Liu Xuzhi, Shi Hanbing, Liu Bo, Li Jianing, Liu Yaxin, Yu Baiquan
Department of Respiratory Medicine, the Third Affiliated Hospital of Qiqihar Medical University, Qiqihar 161000, China.
Department of Respiratory Medicine, the Second Affiliated Hospital of Harbin Medical University, Harbin 150086, China.
Acta Biochim Biophys Sin (Shanghai). 2015 Jun;47(6):431-40. doi: 10.1093/abbs/gmv032. Epub 2015 May 2.
Non-small-cell lung cancer (NSCLC) is one of the most common lung cancers, and microRNAs (miRNAs) have been reported to play essential roles in NSCLC. Recent studies have indicated that miR-330-3p expression is up-regulated in NSCLC samples and in tissues of NSCLC brain metastasis. In this study, up-regulation of miR-330-3p expression was confirmed in NSCLC and 20 NSCLC patient samples. Furthermore, miR-330-3p was over-expressed in NSCLC cell lines A549 and H23, and the promotive function of miR-330-3p was investigated in regulating NSCLC cell proliferation and cell cycle distribution. To identify potential target genes of miR-330-3p in NSCLC, the miRNA target prediction databases were used. Luciferase activity assay and real-time RT-PCR analysis confirmed that miR-330-3p is negatively correlated with the expression of early growth response 2 (EGR2). Moreover, it was also found that EGR2 mRNA contains two potential binding sites for miR-330-3p. Knock-down of EGR2 with siRNA was demonstrated to have a similar effect as the over-expression of miR-330-3p in NSCLC cell lines. Taken together, our results show that EGR2 is a target of miR-330-3p.
非小细胞肺癌(NSCLC)是最常见的肺癌类型之一,据报道,微小RNA(miRNA)在NSCLC中发挥着重要作用。最近的研究表明,miR-330-3p在NSCLC样本和NSCLC脑转移组织中的表达上调。在本研究中,在NSCLC和20例NSCLC患者样本中证实了miR-330-3p表达上调。此外,miR-330-3p在NSCLC细胞系A549和H23中过表达,并研究了miR-330-3p在调节NSCLC细胞增殖和细胞周期分布中的促进作用。为了鉴定NSCLC中miR-330-3p的潜在靶基因,使用了miRNA靶标预测数据库。荧光素酶活性测定和实时RT-PCR分析证实,miR-330-3p与早期生长反应2(EGR2)的表达呈负相关。此外,还发现EGR2 mRNA包含两个miR-330-3p的潜在结合位点。在NSCLC细胞系中,用siRNA敲低EGR2被证明与miR-330-3p过表达具有相似的效果。综上所述,我们的结果表明EGR2是miR-330-3p的靶标。