TSC2
清脆的
结节性硬化
基因剔除小鼠
细胞培养
3T3电池
TSC1
癌症研究
基因敲除
PI3K/AKT/mTOR通路
生物
基因
医学
细胞生物学
病理
信号转导
遗传学
转染
作者
Xu Wang,Yang Zhao,Zhan Wang,Zhangcheng Liao,Yushi Zhang
标识
DOI:10.1007/s12013-022-01094-0
摘要
Tuberous sclerosis complex (TSC) is a rare autosomal dominant disorder involving multiple organ systems. TSC2 gene plays an important role in the development of TSC. The most common kidney manifestation of TSC is renal angiomyolipoma (RAML). TSC-RAML is more likely to be bilateral multiple tumors and tends to destroy the renal structure and damages renal function severely. As a result, patients with TSC-RAML often miss the opportunity for surgical treatment when TSC-RAML is diagnosed, causing difficulty in obtaining tumor specimens through surgery. Due to this difficulty, model cell lines must be constructed for scientific research. In this paper, TSC2 was knocked out in NIH-3T3 cell lines by CRISPR/Cas9 system. PCR, WB and mTOR inhibitor drug sensitivity test showed that the TSC2 knockout NIH-3T3 cells were successfully constructed. The ability of proliferation and invasion in TSC2 KO NIH-3T3 cells were higher than those in wild type group. The constructed KO cell line lay the foundation for further study of TSC.
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