WO2009074364A1 - Nouveau marqueur pronostique du cancer du sein - Google Patents
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- WO2009074364A1 WO2009074364A1 PCT/EP2008/063062 EP2008063062W WO2009074364A1 WO 2009074364 A1 WO2009074364 A1 WO 2009074364A1 EP 2008063062 W EP2008063062 W EP 2008063062W WO 2009074364 A1 WO2009074364 A1 WO 2009074364A1
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- dkk3
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- breast cancer
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- C12Q—MEASURING 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
- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
- C12Q1/6876—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes
- C12Q1/6883—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material
- C12Q1/6886—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material for cancer
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- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
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- C12Q2600/00—Oligonucleotides characterized by their use
- C12Q2600/106—Pharmacogenomics, i.e. genetic variability in individual responses to drugs and drug metabolism
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- C12Q2600/00—Oligonucleotides characterized by their use
- C12Q2600/118—Prognosis of disease development
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING 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
- C12Q2600/00—Oligonucleotides characterized by their use
- C12Q2600/154—Methylation markers
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- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING 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
- C12Q2600/00—Oligonucleotides characterized by their use
- C12Q2600/16—Primer sets for multiplex assays
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N2800/00—Detection or diagnosis of diseases
- G01N2800/52—Predicting or monitoring the response to treatment, e.g. for selection of therapy based on assay results in personalised medicine; Prognosis
Definitions
- breast cancer Many factors contribute to the pathogenesis of breast cancer. These factors include family history, nutrition, age, and epigenetic changes including DNA methylation. About 5 to 10% of breast cancer cases are due to inherited, mutated genes (BRCAl, BRCA2). The majority (90%) of breast cancers are due to genetic abnormalities that happen as a result of the aging process and life in general.
- the present invention further provides a method for the diagnosis and/or prognosis of breast cancer by detecting epigenetic silencing of the DKK3 gene in a test sample, wherein the epigenetic silencing indicates breast cancer or predisposition to breast cancer.
- methylation profile or "methylation status,” when used herein to describe the state of methylation of a genomic sequence, refers to the characteristics of a DNA segment at a particular genomic locus relevant to methylation, i.e. at particular CpG dinucleotides in a CpG island. Such characteristics include, but are not limited to, whether any of the cytosine (C) residues within this DNA sequence are methylated, location of methylated C residue(s), percentage of methylated C at any particular stretch of residues, and allelic differences in methylation due to, e.g., difference in the origin of the alleles.
- methylation profile or “methylation status” also refers to the relative or absolute concentration of methylated C or unmethylated C at any particular stretch of residues in a test sample.
- the methylation status of the differentially methylated CpG islands can provide a variety of information about the disease of breast cancer. It can be used to diagnose breast (pre)cancer in the individual. Alternatively, it can be used to predict the course of the disease in the individual or to predict the susceptibility to the disease, or to stage the progression of the disease in the individual. Importantly, it can help to predict the likelihood of overall survival, cause-specific survival, disease-free survival, or predict the likelihood of reoccurrence of breast cancer, and determine the effectiveness of a treatment course undergone by the individual. Increase or decrease of methylation levels in comparison with a reference level, and alterations in the increased/decreased detected levels provide valuable prognostic and diagnostic information.
- the method of selecting a suitable treatment for breast (pre)cancer involves as well the discrimination between potential drugs, in the sense that a drug selected from a DNA demethylating agent, a DNA methyltransferase inhibitor, a HDAC inhibitor, and a combination thereof, is contra-indicated for treatment if increased expression of the DKK3 gene, and/or reduced or no methylation of the DKK3 gene, of a region thereof, or of a regulatory region thereof, is detected.
