WO2012019192A3 - Cell-permeable molecules as growth factor receptor antagonists - Google Patents
Cell-permeable molecules as growth factor receptor antagonists Download PDFInfo
- Publication number
- WO2012019192A3 WO2012019192A3 PCT/US2011/046956 US2011046956W WO2012019192A3 WO 2012019192 A3 WO2012019192 A3 WO 2012019192A3 US 2011046956 W US2011046956 W US 2011046956W WO 2012019192 A3 WO2012019192 A3 WO 2012019192A3
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- growth factor
- factor receptor
- cell
- molecules
- receptor antagonists
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Ceased
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/475—Growth factors; Growth regulators
- C07K14/485—Epidermal growth factor [EGF], i.e. urogastrone
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/74—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving hormones or other non-cytokine intercellular protein regulatory factors such as growth factors, including receptors to hormones and growth factors
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N2333/00—Assays involving biological materials from specific organisms or of a specific nature
- G01N2333/435—Assays involving biological materials from specific organisms or of a specific nature from animals; from humans
- G01N2333/475—Assays involving growth factors
- G01N2333/485—Epidermal growth factor [EGF] (urogastrone)
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N2333/00—Assays involving biological materials from specific organisms or of a specific nature
- G01N2333/435—Assays involving biological materials from specific organisms or of a specific nature from animals; from humans
- G01N2333/705—Assays involving receptors, cell surface antigens or cell surface determinants
- G01N2333/71—Assays involving receptors, cell surface antigens or cell surface determinants for growth factors; for growth regulators
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N2500/00—Screening for compounds of potential therapeutic value
- G01N2500/02—Screening involving studying the effect of compounds C on the interaction between interacting molecules A and B (e.g. A = enzyme and B = substrate for A, or A = receptor and B = ligand for the receptor)
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N2500/00—Screening for compounds of potential therapeutic value
- G01N2500/10—Screening for compounds of potential therapeutic value involving cells
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Molecular Biology (AREA)
- Engineering & Computer Science (AREA)
- Biochemistry (AREA)
- Immunology (AREA)
- Hematology (AREA)
- General Health & Medical Sciences (AREA)
- Biomedical Technology (AREA)
- Medicinal Chemistry (AREA)
- Urology & Nephrology (AREA)
- Gastroenterology & Hepatology (AREA)
- Organic Chemistry (AREA)
- Endocrinology (AREA)
- Microbiology (AREA)
- Genetics & Genomics (AREA)
- Biotechnology (AREA)
- Cell Biology (AREA)
- Biophysics (AREA)
- Zoology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Toxicology (AREA)
- Food Science & Technology (AREA)
- Physics & Mathematics (AREA)
- Analytical Chemistry (AREA)
- General Physics & Mathematics (AREA)
- Pathology (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Peptides Or Proteins (AREA)
Abstract
The invention provides growth factor receptor inhibitory molecules and methods of identifying such molecules, as well as methods of making such molecules and methods of using such molecules, for example in the treatment of cancer such as breast, colorectal, pancreatic, or lung cancer.
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US37158910P | 2010-08-06 | 2010-08-06 | |
| US61/371,589 | 2010-08-06 | ||
| US201161454209P | 2011-03-18 | 2011-03-18 | |
| US61/454,209 | 2011-03-18 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| WO2012019192A2 WO2012019192A2 (en) | 2012-02-09 |
| WO2012019192A3 true WO2012019192A3 (en) | 2012-05-03 |
Family
ID=45560114
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/US2011/046956 Ceased WO2012019192A2 (en) | 2010-08-06 | 2011-08-08 | Cell-permeable molecules as growth factor receptor antagonists |
Country Status (1)
| Country | Link |
|---|---|
| WO (1) | WO2012019192A2 (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2013163423A1 (en) | 2012-04-25 | 2013-10-31 | Musc Foundation For Research Development | Compositions and methods for wound healing and tissue repair |
| JP2022551467A (en) * | 2019-10-10 | 2022-12-09 | ザ リサーチ ファウンデイション フォー ザ ステイト ユニバーシティー オブ ニューヨーク | Analgesic and narcotic peptides and other drugs |
| WO2024105656A1 (en) * | 2022-11-18 | 2024-05-23 | Ramot At Tel-Aviv University Ltd. | Her receptor derived peptides and methods of use thereof |
-
2011
- 2011-08-08 WO PCT/US2011/046956 patent/WO2012019192A2/en not_active Ceased
Non-Patent Citations (6)
| Title |
|---|
| A. BARDELLI ET AL: "Uncoupling signal transducers from oncogenic MET mutants abrogates cell transformation and inhibits invasive growth", PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES, vol. 95, no. 24, 24 November 1998 (1998-11-24), pages 14379 - 14383, XP055012290, ISSN: 0027-8424, DOI: 10.1073/pnas.95.24.14379 * |
| ANONYMOUS: "EGFR (Epidermal Growth Factor Receptor) inhibitor: Petide Antagonists targeting Juxtamembrane.", 23 July 2009 (2009-07-23), XP002663757, Retrieved from the Internet <URL:http://mssm.technologypublisher.com/technology/3228> [retrieved on 20111116] * |
| CHRISTENSEN J G ET AL: "c-Met as a target for human cancer and characterization of inhibitors for therapeutic intervention", CANCER LETTERS, vol. 225, no. 1, 8 July 2005 (2005-07-08), NEW YORK, NY, US, pages 1 - 26, XP027608071, ISSN: 0304-3835, [retrieved on 20050708] * |
| HOOSHMAND RAD ET AL: "PDGF alpha-receptor mediated cellular responses are not dependent on Src family kinases in endothelial cells.", JOURNAL OF CELL SCIENCE, vol. 111, no. 5, 1 March 1998 (1998-03-01), pages 607 - 614, XP055012379, ISSN: 0021-9533 * |
| JAE-HO LEE ET AL: "A novel germ line juxtamembrane Met mutation in human gastric cancer", ONCOGENE, vol. 19, no. 43, 1 January 2000 (2000-01-01), pages 4947 - 4953, XP055012366, ISSN: 0950-9232, DOI: 10.1038/sj.onc.1203874 * |
| P. M. CHAN ET AL: "Autoinhibition of the Kit Receptor Tyrosine Kinase by the Cytosolic Juxtamembrane Region", MOLECULAR AND CELLULAR BIOLOGY, vol. 23, no. 9, 1 May 2003 (2003-05-01), pages 3067 - 3078, XP055012332, ISSN: 0270-7306, DOI: 10.1128/MCB.23.9.3067-3078.2003 * |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2012019192A2 (en) | 2012-02-09 |
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