Abstract
Gene therapy has become a major focus of current biomedical research. CRISPR (Clustered Regularly Inter spaced Short Palindromic Repeats) systems have been extensively researched for disease treatment applications through genome editing specificity. Compared with Cas9 (CRISPR-associated proteins, Cas), a commonly used tool enzyme for genome editing, Cas13a exhibits RNA-dependent endonuclease activity, including collateral cleavage without obvious potential genetic risks. With its high specificity, Cas13a has significantly improved the sensitivity of viral diagnosis and shown potential to eliminate viruses. However, its efficacy in tumor therapy has not been determined. This review introduces the mechanism and research developments associated with the CRISPR-Cas13a system in tumor treatments and its potential to be used as a new tool for gene therapy. We hope more research would apply Cas13a-based therapy in cancer treatment in the future.


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The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.
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Acknowledgements
The work was financially supported by grants from National Natural Science Foundation of China (Grant No. 21575058), Natural Science Foundation of Guangdong Province (Grant No. 2023A1515011925). We thank J. Iacona, Ph.D., from Liwen Bianji (Edanz) (www.liwenbianji.cn) for editing the English text of a draft of this manuscript.
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Conception: TL and WM. Interpretation or analysis of data: SW and YW. Preparation of the manuscript: YW and YD. Revision for important intellectual: AM and BZ, Content: YW and YD. Supervision: TL. DY, BZ and YW contributed equally to this work.
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Dong, Y., Zhang, B., Wei, Y. et al. Development of Cas13a-based therapy for cancer treatment. Mol Biol Rep 51, 94 (2024). https://doi.org/10.1007/s11033-023-09129-2
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DOI: https://doi.org/10.1007/s11033-023-09129-2


