Ma Qingtong, Zhao Yumei, Wang Shoufeng, Zhang Xiaoyan, Zhang Jinling, Du Mei, Li Liang, Zhang Yun
Department of Urology, Tianjin First Central Hospital, Tianjin, 300192, China.
Tumour Biol. 2014 Feb;35(2):1473-80. doi: 10.1007/s13277-013-1203-3. Epub 2013 Oct 2.
The relationship of bladder cancer with the presence of X-ray cross-complementing group 3(XRCC3) genetic polymorphism Thr241Met has been reported with inconsistent results. The objective of this study was to quantitatively evaluate the association between this polymorphism and bladder cancer susceptibility. A comprehensive research was conducted through PubMed, Medline, Embase, and Web of Science databases up to Aug. 20, 2013. Pooled odds ratio and 95 % confidence interval were calculated using a fixed or random effects model. Statistical analysis was performed with Stata 12.0 software. Of the 18 case-control studies selected for this meta-analysis, a total of 5,667 bladder cancer cases and 7,609 controls were included. The combined results based on all studies suggested that XRCC3 Thr241Met was associated with bladder cancer risk under homozygote and recessive models. When stratifying for ethnicity, significant association was found in Caucasians under homozygote and recessive models. This meta-analysis suggests that XRCC3 Thr241Met polymorphism is a risk factor for bladder cancer risk. However, further well-designed studies are required to confirm our findings.
膀胱癌与X射线交叉互补基因3(XRCC3)基因多态性Thr241Met之间的关系已有报道,但结果并不一致。本研究的目的是定量评估这种多态性与膀胱癌易感性之间的关联。通过检索截至2013年8月20日的PubMed、Medline、Embase和Web of Science数据库进行了全面的研究。使用固定效应模型或随机效应模型计算合并比值比和95%置信区间。使用Stata 12.0软件进行统计分析。在为本荟萃分析选择的18项病例对照研究中,共纳入了5667例膀胱癌病例和7609例对照。基于所有研究的合并结果表明,在纯合子和隐性模型下,XRCC3 Thr241Met与膀胱癌风险相关。按种族分层时,在纯合子和隐性模型下,高加索人群中发现了显著关联。本荟萃分析表明,XRCC3 Thr241Met多态性是膀胱癌风险的一个危险因素。然而,需要进一步设计良好的研究来证实我们的发现。