Department of Hematology, The First Affiliated Hospital of Guangdong Pharmaceutical University, Guangzhou, Guangdong, People's Republic of China.
Department of Cardiology, The Third Affiliated Hospital of SUN YAT-SEN University, Guangzhou, Guangdong, People's Republic of China.
PLoS One. 2019 Jan 25;14(1):e0210943. doi: 10.1371/journal.pone.0210943. eCollection 2019.
We aimed to characterize the clinical significance of epigenetic loss of death-associated protein kinase (DAPK) gene function through promoter methylation in the development and prognosis of lymphoma. PubMed, Web of Science and ProQuest databases were searched for relevant studies. Twelve studies involving 709 patients with lymphoma were identified. The prognostic value of DAPK methylation was expressed as risk ratio (RR) and its corresponding 95% confidence interval (CI), while the associations between DAPK methylation and the clinical characteristics of patients with lymphoma were expressed as odd ratios (ORs) and their corresponding 95% CIs. Meta-analysis showed that the 5-year survival rate was significantly lower in lymphoma patients with hypermethylated DAPK (RR = 0.85, 95% CI (0.73, 0.98), P = 0.025). Sensitivity analysis demonstrated consistent result. However, no associations were found between DAPK methylation and clinicopathological features of lymphoma, in relation to gender (OR = 1.07, 95% CI (0.72, 1.59), P = 0.751), age (OR = 1.01, 95% CI (0.66, 1.55), P = 0.974), international prognostic index (OR = 1.20, 95% CI (0.63, 2.27), P = 0.575), B symptoms (OR = 0.76, 95% CI (0.38, 1.51), P = 0.452), serum lactate dehydrogenase (OR = 1.13, 95% CI (0.62, 2.05), P = 0.683), and BCL-2 expression (OR = 1.55, 95% CI (0.91, 2.66), P = 0.106). Lymphoma patients with hypermethylated DAPK are at risk for poorer 5-year survival rate. DAPK methylation may serve as a negative prognostic biomarker among lymphoma patients, although it may not be associated with the progression of lymphoma.
我们旨在通过启动子甲基化来描述死亡相关蛋白激酶(DAPK)基因功能的表观遗传缺失在淋巴瘤的发生和预后中的临床意义。检索了 PubMed、Web of Science 和 ProQuest 数据库中的相关研究。确定了 12 项涉及 709 例淋巴瘤患者的研究。DAPK 甲基化的预后价值表示为风险比(RR)及其相应的 95%置信区间(CI),而 DAPK 甲基化与淋巴瘤患者临床特征之间的关系表示为比值比(OR)及其相应的 95%CI。荟萃分析显示,DAPK 高甲基化的淋巴瘤患者 5 年生存率显着降低(RR = 0.85,95%CI(0.73,0.98),P = 0.025)。敏感性分析表明结果一致。但是,DAPK 甲基化与淋巴瘤的临床病理特征之间没有关联,与性别(OR = 1.07,95%CI(0.72,1.59),P = 0.751),年龄(OR = 1.01,95%CI(0.66,1.55),P = 0.974),国际预后指数(OR = 1.20,95%CI(0.63,2.27),P = 0.575),B 症状(OR = 0.76,95%CI(0.38,1.51),P = 0.452),血清乳酸脱氢酶(OR = 1.13,95%CI(0.62,2.05),P = 0.683)和 BCL-2 表达(OR = 1.55,95%CI(0.91,2.66),P = 0.106)。DAPK 高甲基化的淋巴瘤患者有 5 年生存率降低的风险。DAPK 甲基化可能是淋巴瘤患者的阴性预后生物标志物,尽管它与淋巴瘤的进展可能无关。