癌变
基因敲除
癌基因
生物
癌症研究
细胞生长
小RNA
体外
细胞培养
细胞
细胞生物学
作者
Yihui Fan,Qing Wang,Minxin Shi,Guanjun Ju,Haimin Lu,Zheng Lu,Jian Chen,Xianshi Zhou,Xiao Tu,Saihua Chen
出处
期刊:Cell Cycle
[Informa]
日期:2022-02-23
卷期号:21 (9): 894-907
被引量:4
标识
DOI:10.1080/15384101.2022.2034093
摘要
Circ_0020123 was highly expressed in NSCLC tissues and cell lines, and knockdown of circ_0020123 abolished cell growth, migration and invasion in vitro and hindered tumor growth in nude mice. Mechanically, circ_0020123 directly targeted miR-940, and KIAA1522 was a target of miR-940. Thereafter, a series of rescue experiments showed that circ_0020123 served its biological functions by miR-940/KIAA1522 axis. In all, circ_0020123 acted as an oncogene to promote the tumorigenesis of NSCLC via miR-940/KIAA1522 axis, suggesting a potential therapeutic target for NSCLC treatment.
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