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CRISPR: A Screener’s Guide

The discovery of CRISPR-Cas9 systems has fueled a rapid expansion of gene editing adoption and has impacted pharmaceutical and biotechnology research substantially. Here, gene editing is used at an industrial scale to identify and validate new biological targets for precision medicines, with functio...

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Detalles Bibliográficos
Autores principales: le Sage, Carlos, Lawo, Steffen, Cross, Benedict C. S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7036479/
https://www.ncbi.nlm.nih.gov/pubmed/31658850
http://dx.doi.org/10.1177/2472555219883621
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author le Sage, Carlos
Lawo, Steffen
Cross, Benedict C. S.
author_facet le Sage, Carlos
Lawo, Steffen
Cross, Benedict C. S.
author_sort le Sage, Carlos
collection PubMed
description The discovery of CRISPR-Cas9 systems has fueled a rapid expansion of gene editing adoption and has impacted pharmaceutical and biotechnology research substantially. Here, gene editing is used at an industrial scale to identify and validate new biological targets for precision medicines, with functional genomic screening having an increasingly important role. Functional genomic strategies provide a crucial link between observed biological phenomena and the genes that influence and drive those phenomena. Although such studies are not new, the use of CRISPR-Cas9 systems in this arena is providing more robust datasets for target identification and validation. CRISPR-based screening approaches are also useful later in the drug development pipeline for understanding drug resistance and sensitivity ahead of entering clinical trials. This review examines the developing landscape for CRISPR screening technologies within the pharmaceutical industry and explores the next steps for this constantly evolving screening platform.
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spelling pubmed-70364792020-03-10 CRISPR: A Screener’s Guide le Sage, Carlos Lawo, Steffen Cross, Benedict C. S. SLAS Discov Review The discovery of CRISPR-Cas9 systems has fueled a rapid expansion of gene editing adoption and has impacted pharmaceutical and biotechnology research substantially. Here, gene editing is used at an industrial scale to identify and validate new biological targets for precision medicines, with functional genomic screening having an increasingly important role. Functional genomic strategies provide a crucial link between observed biological phenomena and the genes that influence and drive those phenomena. Although such studies are not new, the use of CRISPR-Cas9 systems in this arena is providing more robust datasets for target identification and validation. CRISPR-based screening approaches are also useful later in the drug development pipeline for understanding drug resistance and sensitivity ahead of entering clinical trials. This review examines the developing landscape for CRISPR screening technologies within the pharmaceutical industry and explores the next steps for this constantly evolving screening platform. SAGE Publications 2019-10-29 2020-03 /pmc/articles/PMC7036479/ /pubmed/31658850 http://dx.doi.org/10.1177/2472555219883621 Text en © 2019 Society for Laboratory Automation and Screening http://www.creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Review
le Sage, Carlos
Lawo, Steffen
Cross, Benedict C. S.
CRISPR: A Screener’s Guide
title CRISPR: A Screener’s Guide
title_full CRISPR: A Screener’s Guide
title_fullStr CRISPR: A Screener’s Guide
title_full_unstemmed CRISPR: A Screener’s Guide
title_short CRISPR: A Screener’s Guide
title_sort crispr: a screener’s guide
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7036479/
https://www.ncbi.nlm.nih.gov/pubmed/31658850
http://dx.doi.org/10.1177/2472555219883621
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