Translational Research Laboratory, Department of Pathology, Stony Brook University, Stony Brook, NY, USA.
Cell Cycle. 2013 Jan 15;12(2):246-50. doi: 10.4161/cc.23273. Epub 2012 Jan 15.
Autophagy is a catabolic process that allows cellular macromolecules to be broken down and recycled into metabolic precursors. It is a highly conserved, critical process, allowing cells to gain survival advantages under various stress situations due to growth and environmental changes. In the past few years, mounting evidence indicates that the post-transcriptional and translational controls mediated by non-coding miRNAs contribute significantly to autophagy in cancer. Such acute modulation of protein synthesis mediated by miRNAs provides cells with advantages in response to starvation, genotoxic stress and hypoxia. In this review, we highlight some of the important discoveries and molecular insights of miRNAs in regulating autophagy based on various cancer models.
自噬是一种分解代谢过程,允许细胞内的大分子物质被分解并回收成代谢前体。它是一种高度保守的关键过程,使细胞能够在由于生长和环境变化而导致的各种应激情况下获得生存优势。在过去的几年中,越来越多的证据表明,非编码 miRNAs 介导的转录后和翻译调控对癌症中的自噬有重要贡献。miRNAs 对蛋白质合成的这种急性调节为细胞在应对饥饿、遗传毒性应激和缺氧时提供了优势。在这篇综述中,我们根据各种癌症模型强调了 miRNA 在调节自噬方面的一些重要发现和分子见解。