Downregulation of Insulin-like growth factor binding protein 6 is associated with ACTH-secreting pituitary adenoma growth

Pituitary. 2014 Dec;17(6):505-13. doi: 10.1007/s11102-013-0535-8.

Abstract

Background: Adrenocorticotrophic hormone (ACTH)-dependent Cushing's syndrome, called Cushing disease, is caused by a corticotroph tumor of the pituitary gland. Insulin-like growth factor binding protein 6 (IGFBP6), which regulates insulin-like growth factor (IGF) activity and inhibits several IGF2-dependent cancer growths, plays a pivotal role in the tumorigenesis of malignancy, but its roles in ACTH-secreting pituitary adenomas remain unclear.

Objective: To investigate IGFBP6 expression in ACTH-secreting pituitary adenomas, and its involvement in tumor growth.

Methods: Sporadic ACTH-secreting pituitary adenomas specimens (n = 41) and adjacent non-tumorous pituitary tissues (n = 9) were collected by transphenoidal surgery. IGFBP6 expression was assessed by quantitative reverse transcriptase polymerase chain reaction (qRT-PCR) and validated by Western blotting. Associations of IGFBP6 expression with maximum tumor diameter or Ki-67 labeling index were evaluated in ACTH-secreting pituitary adenomas.

Results: IGFBP6 mRNA and protein expression were both decreased in ACTH-secreting pituitary adenomas, compared to adjacent non-tumorous pituitary tissues (P < 0.01). IGFBP6 expression was correlated inversely with maximum tumor diameter (Rho = -0.53, P < 0.0001) and Ki-67 levels (Rho = -0.52, P < 0.05). Moreover, IGFBP6 downregulation activated PI3 K-AKT-mTOR pathway in ACTH-secreting pituitary adenomas.

Conclusions: IGFBP6 attenuation in ACTH-secreting pituitary adenomas is associated with tumor growth, through activation of PI3K-AKT-mTOR pathway. The finding underlies IGFBP6 roles in Cushing disease and would potentially provide a novel target of medical therapies.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • ACTH-Secreting Pituitary Adenoma / metabolism*
  • Adult
  • Biomarkers, Tumor / metabolism
  • Down-Regulation
  • Female
  • Humans
  • In Vitro Techniques
  • Insulin-Like Growth Factor Binding Protein 6 / biosynthesis*
  • Ki-67 Antigen
  • Male
  • Middle Aged
  • Oncogene Protein v-akt / metabolism
  • Phosphatidylinositol 3-Kinases / metabolism
  • Pituitary Neoplasms / metabolism*
  • Signal Transduction
  • TOR Serine-Threonine Kinases / metabolism
  • Young Adult

Substances

  • Biomarkers, Tumor
  • Insulin-Like Growth Factor Binding Protein 6
  • Ki-67 Antigen
  • Oncogene Protein v-akt
  • TOR Serine-Threonine Kinases