Finan Chris, Gaulton Anna, Kruger Felix A, Lumbers R Thomas, Shah Tina, Engmann Jorgen, Galver Luana, Kelley Ryan, Karlsson Anneli, Santos Rita, Overington John P, Hingorani Aroon D, Casas Juan P
Institute of Cardiovascular Science, Faculty of Population Health, University College London, London WC1E 6BT, U.K.
Farr Institute of Health Informatics, University College London, London WC1E 6BT, U.K.
Sci Transl Med. 2017 Mar 29;9(383). doi: 10.1126/scitranslmed.aag1166.
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.
靶点识别(确定针对某种疾病的正确药物靶点)和靶点验证(证明靶点扰动对疾病生物标志物和疾病终点的影响)是药物研发中的重要步骤。编码药物靶点的基因变异的临床相关关联模拟了通过药理学手段修饰相同靶点的效果。为了描绘出这一范式所带来的药物研发(包括药物重新利用)机会,我们将全基因组关联研究中与复杂疾病和生物标志物相关的基因座,与一组更新的编码可成药人类蛋白质的基因、与针对这些靶点具有生物活性的药物以及(在有获批药物的情况下)与临床适应症联系起来。我们利用这组基因来指导新型基因分型芯片的设计,该芯片将能够开展可成药基因的关联研究,以用于人类疾病中药物靶点的选择和验证。