activity are selected. The activity of LIV21 can, for example, be estimated by means of evaluating the ability of the cell to divide, by measuring the expression of the E2F1 gene or by the cytoplasmic and/or nuclear localization of LIV21.
The candidate compound can be a protein, a peptide, a nucleic acid (DNA or RNA), a lipid, or an organic or inorganic compound. In particular, the candidate compound could be an antibody, an antisense, a ribozyme or an siRNA.
Other advantages and characteristics of the invention will appear in the examples and the figures which follow, and which are given in a non limiting manner.

EXAMPLES

Example 1

Extraction of Proteins of the Liv21 Complex.

The MCF-7 Cell Line

The MCF-7 line is a non clonal human line of breast denocarcinoma cells. During their differentiation induced by exogenous factors, these cells develop a hypertrophy, membrane protrusions and a tendency to dissociate from one another. They acquire a secretory phenotype which is characterized by the appearance of numerous granules and of secretory canaliculi.
In vivo, these cells are relatively non metastatic and this low invasiveness is thought to be due to a low constitutive activity of the protein kinases C (PKCs) and to a relatively low level of expression of protein kinase C alpha.
This line is used in many studies on proliferation, differentiation and apoptosis. These studies use appropriate drugs, such as TNF for the induction of apoptosis, or TPA (12-O-tetradecanoyl phorbol-13-10 sumoate) for the induction of differentiation and therefore for the study of departure from the cell cycle.

Extraction of Proteins of the Liv21 Complex.

After culture cells MCF7 (ATCC passage 15) and cell extraction, 5 mg of protein are centrifuged after homogenization in 10 ml RIPA buffer, antiprotease added. These protein extracts went loop for seven hours at a peristaltic pump on a column of affinity (HITRAP NHS ACTIV HP 1×5 ml: Article and catalog 17071701) which was set Liv21 antibody. Wash 3 times, 10 ml in RIPA buffer and then a half-eluting fractions of 500 nl in a buffer glycine PH2/HCL, then control gel SDS Page 10% (deposit of 25 nl of the fraction) followed by a 25 western blot to verify. Revelation of a band on gel at 51 kD flanked by two other bands at 50 and 52 kD respectively and a lower trace of a band 80 kD and 100 kD in gel mono dimensional (FIG. 1A). Moreover revelation of 12 spots between 50 kD and 70 kD in bidimensional gel (figure IB and 2), idem cultures of SHSY5Y (i.e. FIG. 7).

	SEQ ID No 1
	Peptide LIV21a RVYGPLTNPKPQ

	SEQ ID No 2
	Peptide LIV21a PLMIIHHLDDCPHSQALK

	SEQ ID No 3
	Peptide LIV21c SYMSMFLLLMAISCVLAK

	SEQ ID No 4
	peptide LIV21d CYRSILHTKV

	SEQ ID No 5
	Peptide Liv21b KFFVFALILALMLSMCGADSHAKR

Example 2

Mass Spectrometry

A mass spectrometry (MALDI) was realized for the LIV21 protein and its complex. The LIV21 protein (polynucleotide Liv21F) was digested with trypsin. The peptides derived from the digestion are solubilized in a solvent: acetonitrile/water (1/1) containing 0.1% of TFA (trifluoroacetic acid). A saturated solution of the alpha-cyano-4-hydroxycinnamic matrix was prepared in the same solvent. The same volume of the two solutions was taken and mixed together and 1 μl was deposited onto the MALDI plate for analysis. The mass spectrometry showed that the LIV21 protein and its complex digested with trypsin reveals hundred peptides following the band of gel extracted between 49 and 54 kD (i.e. FIGS. 3-5). The LIV21 protein was characterized by a molecular weight of 50 kD revealed by Western blotting and by a two-dimensional SDS PAGE gel (FIG. 2). But we find a product of 100 kD at 130 kD which could be a Liv21 dimer. (I.e description FIGS. 4, 5 and 6)
When it changes cell compartment and when it is sumoylated, the LIV21 protein has a molecular weight of approximately 60 kD. When it is phosphorylated in the cytoplasm, it exhibits two forms which differ by a few kilobases. A doublet is then observed.

Example 3

Analysis of Sequences in the Proteomic Databases

Several peptides in the patent in listing of the patent characterize it:

	SEQ ID No 51
	Peptide LIV21b FVFALILALMLSMCG

	SEQ ID No 5
	Peptide LIV21b KFFVFALILALMLSMCGADSHAKR

For example, the inventor obtained a very significant score of 81, hoped: 0.0012 for the histatin 3-2 variant with 52% of overlapping of sequences between the tested sample and histatin, this sequence SEQ ID No5 is commune to Liv21 and HIS3-HUMAN (FIGS. 6 and 7). Using different database and a ppm which differed to 20 to 50 ppm, we obtain the same sequence for the commune part: SEQ ID No 51.

Example 4

Reverse Transcriptions:

After MCF7 cells (ATCC passage 15) had been thawed and cultured up to 2 00 million, they were trypsinized and frozen at −80° C. The RNA was extracted from two pools of 50 million cells with the Nucleospin RNA L kit (Macherey Nagel) ref. 740.962.20, resulting in a pool 1 of 318 μg and a second of 182 μg.
The poly A+ RNA was extracted from 313 μg of total RNA of pool 1 using the oligo Tex mRNA Midi kit (Qiagen) ref.70042.

I Reverse Transcription:

The RNA was reverse transcribed with the Fermentas Revert Aid H minus M MuLV Reverse Transcriptase, ref. EPO451 batch 1124, with 3.64 μg of total RNA and 0.45 μg of mRNA, according to the supplier's conditions, with an oligo dT primer. Reactions were carried out at 2 different temperatures at 45° C. and 55° C. so as to eliminate the RNA structures that may hinder reverse transcription.

