Significance of absent prohormone convertase 1/3 in inducing clinically silent corticotroph pituitary adenoma of subtype I--immunohistochemical study

Pituitary. 2002;5(4):221-3. doi: 10.1023/a:1025321731790.

Abstract

Biologically inactive ACTH-producing pituitary adenoma is known as clinically silent corticotroph adenoma. To search for the mechanism causing clinically silent corticotroph adenoma, we immunohistochemically examined the expression of prohormone convertase 1/3 (PC1/3) in this type of adenoma and compared our results with those obtained for Cushing's disease. All of the Cushing's disease specimens exhibited strongly positive PC1/3 exhibition. On the contrary, the expression of PC1/3 was very weak in the clinically silent corticotroph adenoma specimens. The absence of PC1/3 in clinically silent corticotroph adenoma indicates that silent corticotroph adenomas arise in a different cell type sharing the prohormone pro-opiomelanocortin (POMC), but processing it differently, accounting for the lack of clinical symptoms due to ACTH excess.

Publication types

  • Clinical Trial
  • Comparative Study

MeSH terms

  • Adenoma / enzymology*
  • Adenoma / genetics*
  • Adrenocorticotropic Hormone / blood
  • Adult
  • Aged
  • Cushing Syndrome / enzymology
  • Cushing Syndrome / genetics
  • Female
  • Furin
  • Humans
  • Hydrocortisone / blood
  • Immunohistochemistry
  • Magnetic Resonance Imaging
  • Middle Aged
  • Pituitary Neoplasms / enzymology*
  • Pituitary Neoplasms / genetics*
  • Pro-Opiomelanocortin / metabolism
  • Subtilisins / genetics*

Substances

  • Pro-Opiomelanocortin
  • Adrenocorticotropic Hormone
  • Subtilisins
  • Furin
  • Hydrocortisone