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Dichloroacetate and Salinomycin Exert a Synergistic Cytotoxic Effect in Colorectal Cancer Cell Lines

In the present study, we examined a hypothesis that dichloroacetate, a metabolic inhibitor, might efficiently potentiate the cytotoxic effect of salinomycin, an antibiotic ionophore, on two human colorectal cancer derived cell lines DLD-1 and HCT116. First, we performed a series of dose response exp...

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Autores principales: Skeberdytė, Aistė, Sarapinienė, Ieva, Aleksander-Krasko, Jan, Stankevičius, Vaidotas, Sužiedėlis, Kęstutis, Jarmalaitė, Sonata
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6288092/
https://www.ncbi.nlm.nih.gov/pubmed/30531808
http://dx.doi.org/10.1038/s41598-018-35815-4
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author Skeberdytė, Aistė
Sarapinienė, Ieva
Aleksander-Krasko, Jan
Stankevičius, Vaidotas
Sužiedėlis, Kęstutis
Jarmalaitė, Sonata
author_facet Skeberdytė, Aistė
Sarapinienė, Ieva
Aleksander-Krasko, Jan
Stankevičius, Vaidotas
Sužiedėlis, Kęstutis
Jarmalaitė, Sonata
author_sort Skeberdytė, Aistė
collection PubMed
description In the present study, we examined a hypothesis that dichloroacetate, a metabolic inhibitor, might efficiently potentiate the cytotoxic effect of salinomycin, an antibiotic ionophore, on two human colorectal cancer derived cell lines DLD-1 and HCT116. First, we performed a series of dose response experiments in the 2D cell culture by applying mono- and combination therapy and by using the Chou-Talalay method found that salinomycin in combination with dichloroacetate acted synergistically in both cell lines. Secondly, in order to recapitulate the in vivo tumor architecture, we tested various doses of these compounds, alone and in combination, in the 3D multicellular spheroid culture. The effect of combination of dichloracetate and salinomycin on multicellular spheroid size was stronger than the sum of both monotherapies, particularly in HCT116 cells. Further, we demonstrate that the synergistic effect of compounds may be related to the inhibitory effect of dichloroacetate on multidrug resistance proteins, and in contrast, it is not related to dichloroacetate-induced reduction of intracellular pH. Our findings indicate that the combination therapy of salinomycin and dichloroacetate could be an effective option for colorectal cancer treatment and provide the first mechanistic explanation of the synergistic action of these compounds.
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spelling pubmed-62880922018-12-19 Dichloroacetate and Salinomycin Exert a Synergistic Cytotoxic Effect in Colorectal Cancer Cell Lines Skeberdytė, Aistė Sarapinienė, Ieva Aleksander-Krasko, Jan Stankevičius, Vaidotas Sužiedėlis, Kęstutis Jarmalaitė, Sonata Sci Rep Article In the present study, we examined a hypothesis that dichloroacetate, a metabolic inhibitor, might efficiently potentiate the cytotoxic effect of salinomycin, an antibiotic ionophore, on two human colorectal cancer derived cell lines DLD-1 and HCT116. First, we performed a series of dose response experiments in the 2D cell culture by applying mono- and combination therapy and by using the Chou-Talalay method found that salinomycin in combination with dichloroacetate acted synergistically in both cell lines. Secondly, in order to recapitulate the in vivo tumor architecture, we tested various doses of these compounds, alone and in combination, in the 3D multicellular spheroid culture. The effect of combination of dichloracetate and salinomycin on multicellular spheroid size was stronger than the sum of both monotherapies, particularly in HCT116 cells. Further, we demonstrate that the synergistic effect of compounds may be related to the inhibitory effect of dichloroacetate on multidrug resistance proteins, and in contrast, it is not related to dichloroacetate-induced reduction of intracellular pH. Our findings indicate that the combination therapy of salinomycin and dichloroacetate could be an effective option for colorectal cancer treatment and provide the first mechanistic explanation of the synergistic action of these compounds. Nature Publishing Group UK 2018-12-10 /pmc/articles/PMC6288092/ /pubmed/30531808 http://dx.doi.org/10.1038/s41598-018-35815-4 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Skeberdytė, Aistė
Sarapinienė, Ieva
Aleksander-Krasko, Jan
Stankevičius, Vaidotas
Sužiedėlis, Kęstutis
Jarmalaitė, Sonata
Dichloroacetate and Salinomycin Exert a Synergistic Cytotoxic Effect in Colorectal Cancer Cell Lines
title Dichloroacetate and Salinomycin Exert a Synergistic Cytotoxic Effect in Colorectal Cancer Cell Lines
title_full Dichloroacetate and Salinomycin Exert a Synergistic Cytotoxic Effect in Colorectal Cancer Cell Lines
title_fullStr Dichloroacetate and Salinomycin Exert a Synergistic Cytotoxic Effect in Colorectal Cancer Cell Lines
title_full_unstemmed Dichloroacetate and Salinomycin Exert a Synergistic Cytotoxic Effect in Colorectal Cancer Cell Lines
title_short Dichloroacetate and Salinomycin Exert a Synergistic Cytotoxic Effect in Colorectal Cancer Cell Lines
title_sort dichloroacetate and salinomycin exert a synergistic cytotoxic effect in colorectal cancer cell lines
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6288092/
https://www.ncbi.nlm.nih.gov/pubmed/30531808
http://dx.doi.org/10.1038/s41598-018-35815-4
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