Functional patient-derived cellular models for neuropsychiatric drug discovery

Abstract Mental health disorders are a leading cause of disability worldwide. Challenges such as disease heterogeneity, incomplete characterization of the targets of existing drugs and a limited understanding of functional interactions of complex genetic risk loci and environmental factors have comp...

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Main Authors: Santiago G. Lago, Jakub Tomasik, Sabine Bahn
Format: Article
Language:English
Published: Nature Publishing Group 2021-02-01
Series:Translational Psychiatry
Online Access:https://doi.org/10.1038/s41398-021-01243-8
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spelling doaj-66a0a34b91a84bf5bfe9d2b113ad006f2021-02-21T12:48:02ZengNature Publishing GroupTranslational Psychiatry2158-31882021-02-0111111110.1038/s41398-021-01243-8Functional patient-derived cellular models for neuropsychiatric drug discoverySantiago G. Lago0Jakub Tomasik1Sabine Bahn2Department of Chemical Engineering and Biotechnology, University of CambridgeDepartment of Chemical Engineering and Biotechnology, University of CambridgeDepartment of Chemical Engineering and Biotechnology, University of CambridgeAbstract Mental health disorders are a leading cause of disability worldwide. Challenges such as disease heterogeneity, incomplete characterization of the targets of existing drugs and a limited understanding of functional interactions of complex genetic risk loci and environmental factors have compromised the identification of novel drug candidates. There is a pressing clinical need for drugs with new mechanisms of action which address the lack of efficacy and debilitating side effects of current medications. Here we discuss a novel strategy for neuropsychiatric drug discovery which aims to address these limitations by identifying disease-related functional responses (‘functional cellular endophenotypes’) in a variety of patient-derived cells, such as induced pluripotent stem cell (iPSC)-derived neurons and organoids or peripheral blood mononuclear cells (PBMCs). Disease-specific alterations in cellular responses can subsequently yield novel drug screening targets and drug candidates. We discuss the potential of this approach in the context of recent advances in patient-derived cellular models, high-content single-cell screening of cellular networks and changes in the diagnostic framework of neuropsychiatric disorders.https://doi.org/10.1038/s41398-021-01243-8
collection DOAJ
language English
format Article
sources DOAJ
author Santiago G. Lago
Jakub Tomasik
Sabine Bahn
spellingShingle Santiago G. Lago
Jakub Tomasik
Sabine Bahn
Functional patient-derived cellular models for neuropsychiatric drug discovery
Translational Psychiatry
author_facet Santiago G. Lago
Jakub Tomasik
Sabine Bahn
author_sort Santiago G. Lago
title Functional patient-derived cellular models for neuropsychiatric drug discovery
title_short Functional patient-derived cellular models for neuropsychiatric drug discovery
title_full Functional patient-derived cellular models for neuropsychiatric drug discovery
title_fullStr Functional patient-derived cellular models for neuropsychiatric drug discovery
title_full_unstemmed Functional patient-derived cellular models for neuropsychiatric drug discovery
title_sort functional patient-derived cellular models for neuropsychiatric drug discovery
publisher Nature Publishing Group
series Translational Psychiatry
issn 2158-3188
publishDate 2021-02-01
description Abstract Mental health disorders are a leading cause of disability worldwide. Challenges such as disease heterogeneity, incomplete characterization of the targets of existing drugs and a limited understanding of functional interactions of complex genetic risk loci and environmental factors have compromised the identification of novel drug candidates. There is a pressing clinical need for drugs with new mechanisms of action which address the lack of efficacy and debilitating side effects of current medications. Here we discuss a novel strategy for neuropsychiatric drug discovery which aims to address these limitations by identifying disease-related functional responses (‘functional cellular endophenotypes’) in a variety of patient-derived cells, such as induced pluripotent stem cell (iPSC)-derived neurons and organoids or peripheral blood mononuclear cells (PBMCs). Disease-specific alterations in cellular responses can subsequently yield novel drug screening targets and drug candidates. We discuss the potential of this approach in the context of recent advances in patient-derived cellular models, high-content single-cell screening of cellular networks and changes in the diagnostic framework of neuropsychiatric disorders.
url https://doi.org/10.1038/s41398-021-01243-8
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