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CA2795671A1 - Genetic signatures and gene chips associated with administration of electrically conducted radio frequency current to skin and methods and treatments relating thereto - Google Patents

Genetic signatures and gene chips associated with administration of electrically conducted radio frequency current to skin and methods and treatments relating thereto Download PDF

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Publication number
CA2795671A1
CA2795671A1 CA2795671A CA2795671A CA2795671A1 CA 2795671 A1 CA2795671 A1 CA 2795671A1 CA 2795671 A CA2795671 A CA 2795671A CA 2795671 A CA2795671 A CA 2795671A CA 2795671 A1 CA2795671 A1 CA 2795671A1
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CA
Canada
Prior art keywords
skin
treatment
tissue volume
gene
radio frequency
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.)
Abandoned
Application number
CA2795671A
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French (fr)
Inventor
David John Weisgerber
Nikki Elizabeth Annunziata
Tia Janinne Maurer
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Procter and Gamble Co
Original Assignee
Procter and Gamble Co
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Procter and Gamble Co filed Critical Procter and Gamble Co
Publication of CA2795671A1 publication Critical patent/CA2795671A1/en
Abandoned legal-status Critical Current

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    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12QMEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
    • C12Q1/00Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
    • C12Q1/68Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
    • C12Q1/6876Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12QMEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
    • C12Q1/00Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
    • C12Q1/68Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
    • C12Q1/6813Hybridisation assays
    • C12Q1/6834Enzymatic or biochemical coupling of nucleic acids to a solid phase
    • C12Q1/6837Enzymatic or biochemical coupling of nucleic acids to a solid phase using probe arrays or probe chips
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12QMEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
    • C12Q2600/00Oligonucleotides characterized by their use
    • C12Q2600/158Expression markers

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  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Organic Chemistry (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Zoology (AREA)
  • Wood Science & Technology (AREA)
  • Analytical Chemistry (AREA)
  • Genetics & Genomics (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Biochemistry (AREA)
  • Biotechnology (AREA)
  • Microbiology (AREA)
  • General Health & Medical Sciences (AREA)
  • General Engineering & Computer Science (AREA)
  • Biophysics (AREA)
  • Molecular Biology (AREA)
  • Immunology (AREA)
  • Physics & Mathematics (AREA)
  • Biomedical Technology (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Cosmetics (AREA)
  • Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
  • Apparatus Associated With Microorganisms And Enzymes (AREA)

Abstract

A gene panel comprising genes regulated in mammalian skin in response to generation of a radio frequency current in a tissue volume of the mammalian skin sufficient to heat the tissue volume to a treatment temperature, wherein at least one gene is selected from Table 1 or Table 2 and at least one gene is selected from Table 3. Further there is a method for providing a benefit to mammalian skin, the benefit comprising inducing collagen formation and/or dermal remodeling in a dermal layer of the mammalian skin in the absence of a skin-damaging inflammatory cytokine response, the method comprising generating a radio frequency current in a tissue volume of the mammalian skin for a treatment cycle sufficient to heat the tissue volume to a treatment temperature while avoiding an upregulation in expression of genes listed in Table 3.

Claims (36)

