Network-Based Drug Discovery: Coupling Network Pharmacology with Phenotypic Screening for Neuronal Excitability

被引:36
|
作者
Sidders, Ben [1 ,2 ]
Karlsson, Anna [3 ]
Kitching, Linda [1 ,4 ]
Torella, Rubben [5 ]
Karila, Paul [3 ]
Phelan, Anne [1 ,6 ]
机构
[1] Pfizer Res & Dev, Neusentis, Cambridge CB21 6GS, England
[2] AstraZeneca, IMED Biotech Unit, Biosci, Oncol, Cambridge CB2 0RE, England
[3] Cellectricon, S-43137 Molndal, Sweden
[4] BenevolentAl Cambridge Ltd, Cambridge CB22 3AT, England
[5] Pfizer World Wide Res & Dev, Cambridge, MA 02139 USA
[6] Mission Therapeut, Cambridge CB22 3AT, England
关键词
network-based drug discovery; neuroscience; pain; drug repurposing; PAIN; EXPRESSION; CURRENTS;
D O I
10.1016/j.jmb.2018.07.016
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Diseases such as chronic pain with complex etiologies are unlikely to respond to single, target-specific therapeutics but rather require intervention at multiple points within a perturbed disease system. Such approaches are being enabled by the rise of computational methods to identify key points of intervention and by new screening techniques that focus on a relevant condition or phenotype, rather than a specific target. Here we apply an in silico network pharmacology approach to identify small-molecule compounds with the potential to selectively disrupt the structure of a chronic-pain specific disease network, which we validate using a novel phenotypic screen that recapitulates key aspects of neuronal and pain biology by measuring changes in neuronal excitability in native sensory neurons. The combination of network pharmacology with a phenotypic screen is a powerful approach; we show that hit rates increase from 26% to 42%. This represents a rational approach to the discovery of compounds with a poly-pharmacology based therapeutic value, which will be vital for the discovery of treatments for complex disease. (C) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3005 / 3015
页数:11
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