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Circular RNA circRGNEF promotes bladder cancer progression via miR-548/KIF2C axis regulation
Author(s) -
Chen Yang,
Qiong Li,
Xinan Chen,
Zheyu Zhang,
Zezhong Mou,
Fangdie Ye,
Shengming Jin,
Jun Xiang,
Feng Tang,
Haowen Jiang
Publication year - 2020
Publication title -
aging
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.473
H-Index - 90
ISSN - 1945-4589
DOI - 10.18632/aging.103047
Subject(s) - downregulation and upregulation , gene silencing , cell growth , microrna , cancer research , metastasis , cell migration , biology , luciferase , reporter gene , bladder cancer , cell , microbiology and biotechnology , circular rna , cancer , cell culture , transfection , gene expression , gene , genetics
Circular RNAs (circRNAs) play an important role in bladder cancer (BC). Though circRNA involvement in BC has been reported, the underlying regulatory mechanisms are unknown. In this study, we performed EdU, CCK8, colony formation and Transwell assays to establish the role of circRGNEF in BC cell migration, proliferation, and invasion. We used bioinformatics and luciferase reporter experiments to investigate the regulatory mechanism. Nude mice xenografts and live imaging were used to explore the role of circRGNEF in tumor metastasis and growth. Expression profile analysis of human circRNAs in BC revealed that circRGNEF was upregulated significantly. High circRGNEF expression was correlated with aggressive BC phenotypes. The downregulation of circRGNEF suppressed BC cell metastasis and proliferation by targeting the miR-548/KIF2C axis in vitro and in vivo ; these results were verified with luciferase reporter assays. Our results show that miR-548 downregulation or KIF2C overexpression restored BC cell proliferation, migration, and invasion following silencing of circRGNEF. KIF2C overexpression reversed miR-548-induced cell invasion and migration as well as growth inhibition in vitro . In summary, the data illustrate that circRGNEF suppresses BC progression by functioning as a miR-548 sponge to enhance KIF2C expression. Therefore, circRGNEF might be a candidate BC treatment target.

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