清脆的
基因组编辑
计算生物学
癌症治疗
计算机科学
基因组
生物
癌症
生物信息学
遗传学
基因
作者
Ningke Fan,Xintong Bian,Meng Li,Junman Chen,Haiping Wu,Qiling Peng,Huijie Bai,Wenqian Cheng,Liangsheng Kong,Shijia Ding,Siqiao Li,Wei Cheng
出处
期刊:Science Advances
[American Association for the Advancement of Science (AAAS)]
日期:2022-05-18
卷期号:8 (20)
被引量:21
标识
DOI:10.1126/sciadv.abn7382
摘要
CRISPR-Cas13a holds enormous potential for developing precise RNA editing. However, spatial manipulation of CRISPR-Cas13a activity remains a daunting challenge for elaborately regulating localized RNase function. Here, we designed hierarchical self-uncloaking CRISPR-Cas13a-customized RNA nanococoons (RNCOs-D), featuring tumor-specific recognition and spatial-controlled activation of Cas13a, for precise cancer synergistic therapy. RNCOs-D consists of programmable RNA nanosponges (RNSs) capable of targeted delivery and caging chemotherapeutic drug, and nanocapsules (NCs) anchored on RNSs for cloaking Cas13a/crRNA ribonucleoprotein (Cas13a RNP) activity. The acidic endo/lysosomal microenvironment stimulates the outer decomposition of NCs with concomitant Cas13a RNP activity revitalization, while the inner disassembly through trans-cleavage of RNSs initiated by cis-recognition and cleavage of EGFR variant III (EGFRvIII) mRNA. RNCOs-D demonstrates the effective EGFRvIII mRNA silencing for synergistic therapy of glioblastoma cancer cells in vitro and in vivo. The engineering of RNSs, together with efficient Cas13a activity regulation, holds immense prospect for multimodal and synergistic cancer therapy.
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