Department of Otorhinolaryngology, First Affiliated Hospital of Nanjing Medical University, Nanjing 210029, People's Republic of China.
Breast Cancer Res Treat. 2010 Aug;123(1):213-7. doi: 10.1007/s10549-010-0755-9. Epub 2010 Jan 29.
The A2756G polymorphism in the methionine synthase (MTR) gene has been implicated in breast cancer risk. However, the published findings are inconsistent. We therefore performed a meta-analysis to investigate this relationship. Eleven published case-control studies, including 8,438 breast cancer cases and 10,515 controls were identified. Odds ratios (ORs) and 95% confidence intervals (CIs) were used to assess the strength of the association. Overall, no significant associations between the MTR A2756G polymorphism and breast cancer risk were found for GG versus AA (OR = 0.98, 95% CI: 0.84-1.15), AG versus AA (OR = 0.95, 95% CI: 0.89-1.01), GG/AG versus AA (OR = 0.95, 95% CI = 0.89-1.01), and GG versus AG/AA (OR = 1.00, 95% CI: 0.86-1.17). However, in the stratified analysis, significantly decreased breast cancer risks were found among Europeans (AG versus AA, OR = 0.90, 95% CI = 0.83-0.98; GG/AG versus AA, OR = 0.90, 95% CI = 0.82-0.97) and studies with population-based controls (AG versus AA, OR = 0.93, 95% CI = 0.86-1.00; GG/AG versus AA, OR = 0.93, 95% CI = 0.86-1.00). When stratifying by the menopausal status, no significant result was observed in all genetic models. Taken together, the results suggest that the MTR A2756G polymorphism may contribute to susceptibility to breast cancer among Europeans.
甲硫氨酸合成酶(MTR)基因中的 A2756G 多态性与乳腺癌风险有关。然而,已发表的研究结果并不一致。因此,我们进行了荟萃分析来研究这种关系。共确定了 11 项已发表的病例对照研究,包括 8438 例乳腺癌病例和 10515 例对照。比值比(ORs)和 95%置信区间(CIs)用于评估关联的强度。总体而言,未发现 MTR A2756G 多态性与乳腺癌风险之间存在显著相关性,对于 GG 与 AA(OR=0.98,95%CI:0.84-1.15),AG 与 AA(OR=0.95,95%CI:0.89-1.01),GG/AG 与 AA(OR=0.95,95%CI=0.89-1.01),以及 GG 与 AG/AA(OR=1.00,95%CI:0.86-1.17)。然而,在分层分析中,在欧洲人群中发现乳腺癌风险显著降低(AG 与 AA,OR=0.90,95%CI=0.83-0.98;GG/AG 与 AA,OR=0.90,95%CI=0.82-0.97)和基于人群的对照研究(AG 与 AA,OR=0.93,95%CI=0.86-1.00;GG/AG 与 AA,OR=0.93,95%CI=0.86-1.00)。当按绝经状态分层时,在所有遗传模型中均未观察到显著结果。总的来说,结果表明 MTR A2756G 多态性可能导致欧洲人群乳腺癌易感性增加。