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基于 CRISPR/Cas9 的基因编辑技术在癌症基础研究、诊断和治疗中的应用。

Application of the CRISPR/Cas9-based gene editing technique in basic research, diagnosis, and therapy of cancer.

机构信息

Shanxi Key Laboratory of Otorhinolaryngology Head and Neck Cancer, Shanxi Province Clinical Medical Research Center for Precision Medicine of Head and Neck Cancer, Department of Otolaryngology Head & Neck Surgery, First Hospital of Shanxi Medical University, Taiyuan, 030001, Shanxi, China.

Department of Biochemistry & Molecular Biology, Shanxi Medical University, Taiyuan, 030001, Shanxi, China.

出版信息

Mol Cancer. 2021 Oct 1;20(1):126. doi: 10.1186/s12943-021-01431-6.

DOI:10.1186/s12943-021-01431-6
PMID:34598686
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8484294/
Abstract

The 2020 Nobel Prize in Chemistry was awarded to Emmanuelle Charpentier and Jennifer Doudna for the development of the Clustered regularly interspaced short palindromic repeats/CRISPR-associated nuclease9 (CRISPR/Cas9) gene editing technology that provided new tools for precise gene editing. It is possible to target any genomic locus virtually using only a complex nuclease protein with short RNA as a site-specific endonuclease. Since cancer is caused by genomic changes in tumor cells, CRISPR/Cas9 can be used in the field of cancer research to edit genomes for exploration of the mechanisms of tumorigenesis and development. In recent years, the CRISPR/Cas9 system has been increasingly used in cancer research and treatment and remarkable results have been achieved. In this review, we introduced the mechanism and development of the CRISPR/Cas9-based gene editing system. Furthermore, we summarized current applications of this technique for basic research, diagnosis and therapy of cancer. Moreover, the potential applications of CRISPR/Cas9 in new emerging hotspots of oncology research were discussed, and the challenges and future directions were highlighted.

摘要

2020 年诺贝尔化学奖授予埃马纽埃尔·卡彭蒂耶和詹妮弗·道德纳,以表彰她们开发了用于精确基因编辑的成簇规律间隔短回文重复/CRISPR 相关核酸酶 9(CRISPR/Cas9)基因编辑技术。该技术仅使用一种复杂的核酶蛋白和短 RNA 作为特异性内切酶,就可以靶向几乎任何基因组位点。由于癌症是由肿瘤细胞中的基因组变化引起的,因此 CRISPR/Cas9 可用于癌症研究领域,编辑基因组以探索肿瘤发生和发展的机制。近年来,CRISPR/Cas9 系统已越来越多地用于癌症研究和治疗,并取得了显著的成果。在这篇综述中,我们介绍了基于 CRISPR/Cas9 的基因编辑系统的机制和发展。此外,我们总结了该技术在癌症基础研究、诊断和治疗方面的当前应用。此外,还讨论了 CRISPR/Cas9 在肿瘤学研究新涌现的热点中的潜在应用,并强调了该技术面临的挑战和未来发展方向。

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