Rykov S V, Khodyrev D S, Pronina I V, Kazubskaya T P, Loginov V I, Braga E A
Genetika. 2013 Jul;49(7):896-901. doi: 10.7868/s0016675813070114.
MicroRNAs play an important role in the regulation of expression of many genes and are involved in carcinogenesis. The regulation of miRNA gene expression can involve the methylation of promoter CpG islands. In this work, the methylation of six miRNA genes (mir-107, mir-125b-1, mir-130b, mir-137, mir-375, and mir-1258) in non-small-cell lung cancer (NSCLC) was studied for the first time by methylation-specific PCR using a representative set of specimens (39 cases). Four new genes (mir-125b-1, mir-137, mir-375, and mir-1258) methylated in primary NSCLC tumors were identified with frequencies of 56, 31, 56, and 36%, respectively. The frequencies of miRNA promoter methylation in DNA of tumors and histologically normal tissues differed significantly (P < or = 0.05 by Fisher's test). In lung tissues of 20 donors without a history of cancer, these genes were only methylated in a few cases. It was also shown that the previously unstudied promoter CpG islands of mir-107 and mir-130b were not methylated in NSCLC. The frequencies of mir-125b-1 and mir-137 methylation were shown for the first time to correlate with NSCLC progression (clinical stage and metastasis).
微小RNA在许多基因表达的调控中发挥重要作用,并参与肿瘤发生。微小RNA基因表达的调控可能涉及启动子CpG岛的甲基化。在本研究中,首次采用甲基化特异性PCR方法,利用一组具有代表性的标本(39例)对非小细胞肺癌(NSCLC)中6个微小RNA基因(mir-107、mir-125b-1、mir-130b、mir-137、mir-375和mir-1258)的甲基化情况进行了研究。在原发性NSCLC肿瘤中发现4个新的甲基化基因(mir-125b-1、mir-137、mir-375和mir-1258),其甲基化频率分别为56%、31%、56%和36%。肿瘤组织和组织学正常组织DNA中微小RNA启动子甲基化频率差异有统计学意义(Fisher检验P≤0.05)。在20例无癌症病史供体的肺组织中,这些基因仅在少数病例中发生甲基化。研究还表明,mir-107和mir-130b之前未被研究的启动子CpG岛在NSCLC中未发生甲基化。首次发现mir-125b-1和mir-137的甲基化频率与NSCLC进展(临床分期和转移)相关。