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ESR1 XBAI 与乳腺癌易感性的关联:系统评价和荟萃分析。

Association Between ESR1 XBAI and Breast Cancer Susceptibility: A Systematic Review and Meta-Analysis.

机构信息

Tumor Radiotherapy and Chemotherapy Center, Chengde Central Hospital, Chengde, Hebei, China.

Both authors contributed equally

出版信息

Clin Invest Med. 2022 Mar 23;45(1):E21-34. doi: 10.25011/cim.v45i1.37842.

Abstract

Estrogen receptor 1 (ESR1) XbaI polymorphisms may affect breast cancer susceptibility; however, the results of previously published studies are inconsistent. This meta-analysis aimed to investigate the relationship between ESR1 XbaI polymorphism and breast cancer risk.  Methods: Articles from the PubMed, Embase, Cochrane Library, WoS, Scopus, Wanfang Data, CNKI, CBM and CQVIP databases were systematically searched to determine the association between ESR1 XbaI polymorphism and breast cancer risk. The pooled results were assessed using odds ratios (ORs) and 95% confidence intervals (CIs), followed by subgroup analysis.  Results: Twenty-two studies involving 12,821 cases and 14,739 control subjects were analyzed. The pooled results indicated that ESR1 XbaI polymorphism may decrease risk of breast cancer in AG vs. AA (co-dominant model: OR = 0.88, 95% CI = 0.79-0.97, P = 0.015) and AG + GG vs. AA models (dominant model: OR = 0.89, 95% CI = 0.80-0.98, P = 0.022). Subgroup analysis indicated significant associations between the ESR1 XbaI polymorphism and breast cancer risk were observed in Asian subjects, non-Hardy-Weinberg equilibrium study, post-menopausal status and hospital-based subgroups under the AG vs. AA and AG + GG vs. AA models (all P < 0.05).  Conclusions: Our analysis of pooled data indicated that AG genotype in ESR1 XbaI may be a protective factor for breast cancer patients in some subgroups.

摘要

雌激素受体 1 (ESR1) XbaI 多态性可能影响乳腺癌易感性;然而,先前发表的研究结果并不一致。本荟萃分析旨在研究 ESR1 XbaI 多态性与乳腺癌风险之间的关系。

方法

系统检索 PubMed、Embase、Cochrane 图书馆、WoS、Scopus、万方数据、CNKI、CBM 和 CQVIP 数据库中的文章,以确定 ESR1 XbaI 多态性与乳腺癌风险之间的关联。使用比值比 (ORs) 和 95%置信区间 (CIs) 评估合并结果,并进行亚组分析。

结果

共分析了 22 项研究,涉及 12821 例病例和 14739 例对照。合并结果表明,ESR1 XbaI 多态性可能降低 AG 与 AA 相比 (共显性模型:OR=0.88,95%CI=0.79-0.97,P=0.015) 和 AG+GG 与 AA 模型 (显性模型:OR=0.89,95%CI=0.80-0.98,P=0.022) 的乳腺癌风险。亚组分析表明,在亚洲人群、非 Hardy-Weinberg 平衡研究、绝经后状态和医院为基础的亚组中,ESR1 XbaI 多态性与乳腺癌风险之间存在显著关联,在 AG 与 AA 和 AG+GG 与 AA 模型中均如此(均 P<0.05)。

结论

我们对汇总数据的分析表明,ESR1 XbaI 中的 AG 基因型可能是某些亚组中乳腺癌患者的保护因素。

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