Cardiac glycosides stimulate Ca2+ increases and apoptosis in androgen-independent, metastatic human prostate adenocarcinoma cells

Cancer Res. 2000 Jul 15;60(14):3807-12.

Abstract

Cardiac glycosides are used clinically to increase contractile force in patients with cardiac disorders. Their mechanism of action is well established and involves inhibition of the plasma membrane Na+/K+-ATPase, leading to alterations in intracellular K+ and Ca(2+) levels. Here, we report that the cardiac glycosides oleandrin, ouabain, and digoxin induce apoptosis in androgen-independent human prostate cancer cell lines in vitro. Cell death was associated with early release of cytochrome c from mitochondria, followed by proteolytic processing of caspases 8 and 3. Oleandrin also promoted caspase activation, detected by cleavage poly(ADP-ribose) polymerase and hydrolysis of a peptide substrate (DEVD-pNA). Comparison of the rates of apoptosis in poorly metastatic PC3 M-Pro4 and highly metastatic PC3 M-LN4 subclones demonstrated that cell death was delayed in the latter because of a delay in mitochondrial cytochrome c release. Single-cell imaging of intracellular Ca(2+) fluxes demonstrated that the proapoptotic effects of the cardiac glycosides were linked to their abilities to induce sustained Ca(2+) increases in the cells. Our results define a novel activity for cardiac glycosides that could prove relevant to the treatment of metastatic prostate cancer.

MeSH terms

  • Adenocarcinoma / metabolism
  • Adenocarcinoma / pathology*
  • Apoptosis / drug effects*
  • Calcium / metabolism*
  • Cardenolides / pharmacology
  • Cardiac Glycosides / pharmacology*
  • Cardiotonic Agents / pharmacology
  • Caspase 3
  • Caspase 8
  • Caspase 9
  • Caspases / metabolism
  • Cell Separation
  • Cytochrome c Group / metabolism
  • DNA Fragmentation / drug effects
  • Digoxin / pharmacology
  • Dose-Response Relationship, Drug
  • Flow Cytometry
  • Humans
  • Male
  • Myocardium / metabolism*
  • Ouabain / pharmacology
  • Poly(ADP-ribose) Polymerases / metabolism
  • Prostatic Neoplasms / metabolism
  • Prostatic Neoplasms / pathology*
  • Time Factors
  • Tumor Cells, Cultured

Substances

  • Cardenolides
  • Cardiac Glycosides
  • Cardiotonic Agents
  • Cytochrome c Group
  • Ouabain
  • Digoxin
  • Poly(ADP-ribose) Polymerases
  • CASP3 protein, human
  • CASP8 protein, human
  • CASP9 protein, human
  • Caspase 3
  • Caspase 8
  • Caspase 9
  • Caspases
  • oleandrin
  • Calcium