The TOR Kinases Link Nutrient Sensing to Cell Growth

John Rohde, Joseph Heitman, Maria E. Cardenas

Producción científica: Contribución a una revistaEncuesta cortarevisión exhaustiva

304 Citas (Scopus)

Resumen

Rapamycin is an immunosuppressive natural product that inhibits the proliferation of T-cells in response to nutrients and growth factors. Rapamycin binds to the peptidyl-prolyl isomerase FKBP12 and forms protein-drug complexes that inhibit signal transduction by the TOR kinases. The FKBP12 and TOR proteins are conserved from fungi to humans, and in both organisms the TOR signaling pathway plays a role in nutrient sensing. In response to nitrogen sources or amino acids, TOR regulates both transcription and translation, enabling cells to appropriately respond to growth-promoting signals. Rapamycin is having a profound impact on clinical medicine and was approved as an immunosuppressant for transplant recipients in 1999. Ongoing clinical studies address new clinical applications for rapamycin as an antiproliferative drug for chemotherapy and invasive cardiology.

Idioma originalEnglish
Páginas (desde-hasta)9583-9586
Número de páginas4
PublicaciónJournal of Biological Chemistry
Volumen276
N.º13
DOI
EstadoPublished - mar. 30 2001
Publicado de forma externa

ASJC Scopus Subject Areas

  • Biochemistry
  • Molecular Biology
  • Cell Biology

PubMed: MeSH publication types

  • Journal Article
  • Research Support, U.S. Gov't, P.H.S.
  • Review

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