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Association between fibroblast growth factor receptor-2 gene polymorphism and risk of breast cancer in Chinese populations: A HuGE review and meta-analysis

机译:成纤维细胞生长因子受体2基因多态性与中国人群乳腺癌风险的关联:HuGE综述和荟萃分析

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Aim of study: To evaluate the effect of fibroblast growth factor receptor.2. (FGFR2) on genetic susceptibility for breast cancer. (BC) in Chinese populations. Materials and Methods: A computerized literature search was carried out in PubMed, Chinese Biomedical Database. (CBM), and Chinese National Knowledge Infrastructure. (CNKI) to collect relevant articles. Pooled odds ratio. (OR) and 95% confidence interval. (CI) were used to assess the strength of the associations. Results: A total of 21 articles involving a total of 15 polymorphisms of the FGFR2 gene were included in the meta-analysis. Due to the limited studies for rs17102287, rs2981578, rs3135718, rs3803662, rs3750817, rsl0510097, rsl7542768, rs13387042, and rs1982073; we only pooled the six polymorphisms. (rs11200014, rs1219648, rs2420946, rs2912778, rs2981579, and rs2981582) into this meta.analysis. Overall, significantly increased BC risk was associated with five polymorphisms. (rs2981579, rs2981582, rs1219648, rs2420946, and rs2912778) when all studies were pooled into the meta.analysis. When stratified by ethnicity and source of controls, similar results were also detected. However, for rs2981579 no significant association was found among Chinese Han in all genetic models. Conclusion: Our meta-analysis suggests that FGFR2 is likely an important genetic marker contributing to susceptibility of BC. We recommend that these single nucleotide polymorphisms to be included in future association studies and functional assays.
机译:研究目的:评价成纤维细胞生长因子受体的作用。2。 (FGFR2)对乳腺癌的遗传易感性。 (BC)在中国人口中。材料与方法:在中国生物医学数据库PubMed中进行计算机文献检索。 (CBM)和中国国家知识基础设施。 (CNKI)收集相关文章。汇总赔率。 (OR)和95%置信区间。 (CI)用于评估协会的实力。结果:荟萃分析共纳入21篇涉及FGFR2基因15个多态性的文章。由于对rs17102287,rs2981578,rs3135718,rs3803662,rs3750817,rsl0510097,rsl7542768,rs13387042和rs1982073的研究有限,我们只汇集了六个多态性。 (rs11200014,rs1219648,rs2420946,rs2912778,rs2981579和rs2981582)纳入此元分析。总体而言,BC风险显着增加与五种多态性有关。 (rs2981579,rs2981582,rs1219648,rs2420946和rs2912778),将所有研究汇总到meta.analysis中。当按种族和控制源进行分层时,也检测到类似的结果。然而,对于rs2981579,在所有遗传模型中均未发现中国汉族人之间存在显着关联。结论:我们的荟萃分析表明,FGFR2可能是导致BC易感性的重要遗传标记。我们建议将这些单核苷酸多态性包括在将来的关联研究和功能测定中。

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