State Key Laboratory of Genetic Engineering, Institute of Genetics, School of Life Sciences, Fudan University, Shanghai, People's Republic of China.
Breast Cancer Res Treat. 2010 Jul;122(2):503-7. doi: 10.1007/s10549-009-0717-2. Epub 2010 Jan 6.
Breast cancer is the most prevalent cancer in the world, which is a major public health challenge. To date, many publications have evaluated the correlation between cytochrome P450 1A1 (CYP1A1) T3801C polymorphism and breast cancer risk. However, the results remain inconclusive. In order to derive a more precise estimation of the association, a meta-analysis was performed in this study. By searching Medline, PubMed, and ISI Web of Knowledge databases, 23 studies including 10,520 cases and 14,567 controls were collected for CYP1A1 T3801C polymorphism. The strength of association between CYP1A1 T3801C polymorphism and breast cancer risk was assessed by calculating crude ORs with 95% CIs. The pooled ORs were performed for codominant model, dominant model, and recessive model, respectively. Overall, no significant associations between CYP1A1 T3801C polymorphism and breast cancer susceptibility were found for TT versus CC (OR = 0.93; 95% CI: 0.72-1.19), TC versus CC (OR = 0.95; 95% CI: 0.79-1.14), TT + TC versus CC (OR = 0.93; 95% CI: 0.75-1.15), and TT versus TC + CC (OR = 0.99; 95% CI: 0.87-1.13). In the stratified analysis by ethnicity, menopausal status, and source of controls, no significant associations were detected in all genetic models. In conclusion, this meta-analysis provides strong evidence that CYP1A1 T3801C polymorphism is not associated with breast cancer risk.
乳腺癌是世界上最常见的癌症,是一个主要的公共健康挑战。迄今为止,许多出版物已经评估了细胞色素 P450 1A1(CYP1A1)T3801C 多态性与乳腺癌风险之间的相关性。然而,结果仍不确定。为了更准确地评估这种相关性,本研究进行了荟萃分析。通过搜索 Medline、PubMed 和 ISI Web of Knowledge 数据库,共收集了 23 项研究,包括 10520 例病例和 14567 例对照,用于 CYP1A1 T3801C 多态性。通过计算粗比值比(ORs)及其 95%置信区间(CIs)来评估 CYP1A1 T3801C 多态性与乳腺癌风险之间的关联强度。分别进行了共显性模型、显性模型和隐性模型的汇总 ORs。总的来说,CYP1A1 T3801C 多态性与乳腺癌易感性之间没有显著关联,无论是 TT 与 CC(OR=0.93;95%CI:0.72-1.19)、TC 与 CC(OR=0.95;95%CI:0.79-1.14)、TT+TC 与 CC(OR=0.93;95%CI:0.75-1.15)还是 TT 与 TC+CC(OR=0.99;95%CI:0.87-1.13)。在按种族、绝经状态和对照来源进行的分层分析中,所有遗传模型均未发现显著关联。总之,本荟萃分析提供了强有力的证据表明 CYP1A1 T3801C 多态性与乳腺癌风险无关。