Association of a progesterone receptor gene+331 G/A polymorphism with breast cancer risk: a meta-analysis

被引:7
|
作者
Yang, Dae Sik [2 ]
Sung, Hwa Jung [1 ]
Woo, Ok Hee [3 ]
Park, Kyong Hwa [1 ]
Wood, Sang Uk [4 ]
Kim, Ae-Ree [5 ]
Lee, Eun Sook [4 ]
Lee, Jae-Bok [4 ]
Kim, Yeul Hong [1 ]
Kim, Jun Suk [1 ]
Seo, Jae Hong [1 ]
机构
[1] Korea Univ, Coll Med, Dept Internal Med, Div Med Oncol, Seoul 136705, South Korea
[2] Korea Univ, Coll Med, Dept Radiat Oncol, Seoul 136705, South Korea
[3] Korea Univ, Coll Med, Dept Radiol, Seoul 136705, South Korea
[4] Korea Univ, Coll Med, Dept Surg, Seoul 136705, South Korea
[5] Korea Univ, Coll Med, Dept Pathol, Seoul 136705, South Korea
关键词
OVARIAN-CANCER; FUNCTIONAL POLYMORPHISM; MICE LACKING; B ISOFORM; ESTROGEN; TRANSLATION; INITIATION; PROMOTER; EVENT;
D O I
10.1016/j.cancergencyto.2009.10.005
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Published studies on the association between the progesterone receptor gene +331 G/A polymorphism and breast cancer risk are inconclusive, and meta-analysis is required to verify the association. Six studies, including a total of 6,849 cases and 6,589 controls, were subjected to meta-analysis. When all eligible subjects were pooled for meta-analysis, the AG + AA variant genotype was not associated with a significantly elevated breast cancer risk [odds ratio (OR) = 1.11; 95% confidence interval (95%CI) = 0.99-1.24; P = 0.071]. However, subgroup analysis revealed that the AG + AA variant genotype was associated with an increased risk of breast cancer in American (OR = 1.32; 95%CI = 1.10-1.58; P = 0.003), but not in European or Australian. We could carefully suggest that the progesterone receptor promoter +331 G/A variant polymorphism might increase breast cancer risk, and this effect appeared to be more prominent in Americans than in Europeans and Australians. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:194 / 197
页数:4
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