He Jun, Jiang Bing-Hua
Department of Pathology, Anatomy and Cell Biology, Thomas Jefferson University, Philadelphia, USA.
Curr Pharmacol Rep. 2016 Apr;2(2):82-90. doi: 10.1007/s40495-016-0051-4. Epub 2016 Feb 9.
Since both reactive oxygen species (ROS) production and microRNAs expression signature have been associated with tumor development, progression, metastasis and therapeutic response, it is important to understand the crosstalk between ROS and microRNAs. Indeed, growing evidence suggests a reciprocal connection between ROS signaling and microRNAs pathway, resulting in diverse biological effects in cancer cells. In this mini review, we discussed the ROS-responsive microRNAs that have implications in cancer and the possible mechanisms in which ROS regulate microRNAs. We also highlighted the microRNAs which are able to modify cellular ROS homeostasis during tumorigenesis, their biological targets and subsequent functions. As the use of antioxidants is limited due to the diverse or even opposing roles of ROS signaling in cancer, the discovery of ROS-responsive microRNAs provides a potential new strategy to specifically overcome ROS-mediated tumor progression or benefit from ROS-induced apoptosis.
由于活性氧(ROS)的产生和微小RNA表达特征均与肿瘤的发生、发展、转移及治疗反应相关,因此了解ROS与微小RNA之间的相互作用至关重要。的确,越来越多的证据表明ROS信号传导与微小RNA通路之间存在相互联系,从而在癌细胞中产生多种生物学效应。在本综述中,我们讨论了与癌症相关的ROS反应性微小RNA以及ROS调节微小RNA的可能机制。我们还强调了在肿瘤发生过程中能够改变细胞ROS稳态的微小RNA、它们的生物学靶点及后续功能。由于ROS信号在癌症中具有多种甚至相反的作用,限制了抗氧化剂的使用,因此ROS反应性微小RNA的发现为特异性克服ROS介导的肿瘤进展或从ROS诱导的细胞凋亡中获益提供了一种潜在的新策略。