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Anthracycline Chemotherapy and Cardiotoxicity

Anthracycline chemotherapy maintains a prominent role in treating many forms of cancer. Cardiotoxic side effects limit their dosing and improved cancer outcomes expose the cancer survivor to increased cardiovascular morbidity and mortality. The basic mechanisms of cardiotoxicity may involve direct p...

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Autores principales: McGowan, John V, Chung, Robin, Maulik, Angshuman, Piotrowska, Izabela, Walker, J Malcolm, Yellon, Derek M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5346598/
https://www.ncbi.nlm.nih.gov/pubmed/28185035
http://dx.doi.org/10.1007/s10557-016-6711-0
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author McGowan, John V
Chung, Robin
Maulik, Angshuman
Piotrowska, Izabela
Walker, J Malcolm
Yellon, Derek M
author_facet McGowan, John V
Chung, Robin
Maulik, Angshuman
Piotrowska, Izabela
Walker, J Malcolm
Yellon, Derek M
author_sort McGowan, John V
collection PubMed
description Anthracycline chemotherapy maintains a prominent role in treating many forms of cancer. Cardiotoxic side effects limit their dosing and improved cancer outcomes expose the cancer survivor to increased cardiovascular morbidity and mortality. The basic mechanisms of cardiotoxicity may involve direct pathways for reactive oxygen species generation and topoisomerase 2 as well as other indirect pathways. Cardioprotective treatments are few and those that have been examined include renin angiotensin system blockade, beta blockers, or the iron chelator dexrazoxane. New treatments exploiting the ErbB or other novel pro-survival pathways, such as conditioning, are on the cardioprotection horizon. Even in the forthcoming era of targeted cancer therapies, the substantial proportion of today’s anthracycline-treated cancer patients may become tomorrow’s cardiac patient.
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spelling pubmed-53465982017-03-24 Anthracycline Chemotherapy and Cardiotoxicity McGowan, John V Chung, Robin Maulik, Angshuman Piotrowska, Izabela Walker, J Malcolm Yellon, Derek M Cardiovasc Drugs Ther Review Article Anthracycline chemotherapy maintains a prominent role in treating many forms of cancer. Cardiotoxic side effects limit their dosing and improved cancer outcomes expose the cancer survivor to increased cardiovascular morbidity and mortality. The basic mechanisms of cardiotoxicity may involve direct pathways for reactive oxygen species generation and topoisomerase 2 as well as other indirect pathways. Cardioprotective treatments are few and those that have been examined include renin angiotensin system blockade, beta blockers, or the iron chelator dexrazoxane. New treatments exploiting the ErbB or other novel pro-survival pathways, such as conditioning, are on the cardioprotection horizon. Even in the forthcoming era of targeted cancer therapies, the substantial proportion of today’s anthracycline-treated cancer patients may become tomorrow’s cardiac patient. Springer US 2017-02-09 2017 /pmc/articles/PMC5346598/ /pubmed/28185035 http://dx.doi.org/10.1007/s10557-016-6711-0 Text en © The Author(s) 2017 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Review Article
McGowan, John V
Chung, Robin
Maulik, Angshuman
Piotrowska, Izabela
Walker, J Malcolm
Yellon, Derek M
Anthracycline Chemotherapy and Cardiotoxicity
title Anthracycline Chemotherapy and Cardiotoxicity
title_full Anthracycline Chemotherapy and Cardiotoxicity
title_fullStr Anthracycline Chemotherapy and Cardiotoxicity
title_full_unstemmed Anthracycline Chemotherapy and Cardiotoxicity
title_short Anthracycline Chemotherapy and Cardiotoxicity
title_sort anthracycline chemotherapy and cardiotoxicity
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5346598/
https://www.ncbi.nlm.nih.gov/pubmed/28185035
http://dx.doi.org/10.1007/s10557-016-6711-0
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