Han Yi, Shi Kang, Zhou Shi-Jie, Yu Da-Ping, Liu Zhi-Dong
Department of Thoracic Surgery, Beijing Chest Hospital, Capital Medical University, Beijing, People's Republic of China.
Onco Targets Ther. 2016 Aug 16;9:5081-90. doi: 10.2147/OTT.S106345. eCollection 2016.
The hMLH1 gene plays an essential role in DNA repair. Methylation of the hMLH1 gene is common in many types of cancer and can lead to the loss of hMLH1 expression. However, the association and clinicopathological significance between hMLH1 promoter hypermethylation and non-small-cell lung cancer (NSCLC) is elusive. Here, we investigated the correlation of hMLH1 promoter hypermethylation and NSCLC using 13 studies by comprising 1,056 lung cancer patients via a meta-analysis. We observed that 1) loss of hMLH1 protein expression was significantly associated with its promoter hypermethylation, 2) hMLH1 gene inactivation through hypermethylation contributed to the tumorigenesis of NSCLC, which could be a decisive factor for the pathogenesis of NSCLC due to its high occurrence in NSCLC tissues compared to normal lung tissues, 3) a correlation exists between histologic subtypes/disease stages (TNM I+II vs III+IV) and hypermethylation status of hMLH1 gene, and 4) NSCLC patients with hMLH1 hypermethylation and subsequent low expression levels of hMLH1 have a short overall survival period than those patients with normal expression of hMLH1 gene. hMLH1 mRNA predicts patient survival in lung cancer, and this was confirmed by using a public database. We then discussed the tumor suppressor function of hMLH1 and the clinicopathological significance of hMLH1 in NSCLC. We concluded that hMLH1 hypermethylation should be an early diagnostic marker for NSCLC and also a prognostic index for NSCLC. hMLH1 is an interesting therapeutic target in human lung cancers.
hMLH1基因在DNA修复中起着至关重要的作用。hMLH1基因的甲基化在多种癌症类型中很常见,并可能导致hMLH1表达缺失。然而,hMLH1启动子高甲基化与非小细胞肺癌(NSCLC)之间的关联及临床病理意义尚不清楚。在此,我们通过荟萃分析,纳入13项研究中的1056例肺癌患者,研究hMLH1启动子高甲基化与NSCLC的相关性。我们观察到:1)hMLH1蛋白表达缺失与其启动子高甲基化显著相关;2)通过高甲基化导致的hMLH1基因失活促成了NSCLC的肿瘤发生,由于其在NSCLC组织中的发生率高于正常肺组织,这可能是NSCLC发病机制的一个决定性因素;3)组织学亚型/疾病分期(TNM I+II期与III+IV期)与hMLH1基因的高甲基化状态之间存在相关性;4)hMLH1高甲基化且随后hMLH1表达水平低的NSCLC患者的总生存期比hMLH1基因表达正常的患者短。hMLH1 mRNA可预测肺癌患者的生存情况,这通过使用公共数据库得到了证实。然后我们讨论了hMLH1的肿瘤抑制功能以及hMLH1在NSCLC中的临床病理意义。我们得出结论,hMLH1高甲基化应是NSCLC的早期诊断标志物,也是NSCLC的预后指标。hMLH1是人类肺癌中一个有趣的治疗靶点。