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MDM2基因启动子SNP309 T/G多态性与肝癌风险的关联——一项荟萃分析

Association between MDM2 promoter SNP309 T/G polymorphism and liver cancer risk - a meta-analysis.

作者信息

Ma Hong-Bo, Huang Tao, Han Feng, Chen Wei-Yu

机构信息

Department of Hepatobiliary and Pancreatic Surgery, Henan Tumor Hospital, the Affiliated Tumor Hospital of Zhengzhou University, Zhengzhou, China.

出版信息

Asian Pac J Cancer Prev. 2012;13(6):2841-6. doi: 10.7314/apjcp.2012.13.6.2841.

Abstract

BACKGROUND

Many studies have investigated the association between the MDM2 promoter SNP309 T/G polymorphism and liver cancer risk, but inconsistencies make drawwing definitive conclusions difficult.

METHODS

We therefore searched main databases for articles relating MDM2 SNP309 T/G polymorphism to risk of liver cancer in humans and estimated summary odds ratio (OR) with 95% confidence intervals (95% CI) to assess the possible association in a meta-analysis.

RESULTS

The main analysis revealed no significant heterogeneity, and the pooled ORs of fixed-effects were all significant (for G versus T, OR = 1.59, 95% CI 1.42-1.78; for GG versus TT, OR = 2.45, 95% CI 1.93-3.12; for GT versus TT, OR = 1.70, 95% CI 1.38-2.09; for GG versus GT, OR = 1.49, 95% CI 1.24-1.79; for GG and GT versus TT, OR = 1.95, 95% CI 1.61-2.38; for GG versus TT and GT, OR = 1.73, 95% CI 1.46-2.07). Subgroup analyses by ethnicity and sensitivity analyses both showed associations to remain significant.

CONCLUSION

The present meta-analysis of available data showed a significant association between the MDM2 SNP309 T/G polymorphism and liver cancer risk, the MDM2 SNP309 G allele contributing to increased risk in both Asians and Caucasians in a graded, dose-dependent fashion.

摘要

背景

许多研究调查了MDM2启动子SNP309 T/G多态性与肝癌风险之间的关联,但结果不一致,难以得出明确结论。

方法

因此,我们在主要数据库中搜索了有关MDM2 SNP309 T/G多态性与人类肝癌风险的文章,并估计了汇总比值比(OR)及95%置信区间(95%CI),以在荟萃分析中评估可能的关联。

结果

主要分析显示无显著异质性,固定效应的合并OR均具有显著性(G对T,OR = 1.59,95%CI 1.42 - 1.78;GG对TT,OR = 2.45,95%CI 1.93 - 3.12;GT对TT,OR = 1.70,95%CI 1.38 - 2.09;GG对GT,OR = 1.49,95%CI 1.24 - 1.79;GG和GT对TT,OR = 1.95,95%CI 1.61 - 2.38;GG对TT和GT,OR = 1.73,95%CI 1.46 - 2.07)。按种族进行的亚组分析和敏感性分析均显示关联仍然显著。

结论

目前对现有数据的荟萃分析表明,MDM2 SNP309 T/G多态性与肝癌风险之间存在显著关联,MDM2 SNP309 G等位基因以分级、剂量依赖的方式导致亚洲人和白种人患癌风险增加。

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