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GSTT1 and GSTM1 polymorphisms and prostate cancer risk in Asians: a systematic review and meta-analysis

机译:GSTT1和GSTM1基因多态性与亚洲人前列腺癌的风险:系统评价和荟萃分析

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摘要

Glutathione S-transferases (GSTs) enzymes are involved in conjugation of electrophilic compounds to glutathione, and glutathione S-transferase T 1 (GSTT1) and glutathione S-transferase M 1 (GSTM1) polymorphisms have been implicated as risk factors for prostate cancer. We conducted a systematic review and meta-analysis to define the effect of GSTM1 and GSTT1 null genotypes on prostate cancer risk in Asians. We searched the PubMed and Wanfang Medical databases to identify published case–control studies investigating the associations of GSTM1 and GSTT1 null genotypes with risk of prostate cancer in Asians. Heterogeneity was assessed using Cochran’s Q statistic and odds ratios (OR) with corresponding 95 % confidence intervals (95 % CI) from individual studies were pooled using fixed or random effects models according to the heterogeneity. There were 18 studies (2,046 cases, 2,876 controls) on GSTM1 polymorphism, 15 studies (1,677 cases, 2,431 controls) on GSTT1 polymorphism, and 6 studies (675 cases, 853 controls) on GSTM1/GSTT1 interaction analysis. Overall, GSTM1 null genotype was significantly associated with increased risk of prostate cancer in Asians (random effects OR 1.80, 95 % CI 1.48–2.18, P < 0.001), and GSTT1 null genotype was also significantly associated with increased risk of prostate cancer in Asians (random effects OR 1.40, 95 % CI 1.10–1.80, P < 0.001). In addition, the GSTM1/GSTT dual null genotype was associated with higher risk of prostate cancer in Asians (random effects OR 2.14, 95 % CI 1.59–2.89, P = 0.007). In conclusion, GSTM1 and GSTT1 null genotypes are associated with increased risk of prostate cancer in Asians, and GSTM1 and GSTT1 null genotypes are risk factors for the development of prostate cancer.
机译:谷胱甘肽S-转移酶(GSTs)酶参与了亲电子化合物与谷胱甘肽的偶联,谷胱甘肽S-转移酶T 1(GSTT1)和谷胱甘肽S-转移酶M 1(GSTM1)多态性被认为是前列腺癌的危险因素。我们进行了系统的综述和荟萃分析,以定义GSTM1和GSTT1无效基因型对亚洲人前列腺癌风险的影响。我们搜索了PubMed和Wanfang Medical数据库,以确定已发表的病例对照研究,这些研究调查了GSTM1和GSTT1无效基因型与亚洲人患前列腺癌的关联。使用Cochran的Q统计量评估异质性,并根据异质性使用固定或随机效应模型汇总来自单个研究的具有95%置信区间(95%CI)的比值比(OR)。 GSTM1多态性研究18篇(2,046例,2,876例对照),GSTT1多态性研究15例(1,677例,2,431例对照),GSTM1 / GSTT1相互作用分析6项研究(675例,853例对照)。总体而言,GSTM1无效基因型与亚洲人患前列腺癌的风险显着相关(随机效应或1.80,95%CI 1.48–2.18,P <0.001),而GSTT1无效基因型也与亚洲人前列腺癌的风险增加显着相关(随机效应为1.40,95%CI为1.10-1.80,P 0.001)。此外,GSTM1 / GSTT双无效基因型与亚洲人患前列腺癌的风险更高相关(随机效应OR 2.14,95%CI 1.59-2.89,P = 0.007)。总之,GSTM1和GSTT1无效基因型与亚洲人患前列腺癌的风险增加相关,而GSTM1和GSTT1无效基因型是前列腺癌发展的危险因素。

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