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CRISPR/Cas9 in Cancer Immunotherapy: Animal Models and Human Clinical Trials
K. Khalaf, K. Janowicz, M. Dyszkiewicz-Konwińska, G. Hutchings, C. Dompe, L. Moncrieff, M. Jankowski, M. Machnik, U. Oleksiewicz, I. Kocherova, J. Petitte, P. Mozdziak, JA. Shibli, D. Iżycki, M. Józkowiak, H. Piotrowska-Kempisty, MT. Skowroński,...
Jazyk angličtina Země Švýcarsko
Typ dokumentu časopisecké články, Research Support, U.S. Gov't, Non-P.H.S., přehledy
NLK
Directory of Open Access Journals
od 2010
Free Medical Journals
od 2010
PubMed Central
od 2010
Europe PubMed Central
od 2010
ProQuest Central
od 2010-03-01
Open Access Digital Library
od 2010-01-01
Open Access Digital Library
od 2010-01-01
ROAD: Directory of Open Access Scholarly Resources
od 2010
PubMed
32796761
DOI
10.3390/genes11080921
Knihovny.cz E-zdroje
- MeSH
- CRISPR-Cas systémy * MeSH
- editace genu * MeSH
- genetická terapie * MeSH
- imunoterapie adoptivní MeSH
- imunoterapie * MeSH
- individualizovaná medicína metody MeSH
- klinické zkoušky jako téma MeSH
- lidé MeSH
- modely nemocí na zvířatech MeSH
- nádory etiologie terapie MeSH
- nemoc MeSH
- preklinické hodnocení léčiv MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- přehledy MeSH
- Research Support, U.S. Gov't, Non-P.H.S. MeSH
Even though chemotherapy and immunotherapy emerged to limit continual and unregulated proliferation of cancer cells, currently available therapeutic agents are associated with high toxicity levels and low success rates. Additionally, ongoing multi-targeted therapies are limited only for few carcinogenesis pathways, due to continually emerging and evolving mutations of proto-oncogenes and tumor-suppressive genes. CRISPR/Cas9, as a specific gene-editing tool, is used to correct causative mutations with minimal toxicity, but is also employed as an adjuvant to immunotherapy to achieve a more robust immunological response. Some of the most critical limitations of the CRISPR/Cas9 technology include off-target mutations, resulting in nonspecific restrictions of DNA upstream of the Protospacer Adjacent Motifs (PAM), ethical agreements, and the lack of a scientific consensus aiming at risk evaluation. Currently, CRISPR/Cas9 is tested on animal models to enhance genome editing specificity and induce a stronger anti-tumor response. Moreover, ongoing clinical trials use the CRISPR/Cas9 system in immune cells to modify genomes in a target-specific manner. Recently, error-free in vitro systems have been engineered to overcome limitations of this gene-editing system. The aim of the article is to present the knowledge concerning the use of CRISPR Cas9 technique in targeting treatment-resistant cancers. Additionally, the use of CRISPR/Cas9 is aided as an emerging supplementation of immunotherapy, currently used in experimental oncology. Demonstrating further, applications and advances of the CRISPR/Cas9 technique are presented in animal models and human clinical trials. Concluding, an overview of the limitations of the gene-editing tool is proffered.
Department of Anatomy Poznan University of Medical Sciences 60 781 Poznań Poland
Department of Cancer Diagnostics and Immunology Greater Poland Cancer Centre 61 866 Poznan Poland
Department of Cancer Immunology Poznan University of Medical Sciences 60 408 Poznan Poland
Department of Histology and Embryology Poznan University of Medical Sciences 60 781 Poznań Poland
Department of Toxicology Poznan University of Medical Sciences 61 631 Poznań Poland
Department of Veterinary Surgery Nicolaus Copernicus University in Torun 87 100 Toruń Poland
Physiology Graduate Program North Carolina State University Raleigh NC 27695 USA
Prestage Department of Poultry Science North Carolina State University Raleigh NC 27695 USA
The School of Medicine Medical Sciences and Nutrition University of Aberdeen Aberdeen AB25 2ZD UK
Citace poskytuje Crossref.org
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