Kim Dong Sun, Lee Won Kee, Park Jae Yong
Department of Anatomy, BK21 Plus KNU Biomedical Convergence Program, School of Medicine, Kyungpook National University, Daegu 702-422, Republic of Korea.
Department of Preventive Medicine, School of Medicine, Kyungpook National University, Daegu 702-422, Republic of Korea.
Oncol Lett. 2018 Aug;16(2):2409-2415. doi: 10.3892/ol.2018.8915. Epub 2018 Jun 6.
Lung cancer is the leading cause of cancer-associated mortality due to high incidence and poor survival rates, irrespective of global variations in its biology and treatment. Changes in DNA methylation are frequent in cancer and constitute an important mechanism in tumorigenesis. Normal mucosa of esophagus-specific 1 () is expressed in epithelial tissue and is believed to be a tumor suppressor gene. The present study investigated the methylation status of the promoter in 178 cases of primary non-small cell lung cancer (NSCLC) by pyrosequencing and evaluated the prognostic value of this methylation. NMES1 methylation-positive tumors above the background threshold for non-malignant tissue were found in 15 cases (8.4%) and were detected exclusively in malignant tissues. In addition, univariate and multivariate analyses showed that methylation-positive patients experienced worse overall survival rate (OSR) compared with methylation-negative patients (adjusted hazard ratio, 2.62; 95% confidence interval, 1.20-5.69; P=0.02). Notably, within the methylation-positive group, patients with strong methylation tended to experience worse OSR compared with those with weak methylation (adjusted hazard ratio, 2.45 vs. 3.05; P=0.02). These findings suggest that may serve an important role in lung cancer pathogenesis, and its methylation could be considered a prognostic marker for NSCLC. Further studies with large numbers of samples are required to confirm this conclusion.
肺癌由于其高发病率和低生存率,是癌症相关死亡的主要原因,无论其生物学特性和治疗方法在全球范围内存在何种差异。DNA甲基化变化在癌症中很常见,是肿瘤发生的重要机制。食管特异性1(NMES1)在正常食管黏膜上皮组织中表达,被认为是一种肿瘤抑制基因。本研究通过焦磷酸测序法调查了178例原发性非小细胞肺癌(NSCLC)中NMES1启动子的甲基化状态,并评估了这种甲基化的预后价值。在15例(8.4%)患者中发现NMES1甲基化阳性肿瘤高于非恶性组织的背景阈值,且仅在恶性组织中检测到。此外,单因素和多因素分析表明,与甲基化阴性患者相比,甲基化阳性患者的总生存率(OSR)更差(调整后的风险比,2.62;95%置信区间,1.20 - 5.69;P = 0.02)。值得注意的是,在甲基化阳性组中,甲基化程度高的患者与甲基化程度低的患者相比,OSR往往更差(调整后的风险比,2.45对3.05;P = 0.02)。这些发现表明,NMES1可能在肺癌发病机制中起重要作用,其甲基化可被视为NSCLC的预后标志物。需要进一步进行大量样本研究来证实这一结论。