دورية أكاديمية

Network analysis of coronary artery disease risk genes elucidates disease mechanisms and druggable targets

التفاصيل البيبلوغرافية
العنوان: Network analysis of coronary artery disease risk genes elucidates disease mechanisms and druggable targets
المؤلفون: Lempiäinen, H., Brænne, I., Michoel, T., Tragante, V., Vilne, B., Webb, T.R., Kyriakou, T., Eichner, J., Zeng, L., Willenborg, C., Franzen, O., Ruusalepp, A., Goel, A., Laan, S.W. van der, Biegert, C., Hamby, S., Talukdar, H.A., Foroughi Asl, H., Dichgans, M., Dreker, T., Graettinger, M., Gribbon, P., Kessler, T., Malik, R., Prestel, M., Stiller, B., Schofield, C., Pasterkamp, G., Watkins, H., Samani, N.J., Wittenberger, T., Erdmann, J., Schunkert, H., Asselbergs, F.W., Björkegren, J.L.M.
سنة النشر: 2018
المجموعة: Publikationsdatenbank der Fraunhofer-Gesellschaft
الوقت: 620, 670
الوصف: Art. 3434, 14 S. ; Genome-wide association studies (GWAS) have identified over two hundred chromosomal loci that modulate risk of coronary artery disease (CAD). The genes affected by variants at these loci are largely unknown and an untapped resource to improve our understanding of CAD pathophysiology and identify potential therapeutic targets. Here, we prioritized 68 genes as the most likely causal genes at genome-wide significant loci identified by GWAS of CAD and examined their regulatory roles in 286 metabolic and vascular tissue gene-protein sub-networks ("modules"). The modules and genes within were scored for CAD druggability potential. The scoring enriched for targets of cardiometabolic drugs currently in clinical use and in-depth analysis of the top-scoring modules validated established and revealed novel target tissues, biological processes, and druggable targets. This study provides an unprecedented resource of tissue-defined gene-protein interactions directly affected by genetic variance in CAD risk loci. ; 8
نوع الوثيقة: article in journal/newspaper
اللغة: English
العلاقة: Scientific Reports; https://publica.fraunhofer.de/handle/publica/256959Test
DOI: 10.1038/s41598-018-20721-6
الإتاحة: https://doi.org/10.1038/s41598-018-20721-6Test
https://publica.fraunhofer.de/handle/publica/256959Test
رقم الانضمام: edsbas.CD8556BD
قاعدة البيانات: BASE