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Association between TCF7L2 polymorphisms and breast cancer susceptibility: a meta-analysis

机译:TCF7L2基因多态性与乳腺癌易感性的关联:一项荟萃分析

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摘要

Aim: Our aim was to investigate the relationship between transcription factor 7-like 2 (TCF7L2) polymorphisms and breast cancer susceptibility. Methods: PubMed, Embase and CNKI databases were used to search the related studies investigating the correlation between TCF7L2 polymorphisms and breast cancer susceptibility. Pooled ORs and 95% CIs, based on five genetic models, were applied to estimate the association betweenTCF7L2 polymorphisms and breast cancer. A fixed-effect model or a random-effect model was applied according to the between-study heterogeneity. Results: We analyzed six single nucleotide polymorphisms (SNPs) in TCF7L2 gene, namely rs12255372, rs7903146, rs7900150, rs3750805, rs1225404 and rs7003146. The increased risk of breast cancer was associated with TCF7L2 polymorphisms (22 vs. 11: OR=1.16, 95% CI=1.02-1.32; 22+12 vs. 11: OR=1.06, 95% CI=1.02-1.10; 22 vs. 11+12: OR=1.15, 95% CI=1.04-1.27; 2 vs. 1: OR=1.07, 95% CI=1.02-1.13; 12 vs. 11: OR=1.05, 95% CI=1.01-1.09). Among the locus, rs7903146 polymorphism was significantly associated with the risk for breast cancer under five genetic models (TT vs. CC: OR=1.29, 95% CI=1.08-1.53; TT+CT vs. CC: OR=1.09, 95% CI=1.01-1.18; TT vs. CC+CT: OR=1.24, 95% CI=1.05-1.48; T vs. C: OR=1.11, 95% CI=1.04-1.19; CT vs. CC: OR=1.08, 95% CI=1.00-1.17). Additionally, rs7900150 also showed effects on the susceptibility of breast cancer (TT vs. AA: OR=1.22, 95% CI=1.07-1.39; TT+AT vs. AA: OR=1.06, 95% CI=1.00-1.14; TT vs. AA+AT: OR=1.21, 95% CI=1.07-1.37; T vs. A: OR=1.09, 95% CI=1.02-1.15; AT vs. AA: OR=1.04, 95% CI=1.01-1.33). Meanwhile, we found that rs3750805 polymorphism could increased the risk for breast cancer (TT+AT vs. AA: OR=1.12, 95% CI=1.01-1.24). Conclusion: Our meta-analysis demonstrates that TCF7L2 polymorphisms may increase the risk for breast cancer.
机译:目的:我们的目的是研究转录因子7-like 2(TCF7L2)多态性与乳腺癌易感性之间的关系。方法:使用PubMed,Embase和CNKI数据库搜索有关TCF7L2多态性与乳腺癌易感性之间关系的相关研究。基于五个遗传模型,将汇总的OR和95%CI应用于估计TCF7L2多态性与乳腺癌之间的关联。根据研究之间的异质性,应用固定效应模型或随机效应模型。结果:我们分析了TCF7L2基因中的六个单核苷酸多态性(SNP),即rs12255372,rs7903146,rs7900150,rs3750805,rs1225404和rs7003146。乳腺癌风险增加与TCF7L2多态性相关(22 vs.11:OR = 1.16,95%CI = 1.02-1.32; 22 + 12 vs.11:OR = 1.06,95%CI = 1.02-1.10; 22 vs. 。11 + 12:OR = 1.15,95%CI = 1.04-1.27; 2比1:OR = 1.07,95%CI = 1.02-1.13; 12 vs.11:OR = 1.05,95%CI = 1.01-1.09 )。在基因座中,rs7903146多态性与五个遗传模型下的乳腺癌风险显着相关(TT vs. CC:OR = 1.29,95%CI = 1.08-1.53​​; TT + CT vs. CC:OR = 1.09,95% CI = 1.01-1.18; TT vs.CC + CT:OR = 1.24,95%CI = 1.05-1.48; T vs. C:OR = 1.11,95%CI = 1.04-1.19; CT vs.CC:OR = 1.08 ,95%CI = 1.00-1.17)。此外,rs7900150还显示出对乳腺癌易感性的影响(TT vs.AA:OR = 1.22,95%CI = 1.07-1.39; TT + AT vs.AA:OR = 1.06,95%CI = 1.00-1.14; TT vs.AA + AT:OR = 1.21,95%CI = 1.07-1.37; T vs.AA:OR = 1.09,95%CI = 1.02-1.15; AT vs.AA:OR = 1.04,95%CI = 1.01- 1.33)。同时,我们发现rs3750805多态性可能会增加患乳腺癌的风险(TT + AT与AA:OR = 1.12,95%CI = 1.01-1.24)。结论:我们的荟萃分析表明,TCF7L2多态性可能会增加患乳腺癌的风险。

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