Department of Thoracic Surgery, Peking Union Medical College and Chinese Academy of Medical Sciences, China.
Cancer Biol Ther. 2011 Mar 1;11(5):490-6. doi: 10.4161/cbt.11.5.14550.
Lung cancer is the leading cause of cancer-related death in the world and approximately 30-40% of patients with stage Ⅰ non-small cell lung cancer (NSCLC) die of recurrent disease. miRNA expression profiles can be diagnostic and prognostic markers of lung cancer. Recently, miR-34 family has been shown to be part of the p53 pathway which is frequently involved in lung cancer, and the expression of miR-34 has been reported to be regulated by DNA methylation. In present study, we investigated the correlation between DNA methylation status of miR-34 family and recurrence of stage Ⅰ NSCLC patients. miR-34a and miR-34b/c promoter methylation status were determined by nested methylation-specific PCR in FFPE tumor tissues from 161 patients of stage Ⅰ NSCLC. Furthermore, mature miR-34b and miR-34c expression were analyzed by qRT-PCR in the same panel tissues. Our results revealed that aberrant DNA methylation of miR-34b/c was correlated with a high probability of recurrence (p = 0.026) and associated with poor overall survival (p = 0.010) and disease-free survival (p = 0.017). No significant association was found for miR-34a methylation. Multivariate analysis showed that promoter hypermethylation of miR-34b/c was an independent prognostic factor of stage Ⅰ NSCLC. Moreover, no significant association between mature miR-34b and miR-34c expression and DNA methylation status was found. In conclusion, we have identified promoter hypermethylation of miR-34b/c as a relatively common event in NSCLC and might be a potential prognostic factor for stage Ⅰ NSCLC.
肺癌是全球癌症相关死亡的主要原因,约 30-40%的Ⅰ期非小细胞肺癌 (NSCLC) 患者因疾病复发而死亡。miRNA 表达谱可作为肺癌的诊断和预后标志物。最近,miR-34 家族已被证明是 p53 通路的一部分,该通路常与肺癌有关,并且已经报道 miR-34 的表达受 DNA 甲基化调控。在本研究中,我们调查了 miR-34 家族的 DNA 甲基化状态与Ⅰ期 NSCLC 患者复发之间的相关性。通过嵌套甲基化特异性 PCR 测定了 161 例Ⅰ期 NSCLC 患者 FFPE 肿瘤组织中 miR-34a 和 miR-34b/c 启动子的甲基化状态。此外,还通过 qRT-PCR 分析了相同组织面板中的成熟 miR-34b 和 miR-34c 的表达。我们的结果表明,miR-34b/c 的异常 DNA 甲基化与高复发率相关(p=0.026),并且与总生存期(p=0.010)和无病生存期(p=0.017)较差相关。miR-34a 甲基化与无显著相关性。多因素分析表明,miR-34b/c 启动子的高甲基化是Ⅰ期 NSCLC 的独立预后因素。此外,成熟 miR-34b 和 miR-34c 的表达与 DNA 甲基化状态之间没有显著相关性。总之,我们已经确定 miR-34b/c 的启动子高甲基化为 NSCLC 中相对常见的事件,可能是Ⅰ期 NSCLC 的一个潜在预后因素。