Concise Review: Induced Pluripotent Stem Cell-Based Drug Discovery for Mitochondrial Disease.
Gizem InakCarmen LorenzPawel LisowskiAnnika ZinkBarbara MlodyAlessandro PrigionePublished in: Stem cells (Dayton, Ohio) (2017)
High attrition rates and loss of capital plague the drug discovery process. This is particularly evident for mitochondrial disease that typically involves neurological manifestations and is caused by nuclear or mitochondrial DNA defects. This group of heterogeneous disorders is difficult to target because of the variability of the symptoms among individual patients and the lack of viable modeling systems. The use of induced pluripotent stem cells (iPSCs) might significantly improve the search for effective therapies for mitochondrial disease. iPSCs can be used to generate patient-specific neural cell models in which innovative compounds can be identified or validated. Here we discuss the promises and challenges of iPSC-based drug discovery for mitochondrial disease with a specific focus on neurological conditions. We anticipate that a proper use of the potent iPSC technology will provide critical support for the development of innovative therapies against these untreatable and detrimental disorders. Stem Cells 2017;35:1655-1662.
Keyphrases
- drug discovery
- stem cells
- induced pluripotent stem cells
- mitochondrial dna
- oxidative stress
- end stage renal disease
- copy number
- chronic kidney disease
- ejection fraction
- newly diagnosed
- gene expression
- diabetic rats
- dna methylation
- physical activity
- high glucose
- anti inflammatory
- endothelial cells
- drug induced
- brain injury