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细胞色素P450 2E1基因多态性与肝癌发生的Meta分析。

Meta-analysis of CYP2E1 polymorphisms in liver carcinogenesis.

作者信息

Fu Peiyao, Yang Fan, Li Bo, Zhang Biao, Guan Lianyue, Sheng Jiyao, Ye Yanshuo, Wang Zhanpeng, Li Peidong, Xu Li, Zou Liangjian, Li Wei

机构信息

Department of Hepatobiliary-Pancreatic Surgery, China-Japan Union Hospital of Jilin University, Changchun, China.

Department of Cardiothoracic Surgery, Changhai Hospital of the Second Military Medical University, Shanghai, China.

出版信息

Dig Liver Dis. 2017 Jan;49(1):77-83. doi: 10.1016/j.dld.2016.08.114. Epub 2016 Aug 18.

Abstract

BACKGROUND

The CYP2E1 protein is a monooxygenase with certain polymorphisms linked to liver cancer. However, results from individual studies remain controversial.

AIMS

To evaluate CYP2E1 polymorphisms in liver carcinogenesis through meta-analysis.

METHODS

All studies about CYP2E1 polymorphisms and liver cancer were retrieved from seven major databases. Original data from each study were pooled and re-analyzed.

RESULTS

Total of 16 articles with 4862 cases were selected, including 1820 cases of liver cancer and 3042 cases of controls. The c1 allelic frequency in the cases and controls was 83.3% and 85.3%, respectively. Five genetic variations were compared: dominant c1c2/c2c2 vs. c1/c1 (OR=0.987 (0.853, 1.141)), homozygous c2c2 vs. c1c1 (OR=0.767 (0.526, 1.119)), heterozygous c1c2 vs. c1c1 (OR=1.005 (0.854, 1.182)), recessive c2c2 vs. c1c2/c2c2 (OR=0.771 (0.530, 1.122)), and different alleles c2 vs. c1 (OR=0.947 (0.828, 1.082)). Pooled data were further analyzed based on ethnicity, control sources, and HWE (Hardy-Weinberg equilibrium). These results from stratified groups were similar to that of nonstratified groups.

CONCLUSIONS

Our meta-analysis results suggest that there is no evidence for a major role of CYP2E1 polymorphism in liver carcinogenesis, but do not rule out the possibility in certain cases.

摘要

背景

CYP2E1蛋白是一种单加氧酶,其某些多态性与肝癌相关。然而,个别研究的结果仍存在争议。

目的

通过荟萃分析评估CYP2E1多态性在肝癌发生中的作用。

方法

从七个主要数据库中检索所有关于CYP2E1多态性与肝癌的研究。汇总并重新分析每项研究的原始数据。

结果

共选择了16篇文章,涉及4862例,其中包括1820例肝癌患者和3042例对照。病例组和对照组中c1等位基因频率分别为83.3%和85.3%。比较了五种基因变异:显性c1c2/c2c2与c1/c1(OR = 0.987(0.853,1.141)),纯合子c2c2与c1c1(OR = 0.767(0.526,1.119)),杂合子c1c2与c1c1(OR = 1.005(0.854,1.182)),隐性c2c2与c1c2/c2c2(OR = 0.771(0.530,1.122)),以及不同等位基因c2与c1(OR = 0.947(0.828,1.082))。根据种族、对照来源和哈迪-温伯格平衡(HWE)对汇总数据进行了进一步分析。分层组的这些结果与非分层组的结果相似。

结论

我们的荟萃分析结果表明,没有证据支持CYP2E1多态性在肝癌发生中起主要作用,但不排除在某些情况下存在这种可能性。

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