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首页> 外文期刊>Asian Pacific Journal of Cancer Prevention >Lack of Association of the MDR1 C3435T Polymorphism with Susceptibility to Gastric Cancer and Peptic Ulcer: a Systemic Review and Meta-analysis
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Lack of Association of the MDR1 C3435T Polymorphism with Susceptibility to Gastric Cancer and Peptic Ulcer: a Systemic Review and Meta-analysis

机译:缺乏MDR1 C3435T多态性与胃癌和消化性溃疡易感性的关联:系统评价和荟萃分析

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摘要

Background: The multidrug resistance 1 gene (MDR1) C3435T polymorphism has been demonstrated toinfluence the P-glycoprotein (P-gp) activity level which is related to inflammation and carcinogenesis. Thismeta-analysis was performed to estimate the association between the MDR1 C3435T polymorphism and therisk of gastric cancer (GC) and peptic ulcer (PU). Materials and Methods: A literature search was conductedwith PubMed, Embase and the Cochrane library up to November 2013. Odds ratios (ORs) with 95% confidenceintervals (CIs) were used to assess the strength of association. Data were analyzed using Review Manager (Version5.2), and Stata package (version 12.0) for estimation of publication bias. Results: Six case-control studies wereincluded, of which five were for GC and two for PU. Overall, no evidence was found for any association betweenthe MDR1 C3435T polymorphism and the susceptibility to GC and PU. In the stratified analysis by H. pyloriinfection status, stage and histology classification of GC, and PU type, there was still no significant associationbetween them. Conclusions: This meta-analysis suggested that the MDR1 C3435T polymorphism is not associatedwith susceptibility to GC and PU. Large and well-designed studies are warranted to validate our findings.
机译:背景:已证明多药耐药性1基因(MDR1)C3435T多态性影响P-糖蛋白(P-gp)活性水平,该水平与炎症和致癌作用有关。进行此元分析以估计MDR1 C3435T多态性与胃癌(GC)和消化性溃疡(PU)风险之间的关联。材料和方法:截至2013年11月,使用PubMed,Embase和Cochrane库进行文献检索。使用奇数比(OR)和95%置信区间(CI)评估关联强度。使用Review Manager(Version5.2)和Stata软件包(版本12.0)对数据进行分析,以评估发布偏差。结果:包括六个病例对照研究,其中五个用于GC,两个用于PU。总体而言,未发现MDR1 C3435T多态性与GC和PU敏感性之间存在任何关联的证据。在根据幽门螺杆菌感染状况,GC的分期和组织学分类以及PU类型进行的分层分析中,它们之间仍然没有显着关联。结论:这项荟萃分析表明MDR1 C3435T多态性与GC和PU的敏感性无关。必须进行大型且设计合理的研究以验证我们的发现。

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