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The Multi-Faceted Consequences of NRF2 Activation throughout Carcinogenesis.
Occhiuto, Christopher J; Moerland, Jessica A; Leal, Ana S; Gallo, Kathleen A; Liby, Karen T.
Afiliación
  • Occhiuto CJ; Department of Pharmacology and Toxicology, Michigan State University, East Lansing, MI 48824, USA.
  • Moerland JA; College of Human Medicine, Michigan State University, East Lansing, MI 48824, USA.
  • Leal AS; Department of Pharmacology and Toxicology, Michigan State University, East Lansing, MI 48824, USA.
  • Gallo KA; College of Osteopathic Medicine, Michigan State University, East Lansing, MI 48824, USA.
  • Liby KT; Department of Pharmacology and Toxicology, Michigan State University, East Lansing, MI 48824, USA.
Mol Cells ; 46(3): 176-186, 2023 Mar 31.
Article en En | MEDLINE | ID: mdl-36994476
ABSTRACT
The oxidative balance of a cell is maintained by the Kelch-like ECH-associated protein 1 (KEAP1)/nuclear factor erythroid 2-related factor 2 (NRF2) pathway. This cytoprotective pathway detoxifies reactive oxygen species and xenobiotics. The role of the KEAP1/NRF2 pathway as pro-tumorigenic or anti-tumorigenic throughout stages of carcinogenesis (including initiation, promotion, progression, and metastasis) is complex. This mini review focuses on key studies describing how the KEAP1/NRF2 pathway affects cancer at different phases. The data compiled suggest that the roles of KEAP1/NRF2 in cancer are highly dependent on context; specifically, the model used (carcinogen-induced vs genetic), the tumor type, and the stage of cancer. Moreover, emerging data suggests that KEAP1/NRF2 is also important for regulating the tumor microenvironment and how its effects are amplified either by epigenetics or in response to co-occurring mutations. Further elucidation of the complexity of this pathway is needed in order to develop novel pharmacological tools and drugs to improve patient outcomes.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Factor 2 Relacionado con NF-E2 / Neoplasias Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Mol Cells Asunto de la revista: BIOLOGIA MOLECULAR Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Factor 2 Relacionado con NF-E2 / Neoplasias Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Mol Cells Asunto de la revista: BIOLOGIA MOLECULAR Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos