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Signaling from RAS to RAF: The Molecules and Their Mechanisms.
Jeon, Hyesung; Tkacik, Emre; Eck, Michael J.
Afiliación
  • Jeon H; Department of Cancer Biology, Dana-Farber Cancer Institute, Boston, Massachusetts, USA; email: Michael_Eck@dfci.harvard.edu.
  • Tkacik E; Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, Massachusetts, USA.
  • Eck MJ; Department of Cancer Biology, Dana-Farber Cancer Institute, Boston, Massachusetts, USA; email: Michael_Eck@dfci.harvard.edu.
Annu Rev Biochem ; 93(1): 289-316, 2024 Aug.
Article en En | MEDLINE | ID: mdl-38316136
ABSTRACT
RAF family protein kinases are a key node in the RAS/RAF/MAP kinase pathway, the signaling cascade that controls cellular proliferation, differentiation, and survival in response to engagement of growth factor receptors on the cell surface. Over the past few years, structural and biochemical studies have provided new understanding of RAF autoregulation, RAF activation by RAS and the SHOC2 phosphatase complex, and RAF engagement with HSP90-CDC37 chaperone complexes. These studies have important implications for pharmacologic targeting of the pathway. They reveal RAF in distinct regulatory states and show that the functional RAF switch is an integrated complex of RAF with its substrate (MEK) and a 14-3-3 dimer. Here we review these advances, placing them in the context of decades of investigation of RAF regulation. We explore the insights they provide into aberrant activation of the pathway in cancer and RASopathies (developmental syndromes caused by germline mutations in components of the pathway).
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Transducción de Señal / Proteínas ras / Quinasas raf Límite: Animals / Humans Idioma: En Revista: Annu Rev Biochem Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Transducción de Señal / Proteínas ras / Quinasas raf Límite: Animals / Humans Idioma: En Revista: Annu Rev Biochem Año: 2024 Tipo del documento: Article