Cardiotoxicity of Antineoplastic Therapies and Applications of Induced Pluripotent Stem Cell-Derived Cardiomyocytes

The therapeutic landscape for the treatment of cancer has evolved significantly in recent decades, aided by the development of effective oncology drugs. However, many cancer drugs are often poorly tolerated by the body and in particular the cardiovascular system, causing adverse and sometimes fatal...

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Autores principales: Mo-Fan Huang, Lon Kai Pang, Yi-Hung Chen, Ruiying Zhao, Dung-Fang Lee
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Lenguaje:EN
Publicado: MDPI AG 2021
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Acceso en línea:https://doaj.org/article/d997cfa149d14d118a45b22d671915dd
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spelling oai:doaj.org-article:d997cfa149d14d118a45b22d671915dd2021-11-25T17:07:35ZCardiotoxicity of Antineoplastic Therapies and Applications of Induced Pluripotent Stem Cell-Derived Cardiomyocytes10.3390/cells101128232073-4409https://doaj.org/article/d997cfa149d14d118a45b22d671915dd2021-10-01T00:00:00Zhttps://www.mdpi.com/2073-4409/10/11/2823https://doaj.org/toc/2073-4409The therapeutic landscape for the treatment of cancer has evolved significantly in recent decades, aided by the development of effective oncology drugs. However, many cancer drugs are often poorly tolerated by the body and in particular the cardiovascular system, causing adverse and sometimes fatal side effects that negate the chemotherapeutic benefits. The prevalence and severity of chemotherapy-induced cardiotoxicity warrants a deeper investigation of the mechanisms and implicating factors in this phenomenon, and a consolidation of scientific efforts to develop mitigating strategies. Aiding these efforts is the emergence of induced pluripotent stem cells (iPSCs) in recent years, which has allowed for the generation of iPSC-derived cardiomyocytes (iPSC-CMs): a human-based, patient-derived, and genetically variable platform that can be applied to the study of chemotherapy-induced cardiotoxicity and beyond. After surveying chemotherapy-induced cardiotoxicity and the associated chemotherapeutic agents, we discuss the use of iPSC-CMs in cardiotoxicity modeling, drug screening, and other potential applications. Improvements to the iPSC-CM platform, such as the development of more adult-like cardiomyocytes and ongoing advances in biotechnology, will only enhance the utility of iPSC-CMs in both basic science and clinical applications.Mo-Fan HuangLon Kai PangYi-Hung ChenRuiying ZhaoDung-Fang LeeMDPI AGarticlestem celldisease modelinduced pluripotencyreprogrammingdifferentiationchemotherapyBiology (General)QH301-705.5ENCells, Vol 10, Iss 2823, p 2823 (2021)
institution DOAJ
collection DOAJ
language EN
topic stem cell
disease model
induced pluripotency
reprogramming
differentiation
chemotherapy
Biology (General)
QH301-705.5
spellingShingle stem cell
disease model
induced pluripotency
reprogramming
differentiation
chemotherapy
Biology (General)
QH301-705.5
Mo-Fan Huang
Lon Kai Pang
Yi-Hung Chen
Ruiying Zhao
Dung-Fang Lee
Cardiotoxicity of Antineoplastic Therapies and Applications of Induced Pluripotent Stem Cell-Derived Cardiomyocytes
description The therapeutic landscape for the treatment of cancer has evolved significantly in recent decades, aided by the development of effective oncology drugs. However, many cancer drugs are often poorly tolerated by the body and in particular the cardiovascular system, causing adverse and sometimes fatal side effects that negate the chemotherapeutic benefits. The prevalence and severity of chemotherapy-induced cardiotoxicity warrants a deeper investigation of the mechanisms and implicating factors in this phenomenon, and a consolidation of scientific efforts to develop mitigating strategies. Aiding these efforts is the emergence of induced pluripotent stem cells (iPSCs) in recent years, which has allowed for the generation of iPSC-derived cardiomyocytes (iPSC-CMs): a human-based, patient-derived, and genetically variable platform that can be applied to the study of chemotherapy-induced cardiotoxicity and beyond. After surveying chemotherapy-induced cardiotoxicity and the associated chemotherapeutic agents, we discuss the use of iPSC-CMs in cardiotoxicity modeling, drug screening, and other potential applications. Improvements to the iPSC-CM platform, such as the development of more adult-like cardiomyocytes and ongoing advances in biotechnology, will only enhance the utility of iPSC-CMs in both basic science and clinical applications.
format article
author Mo-Fan Huang
Lon Kai Pang
Yi-Hung Chen
Ruiying Zhao
Dung-Fang Lee
author_facet Mo-Fan Huang
Lon Kai Pang
Yi-Hung Chen
Ruiying Zhao
Dung-Fang Lee
author_sort Mo-Fan Huang
title Cardiotoxicity of Antineoplastic Therapies and Applications of Induced Pluripotent Stem Cell-Derived Cardiomyocytes
title_short Cardiotoxicity of Antineoplastic Therapies and Applications of Induced Pluripotent Stem Cell-Derived Cardiomyocytes
title_full Cardiotoxicity of Antineoplastic Therapies and Applications of Induced Pluripotent Stem Cell-Derived Cardiomyocytes
title_fullStr Cardiotoxicity of Antineoplastic Therapies and Applications of Induced Pluripotent Stem Cell-Derived Cardiomyocytes
title_full_unstemmed Cardiotoxicity of Antineoplastic Therapies and Applications of Induced Pluripotent Stem Cell-Derived Cardiomyocytes
title_sort cardiotoxicity of antineoplastic therapies and applications of induced pluripotent stem cell-derived cardiomyocytes
publisher MDPI AG
publishDate 2021
url https://doaj.org/article/d997cfa149d14d118a45b22d671915dd
work_keys_str_mv AT mofanhuang cardiotoxicityofantineoplastictherapiesandapplicationsofinducedpluripotentstemcellderivedcardiomyocytes
AT lonkaipang cardiotoxicityofantineoplastictherapiesandapplicationsofinducedpluripotentstemcellderivedcardiomyocytes
AT yihungchen cardiotoxicityofantineoplastictherapiesandapplicationsofinducedpluripotentstemcellderivedcardiomyocytes
AT ruiyingzhao cardiotoxicityofantineoplastictherapiesandapplicationsofinducedpluripotentstemcellderivedcardiomyocytes
AT dungfanglee cardiotoxicityofantineoplastictherapiesandapplicationsofinducedpluripotentstemcellderivedcardiomyocytes
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