Zhang Yan, Wu Jiang, Huang Gui, Xu Shouming
Department of Pathology, Huaihe Hospital, Henan University.
School of Life Sciences, Henan University, Kaifeng 475004, People's Republic of China,
Cancer Manag Res. 2018 Dec 12;10:6897-6904. doi: 10.2147/CMAR.S174815. eCollection 2018.
Lung carcinogenesis is related to silencing of tumor suppressor genes and activation of oncogenes. The aim was to investigate the significance of death-associated protein kinase (DAPK) methylation in non-small-cell lung cancer (NSCLC) through a meta-analysis.
A detailed literature search was made in PubMed, Embase, and Web of Science databases. All analysis was performed with Review Manager 5.2.
In total, 28 studies with a total of 2,148 patients were involved. The frequency of DAPK promoter hypermethylation was 40.50% in NSCLC, significantly higher than in nonmalignant lung tissue; the pooled OR was 5.69, <0.00001. Additionally, DAPK promoter hypermethylation was significantly correlated with poor overall survival in patients with NSCLC. However, there was no significant difference found while comparing the rate of DAPK promoter hypermethylation in adenocarcinoma and squamous cell cancer. The rate of DAPK promoter hypermethylation was similar between stage III/IV and stage I/II. In addition, the data showed that DAPK promoter hypermethylation was not associated with smoking behavior in patients with NSCLC.
DAPK promoter hypermethylation is correlated with risk of NSCLC and is a potential biomarker for prediction of poor prognosis in patients with NSCLC.
肺癌发生与肿瘤抑制基因沉默及癌基因激活有关。本研究旨在通过荟萃分析探讨死亡相关蛋白激酶(DAPK)甲基化在非小细胞肺癌(NSCLC)中的意义。
在PubMed、Embase和Web of Science数据库中进行详细的文献检索。所有分析均使用Review Manager 5.2进行。
共纳入28项研究,涉及2148例患者。NSCLC中DAPK启动子高甲基化频率为40.50%,显著高于非恶性肺组织;合并OR为5.69,P<0.00001。此外,DAPK启动子高甲基化与NSCLC患者的总生存期较差显著相关。然而,在比较腺癌和鳞状细胞癌中DAPK启动子高甲基化率时,未发现显著差异。III/IV期和I/II期之间DAPK启动子高甲基化率相似。此外,数据显示NSCLC患者中DAPK启动子高甲基化与吸烟行为无关。
DAPK启动子高甲基化与NSCLC风险相关,是预测NSCLC患者预后不良的潜在生物标志物。