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This includes epigenetic modifications that dictate the promoter accessibility of NFE2L2 /NRF2 or its negative regulators, microRNA-dependent suppression of NRF2 translation, or regulation of NRF2 protein stability, either through interaction with E3 ligase complexes that target it for degradation (i.e., Kelch-like ECH-associated protein 1/Cullin 3/Ring box 1 [KEAP1-CUL3-RBX1], HRD1, and S-phase kinase-associated protein 1-Cullin 1-RBX1/-transducin repeat-containing protein [SCF/-TRCP]) or other binding partners (discussed in more detail below) that stabilize and prevent its degradation (Fig