| Literature DB >> 28356508 |
Chris Finan1,2, Anna Gaulton3, Felix A Kruger1,4, R Thomas Lumbers1,2, Tina Shah1,2, Jorgen Engmann1,2, Luana Galver5, Ryan Kelley5, Anneli Karlsson3, Rita Santos3, John P Overington6,4, Aroon D Hingorani7,2, Juan P Casas8.
Abstract
Target identification (determining the correct drug targets for a disease) and target validation (demonstrating an effect of target perturbation on disease biomarkers and disease end points) are important steps in drug development. Clinically relevant associations of variants in genes encoding drug targets model the effect of modifying the same targets pharmacologically. To delineate drug development (including repurposing) opportunities arising from this paradigm, we connected complex disease- and biomarker-associated loci from genome-wide association studies to an updated set of genes encoding druggable human proteins, to agents with bioactivity against these targets, and, where there were licensed drugs, to clinical indications. We used this set of genes to inform the design of a new genotyping array, which will enable association studies of druggable genes for drug target selection and validation in human disease.Entities:
Mesh:
Year: 2017 PMID: 28356508 PMCID: PMC6321762 DOI: 10.1126/scitranslmed.aag1166
Source DB: PubMed Journal: Sci Transl Med ISSN: 1946-6234 Impact factor: 17.956