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Perspectives Regarding the Intersections between STAT3 and Oxidative Metabolism in Cancer.
Chun, Kyung-Soo; Jang, Jeong-Hoon; Kim, Do-Hee.
Afiliação
  • Chun KS; College of Pharmacy, Keimyung University, Daegu 42601, Korea.
  • Jang JH; Tumor Microenvironment Global Core Research Center, College of Pharmacy, Seoul National University, Seoul 08826, Korea.
  • Kim DH; Department of Chemistry, College of Convergence and Integrated Science, Kyonggi University, Suwon, Gyonggi-do 16277, Korea.
Cells ; 9(10)2020 09 29.
Article em En | MEDLINE | ID: mdl-33003453
ABSTRACT
Signal transducer and activator of transcription 3 (STAT3) functions as a major molecular switch that plays an important role in the communication between cytokines and kinases. In this role, it regulates the transcription of genes involved in various biochemical processes, such as proliferation, migration, and metabolism of cancer cells. STAT3 undergoes diverse post-translational modifications, such as the oxidation of cysteine by oxidative stress, the acetylation of lysine, or the phosphorylation of serine/threonine. In particular, the redox modulation of critical cysteine residues present in the DNA-binding domain of STAT3 inhibits its DNA-binding activity, resulting in the inactivation of STAT3-mediated gene expression. Accumulating evidence supports that STAT3 is a key protein that acts as a mediator of metabolism and mitochondrial activity. In this review, we focus on the post-translational modifications of STAT3 by oxidative stress and how the modification of STAT3 regulates cell metabolism, particularly in the metabolic pathways in cancer cells.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Estresse Oxidativo / Fator de Transcrição STAT3 / Mitocôndrias / Neoplasias Limite: Humans Idioma: En Revista: Cells Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Estresse Oxidativo / Fator de Transcrição STAT3 / Mitocôndrias / Neoplasias Limite: Humans Idioma: En Revista: Cells Ano de publicação: 2020 Tipo de documento: Article
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