Department of Medical Oncology, Shandong Cancer Hospital and Institute, Jinan University, Jinan, Shandong 250117, PR China.
Biochem Biophys Res Commun. 2013 Nov 1;440(4):604-10. doi: 10.1016/j.bbrc.2013.09.111. Epub 2013 Oct 4.
MicroRNAs (miRNAs) have emerged to play important roles in tumorigenesis and drug resistance of human cancer. Fewer studies were explored the roles of miR-92b on human lung cancer cell growth and resistance to cisplatin (CDDP). In this paper, we utilized real-time PCR to verify miR-92b was significantly up-regulated in non-small cell lung cancer (NSCLC) tissues compared to matched adjacent normal tissues. In vitro assay demonstrated that knock-down of miR-92b inhabits cell growth and sensitized the A549/CDDP cells to CDDP. Furthermore, we found miR-92b could directly target PTEN, a unique tumor suppressor gene, which was downregulated in lung cancer tissues compared to the matched adjacent normal tissues. These data indicate that the miR-92b play an oncogene roles by regulates cell growth, cisplatin chemosensitivity phenotype, and could serve as a novel potential maker for NSCLC therapy.
微小 RNA(miRNAs)在人类癌症的发生和耐药中发挥着重要作用。关于 miR-92b 在人肺癌细胞生长和对顺铂(CDDP)耐药中的作用的研究较少。在本文中,我们利用实时 PCR 验证 miR-92b 在非小细胞肺癌(NSCLC)组织中明显上调,与配对的相邻正常组织相比。体外试验表明,敲低 miR-92b 抑制细胞生长并使 A549/CDDP 细胞对 CDDP 敏感。此外,我们发现 miR-92b 可以直接靶向 PTEN,一种独特的肿瘤抑制基因,与配对的相邻正常组织相比,肺癌组织中下调。这些数据表明,miR-92b 通过调节细胞生长、顺铂化疗敏感性表型发挥癌基因作用,并可作为 NSCLC 治疗的新的潜在标志物。