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Translating GWAS Findings to Novel Therapeutic Targets for Coronary Artery Disease

The success of genome-wide association studies (GWAS) has significantly advanced our understanding of the etiology of coronary artery disease (CAD) and opens new opportunities to reinvigorate the stalling CAD drug development. However, there exists remarkable disconnection between the CAD GWAS findi...

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Detalles Bibliográficos
Autores principales: Shu, Le, Blencowe, Montgomery, Yang, Xia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5989327/
https://www.ncbi.nlm.nih.gov/pubmed/29900175
http://dx.doi.org/10.3389/fcvm.2018.00056
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author Shu, Le
Blencowe, Montgomery
Yang, Xia
author_facet Shu, Le
Blencowe, Montgomery
Yang, Xia
author_sort Shu, Le
collection PubMed
description The success of genome-wide association studies (GWAS) has significantly advanced our understanding of the etiology of coronary artery disease (CAD) and opens new opportunities to reinvigorate the stalling CAD drug development. However, there exists remarkable disconnection between the CAD GWAS findings and commercialized drugs. While this could implicate major untapped translational and therapeutic potentials in CAD GWAS, it also brings forward extensive technical challenges. In this review we summarize the motivation to leverage GWAS for drug discovery, outline the critical bottlenecks in the field, and highlight several promising strategies such as functional genomics and network-based approaches to enhance the translational value of CAD GWAS findings in driving novel therapeutics
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spelling pubmed-59893272018-06-13 Translating GWAS Findings to Novel Therapeutic Targets for Coronary Artery Disease Shu, Le Blencowe, Montgomery Yang, Xia Front Cardiovasc Med Cardiovascular Medicine The success of genome-wide association studies (GWAS) has significantly advanced our understanding of the etiology of coronary artery disease (CAD) and opens new opportunities to reinvigorate the stalling CAD drug development. However, there exists remarkable disconnection between the CAD GWAS findings and commercialized drugs. While this could implicate major untapped translational and therapeutic potentials in CAD GWAS, it also brings forward extensive technical challenges. In this review we summarize the motivation to leverage GWAS for drug discovery, outline the critical bottlenecks in the field, and highlight several promising strategies such as functional genomics and network-based approaches to enhance the translational value of CAD GWAS findings in driving novel therapeutics Frontiers Media S.A. 2018-05-30 /pmc/articles/PMC5989327/ /pubmed/29900175 http://dx.doi.org/10.3389/fcvm.2018.00056 Text en Copyright © 2018 Shu, Blencowe and Yang http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cardiovascular Medicine
Shu, Le
Blencowe, Montgomery
Yang, Xia
Translating GWAS Findings to Novel Therapeutic Targets for Coronary Artery Disease
title Translating GWAS Findings to Novel Therapeutic Targets for Coronary Artery Disease
title_full Translating GWAS Findings to Novel Therapeutic Targets for Coronary Artery Disease
title_fullStr Translating GWAS Findings to Novel Therapeutic Targets for Coronary Artery Disease
title_full_unstemmed Translating GWAS Findings to Novel Therapeutic Targets for Coronary Artery Disease
title_short Translating GWAS Findings to Novel Therapeutic Targets for Coronary Artery Disease
title_sort translating gwas findings to novel therapeutic targets for coronary artery disease
topic Cardiovascular Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5989327/
https://www.ncbi.nlm.nih.gov/pubmed/29900175
http://dx.doi.org/10.3389/fcvm.2018.00056
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