Use of Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes in Preclinical Cancer Drug Cardiotoxicity Testing

被引:101
作者
Gintant, Gary [1 ]
Burridge, Paul [3 ]
Gepstein, Lior [4 ]
Harding, Sian [5 ]
Herron, Todd [6 ]
Hong, Charles [7 ]
Jalife, Jose [6 ]
Wu, Joseph C. [2 ]
机构
[1] AbbVie Inc, N Chicago, IL 60064 USA
[2] Stanford Univ, Sch Med, Stanford, CA 94305 USA
[3] Northwestern Univ, Evanston, IL 60208 USA
[4] Technion Israel Inst Technol, Haifa, Israel
[5] Imperial Coll, NHLI, London, England
[6] Univ Michigan, Ann Arbor, MI 48109 USA
[7] Univ Maryland, Sch Med, Baltimore, MD 21201 USA
关键词
AHA Scientific Statements; biomarkers; cardiotoxicity; electrophysiology; human stem cell-derived cardiomyocytes; myocardial contraction; wounds and injuries; FIELD POTENTIAL DURATION; HUMAN MYOCARDIUM; MATURATION; DOXORUBICIN; SURVIVAL; DISEASE; RISK; TRANSCRIPTOME; GENERATION; MICRORNAS;
D O I
10.1161/RES.0000000000000291
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
It is now well recognized that many lifesaving oncology drugs may adversely affect the heart and cardiovascular system, including causing irreversible cardiac injury that can result in reduced quality of life. These effects, which may manifest in the short term or long term, are mechanistically not well understood. Research is hampered by the reliance on whole-animal models of cardiotoxicity that may fail to reflect the fundamental biology or cardiotoxic responses of the human myocardium. The emergence of human induced pluripotent stem cell-derived cardiomyocytes as an in vitro research tool holds great promise for understanding drug-induced cardiotoxicity of oncological drugs that may manifest as contractile and electrophysiological dysfunction, as well as structural abnormalities, making it possible to deliver novel drugs free from cardiac liabilities and guide personalized therapy. This article briefly reviews the challenges of cardio-oncology, the strengths and limitations of using human induced pluripotent stem cell-derived cardiomyocytes to represent clinical findings in the nonclinical research space, and future directions for their further use.
引用
收藏
页码:E75 / E92
页数:18
相关论文
共 118 条
[41]   Three-dimensional cardiac microtissues composed of cardiomyocytes and endothelial cells co-differentiated from human pluripotent stem cells [J].
Giacomelli, Elisa ;
Bellin, Milena ;
Sala, Luca ;
Van Meer, Berend J. ;
Tertoolen, Leon G. J. ;
Orlova, Valeria V. ;
Mummery, Christine L. .
DEVELOPMENT, 2017, 144 (06) :1008-1017
[42]   A Human Population-Based Organotypic In Vitro Model for Cardiotoxicity Screening [J].
Grimm, Fabian A. ;
Blanchette, Alexander ;
House, John S. ;
Ferguson, Kyle ;
Hsieh, Nan-Hung ;
Dalaijamts, Chimeddulam ;
Wright, Alec A. ;
Anson, Blake ;
Wright, Fred A. ;
Chiu, Weihsueh A. ;
Rusyn, Ivan .
ALTEX-ALTERNATIVES TO ANIMAL EXPERIMENTATION, 2018, 35 (04) :441-452
[43]   Precision cardio-oncology: understanding the cardiotoxicity of cancer therapy [J].
Han, Xinqiang ;
Zhou, Yun ;
Liu, Wendi .
NPJ PRECISION ONCOLOGY, 2017, 1
[44]   ENERGETICS OF ISOMETRIC FORCE DEVELOPMENT IN CONTROL AND VOLUME-OVERLOAD HUMAN MYOCARDIUM - COMPARISON WITH ANIMAL SPECIES [J].
HASENFUSS, G ;
MULIERI, LA ;
BLANCHARD, EM ;
HOLUBARSCH, C ;
LEAVITT, BJ ;
ITTLEMAN, F ;
ALPERT, NR .
CIRCULATION RESEARCH, 1991, 68 (03) :836-846
[45]   Extracellular Matrix-Mediated Maturation of Human Pluripotent Stem Cell-Derived Cardiac Monolayer Structure and Electrophysiological Function [J].
Herron, Todd J. ;
Da Rocha, Andre Monteiro ;
Campbell, Katherine F. ;
Ponce-Balbuena, Daniela ;
Willis, B. Cicero ;
Guerrero-Serna, Guadalupe ;
Liu, Qinghua ;
Klos, Matt ;
Musa, Hassan ;
Zarzoso, Manuel ;
Bizy, Alexandra ;
Furness, Jamie ;
Anumonwo, Justus ;
Mironov, Sergey ;
Jalife, Jose .
CIRCULATION-ARRHYTHMIA AND ELECTROPHYSIOLOGY, 2016, 9 (04)
[46]   Functional improvement and maturation of rat and human engineered heart tissue by chronic electrical stimulation [J].
Hirt, Marc N. ;
Boeddinghaus, Jasper ;
Mitchell, Alice ;
Schaaf, Sebastian ;
Boernchen, Christian ;
Mueller, Christian ;
Schulz, Herbert ;
Hubner, Norbert ;
Stenzig, Justus ;
Stoehr, Andrea ;
Neuber, Christiane ;
Eder, Alexandra ;
Luther, Pradeep K. ;
Hansen, Arne ;
Eschenhagen, Thomas .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 2014, 74 :151-161
[47]   Increased afterload induces pathological cardiac hypertrophy: a new in vitro model [J].
Hirt, Marc N. ;
Soerensen, Nils A. ;
Bartholdt, Lena M. ;
Boeddinghaus, Jasper ;
Schaaf, Sebastian ;
Eder, Alexandra ;
Vollert, Ingra ;
Stoehr, Andrea ;
Schulze, Thomas ;
Witten, Anika ;
Stoll, Monika ;
Hansen, Arne ;
Eschenhagen, Thomas .
BASIC RESEARCH IN CARDIOLOGY, 2012, 107 (06)
[48]   Expression Profiling of Human Pluripotent Stem Cell-Derived Cardiomyocytes Exposed to Doxorubicin-Integration and Visualization of Multi-Omics Data [J].
Holmgren, Gustav ;
Sartipy, Peter ;
Andersson, Christian X. ;
Lindahl, Anders ;
Synnergren, Jane .
TOXICOLOGICAL SCIENCES, 2018, 163 (01) :182-195
[49]   The Use of Ratiometric Fluorescence Measurements of the Voltage Sensitive Dye Di-4-ANEPPS to Examine Action Potential Characteristics and Drug Effects on Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes [J].
Hortigon-Vinagre, M. P. ;
Zamora, V. ;
Burton, F. L. ;
Green, J. ;
Gintant, G. A. ;
Smith, G. L. .
TOXICOLOGICAL SCIENCES, 2016, 154 (02) :320-331
[50]   Comparable calcium handling of human iPSC-derived cardiomyocytes generated by multiple laboratories [J].
Hwang, Hyun Seok ;
Kryshtal, Dmytro O. ;
Feaster, T. K. ;
Sanchez-Freire, Veronica ;
Zhang, Jianhua ;
Kamp, Timothy J. ;
Hong, Charles C. ;
Wu, Joseph C. ;
Knollmann, Bjoern C. .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 2015, 85 :79-88