Ouabain at nanomolar concentrations is cytotoxic for biliary tract cancer cells.

Biliary tract cancer is a deadly disease with limited therapeutic options. Ouabain is a well-known inhibitor of the pumping function of Na+/K+-ATPase, though there is evidence that low concentrations of ouabain lead to a reduction of cell viability of cancer cells independent of its inhibition of th...

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Main Authors: Christian Mayr, Tobias Kiesslich, Dino Bekric, Marlena Beyreis, Michael Kittl, Celina Ablinger, Elen Neureiter, Martin Pichler, Felix Prinz, Markus Ritter, Daniel Neureiter, Martin Jakab, Heidemarie Dobias
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2023-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0287769
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author Christian Mayr
Tobias Kiesslich
Dino Bekric
Marlena Beyreis
Michael Kittl
Celina Ablinger
Elen Neureiter
Martin Pichler
Felix Prinz
Markus Ritter
Daniel Neureiter
Martin Jakab
Heidemarie Dobias
author_facet Christian Mayr
Tobias Kiesslich
Dino Bekric
Marlena Beyreis
Michael Kittl
Celina Ablinger
Elen Neureiter
Martin Pichler
Felix Prinz
Markus Ritter
Daniel Neureiter
Martin Jakab
Heidemarie Dobias
author_sort Christian Mayr
collection DOAJ
description Biliary tract cancer is a deadly disease with limited therapeutic options. Ouabain is a well-known inhibitor of the pumping function of Na+/K+-ATPase, though there is evidence that low concentrations of ouabain lead to a reduction of cell viability of cancer cells independent of its inhibition of the pumping function of the Na+/K+-ATPase. Regarding the impact of ouabain on biliary tract cancer, no data is currently available. Therefore, we aimed for a first-time investigation of ouabain as a potential anti-neoplastic biliary tract cancer agent using comprehensive human biliary tract cancer in vitro models. We found that ouabain has a strong cell line-dependent cytotoxic effect with IC50 levels in the (low) nanomolar-range and that this effect was not associated with the mRNA expression levels of the Na+/K+-ATPase α, β and fxyd-subunits. Regarding the mode of cytotoxicity, we observed induction of apoptosis in biliary tract cancer cells upon treatment with ouabain. Interestingly, cytotoxic effects of ouabain at sub-saturating (< μM) levels were independent of cellular membrane depolarization and changes in intracellular sodium levels. Furthermore, using a 3D cell culture model, we found that ouabain disturbs spheroid growth and reduces the viability of biliary tract cancer cells within the tumor spheroids. In summary, our data suggest that ouabain possesses anti-biliary tract cancer potential at low μM-concentration in 2D and 3D in vitro biliary tract cancer models and encourage further detailed investigation.
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spelling doaj.art-ee71fae858cb43a488c0159eb41426f22023-12-12T05:35:22ZengPublic Library of Science (PLoS)PLoS ONE1932-62032023-01-01186e028776910.1371/journal.pone.0287769Ouabain at nanomolar concentrations is cytotoxic for biliary tract cancer cells.Christian MayrTobias KiesslichDino BekricMarlena BeyreisMichael KittlCelina AblingerElen NeureiterMartin PichlerFelix PrinzMarkus RitterDaniel NeureiterMartin JakabHeidemarie DobiasBiliary tract cancer is a deadly disease with limited therapeutic options. Ouabain is a well-known inhibitor of the pumping function of Na+/K+-ATPase, though there is evidence that low concentrations of ouabain lead to a reduction of cell viability of cancer cells independent of its inhibition of the pumping function of the Na+/K+-ATPase. Regarding the impact of ouabain on biliary tract cancer, no data is currently available. Therefore, we aimed for a first-time investigation of ouabain as a potential anti-neoplastic biliary tract cancer agent using comprehensive human biliary tract cancer in vitro models. We found that ouabain has a strong cell line-dependent cytotoxic effect with IC50 levels in the (low) nanomolar-range and that this effect was not associated with the mRNA expression levels of the Na+/K+-ATPase α, β and fxyd-subunits. Regarding the mode of cytotoxicity, we observed induction of apoptosis in biliary tract cancer cells upon treatment with ouabain. Interestingly, cytotoxic effects of ouabain at sub-saturating (< μM) levels were independent of cellular membrane depolarization and changes in intracellular sodium levels. Furthermore, using a 3D cell culture model, we found that ouabain disturbs spheroid growth and reduces the viability of biliary tract cancer cells within the tumor spheroids. In summary, our data suggest that ouabain possesses anti-biliary tract cancer potential at low μM-concentration in 2D and 3D in vitro biliary tract cancer models and encourage further detailed investigation.https://doi.org/10.1371/journal.pone.0287769
spellingShingle Christian Mayr
Tobias Kiesslich
Dino Bekric
Marlena Beyreis
Michael Kittl
Celina Ablinger
Elen Neureiter
Martin Pichler
Felix Prinz
Markus Ritter
Daniel Neureiter
Martin Jakab
Heidemarie Dobias
Ouabain at nanomolar concentrations is cytotoxic for biliary tract cancer cells.
PLoS ONE
title Ouabain at nanomolar concentrations is cytotoxic for biliary tract cancer cells.
title_full Ouabain at nanomolar concentrations is cytotoxic for biliary tract cancer cells.
title_fullStr Ouabain at nanomolar concentrations is cytotoxic for biliary tract cancer cells.
title_full_unstemmed Ouabain at nanomolar concentrations is cytotoxic for biliary tract cancer cells.
title_short Ouabain at nanomolar concentrations is cytotoxic for biliary tract cancer cells.
title_sort ouabain at nanomolar concentrations is cytotoxic for biliary tract cancer cells
url https://doi.org/10.1371/journal.pone.0287769
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