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Tytuł:
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CRISPR-Cas9 therapeutics in cancer: promising strategies and present challenges.
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Autorzy:
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Yi L; National Center for Clinical Laboratories, Beijing Hospital, National Center of Gerontology, Beijing, People's Republic of China; Graduate School, Peking Union Medical College, Chinese Academy of Medical Sciences, Beijing, People's Republic of China; Beijing Engineering Research Center of Laboratory Medicine, Beijing Hospital, Beijing, People's Republic of China.
Li J; National Center for Clinical Laboratories, Beijing Hospital, National Center of Gerontology, Beijing, People's Republic of China; Graduate School, Peking Union Medical College, Chinese Academy of Medical Sciences, Beijing, People's Republic of China; Beijing Engineering Research Center of Laboratory Medicine, Beijing Hospital, Beijing, People's Republic of China. Electronic address: .
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Źródło:
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Biochimica et biophysica acta [Biochim Biophys Acta] 2016 Dec; Vol. 1866 (2), pp. 197-207. Date of Electronic Publication: 2016 Sep 15.
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Typ publikacji:
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Journal Article; Research Support, Non-U.S. Gov't; Review
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Język:
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English
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Imprint Name(s):
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Original Publication: Amsterdam : Elsevier Pub. Co.
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MeSH Terms:
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CRISPR-Cas Systems*/physiology
Neoplasms/*therapy
Animals ; Epigenesis, Genetic ; Gene Editing ; Humans ; Immunotherapy ; Molecular Targeted Therapy ; Neoplasms/genetics ; Oncolytic Virotherapy
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Contributed Indexing:
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Keywords: CRISPR-Cas9; Cancer genome manipulation; Cancer therapy; Gene therapy; Genome editing
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Molecular Sequence:
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ClinicalTrials.gov NCT02793856; NCT02867345; NCT02863913; NCT02867332
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Entry Date(s):
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Date Created: 20160920 Date Completed: 20170615 Latest Revision: 20170922
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Update Code:
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20240104
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DOI:
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10.1016/j.bbcan.2016.09.002
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PMID:
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27641687
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Cancer is characterized by multiple genetic and epigenetic alterations that drive malignant cell proliferation and confer chemoresistance. The ability to correct or ablate such mutations holds immense promise for combating cancer. Recently, because of its high efficiency and accuracy, the CRISPR-Cas9 genome editing technique has been widely used in cancer therapeutic explorations. Several studies used CRISPR-Cas9 to directly target cancer cell genomic DNA in cellular and animal cancer models which have shown therapeutic potential in expanding our anticancer protocols. Moreover, CRISPR-Cas9 can also be employed to fight oncogenic infections, explore anticancer drugs, and engineer immune cells and oncolytic viruses for cancer immunotherapeutic applications. Here, we summarize these preclinical CRISPR-Cas9-based therapeutic strategies against cancer, and discuss the challenges and improvements in translating therapeutic CRISPR-Cas9 into clinical use, which will facilitate better application of this technique in cancer research. Further, we propose potential directions of the CRISPR-Cas9 system in cancer therapy.
(Copyright © 2016 Elsevier B.V. All rights reserved.)
