Abstract
We recently reported that over-expressed Na+/K+-ATPase α 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.
| Original language | English |
|---|---|
| Pages (from-to) | 30-34 |
| Number of pages | 5 |
| Journal | Cancer Letters |
| Volume | 282 |
| Issue number | 1 |
| Early online date | 31 Mar 2009 |
| DOIs | |
| Publication status | Published - 8 Sept 2009 |
Bibliographical note
Copyright:Copyright 2009 Elsevier B.V., All rights reserved.
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- 19-hydroxy-2″oxovoruscharin
- Cardenolide
- Multi-drug resistance (MDR)
- Na/K-ATPase targeting
ASJC Scopus subject areas
- Oncology
- Cancer Research
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