首页> 外文期刊>Trends in Ecology & Evolution >Glutathione S-Transferase P1 313 (A > G) Ile105Val Polymorphism Contributes to Cancer Susceptibility in Indian Population: A Meta-analysis of 39 Case-Control Studies
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Glutathione S-Transferase P1 313 (A > G) Ile105Val Polymorphism Contributes to Cancer Susceptibility in Indian Population: A Meta-analysis of 39 Case-Control Studies

机译:谷胱甘肽S-转移酶P1 313(A> G)ILE105 VAL多态性有助于印度人群的癌症易感性:39例案例对照研究的荟萃分析

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GSTP1 involved in the metabolism of carcinogens and toxins, reduces damage of DNA and act as a suppressor of carcinogenesis. Many studies have reported that 313 A > G polymorphism is associated with different cancer in Indian population, but the results remain conflicting rather than conclusive. Therefore, we have performed meta-analysis to clarify the more precise association of GSPT1 313 A > G polymorphism with cancer risk in Indian population. We retrieved all relevant published literature from PubMed (Medline) and Google scholar web database and included those study only based on the established inclusion criteria. Pooled ORs and 95% CIs were used to appraise the strength of association. Publication bias and sensitivity analysis was also evaluated. A total of 6581 confirmed cancer cases and 8218 controls were included from eligible thirty nine case-controls studies. Pooled analysis suggested that the variant genotypes significantly increased the risk of cancer in allele (G vs. A: OR 1.266, 95% CI 1.129-1.418, p = 0.001), heterozygous (AG vs. AA: OR 1.191, 95% CI 1.047-1.355, p = 0.008), homozygous (GG vs. AA: OR 1.811, 95% CI 1.428-2.297, p = 0.001), dominant (GG + AG vs. AA: OR 1.276, 95% CI 1.110-1.466, p = 0.001) and recessive (GG vs. AG + AA: OR 1.638, 95% CI 1.340-2.002, p = 0.001) genetic models. The stability of these observations was confirmed by a sensitivity analysis. Begger's funnel plot and Egger's test did not reveal any publication bias. This meta-analysis suggests that the GSTP1 313 A > G polymorphism may contribute to genetic susceptibility to cancer in Indian population. However, larger studies and randomized clinical trial will be required to elucidate the biological and molecular mechanism of GSTP1 gene in cancer.
机译:GSTP1参与致癌物质和毒素的代谢,降低了DNA损伤,并充当致癌物的抑制作用。许多研究报告说,313A> G多态性与印度人群不同癌症有关,但结果仍然相互冲突而不是确凿的。因此,我们已经进行了Meta分析,以澄清GSPT1 313 A> G多态性与印度人群癌症风险的更精确关联。我们从PubMed(Medline)和Google Scholar Web数据库中检索了所有相关的发布文献,并根据既定的纳入标准汇集了这些研究。合并的oder和95%的CIS用于评估协会的实力。还评估了出版物偏差和敏感性分析。共有6581例确诊的癌症病例和8218个对照包括符合条件的三十九个病例对照研究。汇总分析表明,变体基因型在等位基因中显着提高了癌症的风险(G对A:或1.266,95%CI 1.129-1.418,P = 0.001),杂合(Ag与AA:或1.191,95%CI 1.047 -1.355,p = 0.008),纯合(gg vs. aa:或1.811,95%ci 1.428-2.297,p = 0.001),显性(gg + ag与aa:或1.276,95%ci 1.110-1.466,p = 0.001)和隐性(GG与Ag + AA:或1.638,95%CI 1.340-2.002,P = 0.001)遗传模型。通过敏感性分析证实了这些观察结果的稳定性。 Begger的漏斗情节和Egger的测试没有透露任何出版物偏见。该Meta分析表明GSTP1 313 A> G多态性可能导致印度人群对癌症的遗传易感性。然而,将需要更大的研究和随机临床试验来阐明癌症GSTP1基因的生物学和分子机制。

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