Department of Urology, The First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi Zhuang Autonomous Region 530021, People's Republic of China.
Med Oncol. 2011 Mar;28(1):365-76. doi: 10.1007/s12032-010-9423-5. Epub 2010 Jan 23.
Studies revealing conflicting results on the role of NAT1 or NAT2 phenotypes on prostate cancer risk led us to perform a meta-analysis to investigate the association of these polymorphisms and prostate cancer risk. The meta-analysis included six studies with NAT1 genotyping (610 prostate cancer cases and 713 controls), and 10 studies with NAT2 genotyping (1,253 cases and 1,722 controls). The fixed effects odds ratio was 0.96 [95% confidence interval (95% CI): 0.75, 1.21; I(2) = 32.9%, P for heterogeneity = 0.189] for the NAT1 genotype, and the random effects odds ratio was 1.10 (95% CI: 0.87, 1.39; I(2) = 49.1%, P for heterogeneity = 0.039) for the NAT2 genotype. For NAT2 polymorphism, a statistically significant association between NAT2 polymorphism and prostate cancer appeared in Asians, but not in Caucasians. In conclusion, the NAT1 or NAT2 phenotypes detoxify carcinogens and their reactive intermediates are unlikely to be the cause of PCa development.
研究揭示了 NAT1 或 NAT2 表型在前列腺癌风险中的作用相互矛盾,这促使我们进行荟萃分析以研究这些多态性与前列腺癌风险的关联。该荟萃分析包括 6 项 NAT1 基因分型研究(610 例前列腺癌病例和 713 例对照)和 10 项 NAT2 基因分型研究(1253 例病例和 1722 例对照)。NAT1 基因型的固定效应比值比为 0.96(95%置信区间[95%CI]:0.75,1.21;I²=32.9%,异质性 P=0.189),NAT2 基因型的随机效应比值比为 1.10(95%CI:0.87,1.39;I²=49.1%,异质性 P=0.039)。对于 NAT2 多态性,NAT2 多态性与前列腺癌之间存在统计学显著关联,但在白种人中则没有。总之,NAT1 或 NAT2 表型可能不会导致 PCa 发展。