CRISPR/Cas9 Delivery System Engineering for Genome Editing in Therapeutic Applications

被引:59
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.
引用
收藏
页数:23
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共 70 条
[1]   Co-encapsulation of Cas9 mRNA and guide RNA in polyplex micelles enables genome editing in mouse brain [J].
Abbasi, Saed ;
Uchida, Satoshi ;
Toh, Kazuko ;
Tockary, Theofilus A. ;
Dirisala, Anjaneyulu ;
Hayashi, Kotaro ;
Fukushima, Shigeto ;
Kataoka, Kazunori .
JOURNAL OF CONTROLLED RELEASE, 2021, 332 :260-268
[2]   Endosomal Escape and Delivery of CRISPR/Cas9 Genome Editing Machinery Enabled by Nanoscale Zeolitic Imidazolate Framework [J].
Alsaiari, Shahad K. ;
Patil, Sachin ;
Alyami, Mram ;
Alamoudi, Kholod O. ;
Aleisa, Fajr A. ;
Merzaban, Jasmeen S. ;
Li, Mo ;
Khashab, Niveen M. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2018, 140 (01) :143-146
[3]   Nucleoside modifications in RNA limit activation of 2'-5'-oligoadenylate synthetase and increase resistance to cleavage by RNase L [J].
Anderson, Bart R. ;
Muramatsu, Hiromi ;
Jha, Babal K. ;
Silverman, Robert H. ;
Weissman, Drew ;
Kariko, Katalin .
NUCLEIC ACIDS RESEARCH, 2011, 39 (21) :9329-9338
[4]   Engineered targeting tLyp-1 exosomes as gene therapy vectors for efficient delivery of siRNA into lung cancer cells [J].
Bai, Jing ;
Duan, Jialun ;
Liu, Rui ;
Du, Yafei ;
Luo, Qian ;
Cui, Yinuo ;
Su, Zhanbo ;
Xu, Jiarui ;
Xie, Ying ;
Lu, Wanliang .
ASIAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2020, 15 (04) :461-471
[5]   PH-responsive strontium nanoparticles for targeted gene therapy against mammary carcinoma cells [J].
Bakhtiar, Athirah ;
Chowdhury, Ezharul Hoque .
ASIAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2021, 16 (02) :236-252
[6]   A peptide nucleic acid-nuclear localization signal fusion that mediates nuclear transport of DNA [J].
Brandén, LJ ;
Mohamed, AJ ;
Smith, CIE .
NATURE BIOTECHNOLOGY, 1999, 17 (08) :784-787
[7]   Targeted activation of diverse CRISPR-Cas systems for mammalian genome editing via proximal CRISPR targeting [J].
Chen, Fuqiang ;
Ding, Xiao ;
Feng, Yongmei ;
Seebeck, Timothy ;
Jiang, Yanfang ;
Davis, Gregory D. .
NATURE COMMUNICATIONS, 2017, 8
[8]   A biodegradable nanocapsule delivers a Cas9 ribonucleoprotein complex for in vivo genome editing [J].
Chen, Guojun ;
Abdeen, Amr A. ;
Wang, Yuyuan ;
Shahi, Pawan K. ;
Robertson, Samantha ;
Xie, Ruosen ;
Suzuki, Masatoshi ;
Pattnaik, Bikash R. ;
Saha, Krishanu ;
Gong, Shaoqin .
NATURE NANOTECHNOLOGY, 2019, 14 (10) :974-+
[9]   Multiplexed activation of endogenous genes by CRISPR-on, an RNA-guided transcriptional activator system [J].
Cheng, Albert W. ;
Wang, Haoyi ;
Yang, Hui ;
Shi, Linyu ;
Katz, Yarden ;
Theunissen, Thorold W. ;
Rangarajan, Sudharshan ;
Shivalila, Chikdu S. ;
Dadon, Daniel B. ;
Jaenisch, Rudolf .
CELL RESEARCH, 2013, 23 (10) :1163-1171
[10]   Selective organ targeting (SORT) nanoparticles for tissue-specific mRNA delivery and CRISPR-Cas gene editing [J].
Cheng, Qiang ;
Wei, Tuo ;
Farbiak, Lukas ;
Johnson, Lindsay T. ;
Dilliard, Sean A. ;
Siegwart, Daniel J. .
NATURE NANOTECHNOLOGY, 2020, 15 (04) :313-+