Construction of TSC2 knockout cell line using CRISPR/Cas9 system and demonstration of its effects on NIH-3T3 cells

被引:0
作者
Wang, Xu [1 ]
Zhao, Yang [1 ]
Wang, Zhan [1 ]
Liao, Zhangcheng [1 ]
Zhang, Yushi [1 ]
机构
[1] Chinese Acad Med Sci & Peking Union Med Coll, Dept Urol, Peking Union Med Coll Hosp, Beijing 100730, Peoples R China
基金
中国国家自然科学基金;
关键词
CRISPR; Cas9; Knockout; TSC; Invasion; Proliferation; TUBEROUS SCLEROSIS COMPLEX; ANGIOMYOLIPOMA; MULTICENTER; MANAGEMENT; EVEROLIMUS; EFFICACY; SAFETY;
D O I
10.1007/s12013-022-01094-0
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
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.
引用
收藏
页码:681 / 687
页数:7
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