Novel pathway for somatostatin analogs in patients with acromegaly

Trends Endocrinol Metab. 2013 May;24(5):238-46. doi: 10.1016/j.tem.2012.11.007. Epub 2012 Dec 25.

Abstract

Acromegaly is a chronic disease with increased morbidity and mortality, where usually multiple treatment modalities are used. The somatostatin analogs (SSAs) are the mainstay of medical therapy but, in many patients, including those with a germline mutation in the aryl hydrocarbon receptor-interacting protein (AIP) gene, disease activity cannot be controlled with these drugs. Previous data have suggested the involvement of the tumor-suppressor gene ZAC1 in the mechanism of action of SSAs, and more recent findings suggested that SSAs could regulate AIP, which in turn can stimulate ZAC1, therefore suggesting the existence of a SSA-AIP-ZAC1-somatostatin effect pathway. The current review discusses these novel observations, highlighting their significance in the treatment of sporadic and familial somatotroph adenomas.

Publication types

  • Review

MeSH terms

  • Acromegaly / drug therapy*
  • Acromegaly / etiology
  • Acromegaly / genetics
  • Acromegaly / metabolism
  • Animals
  • Cell Cycle Proteins / genetics
  • Cell Cycle Proteins / metabolism
  • Combined Modality Therapy
  • Drug Resistance
  • Gene Expression Regulation / drug effects
  • Growth Hormone-Secreting Pituitary Adenoma / genetics
  • Growth Hormone-Secreting Pituitary Adenoma / metabolism
  • Growth Hormone-Secreting Pituitary Adenoma / physiopathology
  • Growth Hormone-Secreting Pituitary Adenoma / therapy
  • Humans
  • Intracellular Signaling Peptides and Proteins / metabolism
  • Liver / drug effects
  • Liver / metabolism
  • Models, Biological*
  • Pituitary Gland / drug effects*
  • Pituitary Gland / metabolism
  • Signal Transduction / drug effects*
  • Somatostatin / analogs & derivatives*
  • Somatostatin / pharmacology
  • Somatostatin / therapeutic use
  • Transcription Factors / genetics
  • Transcription Factors / metabolism
  • Tumor Suppressor Proteins / genetics
  • Tumor Suppressor Proteins / metabolism

Substances

  • Cell Cycle Proteins
  • Intracellular Signaling Peptides and Proteins
  • PLAGL1 protein, human
  • Transcription Factors
  • Tumor Suppressor Proteins
  • aryl hydrocarbon receptor-interacting protein
  • Somatostatin