New mechanisms of adrenostatic compounds in a human adrenocortical cancer cell line

Eur J Clin Invest. 2000 Dec:30 Suppl 3:76-82. doi: 10.1046/j.1365-2362.2000.0300s3076.x.

Abstract

Background: Adrenostatic compounds are frequently used in the treatment of patients with Cushing's syndrome and act via direct inhibition of steroidogenic enzymes. However, additional mechanisms may be involved in the blockade of adrenal steroid secretion. We therefore investigated the effects of aminoglutethimide (AG), metyrapone (MTP) and etomidate (ETO) in the human NCI-h295 adrenocortical carcinoma cell line.

Materials and methods: Cells were incubated with increasing doses of the adrenostatic compounds. Steroid hormone secretion (cortisol, 17-OH-progesterone, DHEA-S) and cAMP synthesis were determined and Northern blot analysis and cell proliferation experiments were performed.

Results: ETO was the most potent adrenostatic compound inhibiting P450c11 hydroxylase at low concentrations (IC50 15 nM), and also blocking P450 side-chain cleavage (scc) enzyme (IC50 400 nM) at higher concentrations. The pattern of enzyme inhibition was similar for MTP with an IC50 of 3-5 microM for P450c11 and 17 microM for P450scc, while AG blocked P450scc with an IC50 of 10 microM. AG significantly suppressed the baseline ACTH-R mRNA expression in a dose-dependent fashion (300 microM AG: 5% +/- 1%; 30 microM AG: 64% +/- 1%; 3 microM AG: 108% +/- 19% compared with control cells: 100% +/- 11%) but increased glucocorticoid receptor mRNA. The reduced ACTH-R mRNA was paralleled by low ACTH-induced cAMP accumulation indicating reduced expression of ACTH-R protein. The simultaneous incubation of hydrocortisone together with AG reversed the inhibitory effect of AG on the ACTH-R expression. AG and ETO inhibited cell proliferation in the NCI-h295 cells, but ETO was much more potent and showed antiproliferative effects at concentrations of 6 microM. The growth inhibition was not reversed by administration of hydrocortisone.

Conclusions: Our data demonstrate that adrenostatic compounds not only act by suppression of steroidogenic enzymes but can also influence both ACTH-R expression and cell proliferation in adrenal cells. As these effects occur in vitro at concentrations that are reached during treatment with these drugs in patients, they are probably also of clinical relevance. Particularly the antiproliferative activity of ETO may be useful in Cushing's syndrome due to adrenocortical cancer. The interaction of steroidogenesis, ACTH-R and glucocorticoid receptor expression as well as cell proliferation provides a new concept of the intra-adrenal response to stress in humans.

Publication types

  • Review

MeSH terms

  • Adrenal Cortex Neoplasms / drug therapy*
  • Adrenal Glands / drug effects*
  • Adrenal Glands / metabolism
  • Aminoglutethimide / pharmacology*
  • Cell Division / drug effects
  • Cholesterol Side-Chain Cleavage Enzyme / antagonists & inhibitors
  • Etomidate / pharmacology*
  • Humans
  • Hydrocortisone / metabolism
  • Metyrapone / pharmacology*
  • RNA, Messenger / analysis
  • Receptors, Corticotropin / drug effects
  • Receptors, Corticotropin / genetics
  • Receptors, Glucocorticoid / drug effects
  • Receptors, Glucocorticoid / genetics
  • Steroids / biosynthesis*
  • Tumor Cells, Cultured

Substances

  • RNA, Messenger
  • Receptors, Corticotropin
  • Receptors, Glucocorticoid
  • Steroids
  • Aminoglutethimide
  • Cholesterol Side-Chain Cleavage Enzyme
  • Hydrocortisone
  • Etomidate
  • Metyrapone