| Literature DB >> 33740432 |
Anna P Hnatiuk1, Francesca Briganti1, David W Staudt2, Mark Mercola3.
Abstract
Human induced pluripotent stem cells (hiPSCs) have emerged as a promising platform for pharmacogenomics and drug development. In cardiology, they make it possible to produce unlimited numbers of patient-specific human cells that reproduce hallmark features of heart disease in the culture dish. Their potential applications include the discovery of mechanism-specific therapeutics, the evaluation of safety and efficacy in a human context before a drug candidate reaches patients, and the stratification of patients for clinical trials. Although this new technology has the potential to revolutionize drug discovery, translational hurdles have hindered its widespread adoption for pharmaceutical development. Here we discuss recent progress in overcoming these hurdles that should facilitate the use of hiPSCs to develop new medicines and individualize therapies for heart disease.Entities:
Keywords: HTS; cardiomyocyte; disease modeling; drug attrition; drug discovery; heart disease; hiPSC; screen
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Year: 2021 PMID: 33740432 PMCID: PMC8054828 DOI: 10.1016/j.chembiol.2021.02.016
Source DB: PubMed Journal: Cell Chem Biol ISSN: 2451-9448 Impact factor: 8.116