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Genetics of Anthracycline-Associated Cardiotoxicity

Anthracyclines are a major component of chemotherapies used in many pediatric and adult malignancies. Anthracycline-associated cardiotoxicity (ACT) is a dose-dependent adverse effect that has substantial impact on morbidity and mortality. Therefore, the identification of genetic variants associated...

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Autores principales: Al-Otaibi, Talal Khalid, Weitzman, Benjamin, Tahir, Usman A., Asnani, Aarti
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9068960/
https://www.ncbi.nlm.nih.gov/pubmed/35528837
http://dx.doi.org/10.3389/fcvm.2022.867873
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author Al-Otaibi, Talal Khalid
Weitzman, Benjamin
Tahir, Usman A.
Asnani, Aarti
author_facet Al-Otaibi, Talal Khalid
Weitzman, Benjamin
Tahir, Usman A.
Asnani, Aarti
author_sort Al-Otaibi, Talal Khalid
collection PubMed
description Anthracyclines are a major component of chemotherapies used in many pediatric and adult malignancies. Anthracycline-associated cardiotoxicity (ACT) is a dose-dependent adverse effect that has substantial impact on morbidity and mortality. Therefore, the identification of genetic variants associated with increased risk of ACT has the potential for significant clinical impact to improve patient care. The goal of this review is to summarize the current evidence supporting genetic variants associated with ACT, identify gaps and limitations in current knowledge, and propose future directions for incorporating genetics into clinical practice for patients treated with anthracyclines. We will discuss mechanisms of ACT that could be illuminated by genetics and discuss clinical applications for the cardiologist/cardio-oncologist.
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spelling pubmed-90689602022-05-05 Genetics of Anthracycline-Associated Cardiotoxicity Al-Otaibi, Talal Khalid Weitzman, Benjamin Tahir, Usman A. Asnani, Aarti Front Cardiovasc Med Cardiovascular Medicine Anthracyclines are a major component of chemotherapies used in many pediatric and adult malignancies. Anthracycline-associated cardiotoxicity (ACT) is a dose-dependent adverse effect that has substantial impact on morbidity and mortality. Therefore, the identification of genetic variants associated with increased risk of ACT has the potential for significant clinical impact to improve patient care. The goal of this review is to summarize the current evidence supporting genetic variants associated with ACT, identify gaps and limitations in current knowledge, and propose future directions for incorporating genetics into clinical practice for patients treated with anthracyclines. We will discuss mechanisms of ACT that could be illuminated by genetics and discuss clinical applications for the cardiologist/cardio-oncologist. Frontiers Media S.A. 2022-04-21 /pmc/articles/PMC9068960/ /pubmed/35528837 http://dx.doi.org/10.3389/fcvm.2022.867873 Text en Copyright © 2022 Al-Otaibi, Weitzman, Tahir and Asnani. https://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 Cardiovascular Medicine
Al-Otaibi, Talal Khalid
Weitzman, Benjamin
Tahir, Usman A.
Asnani, Aarti
Genetics of Anthracycline-Associated Cardiotoxicity
title Genetics of Anthracycline-Associated Cardiotoxicity
title_full Genetics of Anthracycline-Associated Cardiotoxicity
title_fullStr Genetics of Anthracycline-Associated Cardiotoxicity
title_full_unstemmed Genetics of Anthracycline-Associated Cardiotoxicity
title_short Genetics of Anthracycline-Associated Cardiotoxicity
title_sort genetics of anthracycline-associated cardiotoxicity
topic Cardiovascular Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9068960/
https://www.ncbi.nlm.nih.gov/pubmed/35528837
http://dx.doi.org/10.3389/fcvm.2022.867873
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