Abstract

Nuclear factor erythroid 2-related factor 2 (NRF2) is a transcription factor that regulates the cellular defense against toxic and oxidative insults through the expression of genes involved in oxidative stress response and drug detoxification. NRF2 activation renders cells resistant to chemical carcinogens and inflammatory challenges. In addition to antioxidant responses, NRF2 is involved in many other cellular processes, including metabolism and inflammation, and its functions are beyond the originally envisioned. NRF2 activity is tightly regulated through a complex transcriptional and post-translational network that enables it to orchestrate the cell’s response and adaptation to various pathological stressors for the homeostasis maintenance. Elevated or decreased NRF2 activity by pharmacological and genetic manipulations of NRF2 activation is associated with many metabolism- or inflammation-related diseases. Emerging evidence shows that NRF2 lies at the center of a complex regulatory network and establishes NRF2 as a truly pleiotropic transcription factor. Here we summarize the complex regulatory network of NRF2 activity and its roles in metabolic reprogramming, unfolded protein response, proteostasis, autophagy, mitochondrial biogenesis, inflammation, and immunity.

Keywords

ProteostasisTranscription factorCell biologyBiologyKEAP1Cellular stress responseInflammationOxidative stressReprogrammingAutophagyNRF1XBP1GeneticsCellImmunologyGeneBiochemistryFight-or-flight responseRNAApoptosis

MeSH Terms

AnimalsAutophagyGene Expression RegulationHumansInflammationNF-E2-Related Factor 2Oxidative StressUnfolded Protein Response

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Publication Info

Year
2020
Type
review
Volume
21
Issue
13
Pages
4777-4777
Citations
1485
Access
Closed

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Social media, news, blog, policy document mentions

Citation Metrics

1485
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49
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1397
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Cite This

Feng He, Xiaoli Ru, Tao Wen (2020). NRF2, a Transcription Factor for Stress Response and Beyond. International Journal of Molecular Sciences , 21 (13) , 4777-4777. https://doi.org/10.3390/ijms21134777

Identifiers

DOI
10.3390/ijms21134777
PMID
32640524
PMCID
PMC7369905

Data Quality

Data completeness: 90%