Dai Zhiming, Tian Tian, Wang Meng, Liu Xinghan, Lin Shuai, Yang Pengtao, Liu Kang, Zheng Yi, Xu Peng, Liu Meng, Yang Xuewen, Dai Zhijun
Department of Oncology, Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
Department of Anesthesia, Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
PeerJ. 2017 Jan 10;5:e2815. doi: 10.7717/peerj.2815. eCollection 2017.
Previous studies have investigated the association between cytotoxic T-lymphocyte antigen-4 () polymorphisms and breast cancer susceptibility, but the results remained inconsistent. Therefore, we evaluated the relationship between four common polymorphisms and breast cancer risk by a meta-analysis, aiming to derive a comprehensive and precise conclusion. We searched EMBASE, Pubmed, Web of Science, CNKI, and Wanfang databases until July 18th, 2016. Finally, ten eligible studies involving 4,544 breast cancer patients and 4,515 cancer-free controls were included; all these studies were from Asia. Odds ratio (OR) and 95% confidence interval (CI) were used to evaluate the breast cancer risk in five genetic models. The results indicated that the +49A>G (rs231775) polymorphism had a significant association with decreased breast cancer risk in allelic, homozygous, dominant and recessive models. Also, the +6230G>A (rs3087243) polymorphism reduced breast cancer risk especially in the Chinese population under homozygous and recessive models. In contrast, the -1661A>G (rs4553808) polymorphism increased breast cancer risk in allelic, heterozygous and dominant models, whereas -1722 T>C (rs733618) did not relate to breast cancer risk. In conclusion, polymorphisms significantly associate with breast cancer susceptibility in Asian populations, and different gene loci may have different effects on breast cancer development. Further large-scale studies including multi-racial populations are required to confirm our findings.
以往的研究探讨了细胞毒性T淋巴细胞抗原4()基因多态性与乳腺癌易感性之间的关联,但结果仍不一致。因此,我们通过荟萃分析评估了四种常见的基因多态性与乳腺癌风险之间的关系,旨在得出全面而精确的结论。我们检索了EMBASE、Pubmed、Web of Science、中国知网和万方数据库,检索截止至2016年7月18日。最终,纳入了10项符合条件的研究,涉及4544例乳腺癌患者和4515例无癌对照;所有这些研究均来自亚洲。采用比值比(OR)和95%置信区间(CI)在五种遗传模型中评估乳腺癌风险。结果表明,+49A>G(rs231775)多态性在等位基因、纯合子、显性和隐性模型中与降低乳腺癌风险显著相关。此外,+6230G>A(rs3087243)多态性尤其在纯合子和隐性模型下的中国人群中降低了乳腺癌风险。相比之下,-1661A>G(rs4553808)多态性在等位基因、杂合子和显性模型中增加了乳腺癌风险,而-1722 T>C(rs733618)与乳腺癌风险无关。总之,基因多态性在亚洲人群中与乳腺癌易感性显著相关,不同基因位点可能对乳腺癌发展有不同影响。需要进一步开展包括多种族人群的大规模研究来证实我们的发现。