| Literature DB >> 33925625 |
Gabriele Bonaventura1, Rosario Iemmolo1, Giuseppe Antonino Attaguile2, Valentina La Cognata1, Brigida Sabrina Pistone1, Giuseppe Raudino3, Velia D'Agata4, Giuseppina Cantarella2, Maria Luisa Barcellona5, Sebastiano Cavallaro1.
Abstract
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).Entities:
Keywords: AD; ALS; FRAX; PD; drug development; iPSCs
Year: 2021 PMID: 33925625 DOI: 10.3390/ijms22094596
Source DB: PubMed Journal: Int J Mol Sci ISSN: 1422-0067 Impact factor: 5.923