| Literature DB >> 30030026 |
Ben Sidders1, Anna Karlsson2, Linda Kitching3, Rubben Torella4, Paul Karila2, Anne Phelan5.
Abstract
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.Entities:
Keywords: drug repurposing; network-based drug discovery; neuroscience; pain
Mesh:
Year: 2018 PMID: 30030026 DOI: 10.1016/j.jmb.2018.07.016
Source DB: PubMed Journal: J Mol Biol ISSN: 0022-2836 Impact factor: 5.469