Tumour-specific distribution of BRCA1 promoter region methylation supports a pathogenetic role in breast and ovarian cancer

被引:97
作者
Bianco, T
Chenevix-Trench, G
Walsh, DCA
Cooper, JE
Dobrovic, A [1 ]
机构
[1] Univ Adelaide, Dept Haematol Oncol, Adelaide, SA 5005, Australia
[2] Univ Adelaide, Dept Med, Adelaide, SA 5005, Australia
[3] Univ Adelaide, Dept Surg, Adelaide, SA 5005, Australia
[4] Queen Elizabeth Hosp, Dept Histopathol, Woodville, SA 5011, Australia
[5] Queensland Inst Med Res, Herston, Qld 4029, Australia
[6] Univ Queensland, Royal Brisbane Hosp, Herston, Qld 4029, Australia
关键词
D O I
10.1093/carcin/21.2.147
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The role of BRCA1 in sporadic breast and ovarian cancers remains elusive, Direct involvement of BRCA1 in the development of breast and ovarian cancer is suggested by the finding that the BRCA1 promoter region CpG island is methylated in a proportion of breast and ovarian cancers. The aim of this study was to compare the incidence of BRCA1 promoter region methylation in tumours in which loss of BRCA1 has been shown to play a role in pathogenesis (breast and ovarian carcinomas) with the incidence in tumours in which BRCA1 is unlikely to play a role in pathogenesis. Promoter region hypermethylation was significantly more common (P < 0.008) in breast and ovarian cancer (6/38 tumours methylated) than in colon cancer (0/35 tumours methylated) or in leukaemias (0/19 samples methylated). The restriction of BRCA1 promoter region hypermethylation to breast and ovarian cancer is consistent with a pathogenetic role of BRCA1 promoter methylation in these tumours, We suggest that the rarity of observed BRCA1 mutations in sporadic breast and ovarian cancer is due to the greater likelihood of BRCA1 inactivation by non-mutational mechanisms such :ts methylation.
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页码:147 / 151
页数:5
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