Drug screening for human genetic diseases using iPSC models

Hum Mol Genet. 2018 Aug 1;27(R2):R89-R98. doi: 10.1093/hmg/ddy186.

Abstract

Induced pluripotent stem cells (iPSCs) enable the generation of previously unattainable, scalable quantities of disease-relevant tissues from patients suffering from essentially any genetic disorder. This cellular material has proven instrumental for drug screening efforts on these disorders, and has facilitated the identification of novel therapeutics for patients. Here we will review the foundational technologies that have enabled iPSCs, the power and limitations of iPSC-based compound screens along with screening guidelines, and recent examples of screening efforts. Additionally we will provide a brief commentary on the future scientific roadmap using pluripotent- and 3D organoid-based, combinatorial approaches.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Cell Culture Techniques / methods
  • Drug Discovery / methods*
  • Drug Evaluation, Preclinical / methods*
  • Genetic Diseases, Inborn / genetics*
  • Human Genetics / methods
  • Humans
  • Induced Pluripotent Stem Cells / drug effects