The Na+/K+-ATPase is the Achilles heel of multi-drug-resistant cancer cells

Cancer Lett. 2009 Sep 8;282(1):30-4. doi: 10.1016/j.canlet.2009.02.048. Epub 2009 Mar 31.

Abstract

We recently reported that over-expressed Na(+)/K(+)-ATPase alpha subunits are new important anti-cancer targets. Cardiotonic steroids are the natural ligands of Na(+)/K(+)-ATPase and thus potentially potent anti-cancer agents with a novel mechanism of action. We report here that the hemi-synthetic cardenolide 19-hydroxy-2''oxovoruscharin is impressively active in cancer cells expressing diverse forms of multi-drug resistance (MDR) either conferred by the over-expression of selected drug-transporter proteins or induced by a range of chemotherapeutic agents. Together with the inability of tumor cells to acquire resistance to 19-hydroxy-2''oxovoruscharin, our data suggest that this novel compound could be especially applicable to notoriously drug-resistant cancers.

MeSH terms

  • ATP Binding Cassette Transporter, Subfamily B, Member 1 / metabolism
  • Breast Neoplasms
  • Carcinoma, Non-Small-Cell Lung / pathology
  • Carcinoma, Small Cell / pathology
  • Carcinoma, Squamous Cell
  • Cardenolides / pharmacology
  • Cell Line, Tumor / drug effects
  • Cell Survival / drug effects
  • Drug Resistance, Multiple / physiology*
  • HeLa Cells / drug effects
  • Humans
  • Hydroxyurea / pharmacology
  • Ligands
  • Neoplasms / drug therapy*
  • Sodium-Potassium-Exchanging ATPase / drug effects
  • Sodium-Potassium-Exchanging ATPase / metabolism*
  • Thiazoles / pharmacology

Substances

  • 2''-oxovoruscharin
  • ATP Binding Cassette Transporter, Subfamily B, Member 1
  • Cardenolides
  • Ligands
  • Thiazoles
  • UNBS 1450
  • Sodium-Potassium-Exchanging ATPase
  • Hydroxyurea