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Erschienen in: Breast Cancer Research and Treatment 1/2009

01.07.2009 | Epidemiology

Promoter methylation patterns of ATM, ATR, BRCA1, BRCA2 and P53 as putative cancer risk modifiers in Jewish BRCA1/BRCA2 mutation carriers

verfasst von: Tair Kontorovich, Yoram Cohen, Uri Nir, Eitan Friedman

Erschienen in: Breast Cancer Research and Treatment | Ausgabe 1/2009

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Abstract

BRCA1/BRCA2 germline mutations substantially increase breast and ovarian cancer risk, yet penetrance is incomplete. We hypothesized that germline epigenetic gene silencing may affect mutant BRCA1/2 penetrance. To test this notion, we determined the methylation status, using methylation-specific quantitative PCR of the promoter in putative modifier genes: BRCA1, BRCA2, ATM, ATR and P53 in Jewish BRCA1/BRCA2 mutation carriers with (n = 41) or without (n = 48) breast cancer, in sporadic breast cancer (n = 52), and healthy controls (n = 89). Promoter hypermethylation was detected only in the BRCA1 promotor in 5.6–7.3% in each of the four subsets of participants, regardless of health and BRCA1/2 status.Germline promoter hypermethylation in the BRCA1 gene can be detected in about 5% of the female Israeli Jewish population, regardless of the BRCA1/2 status. The significance of this observation is yet to be determined.
Literatur
1.
Zurück zum Zitat Wacholder S, Struewing JP, Hartge P, Greene MH, Tucker MA (2004) Breast cancer risks for BRCA1/2 carriers. Science 306:2187–2191PubMed Wacholder S, Struewing JP, Hartge P, Greene MH, Tucker MA (2004) Breast cancer risks for BRCA1/2 carriers. Science 306:2187–2191PubMed
2.
Zurück zum Zitat Robles-Diaz L, Goldfrank JD, Kauff ND, Robson M, Offit K (2004) Hereditary ovarian cancer in Ashkenazi Jews. Fam Cancer 3:259–264PubMedCrossRef Robles-Diaz L, Goldfrank JD, Kauff ND, Robson M, Offit K (2004) Hereditary ovarian cancer in Ashkenazi Jews. Fam Cancer 3:259–264PubMedCrossRef
3.
Zurück zum Zitat Easton DF, Ford D, Bishop DT (1995) Breast and ovarian cancer incidence in BRCA1 mutation carriers Breast Cancer Linkage Consortium. Am J Hum Genet 56:265–271PubMed Easton DF, Ford D, Bishop DT (1995) Breast and ovarian cancer incidence in BRCA1 mutation carriers Breast Cancer Linkage Consortium. Am J Hum Genet 56:265–271PubMed
4.
Zurück zum Zitat Narod SA, Goldgar D, Cannon-Albright L, Weber BL, Moslehi R, Ives E, Lenoir G, Lynch H (1995) Risk modifiers in carriers of BRCA1 mutations. Int J Cancer 64:394–398PubMedCrossRef Narod SA, Goldgar D, Cannon-Albright L, Weber BL, Moslehi R, Ives E, Lenoir G, Lynch H (1995) Risk modifiers in carriers of BRCA1 mutations. Int J Cancer 64:394–398PubMedCrossRef
5.
Zurück zum Zitat Ford D, Easton DF, Stratton M, Narod S et al (1998) Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families. Am J Hum Genet 62:676–689PubMedCrossRef Ford D, Easton DF, Stratton M, Narod S et al (1998) Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families. Am J Hum Genet 62:676–689PubMedCrossRef
6.
