Wang Jian-Gong, Zhang Yang, Xiao Tian-Lin
Department of Cancer Biotherapy, Cancer Institute, Tangshan People's Hospital, Tangshan, Hebei 063001, P.R. China.
Department of Oncology, Xiangyang Central Hospital, Medical College, Hubei University of Arts and Science, Xiangyang, Hubei 441000, P.R. China.
Oncol Lett. 2015 Feb;9(2):994-998. doi: 10.3892/ol.2014.2796. Epub 2014 Dec 12.
Accumulating evidence indicates that polymorphisms in the gene are important in the development of cancer. The current meta-analysis was performed to investigate the association between polymorphisms 3407 A>G (rs2808630) and 29 A>T (rs1417938), and the risk of developing cancer. A search of the relevant literature was conducted using the PubMed database to identify eligible studies published up until March 25, 2014. Five case-control studies involving 888 cases and 3,167 controls for the 3407 A>G polymorphism, and six case-control studies involving 3,110 cases and 5,951 controls for the 29 A>T polymorphism were included in the current meta-analysis. The pooled odds ratios with 95% confidence intervals were calculated using the fixed- or random-effects model. Meta-analysis identified no association between the 3407 A>G and 29 A>T polymorphisms, and overall cancer risk. Additional stratified analysis by cancer type did not reveal any significant associations in the genetic models investigated. The findings of the present study indicated that 3407 A>G and 29 A>T polymorphisms are not associated with cancer risk.
越来越多的证据表明,该基因的多态性在癌症的发生发展中具有重要意义。本荟萃分析旨在研究3407 A>G(rs2808630)和29 A>T(rs1417938)多态性与患癌风险之间的关联。利用PubMed数据库检索相关文献,以确定截至2014年3月25日发表的符合条件的研究。本荟萃分析纳入了五项病例对照研究,涉及3407 A>G多态性的888例病例和3167例对照,以及六项病例对照研究,涉及29 A>T多态性的3110例病例和5951例对照。采用固定效应模型或随机效应模型计算合并比值比及其95%置信区间。荟萃分析未发现3407 A>G和29 A>T多态性与总体癌症风险之间存在关联。按癌症类型进行的额外分层分析在研究的遗传模型中未显示出任何显著关联。本研究结果表明,3407 A>G和29 A>T多态性与癌症风险无关。