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A novel drug-mouse phenotypic similarity method detects molecular determinants of drug effects.

PLoS Comput. Biol. 12, DOI: 10.1371/journal.pcbi.1005111 (2016)
Verlagsversion Forschungsdaten DOI
Open Access Gold
Creative Commons Lizenzvertrag
The molecular mechanisms that translate drug treatment into beneficial and unwanted effects are largely unknown. We present here a novel approach to detect gene-drug and gene-side effect associations based on the phenotypic similarity of drugs and single gene perturbations in mice that account for the polypharmacological property of drugs. We scored the phenotypic similarity of human side effect profiles of 1,667 small molecules and biologicals to profiles of phenotypic traits of 5,384 mouse genes. The benchmarking with known relationships revealed a strong enrichment of physical and indirect drug-target connections, causative drug target-side effect links as well as gene-drug links involved in pharmacogenetic associations among phenotypically similar gene-drug pairs. The validation by in vitro assays and the experimental verification of an unknown connection between oxandrolone and prokineticin receptor 2 reinforces the ability of this method to provide new molecular insights underlying drug treatment. Thus, this approach may aid in the proposal of novel and personalized treatments.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Korrespondenzautor
Schlagwörter Systematic Identification; Affinity-chromatography; Target Identification; Constitutional Delay; Missense Mutations; In-vitro; Oxandrolone; Discovery; Disease; Pharmacogenomics
ISSN (print) / ISBN 1553-734X
e-ISSN 1553-7358
Quellenangaben Band: 12, Heft: 9 Seiten: , Artikelnummer: , Supplement: ,
Verlag Public Library of Science (PLoS)
Verlagsort San Francisco
Nichtpatentliteratur Publikationen
Begutachtungsstatus Peer reviewed