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Zebrafish small molecule screens: Taking the phenotypic plunge

Target based chemical screens are a mainstay of modern drug discovery, but the effectiveness of this reductionist approach is being questioned in light of declines in pharmaceutical R & D efficiency. In recent years, phenotypic screens have gained increasing acceptance as a complementary/alterna...

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Detalles Bibliográficos
Autores principales: Williams, Charles H., Hong, Charles C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Research Network of Computational and Structural Biotechnology 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5050293/
https://www.ncbi.nlm.nih.gov/pubmed/27721960
http://dx.doi.org/10.1016/j.csbj.2016.09.001
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author Williams, Charles H.
Hong, Charles C.
author_facet Williams, Charles H.
Hong, Charles C.
author_sort Williams, Charles H.
collection PubMed
description Target based chemical screens are a mainstay of modern drug discovery, but the effectiveness of this reductionist approach is being questioned in light of declines in pharmaceutical R & D efficiency. In recent years, phenotypic screens have gained increasing acceptance as a complementary/alternative approach to early drug discovery. We discuss the various model organisms used in phenotypic screens, with particular focus on zebrafish, which has emerged as a leading model of in vivo phenotypic screens. Additionally, we anticipate therapeutic opportunities, particularly in orphan disease space, in the context of rapid advances in human Mendelian genetics, electronic health record (EHR)-enabled genome–phenome associations, and genome editing.
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spelling pubmed-50502932016-10-07 Zebrafish small molecule screens: Taking the phenotypic plunge Williams, Charles H. Hong, Charles C. Comput Struct Biotechnol J Mini Review Target based chemical screens are a mainstay of modern drug discovery, but the effectiveness of this reductionist approach is being questioned in light of declines in pharmaceutical R & D efficiency. In recent years, phenotypic screens have gained increasing acceptance as a complementary/alternative approach to early drug discovery. We discuss the various model organisms used in phenotypic screens, with particular focus on zebrafish, which has emerged as a leading model of in vivo phenotypic screens. Additionally, we anticipate therapeutic opportunities, particularly in orphan disease space, in the context of rapid advances in human Mendelian genetics, electronic health record (EHR)-enabled genome–phenome associations, and genome editing. Research Network of Computational and Structural Biotechnology 2016-09-18 /pmc/articles/PMC5050293/ /pubmed/27721960 http://dx.doi.org/10.1016/j.csbj.2016.09.001 Text en http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Mini Review
Williams, Charles H.
Hong, Charles C.
Zebrafish small molecule screens: Taking the phenotypic plunge
title Zebrafish small molecule screens: Taking the phenotypic plunge
title_full Zebrafish small molecule screens: Taking the phenotypic plunge
title_fullStr Zebrafish small molecule screens: Taking the phenotypic plunge
title_full_unstemmed Zebrafish small molecule screens: Taking the phenotypic plunge
title_short Zebrafish small molecule screens: Taking the phenotypic plunge
title_sort zebrafish small molecule screens: taking the phenotypic plunge
topic Mini Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5050293/
https://www.ncbi.nlm.nih.gov/pubmed/27721960
http://dx.doi.org/10.1016/j.csbj.2016.09.001
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