1. A gene panel comprising genes regulated in mammalian skin in response to generation of a radio frequency current in a tissue volume of the mammalian skin sufficient to heat the tissue volume to a treatment temperature, wherein at least one gene is selected from Table 1 or Table 2 and at least one gene is selected from Table 3.
2. A gene panel according to claim 1, wherein at least one gene is selected from Table 1, at least one gene is selected from Table 2, and at least one gene is selected from Table 3.
3. A microarray comprising a set of immobilized nucleic acid probes capable of hybridizing to and detecting genes constituting a gene panel according to claims 1 or 2.
4. A method for providing a benefit to mammalian skin, the benefit comprising inducing collagen formation and/or dermal remodeling in a dermal layer of the mammalian skin in the absence of a skin-damaging inflammatory cytokine response, the method comprising generating a radio frequency current in a tissue volume of the mammalian skin for a treatment cycle sufficient to heat the tissue volume to a treatment temperature while avoiding an upregulation in expression of genes listed in Table 3.
5. The method according to claim 4, wherein the generating step is performed a plurality of times in one treatment cycle.
6. The method according to claim 5, wherein one or more treatment cycles are conducted across a treatment period.
7. The method according to claim 4, wherein a treatment cycle lasts about one minute.
8. The method according to claim 7, wherein a treatment cycle lasts between about 2 and about 6 minutes.
9. The method according to claim 6 wherein the treatment period is at least one week and comprises at least one treatment cycle.
10. The method according to claim 9, wherein the treatment period is between one week and 12 weeks.
11. The method according to claim 10, wherein the treatment period is between 3 and 8 weeks.
12. The method according to claim 11, wherein each week of the treatment period comprises between one and six treatment cycles.
13. The method according to claim 4 wherein the treatment temperature effectuates a skin surface temperature over the tissue volume of less than about 45°C.
14. The method according to claim 4 wherein the treatment temperature effectuates a skin surface temperature over the tissue volume of between about 37°C and about 43°C.
15. The method according to claim 4 further comprising: assessing the benefit by extracting mRNA
from a sample obtained from the tissue volume; and determining an expression profile of a gene panel consisting of at least one gene selected from Table 1 and/or Table 2 and at least one gene selected from Table 3, wherein an expression profile reflecting upregulation of genes selected from Tables 1 and/or 2 combined with substantially no change in expression of genes selected from Table 3 is indicative of a benefit being provided.
16. The method according to claim 15 further comprising optimizing the benefit by adjusting the treatment temperature in response to the expression profile wherein upregulation of the genes selected from Table 1 and/or Table 2 is maximized while expression of genes selected from Table 3 is maintained at substantially no change.
17. The method according to claim 5, wherein the benefit is maintained beyond the treatment period by one or more maintenance treatments, each maintenance treatment comprising at least one maintenance cycle.
18. A method for assessing treatment efficacy of an energy delivery device designed to provide a benefit to skin by heating the skin, the method comprising: treating the skin by application of the energy delivery device; extracting mRNA from a sample of the treated skin; and generating an expression profile for a gene panel according to claims 1 or 2.
19. A method of screening a facial skin treatment regimen for efficacy in providing a collagen and/or dermal remodeling benefit to mammalian skin without stimulating a skin-damaging inflammatory cytokine response, the method comprising: treating facial skin according to a treatment regimen;
extracting mRNA from a sample of the treated facial skin; generating a gene expression profile for a gene panel according to claims 1 or 2; comparing the gene expression profile to a reference profile; and determining that the facial treatment regimen is efficacious where the expression profile reflects upregulation of genes selected from Table 1 and/or Table 2 and a substantial lack of regulation of genes selected from Table 3.
20. The method according to claim 19, wherein the facial skin treatment regimen comprises generating a pulsed radio frequency current through a first tissue volume of the facial skin over a treatment cycle with a radio frequency current generating device.
21. The method according to claim 20, wherein the treatment regimen further comprises moving the radio frequency current generating device and generating a pulsed radio frequency current through a second tissue volume of the facial skin during the treatment cycle.
22. The method according to claim 19, wherein the facial skin comprises periauricular skin and the sample is obtained by biopsy of treated periauricular skin and the reference is obtained by biopsy of pre-treated or non-treated periauricular skin.
23. The method according to claim 22 wherein the pre-treated or non-treated periauricular reference skin comprises skin substantially adjacent to the treated periauricular skin.
24. The method according to claim 19, wherein genes selected from Table 1 demonstrate a statistically greater than one fold increase in expression over the reference.
25. The method according to claims 19 or 24, wherein genes selected from Table 2 demonstrate a statistically greater than one fold increase in expression over the reference.
26. The method according to claim 20, wherein the facial treatment regimen further comprises application of a cosmetic composition to the facial skin in conjunction with generating the pulsed radio frequency current.
27. The method of screening according to claim 26, wherein the method screens for compositions having an enhancing or potentiating effect on the gene expression profile.
28. The method according to claim 21, wherein the treatment regimen includes a plurality of treatment cycles across a treatment period and wherein a cycle comprises generating a pulsed radio frequency current through a tissue volume of the facial skin for a treatment time sufficient to heat the tissue volume to a treatment temperature.
29. The method according to claim 28 wherein a treatment cycle lasts for more than about 1 minute and effectuates a skin surface temperature over the tissue volume of less than about 45°C.
30. The method according to claim 28 wherein a treatment cycle lasts for between about 1 and 8 minutes and effectuates a skin surface temperature over the tissue volume of between about 37°C
and 43°C.
31. The method according to claim 28, wherein a treatment cycle lasts for between about 2 and 6 minutes.
32. The method according to claim 28, wherein between two and six treatment cycles are repeated during a week for at least one week.
33. The method according to claim 28, wherein between two and six treatment cycles are repeated during a week for between 3 and 8 weeks.
34. The method according to claim 20, wherein the device comprises at least two bi-polar electrodes which drive the current through the tissue volume when the electrodes are placed across a skin surface comprising the tissue volume and voltage is applied to the electrodes.
35. The methods according to claims 4 or 20 wherein the radio frequency current is driven through the tissue volume in the absence of electromagnetic radiation in the visible light or infrared frequencies of the electromagnetic spectrum and in the absence of supplemental monochromatic or polychromatic light sources directed toward the tissue volume.
36. A genetic signature of differentially expressed genes suitable for identifying a cosmetic skin benefit, the benefit comprising induction of collagen formation and/or dermal remodeling in a dermal layer of mammalian skin in the absence of a skin-damaging inflammatory cytokine response, the genetic signature comprising at least one gene selected from each of Table 1, Table 2, and Table 3.
CA2795671A 2010-04-19 2011-04-19 Genetic signatures and gene chips associated with administration of electrically conducted radio frequency current to skin and methods and treatments relating thereto Abandoned CA2795671A1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US32563310P 2010-04-19 2010-04-19
US61/325,633 2010-04-19
PCT/US2011/033033 WO2011133538A1 (en) 2010-04-19 2011-04-19 Genetic signatures and gene chips associated with administration of electrically conducted radio frequency current to skin and methods and treatments relating thereto

