| Literature DB >> 35196193 |
Yihui Fan1, Qing Wang1, Minxin Shi1, Guanjun Ju1, Haimin Lu1, Liyun Zheng2, Jian Chen3, Xiaomei Zhou1, Ting Xiao1, Saihua Chen1.
Abstract
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.Entities:
Keywords: KIAA1522; NSCLC; circ_0020123; miR-940; tumorigenesis
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Year: 2022 PMID: 35196193 PMCID: PMC9037485 DOI: 10.1080/15384101.2022.2034093
Source DB: PubMed Journal: Cell Cycle ISSN: 1551-4005 Impact factor: 5.173