Development of a Human iPSC Cardiomyocyte-Based Scoring System for Cardiac Hazard Identification in Early Drug Safety De-risking

被引:43
|
作者
Kopljar, Ivan [1 ]
Lu, Hua Rong [1 ]
Van Ammel, Karel [1 ]
Otava, Martin [2 ]
Tekle, Fetene [2 ]
Teisman, Ard [1 ]
Gallacher, David J. [1 ]
机构
[1] Janssen Res & Dev, Global Safety Pharmacol Nonclin Safety, Turnhoutseweg 30, B-2340 Beerse, Belgium
[2] Janssen Res & Dev, Stat & Decis Sci, Quantitat Sci, Turnhoutseweg 30, B-2340 Beerse, Belgium
来源
STEM CELL REPORTS | 2018年 / 11卷 / 06期
关键词
CELL-DERIVED CARDIOMYOCYTES; PLURIPOTENT STEM-CELLS; CALCIUM TRANSIENT; QT INTERVAL; ACTION-POTENTIALS; RESPONSES; PLATFORM;
D O I
10.1016/j.stemcr.2018.11.007
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) have emerged as a promising cardiac safety platform, demonstrated by numerous validation studies using drugs with known cardiac adverse effects in humans. However, the challenge remains to implement hiPSC-CMs into cardiac de-risking of new chemical entities (NCEs) during preclinical drug development. Here, we used the calcium transient screening assay in hiPSC-CMs to develop a hazard score system for cardiac electrical liabilities. Tolerance interval calculations and evaluation of different classes of cardio-active drugs enabled us to develop a weighted scoring matrix. This approach allowed the translation of various pharmacological effects in hiPSC-CMs into a single hazard label (no, low, high, or very high hazard). Evaluation of 587 internal NCEs and good translation to ex vivo and in vivo models for a subset of these NCEs highlight the value of the cardiac hazard scoring in facilitating the selection of compounds during early drug safety screening.
引用
收藏
页码:1365 / 1377
页数:13
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