Cargando…

Combination of Sulindac and Dichloroacetate Kills Cancer Cells via Oxidative Damage

Sulindac is an FDA-approved non-steroidal anti-inflammatory drug with documented anticancer activities. Our recent studies showed that sulindac selectively enhanced the killing of cancer cells exposed to oxidizing agents via production of reactive oxygen species (ROS) resulting in mitochondrial dysf...

Descripción completa

Detalles Bibliográficos
Autores principales: Ayyanathan, Kasirajan, Kesaraju, Shailaja, Dawson-Scully, Ken, Weissbach, Herbert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3398923/
https://www.ncbi.nlm.nih.gov/pubmed/22866174
http://dx.doi.org/10.1371/journal.pone.0039949
_version_ 1782238343483883520
author Ayyanathan, Kasirajan
Kesaraju, Shailaja
Dawson-Scully, Ken
Weissbach, Herbert
author_facet Ayyanathan, Kasirajan
Kesaraju, Shailaja
Dawson-Scully, Ken
Weissbach, Herbert
author_sort Ayyanathan, Kasirajan
collection PubMed
description Sulindac is an FDA-approved non-steroidal anti-inflammatory drug with documented anticancer activities. Our recent studies showed that sulindac selectively enhanced the killing of cancer cells exposed to oxidizing agents via production of reactive oxygen species (ROS) resulting in mitochondrial dysfunction. This effect of sulindac and oxidative stress on cancer cells could be related to the defect in respiration in cancer cells, first described by Warburg 50 years ago, known as the Warburg effect. We postulated that sulindac might enhance the selective killing of cancer cells when combined with any compound that alters mitochondrial respiration. To test this hypothesis we have used dichloroacetate (DCA), which is known to shift pyruvate metabolism away from lactic acid formation to respiration. One might expect that DCA, since it stimulates aerobic metabolism, could stress mitochondrial respiration in cancer cells, which would result in enhanced killing in the presence of sulindac. In this study, we have shown that the combination of sulindac and DCA enhances the selective killing of A549 and SCC25 cancer cells under the conditions used. As predicted, the mechanism of killing involves ROS production, mitochondrial dysfunction, JNK signaling and death by apoptosis. Our results suggest that the sulindac-DCA drug combination may provide an effective cancer therapy.
format Online
Article
Text
id pubmed-3398923
institution National Center for Biotechnology Information
language English
publishDate 2012
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-33989232012-08-03 Combination of Sulindac and Dichloroacetate Kills Cancer Cells via Oxidative Damage Ayyanathan, Kasirajan Kesaraju, Shailaja Dawson-Scully, Ken Weissbach, Herbert PLoS One Research Article Sulindac is an FDA-approved non-steroidal anti-inflammatory drug with documented anticancer activities. Our recent studies showed that sulindac selectively enhanced the killing of cancer cells exposed to oxidizing agents via production of reactive oxygen species (ROS) resulting in mitochondrial dysfunction. This effect of sulindac and oxidative stress on cancer cells could be related to the defect in respiration in cancer cells, first described by Warburg 50 years ago, known as the Warburg effect. We postulated that sulindac might enhance the selective killing of cancer cells when combined with any compound that alters mitochondrial respiration. To test this hypothesis we have used dichloroacetate (DCA), which is known to shift pyruvate metabolism away from lactic acid formation to respiration. One might expect that DCA, since it stimulates aerobic metabolism, could stress mitochondrial respiration in cancer cells, which would result in enhanced killing in the presence of sulindac. In this study, we have shown that the combination of sulindac and DCA enhances the selective killing of A549 and SCC25 cancer cells under the conditions used. As predicted, the mechanism of killing involves ROS production, mitochondrial dysfunction, JNK signaling and death by apoptosis. Our results suggest that the sulindac-DCA drug combination may provide an effective cancer therapy. Public Library of Science 2012-07-17 /pmc/articles/PMC3398923/ /pubmed/22866174 http://dx.doi.org/10.1371/journal.pone.0039949 Text en Ayyanathan et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Ayyanathan, Kasirajan
Kesaraju, Shailaja
Dawson-Scully, Ken
Weissbach, Herbert
Combination of Sulindac and Dichloroacetate Kills Cancer Cells via Oxidative Damage
title Combination of Sulindac and Dichloroacetate Kills Cancer Cells via Oxidative Damage
title_full Combination of Sulindac and Dichloroacetate Kills Cancer Cells via Oxidative Damage
title_fullStr Combination of Sulindac and Dichloroacetate Kills Cancer Cells via Oxidative Damage
title_full_unstemmed Combination of Sulindac and Dichloroacetate Kills Cancer Cells via Oxidative Damage
title_short Combination of Sulindac and Dichloroacetate Kills Cancer Cells via Oxidative Damage
title_sort combination of sulindac and dichloroacetate kills cancer cells via oxidative damage
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3398923/
https://www.ncbi.nlm.nih.gov/pubmed/22866174
http://dx.doi.org/10.1371/journal.pone.0039949
work_keys_str_mv AT ayyanathankasirajan combinationofsulindacanddichloroacetatekillscancercellsviaoxidativedamage
AT kesarajushailaja combinationofsulindacanddichloroacetatekillscancercellsviaoxidativedamage
AT dawsonscullyken combinationofsulindacanddichloroacetatekillscancercellsviaoxidativedamage
AT weissbachherbert combinationofsulindacanddichloroacetatekillscancercellsviaoxidativedamage