| Literature DB >> 34938908 |
Jialun Duan1, Chunjie Bao1, Ying Xie1, Haitao Guo1, Yixuan Liu1, Jianwei Li1,2, Rui Liu1, Peishan Li1, Jing Bai1, Yan Yan1, Limin Mu1, Xueqi Li1, Guiling Wang1, Wanliang Lu1.
Abstract
Clustered regularly interspaced short palindromic repeats (CRISPR) technology emerges a remarkable potential for cure of refractory cancer like metastatic breast cancer. However, how to efficiently deliver the CRISPR system with non-viral carrier remains a major issue to be solved. Here, we report a kind of targeted core-shell nanoparticles (NPs) carrying dual plasmids (pHR-pCas9) for precise CCCTC-binding factor (CTCF) gene insert to circumvent metastatic breast cancer. The targeted core-shell NPs carrying pHR-pCas9 can accomplish γGTP-mediated cellular uptake and endosomal escape, facilitate the precise insert and stable expression of CTCF gene, inhibit the migration, metastasis, and colonization of metastatic breast cancer cells. Besides, the finding further reveals that the inhibitory mechanism of metastasis could be associated with up-regulating CTCF protein, followed by down-regulating stomatin (STOM) protein. The study offers a universal nanostrategy enabling the robust non-viral delivery of gene-editing system for treatment of severe illness.Entities:
Keywords: CTCF; Core-shell nanoparticles; Metastatic breast cancer; Non-viral gene delivery; Precise gene editing
Year: 2021 PMID: 34938908 PMCID: PMC8661137 DOI: 10.1016/j.bioactmat.2021.10.007
Source DB: PubMed Journal: Bioact Mater ISSN: 2452-199X