RETRACTED: Circular RNA ZNF609 Promoted Hepatocellular Carcinoma Progression by Upregulating PAP2C Expression via Sponging miR-342-3p (Retracted article. See vol. 15, pg. 1389, 2022)

被引:17
|
作者
Liao, Xin [1 ]
Zhan, Wei [2 ]
Tian, Bin [3 ]
Luo, Yilin [3 ]
Gu, Fang [3 ]
Li, Rui [4 ]
机构
[1] Guizhou Med Univ, Imaging Dept, Affiliated Hosp, Guiyang, Peoples R China
[2] Guizhou Med Univ, Colorectal Surg, Affiliated Hosp, Guiyang, Peoples R China
[3] Guizhou Med Univ, Imaging Dept, Guiyang, Peoples R China
[4] Guizhou Prov Peoples Hosp, Dept Tradit Chinese Med, Zhongshan East Rd 83, Guiyang 550002, Peoples R China
来源
ONCOTARGETS AND THERAPY | 2020年 / 13卷
基金
中国国家自然科学基金;
关键词
hepatocellular carcinoma; circular RNA; circZNF609; miR-324-3p; PAP2C; CIRCZNF609; PROMOTES; COLORECTAL-CANCER; MIGRATION; INVASION; GROWTH; PROLIFERATION; DISEASE;
D O I
10.2147/OTT.S253936
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: Emerging evidence has revealed that circular RNAs (circRNAs) participated in hepatocellular carcinoma (HCC) development. However, the roles of most circRNAs have not been studied. Methods: CircZNF609, miR-342-3p and RAP2C expressions were assessed by qPCR or Western blot. Loss-of-function experiments were performed using si-circZNF609 transfection, followed by CCK-8 assay, flow cytometry, wound healing assay and transwell assay. Informatic tools and rescue experiments were carried out to investigate the underlying mechanisms. Results: We showed that circZNF609 was overexpressed in HCC tissues and cells, as well as associated with poor clinical characteristics. Depletion of circZNF609 restrained HCC cell viability, migration and invasion while enhanced cell apoptosis. As to mechanism, miR-342-3p was sponged by circZNF609, and RAP2C was targeted by miR-342-3p. The effects on HCC cells induced by si-circZNF609 could be reversed by miR-342-3p inhibitor or RAP2C. In vivo, circZNF609 knockdown inhibited tumorigenesis of HCC mice, confirming the findings in vitro. Conclusion: CircZNF609 was highly expressed in HCC tissues and driven HCC progression by sponging miR-342-3p and upregulating RAP2C. This study may provide new potential therapeutic targets for HCC treatment.
引用
收藏
页码:7773 / 7783
页数:11
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