ATM variants 7271T>G and IVS10-6T>G among women with unilateral and bilateral breast cancer

被引:38
作者
Bernstein, JL
Bernstein, L
Thompson, WD
Lynch, CF
Malone, KE
Teitelbaum, SL
Olsen, JH
Anton-Culver, H
Boice, JD
Rosenstein, BS
Borresen-Dale, AL
Gatti, RA
Concannon, P
Haile, RW
机构
[1] CUNY Mt Sinai Sch Med, Dept Community & Prevent Med, New York, NY 10029 USA
[2] Univ So Calif, Los Angeles, CA 90033 USA
[3] Univ So Maine, Portland, ME 04104 USA
[4] Univ Iowa, Dept Epidemiol, Iowa City, IA 52242 USA
[5] Fred Hutchinson Canc Res Ctr, Seattle, WA 98109 USA
[6] Danish Canc Soc, DK-2100 Copenhagen, Denmark
[7] Univ Calif Irvine, Irvine, CA 92697 USA
[8] Int Epidemiol Inst, Rockville, MD 20850 USA
[9] Vanderbilt Univ, Nashville, TN 37235 USA
[10] Norwegian Radium Hosp, N-0310 Oslo, Norway
[11] Univ Calif Los Angeles, Los Angeles, CA 90095 USA
[12] Virginia Mason Res Ctr, Seattle, WA 98101 USA
关键词
ATM gene screening; 7271T > G mutation; IVS10-6T > G mutation; breast cancer; bilateral breast cancer;
D O I
10.1038/sj.bjc.6601289
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Recent reports suggest that two ATM gene mutations, 7271T>G and IVS10-6T>G, are associated with a high risk of breast cancer among multiple-case families. To assess the importance of these two mutations in another 'high-risk' group, young women ( under age 51) with multiple primaries, we screened a large population-based series of young women with bilateral breast cancer and compared the frequency of these mutations among similar women diagnosed with unilateral breast cancer. The 1149 women included were enrolled in an ongoing population-based case - control study of the genetic factors that contribute to bilateral breast cancer; they were not selected on the basis of family history of cancer. Screening for 7271T>G and IVS10-6T>G ATM gene mutations was conducted using DHPLC followed by direct sequencing. The 7271T>G mutation was detected in one out of 638 (0.2%) women with unilateral breast cancer and in none of the bilateral cases, and the IVS10-6T>G mutation in one out of 511 ( 0.2%) bilateral and in eight out of 638 (1.3%) unilateral breast cancer cases. Carriers of either mutation were not limited to women with a family history. Given the likelihood that young women with bilateral breast cancer have a genetic predisposition, the observed mutation distribution is contrary to that expected if these two mutations were to play an important role in breast carcinogenesis among individuals at high risk.
引用
收藏
页码:1513 / 1516
页数:4
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