CRISPR / Cas9 System and Its Application in Tumor Therapy

被引:0
作者
Qiao Huan-Huan [1 ]
Zhang Qing-Hao [1 ]
Ming Dong [1 ]
机构
[1] Tianjin Univ, Acad Med Engn & Translat Med, Tianjin 300072, Peoples R China
基金
中国博士后科学基金;
关键词
CRISPR/Cas9; gene editing; nano carrier; tumor treatment; IN-VIVO; MESSENGER-RNA; DELIVERY; GENE; CELLS; RIBONUCLEOPROTEIN; VITRO; GENERATION; KNOCKOUT; IMMUNITY;
D O I
10.16476/j.pibb.2020.0239
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The emerging CRISPR/Cas9 gene editing technology can realize the manipulation of genes at the molecular level. It has the advantages of simple design, easy operation, good specificity and high efficiency. It is widely used in the study of potential mechanisms of tumorigenesis, development and metastasis and clinical treatment. Recent researches into the use of CRISPR/Cas9 for tumor therapy in vivo have focused on developing vectors. Non-viral nano-carriers developed by nanotechnology can efficiently deliver the CRISPR/Cas9 system into the body, providing a new way for the clinical application of CRISPR/Cas9 technology. In this review, we discuss the principle of CRISPR/Cas9, the current delivery forms of CRISPR/Cas9 and commonly used nanodelivery vectors. We highlight several nano-carriers including inorganic nanoparticles, polymer-based nanoparticles, lipid-based nanoparticles and others. We also summarize the characteristics, editing efficiency, applications and new studies of different nano-carriers. The applications and progresses of CRISPR/Cas9 in treating different tumors are also discussed.
引用
收藏
页码:570 / 579
页数:10
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