Zurück zum Zitat Wylie B, Melissa AA (2002) Genetic risk in context: calculating the penetrance of BRCA1 and BRCA2 mutations. J Natl Cancer Inst 94:1185–1187 Wylie B, Melissa AA (2002) Genetic risk in context: calculating the penetrance of BRCA1 and BRCA2 mutations. J Natl Cancer Inst 94:1185–1187
7.
Zurück zum Zitat Begg CB (2002) On the use of familial aggregation in population-based case probands for calculating penentrance. J Natl Cancer Inst 94:1221–1226PubMed Begg CB (2002) On the use of familial aggregation in population-based case probands for calculating penentrance. J Natl Cancer Inst 94:1221–1226PubMed
8.
Zurück zum Zitat Kenneth O (2006) BRCA mutation frequency and penetrance: new data, old debate. J Natl Cancer Inst 98:1675–1677CrossRef Kenneth O (2006) BRCA mutation frequency and penetrance: new data, old debate. J Natl Cancer Inst 98:1675–1677CrossRef
9.
Zurück zum Zitat Narod SA (2006) Modifiers of risk of hereditary breast cancer. Oncogene 25:832–5836CrossRef Narod SA (2006) Modifiers of risk of hereditary breast cancer. Oncogene 25:832–5836CrossRef
10.
Zurück zum Zitat Levy-Lahad E, Friedman E (2007) Cancer risks among BRCA1 and BRCA2 mutation carriers. Br J Cancer 96:11–15PubMedCrossRef Levy-Lahad E, Friedman E (2007) Cancer risks among BRCA1 and BRCA2 mutation carriers. Br J Cancer 96:11–15PubMedCrossRef
11.
Zurück zum Zitat Antoniou AC, Sinilnikova OM, Simard J, Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA) (2007) RAD51 135G→C modifies breast cancer risk among BRCA2 mutation carriers: results from a combined analysis of 19 studies. Am J Hum Genet 81:1186–1200PubMedCrossRef Antoniou AC, Sinilnikova OM, Simard J, Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA) (2007) RAD51 135G→C modifies breast cancer risk among BRCA2 mutation carriers: results from a combined analysis of 19 studies. Am J Hum Genet 81:1186–1200PubMedCrossRef
12.
Zurück zum Zitat Baylin SB, Chen WY (2005) Aberrant gene silencing in tumor progression: implications for control of cancer. Cold Spring Harb Symp Quant Biol 70:427–433PubMedCrossRef Baylin SB, Chen WY (2005) Aberrant gene silencing in tumor progression: implications for control of cancer. Cold Spring Harb Symp Quant Biol 70:427–433PubMedCrossRef
13.
Zurück zum Zitat Bastian PJ, Yegnasubramanian S, Palapattu G, Rogers C, Lin X, Marzo AD, Nelson W (2004) Molecular biomarker in prostate cancer: the role of CpG island hypermethylation. Eur Urol 46:698–708PubMedCrossRef Bastian PJ, Yegnasubramanian S, Palapattu G, Rogers C, Lin X, Marzo AD, Nelson W (2004) Molecular biomarker in prostate cancer: the role of CpG island hypermethylation. Eur Urol 46:698–708PubMedCrossRef
14.
Zurück zum Zitat Feinberg AP (2001) Cancer epigenetics takes center stage. Proc Natl Acad Sci U S A 98:392–394PubMedCrossRef Feinberg AP (2001) Cancer epigenetics takes center stage. Proc Natl Acad Sci U S A 98:392–394PubMedCrossRef
15.
Zurück zum Zitat Baylin SB, Esteller M, Rountree MR, Bachman KE, Schuebel K, Herman JG (2001) Aberrant patterns of DNA methylation, chromatin formation and gene expression in cancer. Hum Mol Genet 10:687–692PubMedCrossRef Baylin SB, Esteller M, Rountree MR, Bachman KE, Schuebel K, Herman JG (2001) Aberrant patterns of DNA methylation, chromatin formation and gene expression in cancer. Hum Mol Genet 10:687–692PubMedCrossRef
17.
