The PI3K/AKT/mTOR pathway in the pathophysiology and treatment of pituitary adenomas

Endocr Relat Cancer. 2014 Aug;21(4):R331-44. doi: 10.1530/ERC-14-0188.

Abstract

Pituitary adenomas are common intracranial neoplasms. Patients with these tumors exhibit a wide range of clinically challenging problems, stemming either from results of sellar mass effect in pituitary macroadenoma or the diverse effects of aberrant hormone production by adenoma cells. While some patients are cured/controlled by surgical resection and/or medical therapy, a proportion of patients exhibit tumors that are refractory to current modalities. New therapeutic approaches are needed for these patients. Activation of the AKT/phophotidylinositide-3-kinase pathway, including mTOR activation, is common in human neoplasia, and a number of therapeutic approaches are being employed to neutralize activation of this pathway in human cancer. This review examines the role of this pathway in pituitary tumors with respect to tumor biology and its potential role as a therapeutic target.

Keywords: RAD001; mTOR; mTOR inhibitor; pituitary adenoma; rapamycin.

Publication types

  • Review

MeSH terms

  • Adenoma / drug therapy
  • Adenoma / metabolism*
  • Animals
  • Antineoplastic Agents / therapeutic use
  • Humans
  • Phosphatidylinositol 3-Kinases / metabolism*
  • Pituitary Neoplasms / drug therapy
  • Pituitary Neoplasms / metabolism*
  • Proto-Oncogene Proteins c-akt / metabolism*
  • Signal Transduction
  • TOR Serine-Threonine Kinases / antagonists & inhibitors
  • TOR Serine-Threonine Kinases / metabolism*

Substances

  • Antineoplastic Agents
  • MTOR protein, human
  • Proto-Oncogene Proteins c-akt
  • TOR Serine-Threonine Kinases