II PCR

The PCRs were carried out with the reverse transcriptions as templates, initially with the primers Al+oligo dT. Nested PCRs were subsequently carried out on these first PCRs, with the primers Al+Splicing, Al+GDBR1, or ATG+Splicing, ATG+GDBR1.
PCR amplification was then carried out with the primers specific for the genes to be detected, using the cDNAs obtained after oligo dT RT.
Enzyme: Fermentas Taq DNA polymerase. Thermocycler: Bio Rad iCycler.
The quality of the cDNAs was tested by amplification of GAPDH, b actin and Histone H3.3 housekeeping genes.

TABLE 1

Primers

		Amplified
		fragment
Reference
	5′-3′ sequence	size

Histone N
	5′-gtg gta aag cac cca gga a-3′	347 bp
Histone I (reverse)	5′-gct agc tgg atg tct ttt gc-3′

Hum GAPDH sense	5′-TGA AGG TCG GAG TCA ACG G-3′	983 bp
Hum GAPDH antisense	5′-CAT GTG GGC CAT GAG GTC-3′

Hum b-actin sense	5′-GGA CTT CGA GCA AGA GATGG-3′	234 bp
Hum b-actin antisense	5*-AGC ACT GTG TTG GCG TAC AG-3′

LIV21 (Al)	5*-TCCTATGCTTTGACTATTAG-3′

LIV21 (A2)	5′-CCTGACATCCCTACATCACCGCA-3*

odT
ATG galgal
	5*-ATGTATATTATATCTAA-3′

Splicing sense histatin	5′-TGTTGGGATTGCTTATATTT-3′

Splicing reverse histatin	5′- AAATATAAGCAATCCC A AC A-3′

GDBR1 reverse
	5′-CTTTATTATTTTGTAAAAT-3*

				Forward	Reverse
		25M Mg
	10 mM	primer	primer
	10×	(1.5 mM final	dNTP		10 uM	10 uM	Taq (ul)	cDNA
H₂O	buffer	concentration)	(Ml)	(Ml)	(Ml)	5 U/ul	(MO

18.3	2.5	1.5	0.5	0.5	0.5	0.2	1

Other oligonucleotides (I e patent in listing of Trail. PCR Cycles Denaturation: 94° C. 2 minutes Denaturation: 94° C. 3 0 seconds 5 Annealing: 52-55° C. 1 minute 35 cycles Elongation: 72° C. 1 minute 3 0 Final elongation: 72° C. 7 minutes Conservation: 4° C.

III Controls

The PCR Products were Subsequently Controlled on Agarose Gels And Analysed with the BIOCAPT 11.01 Software from Vilber Lourmat.

- Gel 1 (ie FIG. 7): control of RNA on agarose gel 15 FIG. 8: RNA pool

FIG. 9: PCR with housekeeping genes and analysis of molecular masses.
FIG. 10: PCR with the primers showing a band of 1400

- bp. 20 FIG. 11: Gel 2 with analysis of molecular masses

FIG. 12: Gel 3 at 55° and analysis of molecular masses
FIG. 13: Gel 4 at 45° and at 55° and analysis of molecular masses. 25 FIG. 14: screening ligation of 400 pb band, clones B1 to B10.
FIG. 15: screening ligation of 1400 pb band, clones CI to C10.
FIG. 16: Gel 5: ligation screening on the five new clones.
FIG. 17: Gel 6: Screening of the S55T and S55M recombinant clones and analysis of molecular masses (i.e. ptenting listing for oligonucleotidic sequences).
Ge12: PCRs carried out using templates from PCRs performed with the primers Al+oligo dT on the RTs carried out at 45° C. on the total RNA and the poly A+ RNA (messenger RNA). The primers used for these PCRs are Al+GDBR1 or Al+Splicing reverse.
On the RTs carried out using the total RNA, a band of 1178 1253 bp is amplified with, the primers Al+GDBR1 and Al+Splicing reverse. The poly A RNA was used to carry out the RT and is weakly observed at the size (FIG. 10) of 1400 by for amplification with the primers Al+G, and of 415 bp with the primers Al+Splicing reverse. In the Al+splicing PCR product, there are other bands, of 860 and 233 bp (FIG. 11).
Gel 3: PCRs carried out using templates from PCRs performed with the primers Al+oligo dT on the RTs carried out at 45° C. on the total RNA and the poly A+ RNA (messenger RNA). The primers used for these PCRs are Al+GDBR1 or 25 Al+Splicing reverse (FIG. 12).
For the PCRs carried out on RTs performed at 55° C., the same overall pattern of bands as that obtained on the RTs performed at 45° C. is found.
No specific amplification is observed when the poly A RNA was used to carry out the RT. On the RTs carried out on the total RNA, a major band of 1554 1609 bp is found with the primers Al+GDBR1 and Al+Splicing reverse. A band at the theoretical size of 1455 bp is expected for an amplification with the primers Al+GDBR1 and a band with the theoretical size of 415 bp is expected with the primers Al+Splicing reverse. In the 2 profiles, very clear bands of 1900-2100 bp and of 1000-1300 bp are found, but with a weaker intensity than that of the band of 1500-1600 bp.
In the Al+splicing reverse PCR product, there is another major band, of 263 bp.
Ge14: Nested PCRs carried out using templates from PCRs 10 performed with the primers Al+GDBR1 or Al+Splicing reverse on the RTs carried out at 45° C. on the total RNA and the poly A+ RNA (messenger RNA). The primers used for these PCRs are ATG+GDBR1 or ATG+Splicing reverse (FIG. 13).
The nested PCRs carried out with the primers ATG+GDBR1 give bands at 1213 bp (RT 45° C.) and 1559+1315 bp (RT at 55° C.); the expected theoretical size is 1455 bp. The PCRs carried with the primers ATG+Splice reverse give more varied band profiles. These PCRs carried out on other PCRs performed with the primers Al+GDBR1 or Al+Splicing reverse. The presence of a band of 400 bp is noted in the profiles obtained from messenger RNA (the band obtained from the reverse transcription carried out at 55° C. is of greater intensity).
The profiles of the ATG+Splice reverse PCRs carried with total RNA at the start give a band of 424 437 bp of very strong intensity. Bands of 614 and 783 bp of very strong intensity are also found in the profile of the RT 45 and a greater number of bands, but of weaker intensity, is found in the profile of the RT 55, bands at 1118, 936 and 749 bp.
The products of these various PCRs were cloned and sequenced.

