首页> 外文期刊>Mutation Research: International Journal on Mutagenesis, Chromosome Breakage and Related Subjects >Candidate gene studies in gallbladder cancer: a systematic review and meta-analysis.
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Candidate gene studies in gallbladder cancer: a systematic review and meta-analysis.

机译:胆囊癌候选基因研究:系统评价和荟萃分析。

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摘要

Gallbladder cancer (GBC) is the most frequent biliary tract malignancy. Wide variations in GBC incidence and familial and epidemiological data suggest involvement of a genetic component in its etiopathogenesis. A systematic review of genetic association studies in GBC was performed by applying a meta-analysis approach and systematically reviewing PubMed database using appropriate terms. Odds ratios (ORs) and 95% confidence intervals (CIs) were appropriately derived for each gene-disease association using fixed and random effect models. Meta-regression with population size and genotyping method was also performed. Study quality was assessed using a 10-point scoring system designed from published guidelines. Following a review of 44 published manuscripts and one unpublished report, 80 candidate gene variants and 173 polymorphisms were analyzed among 1046 cases and 2310 controls. Majority of studies were of intermediate quality. Four polymorphisms with >3 separate studies were included in the meta-analysis [OGG1 (rs1052133), TP53 (rs1042522), CYP1A1 (rs1048943) and GSTM1 null polymorphism]. The meta-analysis demonstrated no significant associations of any of the above polymorphisms with GBC susceptibility except TP53 (rs1042522) polymorphism. To conclude, existing candidate gene studies in GBC susceptibility have so far been insufficient to confirm any association. Future research should focus on a more comprehensive approach utilizing potential gene-gene, gene-environment interactions and high-risk haplotypes.
机译:胆囊癌(GBC)是最常见的胆道恶性肿瘤。 GBC发生率以及家族和流行病学数据的广泛差异表明遗传成分参与了其发病机理。通过应用荟萃分析方法并使用适当的术语系统地审查了PubMed数据库,对GBC中的遗传关联研究进行了系统的综述。使用固定和随机效应模型,针对每种基因-疾病关联性,分别得出了几率(OR)和95%置信区间(CI)。还进行了具有种群规模和基因分型方法的Meta回归分析。使用根据已发布指南设计的10分评分系统评估研究质量。在审查了44篇已发表的手稿和一份未发表的报告之后,在1046例病例和2310例对照中分析了80个候选基因变体和173个多态性。大多数研究属于中等质量。荟萃分析包括四个具有> 3个单独研究的多态性[OGG1(rs1052133),TP53(rs1042522),CYP1A1(rs1048943)和GSTM1无效多态性]。荟萃分析显示,上述任何多态性与GBC易感性均无显着关联,但TP53(rs1042522)多态性除外。总而言之,迄今为止,有关GBC易感性的现有候选基因研究不足以证实任何关联。未来的研究应该集中在利用潜在的基因-基因,基因-环境相互作用和高风险单倍型的更全面的方法上。

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