BRCA2 Arg372His polymorphism and epithelial ovarian cancer risk

被引:35
作者
Auranen, A
Spurdle, AB
Chen, XQ
Lipscombe, J
Purdie, DM
Hopper, JL
Green, A
Healey, CS
Redman, K
Dunning, AM
Pharoah, PD
Easton, DF
Ponder, BAJ
Chenevix-Trench, G
Novik, KL
机构
[1] Strangeways Res Lab, CRC Dept Oncol, Cambridge CB1 4RN, England
[2] Queensland Inst Med Res, Canc & Cell Biol Div, Brisbane, Qld 4006, Australia
[3] Univ Queensland, Brisbane, Qld, Australia
[4] Strangeways Res Lab, CRC Genet Epidemiol Unit, Cambridge CB1 4RN, England
[5] Queensland Inst Med Res, Populat & Clin Sci Div, Brisbane, Qld 4006, Australia
[6] Univ Melbourne, Ctr Genet Epidemiol, Carlton, Vic 3053, Australia
关键词
BRCA2; polymorphism; ovarian cancer;
D O I
10.1002/ijc.10814
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The BRCA2 372 HH genotype defined by the BRCA2 N372H nonconservative amino acid substitution polymorphism was recently reported to be associated with a small increased risk of breast cancer. We investigated whether this polymorphism was associated with ovarian cancer risk by conducting British and Australian case-control comparisons in Para e including a total sample of 1,121 ovarian cancer cases an 2,643 controls. There was no difference in genotype frequency between control groups from the 2 studies (p=0.9). The HH genotype was associated with an increased risk of ovarian cancer in both studies, and the risk estimate for the pooled studies was 1.36 (95% CI 1.04-1.77, p=0.03). There was also a suggestion that this risk may be greater for ovarian cancers of the serous subtype for both studies, with an OR (95% CI) of 1.66 (1.17-2.54) for the 2 studies combined (p=0.005). The BRCA2 372 HH genotype appears to be associated with an increased risk of ovarian cancer of a similar magnitude to that reported for breast cancer. (C) 2002 Wiley-Liss, Inc.
引用
收藏
页码:427 / 430
页数:4
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