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Association between the GSTP1 Ile105Val polymorphism and prostate cancer risk: A systematic review and meta-analysis

机译:GSTP1 Ile105Val多态性与前列腺癌风险之间的关联:系统评价和荟萃分析

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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.
机译: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)风险的作用。但是,这些研究产生了矛盾的结果。因此,我们进行了这项荟萃分析,以研究不同继承模型中GSTP1 Ile105Val多态性与PCa之间的关联。总共13项合格研究纳入了该荟萃分析。对于Ile / Ile与Val / Val比较,GSTP1 Ile158Val变异基因型与PCa之间存在显着相关性[比​​值比(OR)= 0.705; I 2 = 63.7%; 95%置信区间(95%CI)= 0.508-0.977],Ile / Val与Val / Val比较(OR = 0.736; I 2 = 8.0%; 95%CI = 0.613-0.883)和主导模型(OR = 0.712 ; I 2 = 45.5%; 95%CI = 0.555-0.913)。但是,没有发现其他遗传模型的关联。在按种族进行的分层分析中,高加索人中还发现GSTP1 Ile105Val多态性与PCa风险之间存在显着关联(Ile / Ile与Val / Val比较OR = 0.818,I 2 = 0.0%,95%CI = 0.681-0.982; Ile / Val vs Val / Val比较OR = 0.779,I 2 = 0.0%,95%CI = 0.651-0.933;优势模型OR = 0.794,I 2 = 0.0%,95%CI = 0.670-0.941),而没有其他遗传模型的关联。但是,在按种族进行分层时,在亚洲人和非裔美国人中没有发现所有基因模型的关联。总之,我们的荟萃分析表明GSTP1 Ile105Val多态性有助于PCa易感性。但是,需要进行更大样本量的研究来进一步评估GSTP1 Ile105Val多态性与PCa风险之间的基因-环境相互作用。

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