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The Relationship of the TLR9 and TLR2 Genetic Polymorphisms with Cervical Cancer Risk: a Meta-Analysis of Case-Control Studies

机译:TLR9和TLR2遗传多态性与宫颈癌风险的关系:病例对照研究的荟萃分析

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This meta-analysis aimed to assess the association of common TLR9 and TLR2 gene polymorphisms (TLR9 1486T/C, TLR9 G2848A, and TLR2 196 to 174 del/ins) with cervical cancer risk. Studies were searched in Scopus, Pubmed, Embase, and CNKI until December 2017. Both fixed-effects and random-effects models were applied to combine odds ratio (OR) and 95% confidence intervals (95% CI). A total of 11 studies including 7856 participants were identified. The pooled estimation revealed an increased risk of cervical cancer in Caucasian subjects carrying the C allele of the TLR9 1486T/C polymorphism (OR = 1.46, 95% CI: 1.11 1.92, p = 0.007), while there was a decreased risk in Mixed subjects carrying the C allele (OR = 0.35, 95% CI: 0.15 0.82, p = 0.016). Concerning the TLR9 G2848A polymorphism, the A allele was associated with an increased risk of cervical cancer in Caucasians (OR = 1.19, 95% CI: 1.02 1.40, p = 0.030), whereas Asian and Mixed subjects showed no significant associations. No significant associations were demonstrated between the TLR2 196 to 174 del/ins polymorphism and cervical cancer. Our findings suggest that the TLR9 1486T/C and G2848A polymorphisms contribute to cervical cancer risk, but there is no association of the TLR2 196 to 174 del/ins polymorphism with cervical cancer.
机译:该META分析旨在评估常见的TLR9和TLR2基因多态性(TLR9 1486T / C,TLR9 G2848A和TLR2 196至174 DEL / INS)的关联,具有宫颈癌风险。在Scopus,Pubmed,Embase和CNKI中搜查了研究,直到2017年12月。固定效应和随机效应模型均采用差距比(或)和95%置信区间(95%CI)。共有11项研究,包括7856名参与者。汇总估计揭示了携带TLR9 1486T / C多态性的C等位基因(或= 1.46,95%CI:1.11 1.92,P = 0.007)的白种人受试者中宫颈癌的风险增加,而混合受试者风险降低携带C等位基因(或= 0.35,95%CI:0.15 0.82,P = 0.016)。关于TLR9 G2848A多态性,等位基因与高加索人中宫颈癌的风险增加(或= 1.19,95%CI:1.02 1.40,P = 0.030),而亚洲和混合受试者没有显着的关联。在TLR2 196至174 del / Ins多态性和宫颈癌之间没有进行显着的关联。我们的研究结果表明,TLR9 1486T / C和G2848A多态性有助于宫颈癌风险,但没有与宫颈癌的TLR2 196至174 Del / Ins多态性的关联。

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