Human Pluripotent Stem-Cell-Derived Models as a Missing Link in Drug Discovery and Development
- PMID: 34070895
- PMCID: PMC8230131
- DOI: 10.3390/ph14060525
Human Pluripotent Stem-Cell-Derived Models as a Missing Link in Drug Discovery and Development
Abstract
Human pluripotent stem cells (hPSCs), including human embryonic stem cells (hESCs) and human-induced pluripotent stem cells (hiPSCs), have the potential to accelerate the drug discovery and development process. In this review, by analyzing each stage of the drug discovery and development process, we identified the active role of hPSC-derived in vitro models in phenotypic screening, target-based screening, target validation, toxicology evaluation, precision medicine, clinical trial in a dish, and post-clinical studies. Patient-derived or genome-edited PSCs can generate valid in vitro models for dissecting disease mechanisms, discovering novel drug targets, screening drug candidates, and preclinically and post-clinically evaluating drug safety and efficacy. With the advances in modern biotechnologies and developmental biology, hPSC-derived in vitro models will hopefully improve the cost-effectiveness and the success rate of drug discovery and development.
Keywords: drug development; drug discovery; human embryonic stem cells; human pluripotent stem cells; human-induced pluripotent stem cells.
Conflict of interest statement
The authors declare no conflict of interest.
Figures
Similar articles
-
Development of hematopoietic stem and progenitor cells from human pluripotent stem cells.J Cell Biochem. 2015 Jul;116(7):1179-89. doi: 10.1002/jcb.25097. J Cell Biochem. 2015. PMID: 25740540 Free PMC article. Review.
-
The safety of human pluripotent stem cells in clinical treatment.Ann Med. 2015;47(5):370-80. doi: 10.3109/07853890.2015.1051579. Epub 2015 Jul 6. Ann Med. 2015. PMID: 26140342 Review.
-
Application of human pluripotent stem cells and pluripotent stem cell-derived cellular models for assessing drug toxicity.Expert Opin Drug Metab Toxicol. 2019 Jan;15(1):61-75. doi: 10.1080/17425255.2019.1558207. Epub 2018 Dec 17. Expert Opin Drug Metab Toxicol. 2019. PMID: 30526128 Review.
-
A Universal and Robust Integrated Platform for the Scalable Production of Human Cardiomyocytes From Pluripotent Stem Cells.Stem Cells Transl Med. 2015 Dec;4(12):1482-94. doi: 10.5966/sctm.2014-0275. Epub 2015 Oct 28. Stem Cells Transl Med. 2015. PMID: 26511653 Free PMC article.
-
Human Pluripotent Stem Cell Culture: Current Status, Challenges, and Advancement.Stem Cells Int. 2018 Nov 22;2018:7396905. doi: 10.1155/2018/7396905. eCollection 2018. Stem Cells Int. 2018. PMID: 30595701 Free PMC article. Review.
Cited by
-
Current Status and Challenges of Human Induced Pluripotent Stem Cell-Derived Liver Models in Drug Discovery.Cells. 2022 Jan 27;11(3):442. doi: 10.3390/cells11030442. Cells. 2022. PMID: 35159250 Free PMC article. Review.
-
Challenges for the Applications of Human Pluripotent Stem Cell-Derived Liver Organoids.Front Cell Dev Biol. 2021 Oct 1;9:748576. doi: 10.3389/fcell.2021.748576. eCollection 2021. Front Cell Dev Biol. 2021. PMID: 34660606 Free PMC article. Review.
-
Synergistic potential of stem cells and microfluidics in regenerative medicine.Mol Cell Biochem. 2025 Mar;480(3):1481-1493. doi: 10.1007/s11010-024-05108-8. Epub 2024 Sep 16. Mol Cell Biochem. 2025. PMID: 39285093 Free PMC article. Review.
-
iPSCs in Neurodegenerative Disorders: A Unique Platform for Clinical Research and Personalized Medicine.J Pers Med. 2022 Sep 10;12(9):1485. doi: 10.3390/jpm12091485. J Pers Med. 2022. PMID: 36143270 Free PMC article. Review.
-
Advances in hPSC expansion towards therapeutic entities: A review.Cell Prolif. 2022 Aug;55(8):e13247. doi: 10.1111/cpr.13247. Epub 2022 May 31. Cell Prolif. 2022. PMID: 35638399 Free PMC article. Review.
References
-
- Menasché P., Vanneaux V., Hagège A., Bel A., Cholley B., Parouchev A., Cacciapuoti I., Al-Daccak R., Benhamouda N., Blons H., et al. Transplantation of Human Embryonic Stem Cell-Derived Cardiovascular Progenitors for Severe Ischemic Left Ventricular Dysfunction. J. Am. Coll. Cardiol. 2018;71:429–438. doi: 10.1016/j.jacc.2017.11.047. - DOI - PubMed
Publication types
LinkOut - more resources
Full Text Sources
Other Literature Sources