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Plumbagin Modulates Leukemia Cell Redox Status

Plumbagin is a plant naphtoquinone exerting anti-cancer properties including apoptotic cell death induction and generation of reactive oxygen species (ROS). The aim of this study was to elucidate parameters explaining the differential leukemia cell sensitivity towards this compound. Among several le...

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Autores principales: Gaascht, François, Teiten, Marie-Hélène, Cerella, Claudia, Dicato, Mario, Bagrel, Denyse, Diederich, Marc
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6270689/
https://www.ncbi.nlm.nih.gov/pubmed/25014531
http://dx.doi.org/10.3390/molecules190710011
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author Gaascht, François
Teiten, Marie-Hélène
Cerella, Claudia
Dicato, Mario
Bagrel, Denyse
Diederich, Marc
author_facet Gaascht, François
Teiten, Marie-Hélène
Cerella, Claudia
Dicato, Mario
Bagrel, Denyse
Diederich, Marc
author_sort Gaascht, François
collection PubMed
description Plumbagin is a plant naphtoquinone exerting anti-cancer properties including apoptotic cell death induction and generation of reactive oxygen species (ROS). The aim of this study was to elucidate parameters explaining the differential leukemia cell sensitivity towards this compound. Among several leukemia cell lines, U937 monocytic leukemia cells appeared more sensitive to plumbagin treatment in terms of cytotoxicity and level of apoptotic cell death compared to more resistant Raji Burkitt lymphoma cells. Moreover, U937 cells exhibited a ten-fold higher ROS production compared to Raji. Neither differential incorporation, nor efflux of plumbagin was detected. Pre-treatment with thiol-containing antioxidants prevented ROS production and subsequent induction of cell death by apoptosis whereas non-thiol-containing antioxidants remained ineffective in both cellular models. We conclude that the anticancer potential of plumbagin is driven by pro-oxidant activities related to the cellular thiolstat.
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spelling pubmed-62706892018-12-21 Plumbagin Modulates Leukemia Cell Redox Status Gaascht, François Teiten, Marie-Hélène Cerella, Claudia Dicato, Mario Bagrel, Denyse Diederich, Marc Molecules Article Plumbagin is a plant naphtoquinone exerting anti-cancer properties including apoptotic cell death induction and generation of reactive oxygen species (ROS). The aim of this study was to elucidate parameters explaining the differential leukemia cell sensitivity towards this compound. Among several leukemia cell lines, U937 monocytic leukemia cells appeared more sensitive to plumbagin treatment in terms of cytotoxicity and level of apoptotic cell death compared to more resistant Raji Burkitt lymphoma cells. Moreover, U937 cells exhibited a ten-fold higher ROS production compared to Raji. Neither differential incorporation, nor efflux of plumbagin was detected. Pre-treatment with thiol-containing antioxidants prevented ROS production and subsequent induction of cell death by apoptosis whereas non-thiol-containing antioxidants remained ineffective in both cellular models. We conclude that the anticancer potential of plumbagin is driven by pro-oxidant activities related to the cellular thiolstat. MDPI 2014-07-10 /pmc/articles/PMC6270689/ /pubmed/25014531 http://dx.doi.org/10.3390/molecules190710011 Text en © 2014 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Gaascht, François
Teiten, Marie-Hélène
Cerella, Claudia
Dicato, Mario
Bagrel, Denyse
Diederich, Marc
Plumbagin Modulates Leukemia Cell Redox Status
title Plumbagin Modulates Leukemia Cell Redox Status
title_full Plumbagin Modulates Leukemia Cell Redox Status
title_fullStr Plumbagin Modulates Leukemia Cell Redox Status
title_full_unstemmed Plumbagin Modulates Leukemia Cell Redox Status
title_short Plumbagin Modulates Leukemia Cell Redox Status
title_sort plumbagin modulates leukemia cell redox status
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6270689/
https://www.ncbi.nlm.nih.gov/pubmed/25014531
http://dx.doi.org/10.3390/molecules190710011
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