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E-钙黏蛋白(CDH1)基因启动子多态性与结直肠癌风险:荟萃分析。

E-cadherin (CDH1) gene promoter polymorphism and the risk of colorectal cancer : a meta-analysis.

机构信息

Henan Center for Disease Control and Prevention, No. 105 of East Nongye Road, Zhengdong New Area, 450016, Zhengzhou, China.

出版信息

Int J Colorectal Dis. 2012 Feb;27(2):151-8. doi: 10.1007/s00384-011-1320-7. Epub 2011 Oct 14.

Abstract

OBJECTIVE

Published data on the relationship between E-cadherin (CDH1) gene promoter polymorphisms and colorectal cancer (CRC) risk are inconclusive. To derive a more precise estimation of the relationship, a meta-analysis was carried out.

METHODS

In this meta-analysis, we evaluated reported studies of associations between polymorphisms of CDH1 gene promoter -160 C > A and -347 G > GA site, and CRC risk using fixed-effects model and random-effects model.

RESULTS

We found decreased CRC risk among subjects carrying CDH1 -160AA (odds ratio [OR] = 0.86, 95 percent confidence interval [95% CI]: 0.75-0.98) and CA + AA (OR = 0.92, 95% CI: 0.87-0.98), using 4,652/4,428 cases/controls and 7,866/7,689 cases/controls from ten studies, respectively. We found a protective effect of the CDH1 -160CA + AA polymorphisms for CRC in distal site tumor population and population-based control in stratified analysis. We found a protective effect of the CDH1 -160AA and CA + AA polymorphisms for CRC in European and American population (OR = 0.87, 95% CI: 0.76-0.99 and OR = 0.91, 95% CI: 0.85-0.98, respectively). We observed that the CDH1 -347 G/GA + GA/GA carrier had an increased risk of CRC, the summary OR was 1.33 (95% CI: 1.08-1.62).

CONCLUSIONS

Data indicated that certain CDH1 gene promoter -160 C > A and -347 G > GA variants might affect the susceptibility of CRC. Recommendations for further studies include pooling of individual data to facilitate evaluation of multigenic effects and detailed analysis of effect modification by environmental and lifestyle factors.

摘要

目的

关于 E-钙黏蛋白(CDH1)基因启动子多态性与结直肠癌(CRC)风险之间的关系,已有发表的数据尚无定论。为了更准确地评估这种关系,进行了荟萃分析。

方法

在这项荟萃分析中,我们使用固定效应模型和随机效应模型,评估了关于 CDH1 基因启动子-160 C > A 和-347 G > GA 位点多态性与 CRC 风险之间关联的报告研究。

结果

我们发现,携带 CDH1-160AA(比值比[OR] = 0.86,95%置信区间[95%CI]:0.75-0.98)和 CA + AA(OR = 0.92,95%CI:0.87-0.98)的受试者 CRC 风险降低,这是基于十项研究中 4428/4428 例病例/对照和 7689/7689 例病例/对照的数据。我们发现 CDH1-160CA + AA 多态性对远端肿瘤人群和分层分析中基于人群的对照 CRC 有保护作用。我们发现 CDH1-160AA 和 CA + AA 多态性对欧洲和美洲人群的 CRC 有保护作用(OR = 0.87,95%CI:0.76-0.99 和 OR = 0.91,95%CI:0.85-0.98)。我们发现 CDH1-347G/GA + GA/GA 携带者 CRC 风险增加,汇总 OR 为 1.33(95%CI:1.08-1.62)。

结论

数据表明,某些 CDH1 基因启动子-160 C > A 和-347 G > GA 变体可能影响 CRC 的易感性。建议进一步研究包括汇总个体数据,以促进对多基因效应的评估,并详细分析环境和生活方式因素对效应修饰的影响。

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