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Association of CYP1A1 and GSTM1 Polymorphisms With Oral Cancer Susceptibility

机译:CYP1A1和GSTM1多态性与口腔癌易感性的关系

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摘要

Our meta-analysis was aimed to evaluate the association of CYP1A1 and glutathione-S-transferase M1 (GSTM1) polymorphisms with oral cancer susceptibility.The related articles were searched in PubMed, Embase, and CNKI databases. Fifty eligible studies were included in our meta-analysis. Odds ratios (ORs) with 95% confidence intervals (CIs) were used to evaluate the relationship of CYP1A1 (rs4646903 and rs1048943) and GSTM1 polymorphisms with oral cancer risk. A random-effects model or fixed-effects model was employed depending on the heterogeneity.In overall analysis, CYP1A1 rs4646903 polymorphism was associated with the risk of oral cancer (CC vs TT: OR 1.65, 95% CI 1.33–2.05; CC vs TC+TT: OR 1.77, 95% CI 1.48–2.11; C vs T: OR 1.17, 95% CI 1.07–1.28), whereas rs1048943 showed no obvious association with oral cancer susceptibility. Moreover, subgroup analysis by ethnicity demonstrated that rs4646903 and rs1048943 both related with increased risk of oral cancer in Asians. Moreover, the analysis based on source of control suggested that rs4646903 could increase the risk for oral cancer in both population- and hospital-based populations, whereas no remarkable relationship of rs1048943 with oral cancer susceptibility was observed. For GSTM1 gene, null genotype appeared to be a risk factor for oral cancer (null vs present: OR 1.23, 95% CI 1.12–1.34), which was also proved in the subgroup analysis.The results demonstrated that CYP1A1 rs4646903 and null genotype of GSTM1 polymorphisms might serve as risk factors for oral cancer.
机译:我们的荟萃分析旨在评估CYP1A1和谷胱甘肽S-转移酶M1(GSTM1)多态性与口腔癌易感性的相关性。在PubMed,Embase和CNKI数据库中搜索相关文章。我们的荟萃分析包括五十项符合条件的研究。使用具有95%置信区间(CI)的几率(OR)评估CYP1A1(rs4646903和rs1048943)和GSTM1多态性与口腔癌风险的关系。根据异质性,采用随机效应模型或固定效应模型。总的来说,CYP1A1 rs4646903多态性与口腔癌风险相关(CC vs TT:OR 1.65,95%CI 1.33–2.05; CC vs TC + TT:OR 1.77,95%CI 1.48–2.11; C vs T:OR 1.17,95%CI 1.07-1.28),而rs1048943与口腔癌易感性没有明显关联。此外,按种族进行的亚组分析表明,rs4646903和rs1048943都与亚洲人口腔癌风险增加有关。此外,基于控制源的分析表明,rs4646903可能会增加基于人群和医院人群的口腔癌风险,而未观察到rs1048943与口腔癌易感性的显着关系。对于GSTM1基因,无效基因型似乎是口腔癌的危险因素(无效vs存在:OR 1.23,95%CI 1.12–1.34),这也在亚组分析中得到了证实。结果表明CYP1A1 rs4646903和CYP1A1无效基因型GSTM1多态性可能是口腔癌的危险因素。

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