ATM mutations that cause ataxia-telangiectasia are breast cancer susceptibility alleles

被引:542
作者
Renwick, Anthony
Thompson, Deborah
Seal, Sheila
Kelly, Patrick
Chagtai, Tasnim
Ahmed, Munaza
North, Bernard
Jayatilake, Hiran
Barfoot, Rita
Spanova, Katarina
McGuffog, Lesley
Evans, D. Gareth
Eccles, Diana
Easton, Douglas F.
Stratton, Michael R.
Rahman, Nazneen
机构
[1] Inst Canc Res, Sect Canc Genet, Sutton SM2 5NG, Surrey, England
[2] Univ Cambridge, Canc Res UK, Genet Epidemiol Unit, Strangeways Res Labs, Cambridge CB1 8RN, England
[3] St Marys Hosp, Dept Med Genet, Manchester M13 0JH, Lancs, England
[4] Princess Anne Hosp, Wessex Clin Genet Serv, Southampton SO16 6YA, Hants, England
[5] Wellcome Trust Sanger Inst, Canc Genome Project, Cambridge CB10 1SA, England
基金
英国医学研究理事会; 英国惠康基金;
关键词
D O I
10.1038/ng1837
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We screened individuals from 443 familial breast cancer pedigrees and 521 controls for ATM sequence variants and identified 12 mutations in affected individuals and two in controls (P = 0.0047). The results demonstrate that ATM mutations that cause ataxia-telangiectasia in biallelic carriers are breast cancer susceptibility alleles in monoallelic carriers, with an estimated relative risk of 2.37 (95% confidence interval (c.i.) = 1.51 - 3.78, P = 0.0003). There was no evidence that other classes of ATM variant confer a risk of breast cancer.
引用
收藏
页码:873 / 875
页数:3
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