Example 5

The PCR products of lanes 2, 4, 6, 7 and 8 were ligated with the plasmid pGEMT Easy, Promega, and the recombinant clones were screened (FIG. 16).


	Lane 2:	G45T ligations
	Lane 4:	S45T ligations
	Lane 6:	G55T ligations
	Lane 7:	S55M ligations
	Lane 8:	S55T ligations

The recombinant clones obtained were screened (after extraction of the plasmid DNA) by restriction with the Eco RI enzyme, the sites of which border the site of insertion of the PCR products into the pGEMT Easy vector.
Screening of the Recombinant Clones:
The first experiments had been carried out using the ten clones B and the ten clones C, FIGS. 14 and 15, and the results of the sequences of clones B2 and C8 are given in the following example, and exhibit, by sequence comparison between clones, great homology with the clones of the second series of experiments.
Gel 5: screening of the S45T and G45T recombinant clones

Analysis of Molecular Masses

The screening of the clones with Eco RI shows that, out of the 9 S45T clones, 3 have inserts of 100 bp, 216 bp and 410 bp. On the G45T clones, out of the 6 clones tested, 3 have inserts of 57, 71 and 148 bp.
FIG. 17: screening of the S55T and S55M recombinant clones

Analysis of Molecular Masses

The screening with Eco RI shows that, out of the 13 clones screened, 7 have inserts of sizes between 239 and 637 bp. The clones G45T5 (148 bp), S45T9 (410 bp), S45T3 (100 bp), S55M1 (491 bp), S55T6 (251 bp) and S55T9 (637 bp) were extracted so as to be sequenced. Primers used for determining the sequences of the 15 various clones and are described in the patent listing:

ATG galgal 5′atgtatattatatatctaa 3′

INV COMP ttagatatataatatacat

Splicing reverse

5′ AAATATAAGCAATCCCAACA 3′

Splicing reverse 5′ TGTTGGGATTGCTTATATTT 3′

inv comp GDBR1 reverse 5′ CTTTATTATTTTGTAAAAT 3′

GDBR1 reverse 5′ ATTTACAAAATAATAAAG 3′

inverse complement Cloned fragments

The test of the bio-markers on extracts of neuroblastomas and cell cultures SHSY reveals by RT PCR the play of under expression and of on expression following in this example of analysis: Example of 16 biomarkers of interest analyzed by RT PCR which recuts the results obtained by biochip on sensor-chip making it possible to see by SPR the over expression and the under-expression of certain genes of the Liv21 complex and its partners of interaction for example. An under expression of DKK1, SKP2, DKK3, ID2, p21, SKP2, TP531NP1, ID2, P73 is observed whereas an over expression of MYCN, ALK, NLRR1 (the neuronal leucine rich repeat is transactivated), CRABPII, DDX1, LIV21K, AURORA kinase A is observed.

Example 6

From the cloning of the LIV21 gene described above, the new sequences are studied in order to design the most specific and effective siRNAs (ie. listing of siRNAs and FIG. 19) for creating “silencing” of the gene, i.e. inhibiting its expression. In the knowledge that the effect of the inhibition at each injection of siRNA remains short, i.e. most commonly less than one hour, the inventor has developed diagnostic products and therapeutic products from this same tool, namely the siRNA.

Example 6.1

The inventor uses siRNAs labeled with rhodamine or fluorescein or any other label that can be revealed and followed by optical observation with a microscope in order to localize the site, in the cells, tissues or sample labelled, that the labelled siRNA will go to in order to attach to the specific sequence which characterizes it, and thus to indicate the site of the expression of the messenger RNA of the gene of interest. Thus, the specific siRNA can be used as a diagnostic marker as an antibody would be, and can make it possible to localize, in a specific case such as on extemporaneous samples or any other type of sample taken from a patient, for example a cancerous tissue sample, the fluorescence or any other labelling used on the siRNA and found in a cell compartment on the sample.
Thus, a labelled siRNA of LIV21 (FIG. 19) that is found, under a microscope, in the cell nuclei at the periphery of a surgical exeresis, would indicate a diagnosis of complete exeresis of the cancerous tissue; on the other hand, this same marker found in the cytoplasm or the membranes of this same sample would mean that the surgeon would have to perform an enlarged exeresis, immediately if this test can be carried out directly in the operating theatre, which would be the best situation for removing all the cancer cells visible only on this molecular and cellular scale by virtue is the siRNA marker. This could be a more rapid implementation alternative than the other application that the inventor has developed with the antibody or the LIV21 peptide, which can be used in the same manner.

