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Cited by 868

The DOI matches its Crossref record; 119 of the 119 references it cites were found in a registry or an index.

Regulation of Nrf2—an update

Open access
Niture, Suryakant K., Khatri, Raju, Jaiswal, Anil K.·2014·Free Radical Biology and Medicine

Abstract

Nrf2:INrf2 (Keap1) are cellular sensors of oxidative and electrophilic stress. Nrf2 is a nuclear factor that controls the expression and coordinated induction of a battery of genes which encode detoxifying enzymes, drug transporters (MRPs), anti-apoptotic proteins and proteasomes. In the basal state, Nrf2 is constantly degraded in the cytoplasm by its inhibitor, INrf2. INrf2 functions as an adapter for Cul3/Rbx1 E3 ubiquitin ligase mediated degradation of Nrf2. Chemicals including antioxidants, tocopherols including α-tocopherol (vitamin E), phytochemicals and radiations antagonize the Nrf2:INrf2 interaction and leads to the stabilization and activation of Nrf2. The signaling events involve pre-induction, induction and post-induction responses that tightly control Nrf2 activation and repression back to the basal state. Oxidative/electrophilic signals activate unknown tyrosine kinase(s) in a pre-induction response which phosphorylates specific residues on Nrf2 negative-regulators, INrf2, Fyn and Bach1, leading to their nuclear export, ubiquitination and degradation. This prepares nuclei for unhindered import of Nrf2. Oxidative/electrophilic modification of INrf2cysteine151 followed by PKC phosphorylation of Nrf2serine40 in the induction response results in the escape or release of Nrf2 from INrf2. Nrf2 is thus stabilized and translocates to the nucleus resulting in a coordinated activation of gene expression. This is followed by a post-induction response that controls the ‘switching off’ of Nrf2-activated gene expression. GSK3β under the control of AKT and PI3K, phosphorylates Fyn leading to Fyn nuclear localization. Fyn phosphorylates Nrf2Y568 resulting in nuclear export and degradation of Nrf2. The activation and repression of Nrf2 provides protection against oxidative/electrophilic stress and associated diseases, including cancer. However, deregulation of INrf2 and Nrf2 due to mutations may lead to nuclear accumulation of Nrf2 that reduces apoptosis and promotes oncogenesis and drug resistance.

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Metadata

Authors
Niture, S. K., Khatri, R., & Jaiswal, A. K.
Venue
Free Radical Biology and Medicine
Publisher
Elsevier BV
Published
2014-01
Volume
66
Pages
36-44
ISSN
0891-5849 (ISSN-L)
OpenAlex
W1999718232
Cited by
868
References
119
FWCI
27.16
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Regulation of Nrf2—an update. https://app.cochat.ai/papers/10.1016/j.freeradbiomed.2013.02.008
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Niture, S. K., Khatri, R., & Jaiswal, A. K. (2014). Regulation of Nrf2—an update. Free Radical Biology and Medicine. https://doi.org/10.1016/j.freeradbiomed.2013.02.008

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