Dual Roles of Nrf2 in Cancer

Keap1 is a key regulator of the Nrf2 signaling pathway and serves as a molecular switch to turn on and off the Nrf2-mediated antioxidant response. (i) The switch is in off position: under basal conditions, Keap1, functioning as an E3 ubiquitin ligase, constantly targets Nrf2 for ubiquitination and degradation. As a consequence, there are minimal levels of Nrf2. (ii) The switch is turned on: oxidative stress or chemopreventive compounds inhibit activity of the Keap1-Cul3-Rbx1 E3 ubiquitin ligase, resulting in increased levels of Nrf2 and activation of its downstream target genes. (iii) The switch is turned off again: Upon recovery of cellular redox homeostasis, Keap1 travels into the nucleus to remove Nrf2 from the ARE. The Nrf2-Keap1 complex is then transported out of the nucleus by the NES in Keap1. In the cytosol, the Nrf2-Keap1 complex associates with the Cul3-Rbx1 core ubiquitin machinery, leading to degradation of Nrf2. For clarity, the constitutive cytoplasmic-nuclear shuttling of Nrf2, Keap1, and the complex is omitted.

Publication

Dual Roles of Nrf2 in Cancer. () Alexandria Lau, et al. Pharmacol Res. ;58(5-6):262-270. Figure: F1. All organisms Mus musculus Homo sapiens Rattus norvegicus Gallus gallus Drosophila melanogaster

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