转录因子
神经退行性变
KEAP1型
疾病
调节器
背景(考古学)
生物信息学
医学
信号转导
临床试验
神经科学
细胞生物学
癌症研究
生物
计算生物学
药理学
内科学
遗传学
基因
古生物学
作者
Matthew Dodson,Montserrat Rojo de la Vega,Aram B. Cholanians,Cody J. Schmidlin,Eli Chapman,Donna D. Zhang
标识
DOI:10.1146/annurev-pharmtox-010818-021856
摘要
The transcription factor nuclear factor erythroid 2 (NF-E2)-related factor 2 (NRF2) is a central regulator of redox, metabolic, and protein homeostasis that intersects with many other signaling cascades. Although the understanding of the complex nature of NRF2 signaling continues to grow, there is only one therapeutic targeting NRF2 for clinical use, dimethyl fumarate, used for the treatment of multiple sclerosis. The discovery of new therapies is confounded by the fact that NRF2 levels vary significantly depending on physiological and pathological context. Thus, properly timed and targeted manipulation of the NRF2 pathway is critical in creating effective therapeutic regimens. In this review, we summarize the regulation and downstream targets of NRF2. Furthermore, we discuss the role of NRF2 in cancer, neurodegeneration, and diabetes as well as cardiovascular, kidney, and liver disease, with a special emphasis on NRF2-based therapeutics, including those that have made it into clinical trials.
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