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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2021-02-01
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Series: | Translational Psychiatry |
Online Access: | https://doi.org/10.1038/s41398-021-01243-8 |
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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 |
work_keys_str_mv |
AT santiagoglago functionalpatientderivedcellularmodelsforneuropsychiatricdrugdiscovery AT jakubtomasik functionalpatientderivedcellularmodelsforneuropsychiatricdrugdiscovery AT sabinebahn functionalpatientderivedcellularmodelsforneuropsychiatricdrugdiscovery |
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