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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...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
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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. |
format | Online Article Text |
id | pubmed-5584210 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
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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