[Safety and efficacy assessments using human iPS cell-derived cardiomyocytes]

Nihon Yakurigaku Zasshi. 2025;160(1):4-8. doi: 10.1254/fpj.24043.
[Article in Japanese]

Abstract

The delay and loss of drugs are serious problems in Japan. To overcome this issue, it is important to strengthen drug development capabilities. For drug development, the establishment and advancement of non-clinical testing methods are necessary for safe and effective clinical trials. Recently, the movement toward alternatives to animal testing has accelerated internationally. New Approach Methodologies (NAMs), such as human inducible pluripotent stem cell (hiPSC) technology and in silico modeling & simulation, are considered valuable for drug development. It has been demonstrated that hiPSC-derived cardiomyocytes (hiPSC-CMs) are useful tools to assess drug-induced cardiotoxicity, including arrhythmia and cardiac contractile dysfunction, leading to the use of hiPSC-CMs in the drug review process. Advancing hiPSC technologies have enabled the generation of mature hiPSC-CMs and engineered heart tissues, which are expected to provide novel information in drug safety and efficacy evaluation. Furthermore, it would be possible to establish the non-clinical evaluation that takes into account individual differences by developing hiPSCs bearing characteristics specific to certain populations, such as pediatrics or rare disease patients. Here, we present the recent findings and future perspectives on non-clinical evaluation using hiPSC technology.

Publication types

  • Review
  • English Abstract

MeSH terms

  • Animals
  • Cardiotoxicity / etiology
  • Cell Differentiation
  • Drug Evaluation, Preclinical
  • Humans
  • Induced Pluripotent Stem Cells* / cytology
  • Myocytes, Cardiac*