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miRNAs 调控 Nrf2 抗氧化通路:氧化还原平衡调控中的新角色

Regulation of the Nrf2 antioxidant pathway by microRNAs: New players in micromanaging redox homeostasis.

机构信息

Cardiovascular Division, British Heart Foundation Centre for Research Excellence, School of Medicine, King's College London, London, UK.

出版信息

Free Radic Biol Med. 2013 Sep;64:4-11. doi: 10.1016/j.freeradbiomed.2013.07.025. Epub 2013 Jul 21.

Abstract

MicroRNAs are now thought to play a central role in the regulation of many diverse aspects of cell biology; however, it remains to be fully elucidated how microRNAs can orchestrate cellular redox homeostasis, which plays a central role in a multitude of physiological and pathophysiological processes. The redox-sensitive transcription factor nuclear factor erythroid 2-related factor 2 (Nrf2) serves as a "master regulator" of cell survival through the coordinated induction of phase II and antioxidant defense enzymes to counteract oxidative stress and modulate redox signaling events. MicroRNAs are able to "fine-tune" the regulation of processes including those directly interacting with the Nrf2 pathway and the generation of reactive oxygen species (ROS). This review highlights that cellular redox homeostasis can be regulated by microRNAs through their modulation of Nrf2-driven antioxidant gene expression as well as key enzymes that generate ROS, which in turn can alter the biogenesis and processing of microRNAs. Therefore redox sensitive microRNAs or "redoximiRs" add an important regulatory mechanism for redox signaling beyond the well-characterized actions of Nrf2. The potential exists for microRNA-based therapies where diminished antioxidant defenses and dysregulated redox signaling can lead to cardiovascular diseases, cancers, neurodegeneration, and accelerated aging.

摘要

MicroRNAs 现在被认为在细胞生物学的许多不同方面的调节中发挥核心作用;然而,microRNAs 如何协调细胞氧化还原稳态仍有待充分阐明,氧化还原稳态在许多生理和病理生理过程中起着核心作用。氧化还原敏感转录因子红细胞生成素 2 相关因子 2(Nrf2)通过协调诱导 II 相和抗氧化防御酶来抵抗氧化应激并调节氧化还原信号事件,作为细胞存活的“主调控因子”。microRNAs 能够“微调”包括与 Nrf2 途径直接相互作用和产生活性氧(ROS)的那些过程的调节。这篇综述强调,细胞氧化还原稳态可以通过 microRNAs 调节 Nrf2 驱动的抗氧化基因表达以及产生 ROS 的关键酶来调节,这反过来又可以改变 microRNAs 的生物发生和加工。因此,氧化还原敏感的 microRNAs 或“氧化还原 microRNAs”除了 Nrf2 的特征性作用之外,为氧化还原信号增加了一个重要的调节机制。基于 microRNA 的治疗存在的潜力,其中抗氧化防御的减弱和失调的氧化还原信号会导致心血管疾病、癌症、神经退行性变和加速衰老。

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