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Transcriptional Regulation by Nrf2

期刊

ANTIOXIDANTS & REDOX SIGNALING
卷 29, 期 17, 页码 1727-1745

出版社

MARY ANN LIEBERT, INC
DOI: 10.1089/ars.2017.7342

关键词

Nrf2; transcription; antioxidant response

资金

  1. CSHL Association
  2. NIH [5P30CA45508-26, 5P50CA101955-07, 1U10CA180944-03, 5U01CA168409-5, 1R01CA190092-03, 1R01CA188134-01A1]
  3. V Foundation
  4. Thompson Family Foundation
  5. Stand Up to Cancer/KWF
  6. STARR Foundation [I7-A718]
  7. DOD [W81XWH-13-PRCRP-IA]
  8. Precision Medicine Research Associates
  9. American Italian Cancer Foundation
  10. Damon Runyon Cancer Research Foundation [DRG-2165-13]
  11. Human Frontier Science Program [LT000190/2013]

向作者/读者索取更多资源

Significance: Nuclear factor E2-related factor 2 (Nrf2) is a transcription factor that coordinates the basal and stress-inducible activation of a vast array of cytoprotective genes. Understanding the regulation of Nrf2 activity and downstream pathways has major implications for human health. Recent Advances: Nrf2 regulates the transcription of components of the glutathione and thioredoxin antioxidant systems, as well as enzymes involved in phase I and phase II detoxification of exogenous and endogenous products, NADPH regeneration, and heme metabolism. It therefore represents a crucial regulator of the cellular defense mechanisms against xenobiotic and oxidative stress. In addition to antioxidant responses, Nrf2 is involved in other cellular processes, such as autophagy, intermediary metabolism, stem cell quiescence, and unfolded protein response. Given the wide range of processes that Nrf2 controls, its activity is tightly regulated at multiple levels. Here, we review the different modes of regulation of Nrf2 activity and the current knowledge of Nrf2-mediated transcriptional control. Critical Issues: It is now clear that Nrf2 lies at the center of a complex regulatory network. A full comprehension of the Nrf2 program will require an integrated consideration of all the different factors determining Nrf2 activity. Future Directions: Additional computational and experimental studies are needed to obtain a more dynamic global view of Nrf2-mediated gene regulation. In particular, studies comparing how the Nrf2-dependent network changes from a physiological to a pathological condition can provide insight into mechanisms of disease and instruct new treatment strategies.

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