Biosynthetic Nanobubble-Mediated CRISPR/Cas9 Gene Editing of Cdh2 Inhibits Breast Cancer Metastasis.

Biosynthetic Nanobubble-Mediated CRISPR/Cas9 Gene Editing of Cdh2 Inhibits Breast Cancer Metastasis.
复制标题

生物合成纳米气泡介导的 CRISPR/Cas9 基因编辑 Cdh2 抑制乳腺癌转移

DOI:
10.3390/pharmaceutics14071382
复制
发表时间:
2022-06-30
期刊:
影响因子:
5.4
通讯作者:
Liu, Jianhua
Liu, Jianhua
中科院分区:
医学2区
文献类型:
--
作者:
Gao, Ruru;Luo, Qiong;Li, Yang;Song, Liming;Cai, Junnan (Stephen);Xiong, Ying;Yan, Fei;Liu, Jianhua

文献摘要

参考文献

被引文献

相似文献

上皮-间充质转化(EMT)是上皮细胞经历一系列生化变化以获得间充质表型的过程,其与肿瘤转移有关。在这里,我们提出了一种敲除EMT相关Cdh 2基因的新策略,该基因通过CRISPR/Cas9介导的基因编辑编码N-钙粘蛋白,该基因通过超声与生物合成纳米泡(Gas Vesicles,GV)相结合。使用聚乙烯亚胺作为基因递送载体以将sgRNA递送到稳定表达Cas9蛋白的4 T1细胞中,产生稳定的Cdh 2基因敲除细胞系。Western印迹分析证实了在这些Cdh 2基因敲除的4 T1细胞系中不存在N-钙粘蛋白蛋白。与野生型细胞相比,在Cdh 2基因敲除的4 T1细胞中观察到肿瘤细胞迁移显着减少。我们的研究表明,超声结合GV可以有效介导Cdh 2基因的CRISPR/Cas9基因编辑,以抑制肿瘤的侵袭和转移。
The epithelial-mesenchymal transition (EMT), a process in which epithelial cells undergo a series of biochemical changes to acquire a mesenchymal phenotype, has been linked to tumor metastasis. Here, we present a novel strategy for knocking out the EMT-related Cdh2 gene, which encodes N-cadherin through CRISPR/Cas9-mediated gene editing by an ultrasound combined with biosynthetic nanobubbles (Gas Vesicles, GVs). Polyethyleneimine were employed as a gene delivery vector to deliver sgRNA into 4T1 cells that stably express the Cas9 protein, resulting in the stable Cdh2 gene- knockout cell lines. The Western blotting assay confirmed the absence of an N-cadherin protein in these Cdh2 gene-knockout 4T1 cell lines. Significantly reduced tumor cell migration was observed in the Cdh2 gene-knockout 4T1 cells in comparison with the wild-type cells. Our study demonstrated that an ultrasound combined with GVs could effectively mediate CRISPR/Cas9 gene editing of a Cdh2 gene to inhibit tumor invasion and metastasis.
DOI: 10.1038/s41467-020-19821-7
发表时间: 2020-11-27
影响因子: 16.6
作者:
Mancuso P;Chen C;Kaminski R;Gordon J;Liao S;Robinson JA;Smith MD;Liu H;Sariyer IK;Sariyer R;Peterson TA;Donadoni M;Williams JB;Siddiqui S;Bunnell BA;Ling B;MacLean AG;Burdo TH;Khalili K
通讯作者: Khalili K
DOI: 10.1056/nejmoa1817426
发表时间: 2019-09-26
影响因子: 158.5
作者:
Xu, Lei;Wang, Jun;Chen, Hu
通讯作者: Chen, Hu
DOI: 10.3390/life5010385
发表时间: 2015-02-02
期刊: Life (Basel, Switzerland)
影响因子: --
作者:
Pfeifer F
通讯作者: Pfeifer F
DOI: 10.1177/0300060519840890
发表时间: 2019-05-01
影响因子: 1.6
作者:
Cai, Junhong;Huang, Sizhe;Bao, Shan
通讯作者: Bao, Shan
DOI: 10.1073/pnas.1512503112
发表时间: 2015-08-18
影响因子: 11.1
作者:
Schumann, Kathrin;Lin, Steven;Marson, Alexander
通讯作者: Marson, Alexander