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Molecular mechanisms of Nrf2 regulation and how these influence chemical modulation for disease intervention.
Harder, Bryan; Jiang, Tao; Wu, Tongde; Tao, Shasha; Rojo de la Vega, Montserrat; Tian, Wang; Chapman, Eli; Zhang, Donna D.
Afiliación
  • Harder B; Department of Pharmacology and Toxicology, University of Arizona, Tucson, Arizona 85721, U.S.A.
  • Jiang T; Department of Pharmacology and Toxicology, University of Arizona, Tucson, Arizona 85721, U.S.A.
  • Wu T; Department of Pharmacology and Toxicology, University of Arizona, Tucson, Arizona 85721, U.S.A.
  • Tao S; Department of Pharmacology and Toxicology, University of Arizona, Tucson, Arizona 85721, U.S.A.
  • Rojo de la Vega M; Department of Pharmacology and Toxicology, University of Arizona, Tucson, Arizona 85721, U.S.A.
  • Tian W; Department of Pharmacology and Toxicology, University of Arizona, Tucson, Arizona 85721, U.S.A.
  • Chapman E; Department of Pharmacology and Toxicology, University of Arizona, Tucson, Arizona 85721, U.S.A.
  • Zhang DD; Department of Pharmacology and Toxicology, University of Arizona, Tucson, Arizona 85721, U.S.A. Arizona Cancer Center, University of Arizona, Tucson, Arizona 85724, U.S.A. dzhang@pharmacy.arizona.edu.
Biochem Soc Trans ; 43(4): 680-6, 2015 Aug.
Article en En | MEDLINE | ID: mdl-26551712
Nrf2 (nuclear factor erytheroid-derived-2-like 2) transcriptional programmes are activated by a variety of cellular stress conditions to maintain cellular homoeostasis. Under non-stress conditions, Nrf2 is under tight regulation by the ubiquitin proteasome system (UPS). Detailed mechanistic investigations have shown the Kelch-like ECH-associated protein 1 (Keap1)-cullin3 (Cul3)-ring-box1 (Rbx1) E3-ligase to be the primary Nrf2 regulatory system. Recently, both beta-transducin repeat-containing E3 ubiquitin protein ligase (ß-TrCP) and E3 ubiquitin-protein ligase synoviolin (Hrd1) have been identified as novel E3 ubiquitin ligases that negatively regulate Nrf2 through Keap1-independent mechanisms. In addition to UPS-mediated regulation of Nrf2, investigations have revealed a cross-talk between Nrf2 and the autophagic pathway resulting in activation of Nrf2 in a non-canonical manner. In addition to regulation at the protein level, Nrf2 was recently shown to be regulated at the transcriptional level by oncogenic K-rat sarcoma (Ras). A consequence of these differential regulatory mechanisms is the dual role of Nrf2 in cancer: the canonical, protective role and the non-canonical 'dark-side' of Nrf2. Based on the protective role of Nrf2, a vast effort has been dedicated towards identifying novel chemical inducers of Nrf2 for the purpose of chemoprevention. On the other hand, upon malignant transformation, some cancer cells have a constitutively high level of Nrf2 offering a growth advantage, as well as rendering cancer cells resistant to chemotherapeutics. This discovery has led to a new paradigm in cancer treatment; the initially counterintuitive use of Nrf2 inhibitors as adjuvants in chemotherapy. Herein, we will discuss the mechanisms of Nrf2 regulation and how this detailed molecular understanding can be leveraged to develop Nrf2 modulators to prevent diseases, mitigate disease progression or overcome chemoresistance.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Regulación Neoplásica de la Expresión Génica / Factor 2 Relacionado con NF-E2 / Neoplasias Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Biochem Soc Trans Año: 2015 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Regulación Neoplásica de la Expresión Génica / Factor 2 Relacionado con NF-E2 / Neoplasias Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Biochem Soc Trans Año: 2015 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Reino Unido