Example 6.2

For the treatment products which rise directly from the observations made thanks to the results of expression of the biomarkers on the biochips, the interest is well illustrated for the example of the TGF Béta and p27:
The publication of Mr. Lecanda J and Gold Li of March 2009 is very well rich of teaching and famous all the interest of the pharmaco diagnostic biochips as described above.
TGF Béta inhibits cell proliferation by increasing the level of p27 via the activation of the factors of transcription smad 2/3.
TGF Béta thus increases the total level of translocation of p27 in the core accumulates p27 in the cellular core through the activation of smad 2 and smad 3.
All these events are locked by an inhibiter of TGF Béta IH: serine kinase SD208: new centers therapeutic targeted for the carriers.
TGF Beta decreases the level of the components skp2 compared to protein but not the level of mRNA.
TGF Béta thus can mediate the degradation of p27 in the proteasome at the proteinic level because it maintains it in the core but on the other hand the inhibition of the transcription of p27 with a specific siRNA locks TGF beta.
TGFBeta prevents degradation proteasomale kinase cycles dependant inhibiter on p27. (Alvarez Rodriguez R Pon S J that sci 2009 Mar. 1-122).
The gene expression proneural coding for Mash 1 abolishes MYCN (mitotic activity). (2009 Liu W Wuz Guan M, Lu Y).
The inventor uses first labelled siRNAs of the Liv21 complex in order to evidence their expected presence in the cellular compartment and to visualize them. Then the inventor will use non-labelled Liv21 siRNAs solely for their therapeutic role. In a specific case, the injection of siRNA (FIG. 19) directly in a neurodegenerating tissue or any other mean of administration allowing to the siRNA to get to the neurodegenerating tissue (for example the ear, the eye, cephalorachidian liquid, etc.) and to act allowing proliferation until apoptosis and therefore the death of the neurodegenerating cell.
An experiment on human cell cultures then on animal models having a retinopathy generating a vitreo-retinal degeneration (direct injection of the siRNA in the eye) makes it possible to illustrate this method.
The siRNA are also transfected in the cells according to the Invitrogen protocol using the lipofectamine 2000.
The study of the specific role of the PKC epsilon on the nuclear translocation of Liv 21F can use a peptide which inhibits function PKC epsilon and the translocation like previously described but also according to the protocol of reference of Si RNA of PKC epsilon. The profile of expression observed corresponds to a doublet of tapes in the cytoplasm with approximately 51 KD (and with a tape of 64 kD according to the siRNA used) whereas it corresponds only to one simple tape with 50 kD in the nuclear fraction.
The molecules of siRNA resulting from the nucleotidic sequences of the Liv21 complex can be selected in the group made up of the molecules of siRNA understanding any of sequences SEQ ID No 119 to 126 and 171 to 175, and SEQ ID No—the use of a multitherapy based on the combination of several of these siRNA for the processing of cancerous or neurodegenerative pathology. These siRNA and the useful combination deduced from the results from on expression and from under expression of the biochips and RT PCR constitute an auxiliary processing of pathology and can be combined with small doses of chemical molecules having already proven reliable in the processing of pathology.

Example 6.3

The present invention, relates to methods and reagents useful in modulating gene expression associated with Alzheimer disease in a variety of applications, including use in validating therapeutic, diagnostic, target, and applications genomic discovery.
The invention concerns compounds, compositions and methods for the study, diagnosis and treatment of diseases that respond to the modulation of beta secretase (BACE) amyloid, expression and/or activity of protein gene the precursor APP, of pin 1 of presenillin 1 (PS-1) and/or of presenillin 2 (PS-2) in association with modulation of gene and protein complex Liv21. The invention concerns compounds, compositions and methods for the study, diagnosis and treatment of diseases that respond to the modulation of the expression and/or activity of genes involved in complex liv21 and in combination with the genes of the betasecretase (BACE), amyloid protein of precursor APP, pin-1, presenillin 1 (PS-1) and/or presenillin 2 (PS-2).
Specifically, the invention relates to small nucleic acid molecules, such as short nucleic acid interferent (siRNA), bicatener RNA (dsRNA), micro RNA (miRNA), short double spin RNA (shRNA) be able to interfere with RNA of mediation (RNAi) against beta secretase (BACE) mediation, gene expression of the protein precursor APP, of pin-1, of presenillin (PS-1) and/or presenillin 2 (PS-2).
Vectors to Produce siRNAs are Described.
Vectors are also commercially available. For example, the psilencer is available in Gene Therapy System, Inc. and the RNAi system of pSUPER is available in Oligoengine. They deliver compositions of siRNA with coding RNA part.
Xia et all 2002 Zeng et all 2002Thijn et all 2002 Lee et all Biotechnology 19 Nature Mc Manus et all.
Sui et all PNAS 2002, Yu et all 2002 PNAS 99. Shi et all 2003.
The pharmaceutical compositions comprise a pharmaceutically acceptable carrier.
The compositions are also provided with a device for administering the composition in a cell or in a subject or a tumor. For example, a composition may be in a syringe or to a stent.

Example 7

Pharmaco-Diagnostic Test

Based on the observations that follow in annex at the end of the description of the example concerning the properties of the Liv21 complex, the inventor conceived a design for a pharmacodiagnostic test clinically applicable by known technologically means, which can differ according to users and correspond for each mean to a new product. The invention consists in the fabrication of diagnostic DNA, protein and antibody arrays, including the antibodies already known for the different proteins of the complex associated with Liv21 according to the phase of the cell cycle, that is the antibodies, peptides or nucleotide sequences of the following genes: RBP2, E2F4, E2F1, SUMO, INT2, CRB2, HDAC1, TGFbeta, integrin_alpha5 beta2, Myob, MyoD, cycE/cdk2, cdk1, chk1, chk2, TNFalpha, CREB 1 and p300, Rb, p107, p130 from the pocket protein family. But also NFkB, cdc2A, mdm2, p21, p53, p65, p73 RAS, Ki67, CAF1. The protein arrays (FIG. 20) will allow the study of over or under expression of the gene products, the protein interactions and the post-translational modifications, more particularly phosphorylations and methylations of certain proteins, which indicate a specific state of the unhealthy cell that is different form the protein interactions and the metabolism of an healthy cell. The expression and silencing state of certain genes is different.

Example 7.1

pharmacodiagnostic biochip (FIG. 20) conceived based on nucleotide or peptide sequences fixed on classical supports and according to known techniques such as Agilent or Affymetrix or Caliper without restriction thereof and corresponding to known sequences of following genes and proteins listed in the patent, preferably using sequences that, by 3D analysis, show preferably a loop or helix-loop-helix or basic loop or zinc finger 3D structure or a 3D conformation similar to an helix corresponding in most cases to functional sites, or nucleotide sequences corresponding to a region of cystein methylation, methylation of the promoter region of the gene inducing a potential silencing (see general bibliography), as well as new sequences of Liv21F et Liv21K listed in the description and in annex, but also sequences common to certain genes and certain virus thought to be implicated in particular in breast cancer of Chinese population:
Mdm2 and HIV 1:
GAVTSSNIAA; DLDQSV; EGF and HPV16; EWWRLD; KNSLD; MHIESLDS; BCAS3; BCAS4
These sequences may be tested by microfluidic techniques upon fixation on a gold coverslip in order to study the protein interactions with the cell extracts of the patient.
But which can also be studied by a MICAM technique implemented of the biochips which (cavities) bio-markers by piezo electric effect and not by physicochemical fixation.

