Improvement of cardiac efficacy and safety models in drug discovery by the use of stem cell-derived cardiomyocytes

被引:19
作者
Jonsson, Malin K. B. [1 ]
van Veen, Toon A. B. [1 ]
Goumans, Marie-Jose [2 ]
Vos, Marc A. [1 ]
Duker, Goran [3 ]
Sartipy, Peter [4 ]
机构
[1] Univ Med Ctr Utrecht, Div Heart & Lungs, Dept Med Physiol, NL-3584 CM Utrecht, Netherlands
[2] Leiden Univ, Med Ctr, Dept Mol Cell Biol, NL-2300 RC Leiden, Netherlands
[3] AstraZeneca R&D, Integrat Pharmacol, S-43183 Molndal, Sweden
[4] Cellartis AB, S-41346 Gothenburg, Sweden
关键词
arrhythmias; cardiomyocytes; drug discovery; electrophysiology; safety pharmacology; stem cells; TORSADES-DE-POINTES; LONG-QT SYNDROME; III ANTIARRHYTHMIC AGENTS; TO-BEAT VARIABILITY; IN-VITRO MODEL; ACTION-POTENTIALS; HUMAN FIBROBLASTS; D-SOTALOL; DIFFERENTIATION; GENERATION;
D O I
10.1517/17460440902794912
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background: The pharmaceutical industry suffers from high attrition rates during late phases of drug development. Improved models for early evaluation of drug efficacy and safety are needed to address this problem. Recent developments have illustrated that human stem cell-derived cardiomyocytes are attractive for using as a model system for different cardiac diseases and as a model for screening, safety pharmacology and toxicology. Objective: In this review, we discuss contemporary drug discovery models and their characteristics for cardiac efficacy testing and safety assessment. Additionally, we evaluate various sources of stem cells and how these cells could potentially improve early screening and safety models. Conclusion: We conclude that human stem cells offer a source of physiologically relevant cells that show great potential as a future tool in cardiac drug discovery. However, some technical challenges related to cell differentiation and production and also to validation of improved platforms remain and must be overcome before successful application can become a reality.
引用
收藏
页码:357 / 372
页数:16
相关论文
共 113 条
[1]   Unique topographical distribution of m cells underlies reentrant mechanism of torsade de pointes in the long-QT syndrome [J].
Akar, FG ;
Yan, GX ;
Antzelevitch, C ;
Rosenbaum, DS .
CIRCULATION, 2002, 105 (10) :1247-1253
[2]   Transgenic enrichment of cardiomyocytes from human embryonic stem cells [J].
Anderson, David ;
Self, Tim ;
Mellor, Ian R. ;
Goh, Gareth ;
Hill, Stephen J. ;
Denning, Chris .
MOLECULAR THERAPY, 2007, 15 (11) :2027-2036
[3]  
Antzelevitch C, 1997, J ELECTROCARDIOL, V30, P168
[4]   Heterogeneity and cardiac arrhythmias: An overview [J].
Antzelevitch, Charles .
HEART RHYTHM, 2007, 4 (07) :964-972
[5]   Endogenous cardiac stem cells [J].
Barile, Lucio ;
Messina, Elisa ;
Giacomello, Alessandro ;
Marban, Eduardo .
PROGRESS IN CARDIOVASCULAR DISEASES, 2007, 50 (01) :31-48
[6]   3D-model of adult cardiac stem cells promotes cardiac differentiation and resistance to oxidative stress [J].
Bartosh, T. J. ;
Wang, Zhaohui ;
Rosales, Armando A. ;
Dimitrijevich, S. Dan ;
Roque, Rouel S. .
JOURNAL OF CELLULAR BIOCHEMISTRY, 2008, 105 (02) :612-623
[7]   Adult cardiac stem cells are multipotent and support myocardial regeneration [J].
Beltrami, AP ;
Barlucchi, L ;
Torella, D ;
Baker, M ;
Limana, F ;
Chimenti, S ;
Kasahara, H ;
Rota, M ;
Musso, E ;
Urbanek, K ;
Leri, A ;
Kajstura, J ;
Nadal-Ginard, B ;
Anversa, P .
CELL, 2003, 114 (06) :763-776
[8]   Cardiac HCN channels: Structure, function, and modulation [J].
Biel, M ;
Schneider, A ;
Wahl, C .
TRENDS IN CARDIOVASCULAR MEDICINE, 2002, 12 (05) :206-213
[9]   Adaptation of human embryonic stem cells to feeder-free and matrix-free culture conditions directly on plastic surfaces [J].
Bigdeli, Narmin ;
Andersson, Maria ;
Strehl, Raimund ;
Emanuelsson, Katarina ;
Kilmare, Eva ;
Hyllner, Johan ;
Lindahl, Anders .
JOURNAL OF BIOTECHNOLOGY, 2008, 133 (01) :146-153
[10]   ISOLATION AND CULTURE OF INNER CELL MASS CELLS FROM HUMAN BLASTOCYSTS [J].
BONGSO, A ;
FONG, CY ;
NG, SC ;
RATNAM, S .
HUMAN REPRODUCTION, 1994, 9 (11) :2110-2117