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iPSCs: A Preclinical Drug Research Tool for Neurological Disorders

Journal

Publisher

MDPI
DOI: 10.3390/ijms22094596

Keywords

iPSCs; drug development; AD; ALS; PD; FRAX

Funding

  1. European Social Fund operational program for the Sicily region (Italy) Development and application of biosensoristic technologies in genomics [CIP 2014.IT.05.SFOP.014/3/10.4/9.2.10/0008]

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The process of developing and commercializing new drugs involves multiple steps, including target identification, preclinical studies, and clinical trials; stem cells play a crucial role in drug discovery; the advancement of iPSCs technology has enabled the creation of patient-specific disease models for drug screening and development.
The development and commercialization of new drugs is an articulated, lengthy, and very expensive process that proceeds through several steps, starting from target identification, screening new leading compounds for testing in preclinical studies, and subsequently in clinical trials to reach the final approval for therapeutic use. Preclinical studies are usually performed using both cell cultures and animal models, although they do not completely resume the complexity of human diseases, in particular neurodegenerative conditions. To this regard, stem cells represent a powerful tool in all steps of drug discovery. The recent advancement in induced Pluripotent Stem Cells (iPSCs) technology has opened the possibility to obtain patient-specific disease models for drug screening and development. Here, we report the use of iPSCs as a disease model for drug development in the contest of neurological disorders, including Alzheimer's (AD) and Parkinson's disease (PD), Amyotrophic lateral Sclerosis (ALS), and Fragile X syndrome (FRAX).

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