- MSP Bisulphite-modification and methylation-specific PCR
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- General Health & Medical Sciences (AREA)
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
Abstract
L'invention concerne le silençage épigénétique du gène DKK3 dans les cancers du sein, ainsi que les utilisations de ce marqueur dans le diagnostic et le pronostic du cancer du sein et dans le choix de traitements thérapeutiques appropriés.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US1357307P | 2007-12-13 | 2007-12-13 | |
US61/013,573 | 2007-12-13 |
Publications (2)
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WO2009074364A1 true WO2009074364A1 (fr) | 2009-06-18 |
WO2009074364A8 WO2009074364A8 (fr) | 2009-08-13 |
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PCT/EP2008/063062 WO2009074364A1 (fr) | 2007-12-13 | 2008-09-30 | Nouveau marqueur pronostique du cancer du sein |
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WO (1) | WO2009074364A1 (fr) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP3162899A1 (fr) * | 2015-10-29 | 2017-05-03 | Rheinisch-Westfälische Technische Hochschule (RWTH) Aachen | Biomarqueur pour le cancer du sein |
US9856301B2 (en) * | 2012-03-26 | 2018-01-02 | University Of Massachusetts | Anti-tumor properties of Dickkopf 3b |
WO2024216112A1 (fr) * | 2023-04-12 | 2024-10-17 | Guardant Health, Inc. | Détection de méthylation du promoteur |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20020183388A1 (en) * | 2001-02-01 | 2002-12-05 | Gudas Lorraine J. | Use of retinoids plus histone deacetylase inhibitors to inhibit the growth of solid tumors |
WO2005027712A2 (fr) * | 2003-05-30 | 2005-03-31 | Temple University - Of The Commonwealth System Of Higher Education | Methodes de diagnostic, pronostic et de traitement du cancer du sein |
WO2005111232A2 (fr) * | 2004-05-17 | 2005-11-24 | MAX-PLANCK-Gesellschaft zur Förderung der Wissenschaften e.V. | Extinction de genes supresseurs de tumeur par methylation cpg dans un cancer de la prostate |
WO2006008128A2 (fr) * | 2004-07-18 | 2006-01-26 | Epigenomics Ag | Methodes epigenetiques et acides nucleiques permettant de deceler des troubles proliferatifs des cellules du sein |
-
2008
- 2008-09-30 WO PCT/EP2008/063062 patent/WO2009074364A1/fr active Application Filing
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20020183388A1 (en) * | 2001-02-01 | 2002-12-05 | Gudas Lorraine J. | Use of retinoids plus histone deacetylase inhibitors to inhibit the growth of solid tumors |
WO2005027712A2 (fr) * | 2003-05-30 | 2005-03-31 | Temple University - Of The Commonwealth System Of Higher Education | Methodes de diagnostic, pronostic et de traitement du cancer du sein |
WO2005111232A2 (fr) * | 2004-05-17 | 2005-11-24 | MAX-PLANCK-Gesellschaft zur Förderung der Wissenschaften e.V. | Extinction de genes supresseurs de tumeur par methylation cpg dans un cancer de la prostate |
WO2006008128A2 (fr) * | 2004-07-18 | 2006-01-26 | Epigenomics Ag | Methodes epigenetiques et acides nucleiques permettant de deceler des troubles proliferatifs des cellules du sein |
Non-Patent Citations (2)
Title |
---|
DATABASE Geneseq [online] 23 March 2006 (2006-03-23), "Human genomic DNA #24.", XP002515110, retrieved from EBI accession no. GSN:AEF55043 Database accession no. AEF55043 * |
VEECK JÜRGEN ET AL: "Wnt signalling in human breast cancer: expression of the putative Wnt inhibitor Dickkopf-3 (DKK3) is frequently suppressed by promoter hypermethylation in mammary tumours.", BREAST CANCER RESEARCH : BCR 2008, vol. 10, no. 5, 30 September 2008 (2008-09-30), pages R82, XP002515109, ISSN: 1465-542X * |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9856301B2 (en) * | 2012-03-26 | 2018-01-02 | University Of Massachusetts | Anti-tumor properties of Dickkopf 3b |
US11421008B2 (en) | 2012-03-26 | 2022-08-23 | University Of Massachusetts | Anti-tumor properties of Dickkopf 3b |
EP3162899A1 (fr) * | 2015-10-29 | 2017-05-03 | Rheinisch-Westfälische Technische Hochschule (RWTH) Aachen | Biomarqueur pour le cancer du sein |
WO2017072292A1 (fr) * | 2015-10-29 | 2017-05-04 | Rheinisch-Westfälische Technische Hochschule (Rwth) Aachen | Biomarqueur pour le cancer du sein |
WO2024216112A1 (fr) * | 2023-04-12 | 2024-10-17 | Guardant Health, Inc. | Détection de méthylation du promoteur |
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