Example 7.2

microfluidic test, for example type Biacore, using the SPR (plasmonic surface resonance) technique known by those skilled in the art based on a support fixed with a gold film, which allows, once the light beam has been sent to the interface, to obtain an adsorbed energy as a function of the presence and the size of protein complexes (in the case of protein protein or protein antibody interactions) or of protein DNA complexes (in the case of protein DNA interactions) or RNA, or protein or peptide and an evanescent wave perpendicular to the interface axis (use of a prism). The inventor fixes the selected peptide or DNA sequences on gold particles and calculates the rU number as a function of the size of molecules cited in this patent for each interaction complex studied. In microfluidic, the liquid flowing over these gold film arrays may be a cell extract (or a selective one, meaning that it is only made of cell nuclei, or solely cell cytoplasms or solely cytoskeletal proteins etc.) according to extraction, separation and fractionation techniques such as Calbiochem: subcellular proteome extraction or tissue or cell extracts without any other preparation than anti-proteases or cephalorachidian liquid or serum issued from a patient sample in order to study the circling marker (i.e. described nucleotide or peptide sequence list and/or known sequences of genes involved in the proliferation cycle listed).

Example 8

biochip of sequences SEQ ID No 119 to 127 and 180 with compounds with the sequences of microRNA of interest in studied cancer: mir 21, mir 34a, etc. . . . without the biochip being limited to these. The technique of fixing of RNUMS on the supports defers according to the form of mediums, of revelation and biochip used. For example one uses the sequences RNUMS quoted in solution biothynilées then fixed on sensor-chips at the streptavidine, if one tests their interactions with the cellular or plasmatic extracts or of the rachidian fluid cephalo passing in the channels (fluidic microcomputer) of a A100 or T100. It can also be used as described in the US patent 2008 045418 A1 RNAs locked in end 3′ and added a ligase T4 RNA and a “labeled nucleic acid adapter” having a residue 5′ phosphates.

Example 9

Study of the Expression of LIV21 in Breast Cancer and Colon Cancer Biopsies

In order to determine whether the observations obtained above are applicable to human tissues, a large number of cancer biopsies obtained from patients were studied by immunohistochemical reaction with LIV21 specific antibodies. The immunohistochemical determination of LIV21 protein expression was carried out on several biopsies from patients. Moreover, some paraffin slides from patients suffering from bladder cancer and from breast cancer were also studied. The improvement of the invention is due to the fact of standardizing the biopsies or the punctures by a technique of taking away standardized and gauged in order to then allow reliable comparisons between cellular extracts of patients and witnesses or between cytoplasmic and nuclear and membrane fractions. This same standardization implemented to the taking away making it possible to compare the results of overexpression or of under expressions of the bio-markers by RTPCR is essential to obtain reliable and comparable results.
Immunocytochemical Analysis Protocol:
1) Deparaffinize the slides, Rehydrate the tissues.
2) Saturate the nonspecific sites and permeabilize the membranes.
3) Add the antibody in a humid chamber, Reveal the antibody.
Deparaffinize the slides under a hood.
Two successive baths of toluene (rectapur Prolabo) 2×30′ min or 2×20 min; then dehydrate the tissues with rectapur alcohol at 100% for 15 min; then rectapur ethanol at 95% for 10 min; then rectapur 70% for a further 10 min.
Thaw the antibody at the same time. Rehydrate the tissues gently in PBS supplemented with 10% fetal calf serum and 0.1% Triton.
Saturate the nonspecific sites (for example, with ovalbumin) and permeabilize the membranes, Rehydrate for one hour.
Deposit one ml of this “PBS” per section in order to cover the slide without it drying out at any moment (when it is a slide with cells and not tissues, half an hour is sufficient).
Place the pane and the stainless steel cover and water below so as to create a humid chamber.
Add the antibody in the humid chamber.
Dilute the rabbit serum to 1/200 in 4 ml of PBS triton, so as to continue to permeabilize the membranes and FCS.
Place 1 ml on each slide and keep away from the light and avoid evaporation. Leave overnight or for a minimum of three hours.
Then rinse with 1× normal PBS pH 7, carry out two washes of 5 to 10 min so that no trace of the first antibody remains.
While preparing the Alexa 488 green probe (in the cold at 4° and in the dark) diluted to 1/250, therefore 10 μliter in 2.5 ml of PBS, still with 10% FCS and 0.1% Triton,
Rest the slides on the plate. Cover the section again with 2.5 ml in order to maintain a humid chamber for one hour, and then wash with 1×PBS pH 7.
Wash with propidium iodide at 0.5 microgram per microliter to be diluted to 20 microgram per ml and then again to 1/50, but this time, diluted in 1×PBS alone (50 microliters per 2.5 ml of PBS). Drain while taking them out of the PBS and then dispense 2.5 ml of propidium iodide over the four slides for one minute, followed by two rinses with simple PBS. Mount the slides in Moviol before reading.
For an immunolabelling with peroxidase it is mandatory to mask the antigenic sites by a 20 minutes water bath step in order to obtain meaningful results when one is working with paraffined coverslips.
All these results show that the cytoplasmic localization of LIV21 is an indicator of the aggressiveness and of the metastatic potential of the cancer. The detection of LIV21 expression indicates the presence of invasive, aggressive and metastatic cancer cells. These results also show that the nuclear localization of LIV21 is an indicator of normal quiescent cells, that is of well-differentiated tissues.

Annex: Study of the Nuclear Translocation of LIV21 in MCF-7 and SHSY5Y Cells

The study of the subcellular distribution of LIV21 in different tumor lines of various origins showed an plasmonic surface resonance exclusively cytoplasmic localization of this protein.
The presence of putative phosphorylation sites by protein kinases C (PKCs) in the Liv21 sequence directed the study toward an involvement of these proteins with respect to its nuclear translocation. The MCF-7 line treated with TPA modulates PKCs and is used in the present study.