Publications (1)

Publication Number Publication Date
CA2795671A1 true CA2795671A1 (en) 2011-10-27

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CA2795671A Abandoned CA2795671A1 (en) 2010-04-19 2011-04-19 Genetic signatures and gene chips associated with administration of electrically conducted radio frequency current to skin and methods and treatments relating thereto

Country Status (8)

Country Link
EP (1) EP2561092A1 (en)
JP (1) JP2013527756A (en)
KR (1) KR20120137407A (en)
CN (1) CN102869789B (en)
BR (1) BR112012026870A2 (en)
CA (1) CA2795671A1 (en)
MX (1) MX2012012235A (en)
WO (1) WO2011133538A1 (en)

Families Citing this family (11)

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US9671410B2 (en) 2011-01-16 2017-06-06 The Procter & Gamble Company Biomarker-based methods for identifying and formulating compositions that improve skin quality and reduce the visible signs of aging in skin
WO2012135651A1 (en) 2011-03-31 2012-10-04 The Procter & Gamble Company Systems, models and methods for identifying and evaluating skin-active agents effective for treating dandruff/seborrheic dermatitis
US20130261024A1 (en) * 2012-03-30 2013-10-03 The Procter & Gamble Company System for Identifying Connections Between Perturbagens and Genes Associated with a Skin Hyperpigmentation Condition
US9920357B2 (en) 2012-06-06 2018-03-20 The Procter & Gamble Company Systems and methods for identifying cosmetic agents for hair/scalp care compositions
WO2014028569A1 (en) 2012-08-15 2014-02-20 The Procter & Gamble Company Systems, models and methods for identifying and evaluating skin-active agents effective for treating an array of skin disorders
US10966916B2 (en) 2014-11-10 2021-04-06 The Procter And Gamble Company Personal care compositions
MX376115B (en) 2014-11-10 2025-03-07 Procter & Gamble COMPOSITIONS FOR PERSONAL CARE WITH TWO BENEFICIAL PHASES.
CN107106429B (en) 2014-11-10 2021-06-29 宝洁公司 Personal care composition with two benefit phases
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CN113015904B (en) 2018-11-29 2024-06-18 宝洁公司 Methods for Screening Personal Care Products

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Also Published As

Publication number Publication date
KR20120137407A (en) 2012-12-20
JP2013527756A (en) 2013-07-04
BR112012026870A2 (en) 2017-01-10
EP2561092A1 (en) 2013-02-27
CN102869789A (en) 2013-01-09
MX2012012235A (en) 2012-11-23
CN102869789B (en) 2015-09-30
WO2011133538A1 (en) 2011-10-27

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Effective date: 20150609