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死亡相关蛋白激酶(DAPK)启动子甲基化与膀胱癌风险:一项系统评价和荟萃分析

DAPK Promoter Methylation and Bladder Cancer Risk: A Systematic Review and Meta-Analysis.

作者信息

Dai Lihe, Ma Chong, Zhang Zhensheng, Zeng Shuxiong, Liu Anwei, Tang Shijie, Ren Qian, Sun Yinghao, Xu Chuanliang

机构信息

Department of Urology, Changhai Hospital, Second Military Medical University, Shanghai, China.

出版信息

PLoS One. 2016 Dec 1;11(12):e0167228. doi: 10.1371/journal.pone.0167228. eCollection 2016.

Abstract

BACKGROUND

Methylation of tumor suppressor gene promoter leads to transcription inactivation and is involved in tumorigenesis. Several studies demonstrate a potential association between the Death-Associated Protein Kinase (DAPK) gene promoter methylation and bladder cancer risk, tumor stage and histological grade. Due to inconsistent results of these studies, we performed this meta-analysis to ascertain the association.

METHODS

Studies were retrieved from the PubMed, Embase, Web of Science and the Cochrane Library databases. Study selection and data extraction were executed by two reviewers independently. Meta-analysis was performed using Stata 13.0 and Review Manager 5.3 software.

RESULTS

A total of 21 articles involving 15 case control and 8 case series studies were included in this meta-analysis. DAPK promoter methylation was associated with bladder cancer risk (OR: 5.81; 95%CI = 3.83-8.82, P<0.00001). The frequency of DAPK promoter methylation was equal in bladder cancer tissue and paired adjacent normal tissue (OR: 0.87; 95%CI = 0.31-2.48, P = 0.794). Furthermore, DAPK promoter methylation was associated with higher histological grade (OR: 1.52; 95%CI = 1.10-2.09, P = 0.011) but not associated with tumor stage (OR: 1.12; 95%CI = 0.67-1.87, P = 0.668).

CONCLUSIONS

The result suggests that DAPK promoter methylation is significantly increased in bladder cancer patients compared to normal controls. DAPK promoter methylation could serve as a biomarker for bladder cancer detection and management.

摘要

背景

肿瘤抑制基因启动子的甲基化会导致转录失活,并参与肿瘤发生。多项研究表明,死亡相关蛋白激酶(DAPK)基因启动子甲基化与膀胱癌风险、肿瘤分期及组织学分级之间可能存在关联。由于这些研究结果不一致,我们进行了这项荟萃分析以确定这种关联。

方法

从PubMed、Embase、Web of Science和Cochrane图书馆数据库中检索研究。由两名审阅者独立进行研究选择和数据提取。使用Stata 13.0和Review Manager 5.3软件进行荟萃分析。

结果

本荟萃分析共纳入21篇文章,其中包括15项病例对照研究和8项病例系列研究。DAPK启动子甲基化与膀胱癌风险相关(比值比:5.81;95%置信区间=3.83 - 8.82,P<0.00001)。DAPK启动子甲基化在膀胱癌组织和配对的相邻正常组织中的频率相等(比值比:0.87;95%置信区间=0.31 - 2.48,P = 0.794)。此外,DAPK启动子甲基化与较高的组织学分级相关(比值比:1.52;95%置信区间=1.10 - 2.09,P = 0.011),但与肿瘤分期无关(比值比:1.12;95%置信区间=0.67 - 1.87,P = 0.668)。

结论

结果表明,与正常对照相比,膀胱癌患者中DAPK启动子甲基化显著增加。DAPK启动子甲基化可作为膀胱癌检测和管理的生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4325/5132202/784dfe187cae/pone.0167228.g001.jpg

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