Wang Qi, Zhong Meizuo, Liu Wei, Li Jianhuang, Huang Jin, Zheng Le
Department of Oncology, The Third Xiangya Hospital of Central South University, Changsha, Hunan Province, PR China.
Exp Lung Res. 2011 Sep;37(7):427-34. doi: 10.3109/01902148.2011.584263. Epub 2011 Jul 25.
ABSTRACT MicroRNAs (miRNAs) are a class of small, noncoding RNAs that posttranscriptionally regulate genes expression and play crucial roles in diverse biological processes, such as development, differentiation, apoptosis, and proliferation. Accumulating evidence suggests that miRNAs may play a role in chemoresistance and may be involved in the modulation of some drug resistance-related pathways in cancer cells. Here, the authors investigated the possible role of miRNAs in the development of drug resistance in lung cancer cell line. The results showed that 14 miRNAs were presented significantly (>2-fold), including up-regulation of 9 miRNAs and down-regulation of 5 miRNAs in A549/DDP cell line, compared with the parental A549 cell line. Up-regulation of miR-138 increased the sensitivity of A549/DDP cells to cisplatin in in vitro drug sensitivity assay, and increased apoptosis assessed by flow cytometry. The authors also found that excision repair cross-complementation group 1 (ERCC1) was negatively regulated by miR-138 and that down-regulation of ERCC1 at the protein level largely correlated with elevated levels of miR-138 in A549/DDP cells. Taken together, these findings suggest that miR-138 could play an important role in the development of cisplatin resistance in non-small cell lung cancer (NSCLC).
摘要 微小RNA(miRNA)是一类小的非编码RNA,可在转录后调节基因表达,并在多种生物学过程中发挥关键作用,如发育、分化、凋亡和增殖。越来越多的证据表明,miRNA可能在化疗耐药中起作用,并且可能参与癌细胞中一些与耐药相关途径的调节。在此,作者研究了miRNA在肺癌细胞系耐药性发展中的可能作用。结果显示,与亲代A549细胞系相比,A549/DDP细胞系中有14种miRNA呈现出显著变化(>2倍),包括9种miRNA上调和5种miRNA下调。在体外药敏试验中,miR-138的上调增加了A549/DDP细胞对顺铂的敏感性,并通过流式细胞术评估显示凋亡增加。作者还发现,切除修复交叉互补组1(ERCC1)受miR-138负调控,并且在A549/DDP细胞中,ERCC1蛋白水平的下调与miR-138水平的升高在很大程度上相关。综上所述,这些发现表明miR-138可能在非小细胞肺癌(NSCLC)顺铂耐药性的发展中起重要作用。