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Grape seed extracts modify the outcome of oxaliplatin in colon cancer cells by interfering with cellular mechanisms of drug cytotoxicity

Grape seed extracts are commonly utilized as dietary supplements for their antioxidant properties, even from cancer patients. However, whether these natural extracts interfere with chemotherapeutics utilized in colon cancer treatment is still poorly investigated. The cytotoxicity of extracts from It...

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Autores principales: Porcelli, Letizia, Iacobazzi, Rosa Maria, Quatrale, Anna Elisa, Bergamini, Carlo, Denora, Nunzio, Crupi, Pasquale, Antonacci, Donato, Mangia, Anita, Simone, Giovanni, Silvestris, Nicola, Azzariti, Amalia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5584210/
https://www.ncbi.nlm.nih.gov/pubmed/28881609
http://dx.doi.org/10.18632/oncotarget.15139
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author Porcelli, Letizia
Iacobazzi, Rosa Maria
Quatrale, Anna Elisa
Bergamini, Carlo
Denora, Nunzio
Crupi, Pasquale
Antonacci, Donato
Mangia, Anita
Simone, Giovanni
Silvestris, Nicola
Azzariti, Amalia
author_facet Porcelli, Letizia
Iacobazzi, Rosa Maria
Quatrale, Anna Elisa
Bergamini, Carlo
Denora, Nunzio
Crupi, Pasquale
Antonacci, Donato
Mangia, Anita
Simone, Giovanni
Silvestris, Nicola
Azzariti, Amalia
author_sort Porcelli, Letizia
collection PubMed
description Grape seed extracts are commonly utilized as dietary supplements for their antioxidant properties, even from cancer patients. However, whether these natural extracts interfere with chemotherapeutics utilized in colon cancer treatment is still poorly investigated. The cytotoxicity of extracts from Italia and Palieri cultivars either alone or in combination with oxaliplatin was evaluated in colon cancer cells. Grape seed extracts displayed anti-proliferative activity depending on the concentration utilized through apoptosis induction. In combination, they affected the activation of Erk1/2 and counteracted the intrinsic and the extrinsic pathway of apoptosis, the DNA damage and the generation of ROS induced by oxaliplatin. Noteworthy grape seed extracts strongly enhanced the uptake of oxaliplatin into all cells, by affecting the cell transport system of platinum. The addition of these natural extracts to oxaliplatin strongly reduced the cellular response to oxaliplatin and allowed a huge accumulation of platinum into cells. Here, we shed light on the chemical biology underlying the combination of grape seed extracts and oxaliplatin, demonstrating that they might be detrimental to oxaliplatin effectiveness in colon cancer therapy.
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spelling pubmed-55842102017-09-06 Grape seed extracts modify the outcome of oxaliplatin in colon cancer cells by interfering with cellular mechanisms of drug cytotoxicity Porcelli, Letizia Iacobazzi, Rosa Maria Quatrale, Anna Elisa Bergamini, Carlo Denora, Nunzio Crupi, Pasquale Antonacci, Donato Mangia, Anita Simone, Giovanni Silvestris, Nicola Azzariti, Amalia Oncotarget Research Paper Grape seed extracts are commonly utilized as dietary supplements for their antioxidant properties, even from cancer patients. However, whether these natural extracts interfere with chemotherapeutics utilized in colon cancer treatment is still poorly investigated. The cytotoxicity of extracts from Italia and Palieri cultivars either alone or in combination with oxaliplatin was evaluated in colon cancer cells. Grape seed extracts displayed anti-proliferative activity depending on the concentration utilized through apoptosis induction. In combination, they affected the activation of Erk1/2 and counteracted the intrinsic and the extrinsic pathway of apoptosis, the DNA damage and the generation of ROS induced by oxaliplatin. Noteworthy grape seed extracts strongly enhanced the uptake of oxaliplatin into all cells, by affecting the cell transport system of platinum. The addition of these natural extracts to oxaliplatin strongly reduced the cellular response to oxaliplatin and allowed a huge accumulation of platinum into cells. Here, we shed light on the chemical biology underlying the combination of grape seed extracts and oxaliplatin, demonstrating that they might be detrimental to oxaliplatin effectiveness in colon cancer therapy. Impact Journals LLC 2017-02-07 /pmc/articles/PMC5584210/ /pubmed/28881609 http://dx.doi.org/10.18632/oncotarget.15139 Text en Copyright: © 2017 Porcelli et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License 3.0 (http://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Porcelli, Letizia
Iacobazzi, Rosa Maria
Quatrale, Anna Elisa
Bergamini, Carlo
Denora, Nunzio
Crupi, Pasquale
Antonacci, Donato
Mangia, Anita
Simone, Giovanni
Silvestris, Nicola
Azzariti, Amalia
Grape seed extracts modify the outcome of oxaliplatin in colon cancer cells by interfering with cellular mechanisms of drug cytotoxicity
title Grape seed extracts modify the outcome of oxaliplatin in colon cancer cells by interfering with cellular mechanisms of drug cytotoxicity
title_full Grape seed extracts modify the outcome of oxaliplatin in colon cancer cells by interfering with cellular mechanisms of drug cytotoxicity
title_fullStr Grape seed extracts modify the outcome of oxaliplatin in colon cancer cells by interfering with cellular mechanisms of drug cytotoxicity
title_full_unstemmed Grape seed extracts modify the outcome of oxaliplatin in colon cancer cells by interfering with cellular mechanisms of drug cytotoxicity
title_short Grape seed extracts modify the outcome of oxaliplatin in colon cancer cells by interfering with cellular mechanisms of drug cytotoxicity
title_sort grape seed extracts modify the outcome of oxaliplatin in colon cancer cells by interfering with cellular mechanisms of drug cytotoxicity
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5584210/
https://www.ncbi.nlm.nih.gov/pubmed/28881609
http://dx.doi.org/10.18632/oncotarget.15139
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