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Nat Commun ; 9(1): 3561, 2018 09 03.
Article in English | MEDLINE | ID: mdl-30177815

ABSTRACT

The identification of drug targets is highly challenging, particularly for diseases of the brain. To address this problem, we developed and experimentally validated a general computational framework for drug target discovery that combines gene regulatory information with causal reasoning ("Causal Reasoning Analytical Framework for Target discovery"-CRAFT). Using a systems genetics approach and starting from gene expression data from the target tissue, CRAFT provides a predictive framework for identifying cell membrane receptors with a direction-specified influence over disease-related gene expression profiles. As proof of concept, we applied CRAFT to epilepsy and predicted the tyrosine kinase receptor Csf1R as a potential therapeutic target. The predicted effect of Csf1R blockade in attenuating epilepsy seizures was validated in three pre-clinical models of epilepsy. These results highlight CRAFT as a systems-level framework for target discovery and suggest Csf1R blockade as a novel therapeutic strategy in epilepsy. CRAFT is applicable to disease settings other than epilepsy.


Subject(s)
Anticonvulsants/pharmacology , Epilepsy, Temporal Lobe/genetics , Epilepsy/genetics , Receptors, Granulocyte-Macrophage Colony-Stimulating Factor/genetics , Animals , Computer Simulation , Disease Models, Animal , Drug Discovery , Epilepsy/chemically induced , Epilepsy/drug therapy , Gene Expression Profiling , Gene Expression Regulation , Genetic Association Studies , High-Throughput Nucleotide Sequencing , Humans , Mice , Molecular Targeted Therapy , Muscarinic Agonists/toxicity , Pilocarpine/toxicity , Receptors, Granulocyte-Macrophage Colony-Stimulating Factor/antagonists & inhibitors , Sequence Analysis, RNA , Systems Biology
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