Zhou Chengzhi, Qin Yinyin, Xie Zhanhong, Zhang Jiexia, Yang Mingou, Li Shiyue, Chen Rongchang
Department of Medicine, Guangzhou Institute of Respiratory Disease, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou Medical University, Guangzhou 510120, China.
Department of Medicine, Guangzhou Institute of Respiratory Disease, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou Medical University, Guangzhou 510120, China.
Biochem Biophys Res Commun. 2015 Mar 6;458(2):381-6. doi: 10.1016/j.bbrc.2015.01.124. Epub 2015 Jan 31.
CpG island hypermethylation of gene promoters is a well-known mechanism of epigenetic regulation of tumor related-genes and is directly linked to lung carcinogenesis. Alterations in the pattern of methylation of the NPTX1 gene have not yet been studied in detail in human lung cancer.
Methylation-specific PCR (MSP) and bisulfite sequencing PCR (BSP) were used to analyze promoter methylation status, and real-time quantitative reverse transcription-PCR (qRT-PCR) examined mRNA levels. Subsequently, we compared the methylation profile of NPTX1 in samples of neoplastic and non-neoplastic lung tissue taken from the same patients by using quantitative methylation specific PCR (QMSP).
CpG island hypermethylation in promoter of NPTX1 was confirmed in lung cancer cell lines. A significant increase in NPTX1 methylation was identified in lung cancer specimens compared to adjacent noncancerous tissues and that it was negatively correlated with its mRNA expression. The overall survival time among patients carrying methylated NPTX1 tumors was significantly shorter as compared to those with unmethylated NPTX1 tumors (P = 0.011). Moreover, methylation of NPTX1 gene was found to be an independent prognostic factor for poor overall survival based on multivariate analysis models (p = 0.021), as was age ≥60 years old (p = 0.012) and TNM stage (p < 0.001).
These results suggest that NPTX1 hypermethylation and consequent mRNA changes might be an important molecular mechanism in lung cancer. Epigenetic alterations in NPTX1 may serve as potential diagnostic and prognostic biomarkers in lung cancer.
基因启动子的CpG岛高甲基化是肿瘤相关基因表观遗传调控的一种众所周知的机制,并且与肺癌发生直接相关。NPTX1基因甲基化模式的改变在人类肺癌中尚未得到详细研究。
采用甲基化特异性PCR(MSP)和亚硫酸氢盐测序PCR(BSP)分析启动子甲基化状态,实时定量逆转录PCR(qRT-PCR)检测mRNA水平。随后,我们通过定量甲基化特异性PCR(QMSP)比较了取自同一患者的肿瘤性和非肿瘤性肺组织样本中NPTX1的甲基化谱。
在肺癌细胞系中证实了NPTX1启动子的CpG岛高甲基化。与相邻的非癌组织相比,肺癌标本中NPTX1甲基化显著增加,并且与mRNA表达呈负相关。携带甲基化NPTX1肿瘤的患者的总生存时间明显短于携带未甲基化NPTX1肿瘤的患者(P = 0.011)。此外,基于多变量分析模型,发现NPTX1基因甲基化是总生存不良的独立预后因素(p = 0.021),年龄≥60岁(p = 0.012)和TNM分期(p < 0.001)也是如此。
这些结果表明,NPTX1高甲基化及随之而来的mRNA变化可能是肺癌中的一种重要分子机制。NPTX1的表观遗传改变可能作为肺癌潜在的诊断和预后生物标志物。