Recent Advances in Therapeutic Genome Editing in China

被引:5
|
作者
Yang, Yang [1 ,2 ]
Wang, Qingnan [1 ,2 ]
Li, Qian [1 ,2 ]
Men, Ke [1 ,2 ]
He, Zhiyao [2 ,3 ]
Deng, Hongxin [1 ,2 ]
Ji, Weizhi [4 ]
Wei, Yuquan [1 ,2 ]
机构
[1] Sichuan Univ, State Key Lab Biotherapy, West China Hosp, Ke Yuan Rd 4,1 Gao Peng St, Chengdu 610041, Sichuan, Peoples R China
[2] Sichuan Univ, Ctr Canc, West China Hosp, Ke Yuan Rd 4,1 Gao Peng St, Chengdu 610041, Sichuan, Peoples R China
[3] Sichuan Univ, Dept Pharm, West China Hosp, Chengdu, Sichuan, Peoples R China
[4] Kunming Univ Sci & Technol, Inst Primate Translat Med, Yunnan Key Lab Primate Biomed Res, Kunming, Yunnan, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
genome editing; gene therapy; CRISPR-Cas9; PLURIPOTENT STEM-CELLS; HEPATITIS-B-VIRUS; BETA-THALASSEMIA; GENE-THERAPY; T-CELLS; CRISPR-CAS9; NUCLEASES; CRISPR/CAS9; MUTATION; DISEASE; DNA;
D O I
10.1089/hum.2017.210
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Editing of the genome to correct disease-causing mutations is a promising approach for the treatment of human diseases. Recent advances in the development of programmable nuclease-based genome editing tools have substantially improved the ability to make precise changes in the human genome. Genome editing technologies are already being used to correct genetic mutations in affected tissues and cells to treat diseases that are refractory to traditional gene therapies. Chinese scientists have made remarkable breakthroughs in the field of therapeutic genome editing, particularly with the first clinical trial involving the clustered regularly interspaced short palindromic repeats-caspase 9 system that began in China. Herein, current progress toward developing programmable nuclease-based gene therapies is introduced, as well as future prospects and challenges in China.
引用
收藏
页码:136 / 145
页数:10
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