CRISPR/Cas9 for cancer research and therapy

CRISPR/Cas9 has become a powerful method for making changes to the genome of many organisms. First discovered in bacteria as part of an adaptive immune system, CRISPR/Cas9 and modified versions have found a widespread use to engineer genomes and to activate or to repress the expression of genes. As...

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Main Authors: Zhan, Tianzuo (Author) , Rindtorff, Niklas (Author) , Betge, Johannes (Author) , Ebert, Matthias (Author) , Boutros, Michael (Author)
Format: Article (Journal)
Language:English
Published: 2019
In: Seminars in cancer biology
Year: 2018, Volume: 55, Pages: 106-119
ISSN:1096-3650
DOI:10.1016/j.semcancer.2018.04.001
Online Access:Verlag, Volltext: https://doi.org/10.1016/j.semcancer.2018.04.001
Verlag, Volltext: http://www.sciencedirect.com/science/article/pii/S1044579X17302742
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Author Notes:Tianzuo Zhan, Niklas Rindtorff, Johannes Betge, Matthias P. Ebert, Michael Boutros
Description
Summary:CRISPR/Cas9 has become a powerful method for making changes to the genome of many organisms. First discovered in bacteria as part of an adaptive immune system, CRISPR/Cas9 and modified versions have found a widespread use to engineer genomes and to activate or to repress the expression of genes. As such, CRISPR/Cas9 promises to accelerate cancer research by providing an efficient technology to dissect mechanisms of tumorigenesis, identify targets for drug development, and possibly arm cells for cell-based therapies. Here, we review current applications of the CRISPR/Cas9 technology for cancer research and therapy. We describe novel Cas9 variants and how they are used in functional genomics to discover novel cancer-specific vulnerabilities. Furthermore, we highlight the impact of CRISPR/Cas9 in generating organoid and mouse models of cancer. Finally, we provide an overview of the first clinical trials that apply CRISPR/Cas9 as a therapeutic approach against cancer.
Item Description:Available online 16 April 2018
Gesehen am 27.05.2019
Physical Description:Online Resource
ISSN:1096-3650
DOI:10.1016/j.semcancer.2018.04.001