The Effect of TPA on the MCF-7 Line

TPA is a known activator of PKCs. It activates the growth of normal breast cells, does not modify the proliferation of the cells of benign tumors from this same tissue, but drastically inhibits the proliferation of the cells of human mammary tumor lines such as the MCF-7 line. It reduces the cell growth of this line by positively controlling the c-erb-2 receptor and negatively controlling the retinoic acid receptor a, which are both expressed in particularly large amount in these cells. The TPA greatly and rapidly inhibits the expression and the function of estrogen receptors (ERs) and it induces the time- and dose-dependent translocation of protein kinases C (PKCs) from the cytosol to the membranes. Furthermore, TPA increases the migratory capacity of MCF-7 cells in vitro and a short period of treatment of these cells with TPA induces cellular expansion and microtubule organization characteristic of their differentiation.

Expression of LIV21 in MCF-7 Cells and in the SHSY5Y Cells

Firstly, the inventor verified the expression of LIV21 in these cells at the transcriptional level and at the protein level.
The expression of the LIV21 mRNA was demonstrated by RT-PCR (sense primer: (CCTGACATCCCTACATCACCCAT) (SEQ ID No 3, SEQ ID No 217 and SEQ ID No 127 to 171) and antisense primer: (TCCTATGCTTGACTATTGC) (SEQ ID No 4) in these cells compared with the cells from breast tissues (FIG. 2A). An mRNA of the same size as the mRNA detected in the breast tissues and specific for LIV21 was detected. However, the level of expression of LIV21 in the MCF 7 cells is lower than in the breast tissues. This first result shows that the MCF 7 line expresses the LIV21 mRNA.
The inventor tackled the study of the expression of the LIV21 protein through the Western blotting technique, with an anti-LIV21 antibody, in MCF-7 cells compared with mammary tissues. The anti-LIV21 antibodies were obtained by the method described below. In this line, LIV21 is expressed, both in the mammary tissues and in the MCF-7 cells, in the form of a doublet which migrates at an apparent molecular weight of 51 kDa.

Production of Purified Anti-LIV21 Serum

The specific peptide sequences are the sequences No. 1 and No. 2 and No. 180.
These peptides were injected into rabbits (NZ W ESD 75 female, 2.3 kg at day 0), in agreement with standard immunization procedures,
The effect of the inhibitors on the cells of neuroblastomas
Study of the Influence of PKCs on the Nuclear Translocation of LIV21

Effect of TPA on PKC Expression

Western blotting study: Given that the protein sequence of LIV21 has putative PKC phosphorylation sites, including two specific for PKC, the inventor tested the variation in the expression of this PKC as a function of the duration of TPA treatment. It was observed that TPA acts very rapidly on PKC expression, which decreases from 30 min. The expression of PKCzeta (PKCζ) is used as an internal control since it is not sensitive to TPA.

P65L26 Immunocyto . . . P66L4 Nucleaire de LIV21

Study of the specific role of PKC on the nuclear translocation of LIV21 using an inhibiting peptide of the function and translocation of PKC.
To determine the specific action of PKC on the translocation of LIV21, the crops were discussed with a peptide, selective antagonist of the function and translocation of this PKC (EAVSLKPT (SEQ ID No 6), and the results were compared with those obtained by processing with TP A. This peptide is recognized by the enzyme and links themselves as a substrate amended to the level of its catalytic site. Not phosphorylable, he acts as a specific inhibiter of the activity of PKC.
The effect of the selective inhibition of the activity of PKC on the nuclear translocation of LIV21 was studied by immunocytochemistry. These experiments were carried out on nontreated cultures or cultures treated for 12 h with TPA at 25 nM or with the peptide at two different concentrations, 1 and 2 μM (the peptide used at the concentration of 2 μM has an effect identical to that of TPA on the nuclear translocation of LIV21).
These results were supported by cell fractionation experiments on cultures treated with the PKC inhibiting peptide at 2 μM, compared with TPA-treated cultures. The same LIV21 expression profile was observed in the form of a doublet in the cytoplasm and of a single band in the nuclear fraction.
The specific inhibition of PKC induces a nuclear translocation of LIV21, which suggests that LIV21 could be the target of PKC, which would maintain it in the cytoplasm in a phosphorylated form.

