Genetic Variation an CYP19A1 and Risk of Breast Cancer and Fibrocystic Breast Conditions among Women in Shanghai, China

被引:10
|
作者
Chen, Chu [1 ,5 ,7 ]
Sakoda, Lori C. [1 ,5 ]
Doherty, Jennifer A. [1 ]
Loomis, Melissa M. [1 ]
Fish, Sherianne [1 ]
Ray, Roberta M. [1 ]
Lin, Ming Gang [2 ,4 ]
Fan, Wenhong [3 ]
Zhao, Lue Ping [3 ,6 ]
Gao, Dao Li [8 ]
Stalsberg, Helge [9 ]
Feng, Ziding [3 ,6 ]
Thomas, David B. [1 ,5 ]
机构
[1] Fred Hutchinson Canc Res Ctr, Div Publ Hlth Sci, Program Epidemiol, Seattle, WA 98109 USA
[2] Fred Hutchinson Canc Res Ctr, Div Publ Hlth Sci, Program Canc Biol, Seattle, WA 98109 USA
[3] Fred Hutchinson Canc Res Ctr, Div Publ Hlth Sci, Program Biostat, Seattle, WA 98109 USA
[4] Fred Hutchinson Canc Res Ctr, Div Human Biol, Seattle, WA 98109 USA
[5] Univ Washington, Sch Publ Hlth & Community Med, Dept Epidemiol, Seattle, WA 98195 USA
[6] Univ Washington, Sch Publ Hlth & Community Med, Dept Biostat, Seattle, WA 98195 USA
[7] Univ Washington, Dept Otolaryngol Head & Neck Surg, Sch Med, Seattle, WA 98195 USA
[8] Fudan Univ, Zhongshan Hosp Canc Ctr, Dept Epidemiol, Shanghai 200433, Peoples R China
[9] Univ Tromso, Inst Med Biol, Tromso, Norway
基金
美国国家卫生研究院;
关键词
D O I
10.1158/1055-9965.EPI-08-0517
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
CYP19A1 encodes for aromatase, which irreversibly converts androgens to estrogens; variation in this gene may affect individual susceptibility to breast cancer and other sex hormone-dependent outcomes. In a case-control study nested within a breast self-examination trial conducted in China, we examined whether CYP19A1 polymorphisms (rs7870049, rs1004982, rs28566535, rs936306, rs11636639, rs767199, rs4775936, rs11575899, rs10046, and rs4646) were associated with risk of breast cancer and fibrocystic breast conditions. Cases were diagnosed with breast cancer (n = 614) or fibrocystic breast conditions (n = 465) during 1989 to 2000. Controls were free of breast disease during the same period (n = 879). Presence of proliferative changes within the extratumoral tissue of women with breast cancer and the lesions of women with fibrocystic conditions only was assessed. None of the polymorphisms were associated with overall risk of breast cancer or fibrocystic breast conditions. Differences in breast cancer risk, however, were observed by proliferation status. The risk of breast cancer with (but not without) proliferative fibrocystic conditions was increased among women homozygous for the minor allele of rs1004982 (C), rs28566535 (C), rs936306 (T), and rs4775936 (C) relative to those homozygous for the major allele [age-adjusted odds ratios (95% confidence intervals), 2.19 (1.24-3.85), 2.20 (1.27-3.82), 1.94 (1.13-3.30), and 1.95 (1.07-3.58), respectively]. Also, haplotypes inferred using all polymorphisms were not associated with overall risk of either outcome, although some block-specific haplotypes were associated with an increased risk of breast cancer with concurrent proliferative fibrocystic conditions. Our findings suggest that CYP19A1 variation may enhance breast cancer development in some women, but further confirmation is warranted. (Cancer Epidemiol Biomarkers Prev 2008;17(12):3457-66)
引用
收藏
页码:3457 / 3466
页数:10
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