Department of Pharmacology and Toxicology, University of Arizona, Tucson, AZ, USA.
University of Arizona Cancer Center, University of Arizona, Tucson, AZ, USA.
Arch Pharm Res. 2020 Mar;43(3):361-369. doi: 10.1007/s12272-019-01177-2. Epub 2019 Aug 1.
Kidney disease affects ~ 10% of the population worldwide, resulting in millions of deaths each year. Mechanistically, oxidative stress is a major driver of various kidney diseases, and promotes the progression from acute to chronic injury, as well as renal cancer development. NRF2, the master regulator of redox balance, has been shown to protect against kidney disease through its negation of reactive oxygen species (ROS). However, many kidney diseases exhibit high levels of ROS as a result of decreased NRF2 protein levels and transcriptional activity. Many studies have tested the strategy of using NRF2 inducing compounds to alleviate ROS to prevent or slow down the progression of kidney diseases. Oppositely, in specific subsets of renal cancer, NRF2 is constitutively activated and contributes to tumor burden and overall poor prognosis; therefore, there has been a recent interest in studies investigating the benefits of NRF2 inhibition. In this review, we summarize recent literature investigating the role of NRF2 and oxidative stress in various kidney diseases, and how pharmacological modification of NRF2 signaling could play a protective role.
肾脏疾病影响着全球约 10%的人口,每年导致数百万人死亡。从机制上讲,氧化应激是多种肾脏疾病的主要驱动因素,它促进了从急性损伤向慢性损伤以及肾癌发展的转变。NRF2 是氧化还原平衡的主要调节因子,通过否定活性氧(ROS)来保护肾脏免受疾病侵害。然而,许多肾脏疾病由于 NRF2 蛋白水平和转录活性降低而表现出高水平的 ROS。许多研究已经测试了使用 NRF2 诱导化合物来减轻 ROS 以预防或减缓肾脏疾病进展的策略。相反,在特定的肾癌亚群中,NRF2 持续激活,导致肿瘤负担增加和整体预后不良;因此,最近人们对研究 NRF2 抑制的益处产生了兴趣。在这篇综述中,我们总结了最近研究 NRF2 和氧化应激在各种肾脏疾病中的作用的文献,以及 NRF2 信号的药理学修饰如何发挥保护作用。