Publication | Open Access
Triterpenoid CDDO-Me Blocks the NF-κB Pathway by Direct Inhibition of IKKβ on Cys-179
231
Citations
25
References
2006
Year
Chemoprevention StrategyApoptosisImmunologyCell DeathDirect InhibitionCddo-me Form AdductsOxidative StressInflammationSignaling PathwayReceptor Tyrosine KinaseRedox BalanceAnti-cancer AgentNf-κb PathwayCell SignalingMolecular SignalingNovel Oleanane TriterpenoidTriterpenoid Cddo-me BlocksMolecular PathwayImmune FunctionPharmacologyCell BiologyTumor MicroenvironmentAnti-inflammatorySignal TransductionCellular BiochemistryMedicine
The novel oleanane triterpenoid 2-cyano-3,12-dioxooleana-1,9,-dien-28-oic acid (CDDO) and the C-28 methyl ester (CDDO-Me) induce apoptosis of human tumor cells by disruption of redox balance and are currently in clinical trials. The present studies show that CDDO and CDDO-Me block tumor necrosis factoralpha-induced targeting of NF-kappaB p65 to the nucleus. CDDO-Me also blocked tumor necrosis factor alpha-induced phosphorylation of IkappaBalpha. In concert with these results, we found that CDDO-Me inhibits IkappaBalpha kinasebeta (IKKbeta) activity in cells. In support of a direct mechanism, CDDO-Me inhibited recombinant IKKbeta activity in vitro. The results also demonstrate that (i) CDDO and CDDO-Me form adducts with IKKbeta, but not IKKbeta with mutation of Cys-179 to Ala, and (ii) CDDO-Me inhibits IKKbeta by a mechanism dependent on oxidation of Cys-179. These findings indicate that CDDO and CDDO-Me directly block IKKbeta activity and thereby the NF-kappaB pathway by interacting with Cys-179 in the IKKbeta activation loop.
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2000 | 1.3K | |
Extremely potent triterpenoid inducers of the phase 2 response: Correlations of protection against oxidant and inflammatory stress Albena T. Dinkova‐Kostova, Karen T. Liby, Katherine K. Stephenson, Proceedings of the National Academy of Sciences Lipid PeroxidationCell DeathPotent Triterpenoid InducersRedox BiologyOxidative Stress | 2005 | 560 |
2004 | 327 | |
1999 | 283 | |
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2006 | 148 | |
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2004 | 136 |
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