Example

Western Blotting Analysis

This example describes the conditions used for a Western blotting analysis of cancerous brain cells.
The protein extracts are heated at 80° C. for 5 minutes in a Laemmli buffer (pH 7.4, 0.06 M Tris, 3% SDS, 10% 3 5 glycerol, 1 mM PMSF, β-mercaptoethanol). The migration is carried out by SDS-PAGE (sodium dodecyl sulfate-polyacrylamide gel electrophoresis). 10 to 20 μg of proteins migrate in a 12% polyacrylamide gel for 1 h under denaturing conditions (migration buffer: 25 mM Tris base, 192 mM glycine, 1% SDS, pH 8.3). The proteins are then transferred onto a nitrocellulose membrane (Schleicher & Schuell) for one hour by liquid 5 transfer, in a transfer membrane (25 mM Tris, 192 mM glycine, 20% methanol, pH 8.3). The membranes, saturated in PBS-0.1% Tween-0.1% Triton X100-5% skimmed milk for one hour, are brought into contact with the primary antibody diluted in PBS-0.1% Tween-0.1% Triton X100-1% milk at ambient temperature with gentle agitation for one hour to two hours. After washing, the peroxidase-coupled secondary antibody is incubated with the membranes for 1 h. Revelation is carried out by means of a chemiluminescence reaction using the ECL kit according to the supplier's protocol (Amersham).
The primary antibodies used are:
The anti-LIV21 serum which was produced using two synthetic peptides based on the sequence of LIV21F: peptide LIV21a (SEQ ID No 1) and peptide LIV21b (SEQ ID No 2) and/or peptide Liv21e (SEQ ID No 51). The peptides were coupled to hemocyanin before being injected into rabbits for the immunization. The polyclonal antibody was obtained from these two peptides by having immunized two rabbits and having bled one rabbit so as to have a preimmune serum (in order to be sure that this antibody did not already exist in this rabbit).
The rabbit anti-CDK2 polyclonal antibody (Santa-Cruz technology sc-163) diluted to 1/200.
The mouse anti-p21 monoclonal antibody (Dako, M72 02) diluted to 1/150.
The mouse anti-p27 monoclonal antibody (Santa-Cruz technology sc-1641) diluted to 1/100.
It was shown before that protein LIV21 is associated with bodies PML and that, at the time of the sumoylation, LIV21 passes from a molecular weight of 50 kd to 60 kd. By immuno-precipitation, the inventor showed a Co-localization of L1V21 with SUMO in complex PML—SUMO/LIV21. (FIG. 12)
Antitumor role of PML bodies: At the proliferation stage, there are visualized modifications in the PML bodies since these PML bodies dissociate and degrade: (speckles), proteins then become available in the nucleus for ensuring transcription, proliferation, immune reactions and everything that is required for gene transcription. It has been shown that PML associates with SUMO and with HDAC-1 (histone deacetylase 1) and that its complex acts on the expression of E2F1 and PML thus acts on the arrest of proliferation by blocking E2F1. Thus, the PML/HDAC-1 complex down-regulates E2F1 expression. PML associated with Rb (p130) binds to the deacetylated histones and blocks E2F1 by binding to the chromatin.
In acute promyelocytic leukemias, PML is truncated and becomes a fusion protein with the retinoic acid receptor. This fusion protein (PMLRARalpha) is due to a 15/17 chromosomal translocation. A new treatment for this disease by combining arsenic and retinoic acid in order to induce cancer cells into apoptosis has been reported in the literature. The PML protein is thought to regulate proliferation in cancers and lymphomas. The inventor has shown, by immunoprecipitation, the association SUMO-PML in which LIV21 is located.
In the above patents, it was shown that LIV21 is phosphorylated by PKC. The TPA-treated MCF-7 lines show an inhibition of cancerous proliferation and a cell differentiation, and LIV21 is translocated into the nucleus. If a PKC-specific inhibitory peptide was used, it was the activity and not the expression of PKC which was inhibited.
During this TPA treatment (25 nM), when E2F4, p130 and LIV21 were studied (green fluorescence) in the nuclei labelled (DNA) with propidium iodide (red fluorescence), the following were observed:
After 12 h, intranuclear green fluorescence signals with the same pattern for E2F4, p130 and LIV21;
After 48 h, when the proliferation begins, E2F4 has a comparable localization; but at 72 h, it disappears from the nucleus (to the benefit of E2F1).
By observing, by double labeling, the co-localization of PML and of LIV21 at 24 h of PKC treatment (i.e. merge: yellow fluorescence), it was observed that they are co-localized in the nuclei. At 48 h, the co-localization between LIV21 and SUMO (i.e.). The hypothesis is that SUMO, which binds to LIV21, in fact targets LIV21 into the PML bodies and that LIV21 is involved in the PML/SUMO/Rb/HDAC-1 complexes. LIV21 is physically associated with PML and SUMO in the nuclear bodies, by immunoprecipitation and by colocalization by immuno cytochemistry (Rb, p130 and p107 are pocket proteins which have the same binding site). The Rb proteins repress cell growth (Fabbro, Regazzi R, Bioch Biophys Res Comm 1986 Feb. 2; 135 (1): 65-73).
Physical Interaction of LIV21 with the Proteins of the E2F Family
Coimmunoprecipitation experiments carried out using anti-LIV21, anti-E2F1 and anti-E2F4 antibodies made it possible to demonstrate that LIV21 associates with E2F4.
It was shown that BRCA1 also re-entered in interaction with family members E2F and thus complex LIV21. Indeed, E2F1 interacts with BRCA1 and Brca1 interacts with MYC, ESR1, CHEK1 and MAP3K3.
The members of the E2F family are transcription factors whose role has been widely described in the literature as being key molecules in the positive or negative control of the cell cycle (Slansky JE and Farnham PJ 1996; Helin K 1998 and Yamasaki L, 1998), by virtue of their association with the pRb protein (WuCL, Zukerberg LR) or pocket proteins. E2F1 positively controls the cell cycle by transactivating 3 5 the promoter of the genes responsible for cell proliferation (DNA polymerase alpha, thymidine kinase, DHFR, etc.), whereas E2F4 is described as one of the members of the EF family which negatively controls the cycle. Furthermore, a high expression of E2F1 in embryonic mammary tissues has been shown (Espanel X, Gillet G 1998), whereas it is no longer expressed in post-mitotic mammary tissues, to the benefit of a large increase in E2F4 expression (Kastner A Brun G 1998).
The identification of antigens has been carried out in cell lysates by immunoprecipitation. The analysis of the physical interaction of various proteins associated with E2F4 and E2F1 was demonstrated by coimmuno-precipitation of protein complexes. The complex was studied using U. MACS PROTEIN with MICROBEADS (MILTENYIBIOTEC). When lysates of S aureus are added, the proteins A interact with the Fc portion of the specific antibodies and the immunocomplexes become insoluble and are therefore recovered by centrifugation. After breaking of the bonds (heating) between AG/AC and protein A-rich membranes, Western blotting was carried out. These results suggest that the LIV21/E2F4 complex appears to play an important Role in establishing cell quiescence. A study of co immunoprecipitation is following also with the profound mammalian kit Pierce.
Functional interaction of LIV21 with the proteins of the E2F family
It was demonstrated that blocking the expression of the LIV21 protein was correlated with a decrease in the expression of E2F4 and with an increase in the expression of E2F1. In parallel, the functional aspect of the increase in E2F1 was verified by studying the transcription of two of its target genes, DHFR and DNA polymerase a.
In conclusion, these results suggest that the LIV21/E2F4 complex acts as a complex which inhibits the expression of the E2F1 gene. This complex could 3 5 correspond to a new point of control in the arrest of cell proliferation.

REFERENCES

Arya R, Kedar V, Hwang J R, McDonough H, Li H H, Taylor J, Patterson C. Muscle ring finger protein-1 inhibits PKC{epsilon} activation and prevents cardiomyocyte hypertrophy. J Cell Biol. 2004 Dec. 20; 167(6): 1147-59. Epub 2004 December
Aurelian Radu, Nicolae Ghinea (2010)
Expression of FSH receptor in tuymor blood vessels N England J Med (363:1621-16802010)
Stevaux O, Dyson N J. A revised picture of the E2F transcriptional network and RB function. (2002) Curr Opin Cell Biol, 14 (6): 684-91.
Yamasaki L. Growth regulation by the E2F and DP transcription factor families. (1998) Results Probl Cell Differ, 22:199-227.

