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 accessAbstract
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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Cites
10 retracted
Niture, S. K., Jain, A. K., & Jaiswal, A. K. (2009) · Journal of Cell Science · doi:10.1242/jcs.058537 · Cited by 192
Self-citationRetractedPhosphorylation of Tyrosine 568 Controls Nuclear Export of Nrf2
Jain, A. K., & Jaiswal, A. K. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m511198200 · Cited by 172
Self-citationRetractedLong, D. J., Gaikwad, A. S., Multani, A. S., Pathak, S., Montgomery, C. A., Gonzalez, F. J., & Jaiswal, A. K. (2018) · Cancer Research · doi:10.1158/0008-5472.can-18-2455 · Cited by 112
Self-citationRetractedINrf2 (Keap1) targets Bcl-2 degradation and controls cellular apoptosis
Niture, S. K., & Jaiswal, A. K. (2010) · Cell Death and Differentiation · doi:10.1038/cdd.2010.114 · Cited by 90
Self-citationRetractedNiture, S. K., Jain, A. K., Shelton, P. M., & Jaiswal, A. K. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.255042 · Cited by 83
Self-citationRetractedNiture, S. K., & Jaiswal, A. K. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.275073 · Cited by 74
Self-citationRetractedProthymosin-α Mediates Nuclear Import of the INrf2/Cul3·Rbx1 Complex to Degrade Nuclear Nrf2
Niture, S. K., & Jaiswal, A. K. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m808084200 · Cited by 69
Self-citationRetractedKaspar, J. W., Niture, S. K., & Jaiswal, A. K. (2012) · Journal of Cell Science · doi:10.1242/jcs.097295 · Cited by 44
Self-citationRetractedHsp90 Interaction with INrf2(Keap1) Mediates Stress-induced Nrf2 Activation
Niture, S. K., & Jaiswal, A. K. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.175802 · Cited by 41
Self-citationRetractedIskander, K. S., Barrios, R. J., & Jaiswal, A. K. (2009) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-08-1783 · Cited by 13
Self-citationRetracted
Cited by
Kurutas, E. B. (2015) · Nutrition Journal · doi:10.1186/s12937-016-0186-5 · Cited by 2,152
Oxidative stress response and Nrf2 signaling in aging
Zhang, H., Davies, K. J. A., & Forman, H. J. (2015) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2015.05.036 · Cited by 804
Sivandzade, F., Prasad, S., Bhalerao, A., & Cucullo, L. (2019) · Redox Biology · doi:10.1016/j.redox.2018.11.017 · Cited by 639
Redox activation of Nrf2 & NF-κB: A double end sword?
Buelna-Chontal, M., & Zazueta, C. (2013) · Cellular Signalling · doi:10.1016/j.cellsig.2013.08.007 · Cited by 239
Effects of Glucagon-Like Peptide-1 on Oxidative Stress and Nrf2 Signaling
Oh, Y., & Jun, H.-S. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms19010026 · Cited by 217
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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