Shead Kyle D, Huethorst Eline, Burton Francis, Lang Ninian N, Myles Rachel C, Smith Godfrey L
School of Cardiovascular and Metabolic Health, University of Glasgow, Glasgow, United Kingdom.
JACC CardioOncol. 2024 Sep 10;6(5):678-683. doi: 10.1016/j.jaccao.2024.07.012. eCollection 2024 Oct.
• hiPSC-CM offer an alternative to in vivo models for predicting cardiotoxicity. • hiPSC-CM monolayers detect pro-arrhythmic effects; inotropic detection is less established. • Cardiac spheroids and engineered tissue may suit chronic cardiotoxicity studies (>2 weeks). • Cardiac assays with non-myocyte cells may be key to identifying some cardiotoxicity forms. • hiPSC-CM technologies are well placed to develop patient-specific assays in the future.
• 人诱导多能干细胞来源的心肌细胞(hiPSC-CM)为预测心脏毒性的体内模型提供了一种替代方案。
• hiPSC-CM单层可检测促心律失常作用;变力性检测的方法尚不完善。
• 心脏球体和工程组织可能适用于慢性心脏毒性研究(>2周)。
• 非心肌细胞的心脏检测可能是识别某些心脏毒性形式的关键。
• hiPSC-CM技术在未来很适合开发针对患者的检测方法。