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.

Details

Title
A systems-level framework for drug discovery identifies Csf1R as an anti-epileptic drug target
Author
Srivastava, Prashant K 1 ; Jonathan van Eyll 2   VIAFID ORCID Logo  ; Godard, Patrice 3   VIAFID ORCID Logo  ; Mazzuferi, Manuela 2 ; Delahaye-Duriez, Andree 4   VIAFID ORCID Logo  ; Juliette Van Steenwinckel 5 ; Gressens, Pierre 6 ; Danis, Benedicte 2 ; Vandenplas, Catherine 2 ; Foerch, Patrik 2 ; Leclercq, Karine 2 ; Mairet-Coello, Georges 2 ; Cardenas, Alvaro 2 ; Vanclef, Frederic 2 ; Laaniste, Liisi 1 ; Niespodziany, Isabelle 2 ; Keaney, James 2 ; Gasser, Julien 2 ; Gillet, Gaelle 2 ; Shkura, Kirill 1 ; Seon-Ah Chong 2 ; Behmoaras, Jacques 7 ; Kadiu, Irena 2 ; Petretto, Enrico 8   VIAFID ORCID Logo  ; Kaminski, Rafal M 2   VIAFID ORCID Logo  ; Johnson, Michael R 1 

 Division of Brain Sciences, Imperial College London, London, UK 
 UCB Pharma, Braine-l’Alleud, Belgium 
 Clarivate Analytics (formerly the IP & Science Business of Thomson Reuters), Carlsbad, CA, USA 
 Division of Brain Sciences, Imperial College London, London, UK; UFR de Santé, Médecine et Biologie Humaine, Sorbonne Paris Cité, Université Paris 13, Bobigny, France; PROTECT, INSERM, Sorbonne Paris Cité, Université Paris Diderot, Paris, France 
 PROTECT, INSERM, Sorbonne Paris Cité, Université Paris Diderot, Paris, France 
 PROTECT, INSERM, Sorbonne Paris Cité, Université Paris Diderot, Paris, France; School of Biomedical Engineering & Imaging Sciences, Centre for the Developing Brain, King’s College London, London, UK 
 Centre for Complement and Inflammation Research, Imperial College London, London, UK 
 Duke-NUS Medical School, Centre for Computational Biology, Singapore, Republic of Singapore; Faculty of Medicine, MRC Clinical Sciences Centre, Imperial College London, London, UK 
Pages
1-15
Publication year
2018
Publication date
Sep 2018
Publisher
Nature Publishing Group
e-ISSN
20411723
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2099030081
Copyright
© 2018. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.