BACKGROUND:FAS cell surface death receptor (FAS) gene has 2 common single nucleotide polymorphisms (SNPs) in its promoter, FAS-1377G > A (rs2234767) and FAS-670A > G (rs1800682). Several studies have investigated the role of these 2 polymorphisms in etiology of breast cancer in Asian population while the outcomes are inconsistent. To derive a more precise assessment of the association between breast cancer susceptibility with FAS gene promoter SNPs, a meta-analysis of published studies was performed. MATERIAL AND METHODS:We systematically searched PubMed, Embase, Web of Science, and the Chinese biomedical database (CBM) for papers published until November 1, 2018. Odds ratio (OR) with 95% confidential interval (95%CI) was conducted to evaluate the associations. Statistical analysis was conducted using Stata13.0 software. A total of 8 studies covering 2564 cases and 2633 controls were included. RESULTS:The integrated results suggest the following: For the FAS-1377G/A polymorphism, we only found significant associations for allele G vs allele A (OR = 1.100, 95%CI = 1.004-1.206, P = .040). After stratification by ethnicity, a significant association was observed only for the AA+GA vs GG genotype in East Asian populations (OR = 1.177, 95% CI = 1.010-1.371, P = .037). The association was not found in West Asian populations. For the FAS -670A/G polymorphism, no association with cancer risk was found in any comparison model. Sensitivity analysis suggests that the meta-analysis results obtained after excluding any single study were similar to the original ones, suggesting that the meta-analysis results were not significantly affected by any single study. CONCLUSION:These results indicated that FAS-1377G/A polymorphism may contribute to the increased breast cancer susceptibility and could be a promising target for cancer risk prediction. Further studies are needed to determine if the FAS gene confers a risk of breast cancer in other ethnic groups, such as Africans and Latin Americans.

译文

背景:FAS细胞表面死亡受体(FAS)基因在其启动子中有2种常见的单核苷酸多态性(SNP),分别为FAS-1377G> A(rs2234767)和FAS-670A> G(rs1800682)。几项研究调查了这两种多态性在亚洲人群乳腺癌病因中的作用,但结果不一致。为了更精确地评​​估乳腺癌易感性与FAS基因启动子SNP之间的关联,对已发表的研究进行了荟萃分析。
材料与方法:我们系统地搜索了PubMed,Embase,Web of Science和中国生物医学数据库(CBM),直至2018年11月1日为止发表的论文。对机率为95%的机率(OR)为95%CI评估关联。使用Stata13.0软件进行统计分析。总共包括8项研究,涵盖2564例和2633例对照。
结果:综合结果表明:对于FAS-1377G / A多态性,我们仅发现等位基因G与等位基因A有显着关联(OR = 1.100,95%CI = 1.004-1.206,P = 0.040)。按种族分层后,仅在东亚人群中观察到AA GA和GG基因型之间存在显着关联(OR = 1.177,95%CI = 1.010-1.371,P = .037)。在西亚人口中未发现该关联。对于FAS -670A / G多态性,在任何比较模型中均未发现与癌症风险相关。敏感性分析表明,排除任何一项单独研究后获得的荟萃分析结果与原始研究相似,这表明任何一项单独研究均未显着影响荟萃分析结果。
结论:这些结果表明,FAS-1377G / A基因多态性可能有助于增加乳腺癌的易感性,并可能成为癌症风险预测的有希望的目标。需要进一步的研究以确定FAS基因是否赋予其他种族群体(例如非洲人和拉丁美洲人)患乳腺癌的风险。

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