Suppr超能文献

CHEK2 1100delC 变异与结直肠癌易感性的荟萃分析。

Meta-analysis of CHEK2 1100delC variant and colorectal cancer susceptibility.

机构信息

Emergency Department of The Second Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China.

出版信息

Eur J Cancer. 2011 Nov;47(17):2546-51. doi: 10.1016/j.ejca.2011.03.025. Epub 2011 Jul 30.

Abstract

Cell cycle checkpoint kinase 2 (CHEK2) gene has been inconsistently associated with colorectal cancer (CRC), particularly the 1100delC variant. To generate large-scale evidence on whether the CHEK2 1100delC variant is associated with CRC susceptibility we have conducted a meta-analysis. Data were collected from the following electronic databases: PubMed, Excerpta Medica Database and Chinese Biomedical Literature Database, with the last report up to November 2010. The odds ratio (OR) and its 95% confidence interval (95% CI) were used to assess the strength of association. We evaluated the contrast of carriers versus non-carriers. Meta-analysis was performed in a fixed/random effect model by using the software Review Manager 4.2. A total of six studies including 4194 cases and 10,010 controls based on the search criteria were involved in this meta-analysis. A significant association of the CHEK2 1100delC variant with unselected CRC was found (OR=2.11, 95% CI=1.41-3.16, P=0.0003). We also found an association of the CHEK2 1100delC variant with familial CRC (OR=2.80, 95% CI=1.74-4.51, P<0.0001). However, the association was not established for sporadic CRC (OR=1.45, 95% CI=0.49-4.30, P=0.50). This meta-analysis demonstrates that the CHEK2 1100delC variant may be an important CRC-predisposing gene, which increases CRC risk.

摘要

细胞周期检查点激酶 2(CHEK2)基因与结直肠癌(CRC)的相关性不一致,特别是 1100delC 变异。为了产生关于 CHEK2 1100delC 变异是否与 CRC 易感性相关的大规模证据,我们进行了荟萃分析。数据来自以下电子数据库:PubMed、Excerpta Medica Database 和中国生物医学文献数据库,最后报告截止到 2010 年 11 月。使用比值比(OR)及其 95%置信区间(95%CI)来评估关联的强度。我们评估了携带者与非携带者的对比。使用 Review Manager 4.2 软件,采用固定/随机效应模型进行荟萃分析。根据搜索标准,共有六项研究包括 4194 例病例和 10010 例对照纳入本荟萃分析。CHEK2 1100delC 变异与非选择性 CRC 存在显著相关性(OR=2.11,95%CI=1.41-3.16,P=0.0003)。我们还发现 CHEK2 1100delC 变异与家族性 CRC 相关(OR=2.80,95%CI=1.74-4.51,P<0.0001)。然而,对于散发性 CRC,这种相关性并未建立(OR=1.45,95%CI=0.49-4.30,P=0.50)。本荟萃分析表明,CHEK2 1100delC 变异可能是一个重要的 CRC 易感基因,增加 CRC 风险。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验