Functional patient-derived cellular models for neuropsychiatric drug discovery

被引:9
|
作者
Lago, Santiago G. [1 ]
Tomasik, Jakub [1 ]
Bahn, Sabine [1 ]
机构
[1] Univ Cambridge, Dept Chem Engn & Biotechnol, Cambridge, England
关键词
BLOOD MONONUCLEAR-CELLS; SCHIZOPHRENIA; NEURONS; BRAIN; DISORDERS; LITHIUM; CONNECTIVITY; METAANALYSIS; LYMPHOCYTES; PREVALENCE;
D O I
10.1038/s41398-021-01243-8
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
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.
引用
收藏
页数:11
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