Vincent Kimberly, Pichler Martin, Lee Gyeong-Won, Ling Hui
Department of Experimental Therapeutics, the University of Texas MD Anderson Cancer Center, Houston, TX 77054, USA.
Division of Hematology-Oncology, Department of Internal Medicine, Gyeongsang National University Hospital, Gyeongsang National University School of Medicine, Jinju 660-702, Korea.
Int J Mol Sci. 2014 Aug 20;15(8):14475-91. doi: 10.3390/ijms150814475.
MicroRNAs (miRNAs) are small non-coding RNA transcripts approximately 20 nucleotides in length that regulate expression of protein-coding genes via complementary binding mechanisms. The last decade has seen an exponential increase of publications on miRNAs, ranging from every aspect of basic cancer biology to diagnostic and therapeutic explorations. In this review, we summarize findings of miRNA involvement in genomic instability, an interesting but largely neglected topic to date. We discuss the potential mechanisms by which miRNAs induce genomic instability, considered to be one of the most important driving forces of cancer initiation and progression, though its precise mechanisms remain elusive. We classify genomic instability mechanisms into defects in cell cycle regulation, DNA damage response, and mitotic separation, and review the findings demonstrating the participation of specific miRNAs in such mechanisms.
微小RNA(miRNA)是长度约为20个核苷酸的小型非编码RNA转录本,其通过互补结合机制调控蛋白质编码基因的表达。在过去十年中,关于miRNA的出版物呈指数级增长,涵盖了从基础癌症生物学的各个方面到诊断和治疗探索等诸多领域。在本综述中,我们总结了miRNA参与基因组不稳定的研究结果,这是一个有趣但迄今为止在很大程度上被忽视的主题。我们讨论了miRNA诱导基因组不稳定的潜在机制,基因组不稳定被认为是癌症发生和发展的最重要驱动力之一,尽管其确切机制仍不清楚。我们将基因组不稳定机制分为细胞周期调控缺陷、DNA损伤反应和有丝分裂分离缺陷,并综述了表明特定miRNA参与这些机制的研究结果。