Cornerstones of CRISPR-Cas in drug discovery and therapy

被引:346
作者
Fellmann, Christof [1 ]
Cowen, Benjamin C. [1 ,2 ]
Lin, Pei-Chun [1 ,2 ,3 ]
Doudna, Jennifer A. [1 ,4 ,5 ,6 ,7 ]
Corn, Jacob E. [1 ,2 ]
机构
[1] Univ Calif Berkeley, Dept Mol & Cell Biol, 229 Stanley Hall, Berkeley, CA 94720 USA
[2] Univ Calif Berkeley, Innovat Genom Inst, Berkeley, CA 94720 USA
[3] Univ Calif San Francisco, Helen Diller Family Comprehens Canc Ctr, San Francisco, CA 94158 USA
[4] Univ Calif Berkeley, Dept Chem, Berkeley, CA 94720 USA
[5] Univ Calif Berkeley, Howard Hughes Med Inst, Berkeley, CA 94720 USA
[6] Univ Calif Berkeley, Li Ka Shing Biomed & Hlth Sci Ctr, Berkeley, CA 94720 USA
[7] Lawrence Berkeley Natl Lab, MBIB Div, Berkeley, CA 94720 USA
基金
美国国家卫生研究院;
关键词
EMBRYONIC STEM-CELLS; HEMATOPOIETIC STEM/PROGENITOR CELLS; GENOME-EDITING SPECIFICITY; ZINC-FINGER NUCLEASES; VIRUS ENTRY REQUIRES; DOUBLE-STRAND BREAKS; HUMAN CANCER-CELLS; OFF-TARGET SITES; IN-VIVO; T-CELLS;
D O I
10.1038/nrd.2016.238
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The recent development of CRISPR-Cas systems as easily accessible and programmable tools for genome editing and regulation is spurring a revolution in biology. Paired with the rapid expansion of reference and personalized genomic sequence information, technologies based on CRISPR-Cas are enabling nearly unlimited genetic manipulation, even in previously difficult contexts, including human cells. Although much attention has focused on the potential of CRISPR-Cas to cure Mendelian diseases, the technology also holds promise to transform the development of therapies to treat complex heritable and somatic disorders. In this Review, we discuss how CRISPR-Cas can affect the next generation of drugs by accelerating the identification and validation of high-value targets, uncovering high-confidence biomarkers and developing differentiated breakthrough therapies. We focus on the promises, pitfalls and hurdles of this revolutionary gene-editing technology, discuss key aspects of different CRISPR-Cas screening platforms and offer our perspectives on the best practices in genome engineering.
引用
收藏
页码:89 / 100
页数:12
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