The First Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou University of Chinese Medicine, Guangzhou, 510405, China.
Centre for Clinical Pharmacology and Precision Medicine, William Harvey Research Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, Heart Centre, Charterhouse Square, London, EC1M 6BQ, UK.
Cell Biol Toxicol. 2023 Dec;39(6):2527-2549. doi: 10.1007/s10565-023-09835-4. Epub 2023 Oct 27.
Cardiovascular disease (CVD) caused by anti-cancer drug-induced cardiotoxicity is now the second leading cause of mortality among cancer survivors. It is necessary to establish efficient in vitro models for early predicting the potential cardiotoxicity of anti-cancer drugs, as well as for screening drugs that would alleviate cardiotoxicity during and post treatment. Human induced pluripotent stem cells (hiPSCs) have opened up new avenues in cardio-oncology. With the breakthrough of tissue engineering technology, a variety of hiPSC-derived cardiac microtissues or organoids have been recently reported, which have shown enormous potential in studying cardiotoxicity. Moreover, using hiPSC-derived heart-on-chip for studying cardiotoxicity has provided novel insights into the underlying mechanisms. Herein, we summarize different types of anti-cancer drug-induced cardiotoxicities and present an extensive overview on the applications of hiPSC-derived cardiac microtissues, cardiac organoids, and heart-on-chips in cardiotoxicity. Finally, we highlight clinical and translational challenges around hiPSC-derived cardiac microtissues/organoids/heart-on chips and their applications in anti-cancer drug-induced cardiotoxicity. • Anti-cancer drug-induced cardiotoxicities represent pressing challenges for cancer treatments, and cardiovascular disease is the second leading cause of mortality among cancer survivors. • Newly reported in vitro models such as hiPSC-derived cardiac microtissues/organoids/chips show enormous potential for studying cardio-oncology. • Emerging evidence supports that hiPSC-derived cardiac organoids and heart-on-chip are promising in vitro platforms for predicting and minimizing anti-cancer drug-induced cardiotoxicity.
抗癌药物引起的心脏毒性导致的心血管疾病(CVD)现在是癌症幸存者死亡的第二大主要原因。有必要建立有效的体外模型,以便早期预测抗癌药物的潜在心脏毒性,并筛选在治疗期间和治疗后减轻心脏毒性的药物。人诱导多能干细胞(hiPSC)为心脏肿瘤学开辟了新途径。随着组织工程技术的突破,最近已经报道了多种 hiPSC 衍生的心脏微组织或类器官,它们在研究心脏毒性方面显示出了巨大的潜力。此外,使用 hiPSC 衍生的心脏芯片进行心脏毒性研究为深入了解潜在机制提供了新的视角。本文总结了不同类型的抗癌药物引起的心脏毒性,并广泛概述了 hiPSC 衍生的心脏微组织、心脏类器官和心脏芯片在心脏毒性研究中的应用。最后,我们强调了 hiPSC 衍生的心脏微组织/类器官/芯片及其在抗癌药物引起的心脏毒性中的应用所面临的临床和转化挑战。• 抗癌药物引起的心脏毒性对癌症治疗构成了紧迫挑战,心血管疾病是癌症幸存者死亡的第二大主要原因。• 最近报道的体外模型,如 hiPSC 衍生的心脏微组织/类器官/芯片,在研究心脏肿瘤学方面显示出巨大的潜力。• 新兴证据表明,hiPSC 衍生的心脏类器官和心脏芯片是预测和最小化抗癌药物引起的心脏毒性的有前途的体外平台。