Claims

1. A Human Liv 21 complex characterized in that it comprises:

a nucleotide sequences selected from SEQ ID No 171 to 175 and SEQ ID 217

an siRNA sequence derived from one of the RNA sequences seq120 and 121 and 171 to 175 and all siRNA sequences (SEQ ID 91 to 118)

a protein fraction comprising at least sequence SEQ ID 1 to 181 or a sequence having 90%, and preferably 80%, and more preferably 70% identity with said SEQ ID 1 to 181 and SEQ ID No 183 and SEQ ID No 215 to 220 or a sequence having 70, 80 or 90% identity with said sequence SEQ ID 183 and 215 to 220 and SEQ ID 230.

2. Liv 21 human complex according to claim 1, further comprising:

A nucleotide sequences SEQ ID No 123, 124, 127 and the protein fractions comprising at least sequence SEQ ID No. 1 or a sequence having 70, 80 or 90% identity with said sequence SEQ ID No 1 and the sequences 181 to 185.

3. The Liv21 human complex is further comprising:

The nucleotide sequences of any one or ribonucleotide sequence SEQ ID No 119 to 126 or 127, or a sequence having 90%, and preferably 80%, and more preferably 70% identity with said sequence SEQ ID No 119 to 127,

or a sequence having 90%, and preferably 80%, and more preferably 70% identity with said sequence SEQ ID No 119 to 127, or UUGGUAACGACCAUGCCAC or UUCACUUAGAAUAAUGUCC or UCUUUGUGAAUUUGACAAC or UCAAGGUCCAGGCUACAAC or

any of the following siRNA sequences SEQ ID No 60 to 88 and 92 to 118, and

GUGGCAUGGUCGUUACCAA dTdT

DTdT CACCGUACCAGCAAUGGUU

GGACAUUAUUCUAAGUGAA dTdT

4. Liv21 human complex according to claim 1, further comprises at least one of:

Any one of the nucleotide sequences SEQ ID No. 123, 124 and SEQ ID No 127 to 149 or

Any one of amino acid sequences SEQ ID No 1 to 118 and SEQ ID No 150 to 170 and SEQ ID No 180 to 185: or a sequence having 90%, and preferably 80%, and more preferably 70% identity with said sequences SEQ ID No: 1 to 185.

5. Liv21 human complex according to any one of claims 1 to 3, characterized in that it interacts with at least one of the partners associated, said at least one of these being associated partners selected from the group consisting of;

any of the following proteins: RBP2, TNF alpha crb2, cmd2, cycE/cdk2, cdk1, CREB1 and p300, Rb, p107, p130 of family of pocket proteins, NFkB, cdc2A, mdm2, p21, p53, p65, p73, CyclinA and D1, BCAS3, BCAS4, Solute Carrier; or

a antibody of any one of the following proteins: RBP2, E2F4, E2F1, E2F2, SUMO, HDAC1, crb2, Int2, cmd2, cycE/cdk2, cdk1, CREB1 and p300, Rb, p107, p130 of family of pocket proteins, NFkB, cdc2A, mdm2, p21, p53, p65, Ki67, CAF1, CyclinA and D1, CHUK, BCAS3, BCAS4, Solute Carrier.

6. Method of detecting the complex human Liv21, characterized in that it comprises the implementation of at least one probe specific for at least one sequence of said human Liv21 complex according to claim 1.

7. Method of detecting the complex human Liv21, characterized in that it comprises the implementation of at least one probe specific for at least one sequence of said human Liv21 complex according to claim 2.

8. Method of detecting the human complex Liv21 according to claim 6, further comprising the implementation of at least one probe specific for at least one of said complex sequence of these Liv21 human complex and associated partners according to claim 3.

9. Method of detecting the human complex Liv21 according to claim 6, further comprising the implementation of at least one probe specific for at least one of said complex sequence of these Liv21 human complex and associated partners according to claim 4.

10. Detection method according to claim 5, comprises at least the following steps:

A step of extracting biological material from a biological sample taken from a patient,

A step of contacting said biological material with at least said specific probe of any one of said sequences of said human complex Liv21 or human Liv21 complex and its content partners, and at least one control and

A step of detecting the expression products of gene expression said complex Liv21 or said human Liv21 complex and its associated partners, said products being comprised of expression of messenger RNA, or peptides, or proteins.

11. Method detection according to claim 10, wherein screening a candidate compound is capable of modulating the activity of said human complex Liv21, and in that it further comprises:

a step of contacting said biological material with said candidate compound, and a step of selecting said candidate compound.

12. Method according to claim 11, wherein said biological sample is taken from a cancer patient and in a healthy patient, and in that said material comprises nuclear cell extracts, cell extracts and cytoplasmic or cell extracts membrane, and in that it further comprises a step of determining the sub-expression and overexpression of the gene products of said complex or said complex Liv21 or said Liv21 human complex and associated partners said biological extracts.

13. Method according to claim 12, and further comprises a step of determining said radio sub-expression and overexpression of said gene products:

cell nuclear extracts and cytoplasmic cell extracts, cell extracts or membrane, and that it further comprises a step of analyzing combined radio said biological material taken from a cancer patient and in a healthy patient

14. Method according to any one of claim 10, characterized in that it uses a biochip on which is deposited at least one sequence-specific probes from said complex Liv21 human according to claim 1.

15. Method according to claim 10, characterized in that it applies to brain cancer, neuroblastoma, glioblastoma, without being limited there and breast cancer, bladder, skin and prostate and Alzheimer disease.

16. Method of treating cancers using an siRNA selected from siRNA SEQ ID NO: 91 to 118.

17. Method of treating cancers by injection of a peptide selected from a vectorized peptide of SEQ ID No: 215 to 220.