生物发光成像
肝细胞癌
荧光素酶
癌症研究
生物发光
PTEN公司
睡美人转座系统
清脆的
医学
生物
基因
转座因子
细胞生物学
转染
突变体
信号转导
PI3K/AKT/mTOR通路
生物化学
生态学
作者
Xiangyi Cao,Yulong Zhang,Qianqian Zhou,Sun Sujing,Minwei He,Xiaohui Wang,Ping Ma,Xiaoang Yang,Li‐Ping Lv,Linsheng Zhan
标识
DOI:10.3389/fonc.2022.794101
摘要
In this study, a novel mouse model of hepatocellular carcinoma (HCC) was established by simultaneously knocking out Pten and p53 suppressor genes and overexpressing c-Met and △90-β-catenin proto-oncogenes in the livers of mice via hydrodynamic injection (HDI). The mutations were introduced using the CRISPR/Cas9 and Sleeping Beauty transposon systems. In this way, a primary liver cancer model was established within six weeks. In addition, macrophages expressing arginase-1(Arg1) promoter coupled with firefly luciferase were engineered for bioluminescence imaging (BLI) of the tumor microenvironment. This novel, rapidly-generated model of primary hepatocellular carcinoma can be monitored noninvasively, which can facilitate not only applications of the model, but also the development of new drugs and treatment strategies of HCC.
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