Yu Zhuo, Li Zhong, Cai Bing, Wang Ziming, Gan Weimin, Chen Haiwen, Li Hecheng, Zhang Peng, Li Hongliang
Department of Medical Oncology, The Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, 310009, China.
Tumour Biol. 2013 Jun;34(3):1855-63. doi: 10.1007/s13277-013-0727-x. Epub 2013 Mar 14.
Many studies have reported the role of glutathione S-transferase P1 (GSTP1) Ile105Val polymorphism with prostate cancer (PCa) risk. However, these studies have yielded conflicting results. Hence, we performed this meta-analysis to investigate the association between GSTP1 Ile105Val polymorphism and PCa in different inheritance models. A total of 13 eligible studies were pooled into this meta-analysis. There was significant association between the GSTP1 Ile158Val variant genotypes and PCa for Ile/Ile vs Val/Val comparison [odds ratio (OR) =0.705; I (2) =63.7 %; 95 % confidence interval (95 % CI) = 0.508-0.977], Ile/Val vs Val/Val comparison (OR=0.736; I (2) =8.0 %; 95 % CI=0.613-0.883), and dominant model (OR=0.712; I (2) =45.5 %; 95 % CI=0.555-0.913). However, no associations were detected for other genetic models. In the stratified analysis by ethnicity, significant associations between GSTP1 Ile105Val polymorphism and PCa risk were also found among Caucasians (Ile/Ile vs Val/Val comparison OR=0.818, I (2) =0.0 %, 95 % CI=0.681-0.982; Ile/Val vs Val/Val comparison OR=0.779, I (2) =0.0 %, 95 % CI=0.651-0.933; and dominant model OR=0.794, I (2) =0.0 %, 95 % CI=0.670-0.941), while there were no associations found for other genetic models. However, no associations were found in Asians and African-Americans for all genetic models when stratified by ethnicity. In conclusion, our meta-analysis indicates that GSTP1 Ile105Val polymorphisms contributed to the PCa susceptibility. However, a study with the larger sample size is needed to further evaluate gene-environment interaction on GSTP1 Ile105Val polymorphisms and PCa risk.
许多研究报告了谷胱甘肽S-转移酶P1(GSTP1)Ile105Val多态性与前列腺癌(PCa)风险的关系。然而,这些研究结果相互矛盾。因此,我们进行了这项荟萃分析,以研究GSTP1 Ile105Val多态性与不同遗传模型中PCa之间的关联。共有13项符合条件的研究被纳入该荟萃分析。在Ile/Ile与Val/Val比较中,GSTP1 Ile158Val变异基因型与PCa之间存在显著关联[比值比(OR)=0.705;I²=63.7%;95%置信区间(95%CI)=0.508 - 0.977],Ile/Val与Val/Val比较(OR = 0.736;I² = 8.0%;95%CI = 0.613 - 0.883),以及显性模型(OR = 0.712;I² = 45.5%;95%CI = 0.555 - 0.913)。然而,在其他遗传模型中未检测到关联。在按种族进行的分层分析中,在白种人中也发现GSTP1 Ile105Val多态性与PCa风险之间存在显著关联(Ile/Ile与Val/Val比较OR = 0.818,I² = 0.0%,95%CI = 0.681 - 0.982;Ile/Val与Val/Val比较OR = 0.779,I² = 0.0%,95%CI = 0.651 - 0.933;显性模型OR = 0.794,I² = 0.0%,95%CI = 0.670 - 0.941),而在其他遗传模型中未发现关联。然而,按种族分层时,在亚洲人和非裔美国人中,所有遗传模型均未发现关联。总之,我们的荟萃分析表明,GSTP1 Ile105Val多态性与PCa易感性有关联。然而,需要更大样本量的研究来进一步评估基因 - 环境相互作用对GSTP1 Ile105Val多态性和PCa风险的影响。