The C19007T polymorphism of ERCC1 and its correlation with the risk of epithelial ovarian and endometrial cancer in Korean women

被引:15
作者
Jo, Hoenil
Kang, Sokbom
Kim, Sung Il
Kim, Jae Weon [1 ]
Park, Noh Hyun
Song, Yong Sang
Park, Sang-Yoon
Kang, Soon Beom
Lee, Hyo Pyo
机构
[1] Seoul Natl Univ, Dept Obstet & Gynecol, 28 Yungun Dong, Seoul 110744, South Korea
[2] Seoul Natl Univ, Canc Res Inst, Seoul 110744, South Korea
[3] Seoul Natl Univ, Human Genome Res Inst, Seoul, South Korea
[4] Natl Canc Ctr, Res Inst & Hosp, Goyang, Gyeonggi, South Korea
关键词
excision repair cross-complementing group 1; DNA repair gene; polymorphism; ovarian cancer; endometrial cancer;
D O I
10.1159/000100008
中图分类号
R71 [妇产科学];
学科分类号
100211 [妇产科学];
摘要
Background: Excision repair cross-complementing group 1 (ERCC1) is a major DNA repair protein. Recent studies have addressed the association between ERCC1 polymorphism and carcinogenesis. Methods: We investigated a polymorphism of ERCC1 at nucleotide 19007(C -> T, Asn118Asn) in 94 epithelial ovarian cancer patients, 102 endometrial cancer patients, and in 329 control subjects. Results: We observed no evidence of associations between the C19007T ERCC1 polymorphism and risk of epithelial ovarian or endometrial cancer, which had the same adjusted odds ratios of 0.91 (p = 0.711, 0.691 respectively). Conclusion: Our findings suggest that the C19007T ERCC1 polymorphism is unlikely to play an important role in epithelial ovarian or endometrial cancer in Korean women. Copyright (c) 2007 S. Karger AG, Basel.
引用
收藏
页码:84 / 88
页数:5
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