Dexamethasone and medroxyprogesterone acetate elevate Nm23-H1 metastasis suppressor gene expression in metastatic human breast carcinoma cells: new uses for old compounds

Clin Cancer Res. 2003 Sep 1;9(10 Pt 1):3763-72.

Abstract

Purpose: Long-term elevation of metastasis suppressor gene expression in micrometastases represents a novel therapeutic strategy for breast and other cancers. We searched for well-tolerated compounds that could elevate Nm23 metastasis suppressor expression in metastatic human breast cancer cell lines.

Experimental design: MDA-MB-435 and MDA-MB-231 human breast carcinoma cells were treated with dexamethasone or medroxyprogesterone acetate (MPA) in cultures containing either charcoal-stripped serum or FCS. Aspects of nm23 expression and function were determined.

Results: Previous investigation of the nm23-H1 promoter suggested that glucocorticoids may contribute to the elevation of Nm23-H1 expression. Dexamethasone elevated Nm23-H1 and Nm23-H2 protein levels in two metastatic human breast carcinoma cell lines 2-3-fold over a 4-day time course when cultured in steroid-free culture medium, with high-dose inhibition, via a traditional transcriptional mechanism. Elevation of Nm23-H1 expression was not observed using FCS-containing culture medium, which contains endogenous levels of corticosteroids, limiting the potential in vivo use of dexamethasone. MPA was investigated as a glucocorticoid receptor agonist. MPA elevated breast carcinoma Nm23-H1 protein expression 3-fold over a 10 nM to 1 micro M dose range when cultured in steroid-free or FCS-containing medium, with a shorter time course. Elevation of Nm23-H1 expression in the presence of endogenous corticosteroids found in FCS involved a distinct, glucocorticoid receptor-dependent, posttranscriptional mechanism of action. MPA had no effect on proliferation in vitro but reduced the soft agar colonization of metastatic breast cancer cell lines by approximately 50%.

Conclusions: MPA represents a first generation lead agent for the elevation of Nm23-H1 metastasis suppressor expression and the inhibition of metastatic colonization.

MeSH terms

  • Agar / chemistry
  • Antineoplastic Agents, Hormonal / pharmacology
  • Blotting, Western
  • Breast Neoplasms / drug therapy
  • Breast Neoplasms / metabolism*
  • Breast Neoplasms / therapy
  • Cell Division
  • Cell Line, Tumor
  • Contraceptives, Oral, Synthetic / pharmacology
  • Dexamethasone / metabolism
  • Dexamethasone / pharmacology*
  • Dose-Response Relationship, Drug
  • Gene Expression Regulation, Neoplastic*
  • Glucocorticoids / metabolism
  • Humans
  • Medroxyprogesterone / pharmacology*
  • Medroxyprogesterone Acetate / metabolism
  • Mutagenesis
  • NM23 Nucleoside Diphosphate Kinases
  • Neoplasm Metastasis
  • Nucleoside-Diphosphate Kinase*
  • Promoter Regions, Genetic
  • Protein Biosynthesis*
  • RNA Processing, Post-Transcriptional
  • Time Factors
  • Transcription, Genetic
  • Transfection

Substances

  • Antineoplastic Agents, Hormonal
  • Contraceptives, Oral, Synthetic
  • Glucocorticoids
  • NM23 Nucleoside Diphosphate Kinases
  • Dexamethasone
  • Agar
  • Medroxyprogesterone Acetate
  • NME1 protein, human
  • Nucleoside-Diphosphate Kinase
  • Medroxyprogesterone