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Association Between p21 Ser31Arg Polymorphism and Gastrointestinal Tract Tumor Risk: A Meta-analysis

机译:p21 Ser31Arg基因多态性与胃肠道肿瘤风险之间的关联:荟萃分析。

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Human p21 gene is characterized by a polymorphism at codon 31 leading to a Serine-to- Arginine (S/R), two different alleles of p21 Ser31Arg (rs 1801270) polymorphism have been shown to differ significantly in their transcriptional efficiency. More and more investigations are now being carried out to examine a possible link between the p21 Ser31Arg polymorphism and cancer. However, the results were inconclusive. Therefore, we carried out a systematic review and meta-analysis to examine whether this polymorphism is associated with gastrointestinal tract tumor in Asian. Seven studies (n = 2690), comprising 967 cases and 1723 controls in Asian population, were included in our study. The meta-analysis showed significant association between Ser-allele or Ser/Ser genotype and the susceptibility to gastrointestinal tract tumor in overall studies (Ser-allele vs. Arg-allele: OR = 1.17, 95% CI: 1.04-1.31; Ser/Ser vs. Arg/Arg: OR = 1.38, 95% CI: 1.09-1.75; Ser/Ser vs. Arg/Ser: OR = 1.27, 95% CI: 1.05-1.53; Ser/Ser vs. Arg/Ser + Arg/Arg: OR = 1.29, 95% CI: 1.07-1.54). Despite the limitations, the results of the present meta-analysis suggested that, in the p21 Ser31Arg polymorphism, Ser-allele and Ser/Ser genotype might be risk factors for gastrointestinal tract tumor in Asian populations.
机译:人p21基因的特征是在31位密码子处多态性导致丝氨酸转精氨酸(S / R),p21 Ser31Arg(rs 1801270)多态性的两个不同等位基因已显示出其转录效率显着不同。现在正在进行越来越多的研究,以检查p21 Ser31Arg多态性与癌症之间的可能联系。但是,结果尚无定论。因此,我们进行了系统的审查和荟萃分析,以检查这种多态性是否与亚洲人的胃肠道肿瘤有关。我们的研究包括7项研究(n = 2690),包括967例和1723例亚洲人群的对照。荟萃分析显示,在总体研究中,Ser等位基因或Ser / Ser基因型与胃肠道肿瘤易感性之间存在显着相关性(Ser等位基因与Arg等位基因:OR = 1.17,95%CI:1.04-1.31; Ser / Ser vs.Arg / Arg:OR = 1.38,95%CI:1.09-1.75; Ser / Ser vs.Arg / Ser:OR = 1.27,95%CI:1.05-1.53​​; Ser / Ser vs.Arg / Ser + Arg / Arg:OR = 1.29,95%CI:1.07-1.54)。尽管存在局限性,本荟萃分析的结果表明,在p21 Ser31Arg多态性中,Ser等位基因和Ser / Ser基因型可能是亚洲人群胃肠道肿瘤的危险因素。

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