Department of Urology, Tianjin First Central Hospital, Tianjin 300192, China.
Gene. 2013 Nov 10;530(2):309-14. doi: 10.1016/j.gene.2013.08.053. Epub 2013 Aug 23.
Many studies have reported the role of xeroderma pigmentosum group D (XPD) with prostate cancer risk, but the results remained controversial. To derive a more precise estimation of the relationship, a meta-analysis was performed. Odds ratios (ORs) with 95% confidence intervals (CIs) were estimated to assess the association between XPD Asp312Asn and Lys751Gln polymorphisms and prostate cancer risk. A total of 8 studies including 2620 cases and 3225 controls described Asp312Asn genotypes, among which 10 articles involving 3230 cases and 3582 controls described Lys751Gln genotypes and were also involved in this meta-analysis. When all the eligible studies were pooled into this meta-analysis, a significant association between prostate cancer risk and XPD Asp312Asn polymorphism was found. For Asp312Asn polymorphism, in the stratified analysis by ethnicity and source of controls, prostate cancer risk was observed in co-dominant, dominant and recessive models, while no evidence of any associations of XPD Lys751Gln polymorphism with prostate cancer was found in the overall or subgroup analyses. Our meta-analysis supports that the XPD Asp312Asn polymorphism contributed to the risk of prostate cancer from currently available evidence. However, a study with a larger sample size is needed to further evaluate gene-environment interaction on XPD Asp312Asn and Lys751Gln polymorphisms and prostate cancer risk.
许多研究报道了 Xeroderma pigmentosum 组 D(XPD)与前列腺癌风险的关系,但结果仍存在争议。为了得出更精确的估计,进行了荟萃分析。使用优势比(OR)及其 95%置信区间(CI)来评估 XPD Asp312Asn 和 Lys751Gln 多态性与前列腺癌风险之间的关系。共有 8 项研究包括 2620 例病例和 3225 例对照描述了 Asp312Asn 基因型,其中 10 项研究涉及 3230 例病例和 3582 例对照描述了 Lys751Gln 基因型,也包含在这项荟萃分析中。当将所有符合条件的研究纳入荟萃分析时,发现 XPD Asp312Asn 多态性与前列腺癌风险之间存在显著关联。对于 Asp312Asn 多态性,在按种族和对照来源进行的分层分析中,在共显性、显性和隐性模型中观察到前列腺癌风险,而在总体或亚组分析中均未发现 XPD Lys751Gln 多态性与前列腺癌之间存在任何关联。我们的荟萃分析支持目前的证据表明 XPD Asp312Asn 多态性导致前列腺癌的风险增加。然而,需要进行更大样本量的研究来进一步评估 XPD Asp312Asn 和 Lys751Gln 多态性与前列腺癌风险的基因-环境相互作用。