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Updates in Anthracycline-Mediated Cardiotoxicity

Cardiotoxicity is one of the main adverse effects of chemotheraphy, affecting the completion of cancer therapies and the short- and long-term quality of life. Anthracyclines are currently used to treat many cancers, including the various forms of leukemia, lymphoma, melanoma, uterine, breast, and ga...

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Detalles Bibliográficos
Autores principales: Nebigil, Canan G., Désaubry, Laurent
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6240592/
https://www.ncbi.nlm.nih.gov/pubmed/30483123
http://dx.doi.org/10.3389/fphar.2018.01262
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author Nebigil, Canan G.
Désaubry, Laurent
author_facet Nebigil, Canan G.
Désaubry, Laurent
author_sort Nebigil, Canan G.
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description Cardiotoxicity is one of the main adverse effects of chemotheraphy, affecting the completion of cancer therapies and the short- and long-term quality of life. Anthracyclines are currently used to treat many cancers, including the various forms of leukemia, lymphoma, melanoma, uterine, breast, and gastric cancers. World Health Organization registered anthracyclines in the list of essential medicines. However, anthracyclines display a major cardiotoxicity that can ultimately culminate in congestive heart failure. Taking into account the growing rate of cancer survivorship, the clinical significance of anthracycline cardiotoxicity is an emerging medical issue. In this review, we focus on the key progenitor cells and cardiac cells (cardiomyocytes, fibroblasts, and vascular cells), focusing on the signaling pathways involved in cellular damage, and the clinical biomarkers in anthracycline-mediated cardiotoxicity.
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spelling pubmed-62405922018-11-27 Updates in Anthracycline-Mediated Cardiotoxicity Nebigil, Canan G. Désaubry, Laurent Front Pharmacol Pharmacology Cardiotoxicity is one of the main adverse effects of chemotheraphy, affecting the completion of cancer therapies and the short- and long-term quality of life. Anthracyclines are currently used to treat many cancers, including the various forms of leukemia, lymphoma, melanoma, uterine, breast, and gastric cancers. World Health Organization registered anthracyclines in the list of essential medicines. However, anthracyclines display a major cardiotoxicity that can ultimately culminate in congestive heart failure. Taking into account the growing rate of cancer survivorship, the clinical significance of anthracycline cardiotoxicity is an emerging medical issue. In this review, we focus on the key progenitor cells and cardiac cells (cardiomyocytes, fibroblasts, and vascular cells), focusing on the signaling pathways involved in cellular damage, and the clinical biomarkers in anthracycline-mediated cardiotoxicity. Frontiers Media S.A. 2018-11-12 /pmc/articles/PMC6240592/ /pubmed/30483123 http://dx.doi.org/10.3389/fphar.2018.01262 Text en Copyright © 2018 Nebigil and Désaubry. 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) and the copyright owner(s) 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
Nebigil, Canan G.
Désaubry, Laurent
Updates in Anthracycline-Mediated Cardiotoxicity
title Updates in Anthracycline-Mediated Cardiotoxicity
title_full Updates in Anthracycline-Mediated Cardiotoxicity
title_fullStr Updates in Anthracycline-Mediated Cardiotoxicity
title_full_unstemmed Updates in Anthracycline-Mediated Cardiotoxicity
title_short Updates in Anthracycline-Mediated Cardiotoxicity
title_sort updates in anthracycline-mediated cardiotoxicity
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6240592/
https://www.ncbi.nlm.nih.gov/pubmed/30483123
http://dx.doi.org/10.3389/fphar.2018.01262
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