[PI3K-AKT-mTOR pathway and cancer]

Bull Cancer. 2012 Feb 1;99(2):173-80. doi: 10.1684/bdc.2011.1384.
[Article in French]

Abstract

PI3K/AKT/mTOR pathway is an intracellular signalling pathway composed of different kinases. Many protein mutations are described in that pathway, and are responsible of dysregulation of cell growth, proliferation, survival and angiogenesis. Rapamycin is an antibiotic inhibiting mTOR. Different analogs of rapamycin are developed or being developed in antitumoral therapy, in which temsirolimus, everolimus and deforolimus, demonstrated antitumoral activity in renal cancer and mantle cell lymphoma, and many clinical trials are in progress in other tumors. In the future, predictive factors of response need to be identified; patient selection and associations with chemotherapy or with other targeted therapies should be explored.

Publication types

  • Review

MeSH terms

  • Carcinoma, Renal Cell / drug therapy*
  • Everolimus
  • Humans
  • Kidney Neoplasms / blood supply
  • Kidney Neoplasms / drug therapy*
  • Kidney Neoplasms / metabolism
  • Lymphoma, Mantle-Cell / drug therapy*
  • Neovascularization, Pathologic / drug therapy
  • Neovascularization, Pathologic / etiology
  • Oncogene Protein v-akt / antagonists & inhibitors*
  • Oncogene Protein v-akt / physiology
  • Phosphatidylinositol 3-Kinases / physiology
  • Phosphoinositide-3 Kinase Inhibitors*
  • Signal Transduction / drug effects*
  • Signal Transduction / physiology
  • Sirolimus / analogs & derivatives
  • Sirolimus / pharmacology
  • TOR Serine-Threonine Kinases / antagonists & inhibitors*
  • TOR Serine-Threonine Kinases / physiology

Substances

  • Phosphoinositide-3 Kinase Inhibitors
  • ridaforolimus
  • temsirolimus
  • Everolimus
  • MTOR protein, human
  • Oncogene Protein v-akt
  • TOR Serine-Threonine Kinases
  • Sirolimus