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CRISPR/Cas9 Delivery System Engineering for Genome Editing in Therapeutic Applications
被引:52
|作者:
Cheng, Hao
[1
]
Zhang, Feng
[1
]
Ding, Yang
[1
]
机构:
[1] China Pharmaceut Univ, NMPA Key Lab Res & Evaluat Pharmaceut Preparat &, Nanjing 210009, Peoples R China
基金:
中国国家自然科学基金;
关键词:
CRISPR/Cas9;
genome editing;
site-specific trafficking;
overcome off-target risks;
therapeutic applications;
CAS9;
MESSENGER-RNA;
NANOPARTICLE DELIVERY;
CRISPR-CAS9;
SYSTEM;
DONOR DNA;
GENE;
BASE;
CELLS;
SPECIFICITY;
INTEGRATION;
ACTIVATION;
D O I:
10.3390/pharmaceutics13101649
中图分类号:
R9 [药学];
学科分类号:
1007 ;
摘要:
The clustered regularly interspaced short palindromic repeats (CRISPR)/associated protein 9 (CRISPR/Cas9) systems have emerged as a robust and versatile genome editing platform for gene correction, transcriptional regulation, disease modeling, and nucleic acids imaging. However, the insufficient transfection and off-target risks have seriously hampered the potential biomedical applications of CRISPR/Cas9 technology. Herein, we review the recent progress towards CRISPR/Cas9 system delivery based on viral and non-viral vectors. We summarize the CRISPR/Cas9-inspired clinical trials and analyze the CRISPR/Cas9 delivery technology applied in the trials. The rational-designed non-viral vectors for delivering three typical forms of CRISPR/Cas9 system, including plasmid DNA (pDNA), mRNA, and ribonucleoprotein (RNP, Cas9 protein complexed with gRNA) were highlighted in this review. The vector-derived strategies to tackle the off-target concerns were further discussed. Moreover, we consider the challenges and prospects to realize the clinical potential of CRISPR/Cas9-based genome editing.
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页数:23
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