Zurück zum Zitat Attwood JT, Yung RL, Richardson BC (2002) DNA methylation and the regulation of gene transcription. Cell Mol Life Sci 59:241–257PubMedCrossRef Attwood JT, Yung RL, Richardson BC (2002) DNA methylation and the regulation of gene transcription. Cell Mol Life Sci 59:241–257PubMedCrossRef
18.
Zurück zum Zitat Jones PA, Baylin SB (2002) The fundamental role of epigenetic events in cancer. Nat Rev Genet 3:415–428PubMedCrossRef Jones PA, Baylin SB (2002) The fundamental role of epigenetic events in cancer. Nat Rev Genet 3:415–428PubMedCrossRef
19.
Zurück zum Zitat Herman JG, Baylin SB (2003) Gene silencing in cancer in association with promoter hypermethylation. N Engl J Med 349:2042–2054PubMedCrossRef Herman JG, Baylin SB (2003) Gene silencing in cancer in association with promoter hypermethylation. N Engl J Med 349:2042–2054PubMedCrossRef
20.
Zurück zum Zitat Bird A, Taggart M, Frommer M, Miller OJ, Macleod D (1985) A fraction of the mouse genome that is derived from islands of nonmethylated, CpG-rich DNA. Cell 40:91–99PubMedCrossRef Bird A, Taggart M, Frommer M, Miller OJ, Macleod D (1985) A fraction of the mouse genome that is derived from islands of nonmethylated, CpG-rich DNA. Cell 40:91–99PubMedCrossRef
21.
Zurück zum Zitat Dobrovic A, Simpfendorfer D (1997) Methylation of the BRCA1 gene in sporadic breast cancer. Cancer Res 57:3347–3350PubMed Dobrovic A, Simpfendorfer D (1997) Methylation of the BRCA1 gene in sporadic breast cancer. Cancer Res 57:3347–3350PubMed
22.
Zurück zum Zitat Suter CM, Martin DI, Ward RL (2004) Germline epimutation of MLH1 in individuals with multiple cancers. Nat Genet 36:497–501PubMedCrossRef Suter CM, Martin DI, Ward RL (2004) Germline epimutation of MLH1 in individuals with multiple cancers. Nat Genet 36:497–501PubMedCrossRef
23.
Zurück zum Zitat Chan TL, Yuen ST, Kong CK, Chan YW, Chan AS, Ng WF, Tsui WY, Lo MW, Tam WY, Li WY, Leung SY (2006) Heritable germline epimutation of MSH2 in a family with hereditary nonpolyposis colorectal cancer. Nat Genet 38:1178–1183PubMedCrossRef Chan TL, Yuen ST, Kong CK, Chan YW, Chan AS, Ng WF, Tsui WY, Lo MW, Tam WY, Li WY, Leung SY (2006) Heritable germline epimutation of MSH2 in a family with hereditary nonpolyposis colorectal cancer. Nat Genet 38:1178–1183PubMedCrossRef
24.
Zurück zum Zitat Weisenberger DJ, Siegmund DK, Campan M et al (2006) CpG island methylator phenotype underlies sporadic microsatellite instability and is tightly associated with BRAF mutation in colorectal cancer. Nat Genet 38:787–793PubMedCrossRef Weisenberger DJ, Siegmund DK, Campan M et al (2006) CpG island methylator phenotype underlies sporadic microsatellite instability and is tightly associated with BRAF mutation in colorectal cancer. Nat Genet 38:787–793PubMedCrossRef
25.
Zurück zum Zitat Chan KY, Ozçelik H, Cheung AN, Ngan HY, Khoo US (2002) Epigenetic Factors Controlling the BRCA1 and BRCA2 Genes in Sporadic Ovarian Cancer. Cancer Res 62:4151–4156PubMed Chan KY, Ozçelik H, Cheung AN, Ngan HY, Khoo US (2002) Epigenetic Factors Controlling the BRCA1 and BRCA2 Genes in Sporadic Ovarian Cancer. Cancer Res 62:4151–4156PubMed
26.
