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iPSCs: A Preclinical Drug Research Tool for Neurological Disorders
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 fin...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8123805/ https://www.ncbi.nlm.nih.gov/pubmed/33925625 http://dx.doi.org/10.3390/ijms22094596 |
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author | Bonaventura, Gabriele Iemmolo, Rosario Attaguile, Giuseppe Antonino La Cognata, Valentina Pistone, Brigida Sabrina Raudino, Giuseppe D’Agata, Velia Cantarella, Giuseppina Barcellona, Maria Luisa Cavallaro, Sebastiano |
author_facet | Bonaventura, Gabriele Iemmolo, Rosario Attaguile, Giuseppe Antonino La Cognata, Valentina Pistone, Brigida Sabrina Raudino, Giuseppe D’Agata, Velia Cantarella, Giuseppina Barcellona, Maria Luisa Cavallaro, Sebastiano |
author_sort | Bonaventura, Gabriele |
collection | PubMed |
description | 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). |
format | Online Article Text |
id | pubmed-8123805 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-81238052021-05-16 iPSCs: A Preclinical Drug Research Tool for Neurological Disorders Bonaventura, Gabriele Iemmolo, Rosario Attaguile, Giuseppe Antonino La Cognata, Valentina Pistone, Brigida Sabrina Raudino, Giuseppe D’Agata, Velia Cantarella, Giuseppina Barcellona, Maria Luisa Cavallaro, Sebastiano Int J Mol Sci Review 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). MDPI 2021-04-27 /pmc/articles/PMC8123805/ /pubmed/33925625 http://dx.doi.org/10.3390/ijms22094596 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Bonaventura, Gabriele Iemmolo, Rosario Attaguile, Giuseppe Antonino La Cognata, Valentina Pistone, Brigida Sabrina Raudino, Giuseppe D’Agata, Velia Cantarella, Giuseppina Barcellona, Maria Luisa Cavallaro, Sebastiano iPSCs: A Preclinical Drug Research Tool for Neurological Disorders |
title | iPSCs: A Preclinical Drug Research Tool for Neurological Disorders |
title_full | iPSCs: A Preclinical Drug Research Tool for Neurological Disorders |
title_fullStr | iPSCs: A Preclinical Drug Research Tool for Neurological Disorders |
title_full_unstemmed | iPSCs: A Preclinical Drug Research Tool for Neurological Disorders |
title_short | iPSCs: A Preclinical Drug Research Tool for Neurological Disorders |
title_sort | ipscs: a preclinical drug research tool for neurological disorders |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8123805/ https://www.ncbi.nlm.nih.gov/pubmed/33925625 http://dx.doi.org/10.3390/ijms22094596 |
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