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Association of TNFAIP8 gene polymorphisms with cancer risk in Chinese population

机译:TNFAIP8基因多态性与中国人群癌症风险的相关性

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Abstract As TNFAIP8 plays an important role in the development of cancer, several studies have analyzed the relationship between potential functional polymorphic loci of the TNFAIP8 gene and cancer risk. However, some results were inconsistent. Therefore, the current study aims to systematically assess the relationship between these genetic polymorphisms and cancer risk using a meta-analysis approach. Relevant studies were obtained from CNKI, Embase, Web of Science, and PubMed databases. RevMan software was used to conduct data analysis. The combined analysis containing four studies with 2786 cancer patients and 2550 control individuals indicated that rs11064 polymorphism was not associated with cancer risk. The pooled analysis containing three studies with 950 cancer patients and 1036 control individuals showed that rs1045241 polymorphism was associated with cancer risk in the heterozygous model (CT vs. CC: OR = 1.34, 95CI = 1.10‐1.62, Pz=0.003) and dominant model (TT?+?CT) vs. CC: OR = 1.38, 95 CI = 1.15-1.66, Pz=0.0006, but not in other models. The pooled analysis containing two studies 436 cancer patients and 479 control individuals showed that rs1045242 polymorphism was associated with cancer risk in the heterozygous model (AG vs. AA: OR = 1.52, 95CI = 1.14-2.03, Pz=0.005), dominant model (GG?+?AG) vs. AA: OR = 1.56, 95 CI = 1.18-2.07, Pz=0.002 and allelic model (G vs. A: OR = 1.48, 95CI = 1.16-1.90, Pz=0.002).In conclusion, the current findings suggest that the rs1045241 and rs1045242 polymorphisms located on the TNFAIP8 gene were associated with cancer risk in Chinese population, and may serve as valuable genetic susceptibility markers.
机译:摘要 由于TNFAIP8在癌症发展中起着重要作用,多项研究分析了TNFAIP8基因潜在功能多态性位点与癌症风险的关系。然而,有些结果并不一致。因此,本研究旨在使用荟萃分析方法系统地评估这些遗传多态性与癌症风险之间的关系。相关研究来源于CNKI、Embase、Web of Science和PubMed数据库。采用RevMan软件进行数据分析。包含四项研究(2786 名癌症患者和 2550 名对照个体)的联合分析表明,rs11064 多态性与癌症风险无关。包含3项研究的汇总分析,涉及950名癌症患者和1036名对照个体,结果显示rs1045241多态性与杂合模型(CT与CC:OR=1.34,95%CI=1.10-1.62,Pz=0.003)和显性模型[(TT?+?CT)与CC:OR=1.38,95%CI=1.15-1.66,Pz=0.0006],但在其他模型中则不然。包含两项研究(436 名癌症患者和 479 名对照个体)的汇总分析表明,rs1045242 多态性与杂合模型(AG vs. AA:OR = 1.52,95%CI = 1.14-2.03,Pz=0.005)、显性模型 [(GG?+?AG)与AA:OR=1.56,95%CI=1.18-2.07,Pz=0.002]和等位基因模型(G与A:OR=1.48,95%CI=1.16-1.90,Pz=0.002)。综上所述,目前的研究结果表明,位于TNFAIP8基因上的rs1045241和rs1045242多态性与中国人群的癌症风险相关,并可能作为有价值的遗传易感性标志物。

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