Zurück zum Zitat Kang JH, Kim SJ, Noh D, Park IA, Choe KJ, Yoo OJ, Kang H (2001) Methylation in the p53 promoter is a supplementary route to breast carcinogenesis: correlation between CpG methylation in the p53 promoter and the mutation of the p53 gene in the progression from ductal carcinoma in situ to invasive ductal carcinoma. Lab Invest 81:573–579PubMed Kang JH, Kim SJ, Noh D, Park IA, Choe KJ, Yoo OJ, Kang H (2001) Methylation in the p53 promoter is a supplementary route to breast carcinogenesis: correlation between CpG methylation in the p53 promoter and the mutation of the p53 gene in the progression from ductal carcinoma in situ to invasive ductal carcinoma. Lab Invest 81:573–579PubMed
27.
Zurück zum Zitat Treilleux I, Chapot B, Goddard S, Pisani P, Ange`le S, Hall J (2007) The molecular causes of low ATM protein expression in breast carcinoma; promoter methylation and levels of the catalytic subunit of DNA-dependent protein kinase. Histopathology 51:63–69PubMedCrossRef Treilleux I, Chapot B, Goddard S, Pisani P, Ange`le S, Hall J (2007) The molecular causes of low ATM protein expression in breast carcinoma; promoter methylation and levels of the catalytic subunit of DNA-dependent protein kinase. Histopathology 51:63–69PubMedCrossRef
28.
Zurück zum Zitat Wei M, Grushko TA, Dignam J, Hagos F, Nanda R, Sveen L, Xu J, Fackenthal J, Tretiakova M, Das S, Olopade OI (2005) BRCA1 Promoter Methylation in Sporadic Breast Cancer Is Associated with Reduced BRCA1 Copy Number and Chromosome 17 Aneusomy. Cancer Res 65:10692–10699PubMedCrossRef Wei M, Grushko TA, Dignam J, Hagos F, Nanda R, Sveen L, Xu J, Fackenthal J, Tretiakova M, Das S, Olopade OI (2005) BRCA1 Promoter Methylation in Sporadic Breast Cancer Is Associated with Reduced BRCA1 Copy Number and Chromosome 17 Aneusomy. Cancer Res 65:10692–10699PubMedCrossRef
29.
Zurück zum Zitat Snell C, Krypuy M, Wong EM, kConFab investigators, Loughrey MB, Dobrovic A (2008) BRCA1 promoter methylation in peripheral blood DNA of mutation negative familial breast cancer patients with a BRCA1 tumour phenotype. Breast Cancer Res 10:R12PubMedCrossRef Snell C, Krypuy M, Wong EM, kConFab investigators, Loughrey MB, Dobrovic A (2008) BRCA1 promoter methylation in peripheral blood DNA of mutation negative familial breast cancer patients with a BRCA1 tumour phenotype. Breast Cancer Res 10:R12PubMedCrossRef
30.
Zurück zum Zitat Chen Y, Amanda E, McLennan TJ, Fridlyand J, Crawford B, Costello JF, John LZ (2006) Lack of germ-line promoter methylation in BRCA1-negative families with familial breast cancer. Genet Test 10:281–284PubMedCrossRef Chen Y, Amanda E, McLennan TJ, Fridlyand J, Crawford B, Costello JF, John LZ (2006) Lack of germ-line promoter methylation in BRCA1-negative families with familial breast cancer. Genet Test 10:281–284PubMedCrossRef
Metadaten
Titel
Promoter methylation patterns of ATM, ATR, BRCA1, BRCA2 and P53 as putative cancer risk modifiers in Jewish BRCA1/BRCA2 mutation carriers
verfasst von
Tair Kontorovich
Yoram Cohen
Uri Nir
Eitan Friedman
Publikationsdatum
01.07.2009
Verlag
Springer US
Erschienen in
Breast Cancer Research and Treatment / Ausgabe 1/2009
Print ISSN: 0167-6806
Elektronische ISSN: 1573-7217
DOI
https://doi.org/10.1007/s10549-008-0121-3

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