HIF-1alpha and calcium signaling as targets for treatment of prostate cancer by cardiac glycosides

Curr Cancer Drug Targets. 2009 Nov;9(7):881-7. doi: 10.2174/156800909789760249.

Abstract

Prostate cancer possesses its unique feature of low proliferation rate and slow growth. Ca(2+)-induced apoptosis is not dependent on cell cycle progression and targeting this pathway could circumvent the problems encountered using current cytotoxic chemotherapies for prostate cancer. Hypoxia-inducible factor 1alpha (HIF-1alpha) is another novel cancer drug target and inhibitors of hypoxia-response pathway are being developed. Digoxin and other cardiac glycosides, known inhibitors of the alpha-subunit of sarcolemmal Na(+)K(+)-ATPase, were recently found to block tumor growth via the inhibition of HIF-1alpha synthesis. Thus, cardiac glycosides disrupt two important cellular pathways and, therefore, may be useful as an anticancer therapy. This review will focus on HIF-1alpha and calcium signaling as novel cancer drug targets in prostate cancer. The possible application of digoxin and other cardiac glycosides in cancer therapeutics especially in prostate cancer is discussed.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Antineoplastic Agents / pharmacology
  • Antineoplastic Agents / therapeutic use
  • Calcium Signaling / drug effects*
  • Calcium Signaling / physiology
  • Cardiac Glycosides / pharmacology*
  • Cardiac Glycosides / therapeutic use
  • Clinical Trials as Topic
  • Drug Delivery Systems
  • Humans
  • Hypoxia / metabolism
  • Hypoxia-Inducible Factor 1, alpha Subunit / antagonists & inhibitors*
  • Hypoxia-Inducible Factor 1, alpha Subunit / metabolism
  • Male
  • Models, Biological
  • Prostatic Neoplasms / drug therapy*
  • Prostatic Neoplasms / metabolism
  • Receptor Cross-Talk
  • Receptors, Androgen / metabolism
  • Signal Transduction / drug effects

Substances

  • Antineoplastic Agents
  • Cardiac Glycosides
  • Hypoxia-Inducible Factor 1, alpha Subunit
  • Receptors, Androgen