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The Blood Flow Shutdown Induced by Combretastatin A4 Impairs Gemcitabine Delivery in a Mouse Hepatocarcinoma
In recent clinical studies, vascular disrupting agents (VDAs) are mainly used in combination with chemotherapy. However, an often overlooked concern in treatment combination is the VDA-induced impairment of chemotherapy distribution in the tumor. The work presented here investigated the impact of bl...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5179558/ https://www.ncbi.nlm.nih.gov/pubmed/28066252 http://dx.doi.org/10.3389/fphar.2016.00506 |
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author | Fruytier, Anne-Catherine Le Duff, Cecile S. Po, Chrystelle Magat, Julie Bouzin, Caroline Neveu, Marie-Aline Feron, Olivier Jordan, Benedicte F. Gallez, Bernard |
author_facet | Fruytier, Anne-Catherine Le Duff, Cecile S. Po, Chrystelle Magat, Julie Bouzin, Caroline Neveu, Marie-Aline Feron, Olivier Jordan, Benedicte F. Gallez, Bernard |
author_sort | Fruytier, Anne-Catherine |
collection | PubMed |
description | In recent clinical studies, vascular disrupting agents (VDAs) are mainly used in combination with chemotherapy. However, an often overlooked concern in treatment combination is the VDA-induced impairment of chemotherapy distribution in the tumor. The work presented here investigated the impact of blood flow shutdown induced by Combretastatin A4 (CA4) on gemcitabine uptake into mouse hepatocarcinoma. At 2 h after CA4 treatment, using DCE-MRI, a significant decrease in the perfusion-relevant parameters K(trans) and Vp were observed in treated group compared with the control group. The blood flow shutdown was indeed confirmed by a histology study. In a third experiment, the total gemcitabine uptake was found to be significantly lower in treated tumors, as assessed in a separate experiment using ex vivo fluorine nuclear magnetic resonance spectroscopy. The amount of active metabolite gemcitabine triphosphate was also lower in treated tumors. In conclusion, the blood flow shutdown induced by VDAs can impact negatively on the delivery of small cytotoxic agents in tumors. The present study outlines the importance of monitoring the tumor vascular function when designing drug combinations. |
format | Online Article Text |
id | pubmed-5179558 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-51795582017-01-06 The Blood Flow Shutdown Induced by Combretastatin A4 Impairs Gemcitabine Delivery in a Mouse Hepatocarcinoma Fruytier, Anne-Catherine Le Duff, Cecile S. Po, Chrystelle Magat, Julie Bouzin, Caroline Neveu, Marie-Aline Feron, Olivier Jordan, Benedicte F. Gallez, Bernard Front Pharmacol Pharmacology In recent clinical studies, vascular disrupting agents (VDAs) are mainly used in combination with chemotherapy. However, an often overlooked concern in treatment combination is the VDA-induced impairment of chemotherapy distribution in the tumor. The work presented here investigated the impact of blood flow shutdown induced by Combretastatin A4 (CA4) on gemcitabine uptake into mouse hepatocarcinoma. At 2 h after CA4 treatment, using DCE-MRI, a significant decrease in the perfusion-relevant parameters K(trans) and Vp were observed in treated group compared with the control group. The blood flow shutdown was indeed confirmed by a histology study. In a third experiment, the total gemcitabine uptake was found to be significantly lower in treated tumors, as assessed in a separate experiment using ex vivo fluorine nuclear magnetic resonance spectroscopy. The amount of active metabolite gemcitabine triphosphate was also lower in treated tumors. In conclusion, the blood flow shutdown induced by VDAs can impact negatively on the delivery of small cytotoxic agents in tumors. The present study outlines the importance of monitoring the tumor vascular function when designing drug combinations. Frontiers Media S.A. 2016-12-23 /pmc/articles/PMC5179558/ /pubmed/28066252 http://dx.doi.org/10.3389/fphar.2016.00506 Text en Copyright © 2016 Fruytier, Le Duff, Po, Magat, Bouzin, Neveu, Feron, Jordan and Gallez. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Pharmacology Fruytier, Anne-Catherine Le Duff, Cecile S. Po, Chrystelle Magat, Julie Bouzin, Caroline Neveu, Marie-Aline Feron, Olivier Jordan, Benedicte F. Gallez, Bernard The Blood Flow Shutdown Induced by Combretastatin A4 Impairs Gemcitabine Delivery in a Mouse Hepatocarcinoma |
title | The Blood Flow Shutdown Induced by Combretastatin A4 Impairs Gemcitabine Delivery in a Mouse Hepatocarcinoma |
title_full | The Blood Flow Shutdown Induced by Combretastatin A4 Impairs Gemcitabine Delivery in a Mouse Hepatocarcinoma |
title_fullStr | The Blood Flow Shutdown Induced by Combretastatin A4 Impairs Gemcitabine Delivery in a Mouse Hepatocarcinoma |
title_full_unstemmed | The Blood Flow Shutdown Induced by Combretastatin A4 Impairs Gemcitabine Delivery in a Mouse Hepatocarcinoma |
title_short | The Blood Flow Shutdown Induced by Combretastatin A4 Impairs Gemcitabine Delivery in a Mouse Hepatocarcinoma |
title_sort | blood flow shutdown induced by combretastatin a4 impairs gemcitabine delivery in a mouse hepatocarcinoma |
topic | Pharmacology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5179558/ https://www.ncbi.nlm.nih.gov/pubmed/28066252 http://dx.doi.org/10.3389/fphar.2016.00506 |
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