期刊论文详细信息
Cancer Cell International
CircRFX3 contributes to glioma progression through the circRFX3-miR-1179/miR-1229-VASP axis
Hongli Li1  Huiqin Song2  Yiwei Zhang3  Li Li3 
[1] Department of Neurology, Huaihe Hospital, Henan University, Kaifeng, Henan, China;Department of Pathology, The First Affiliated Hospital of Henan University, Kaifeng, Henan, China;School of Nursing and Health, North Section of Jinming Avenue, Henan University, 475001, Kaifeng, Henan, China;
关键词: Glioma;    circRFX3;    miR-1179;    miR-1229;    VASP;   
DOI  :  10.1186/s12935-021-02293-0
来源: Springer
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【 摘 要 】

BackgroundCircular RNAs (circRNAs) are implicated in the carcinogenesis of human cancers. However, the functional roles of circRFX3 in glioma are not elucidated.MethodsQuantitative real-time polymerase chain reaction (qRT-PCR) assay was performed for the levels of circRFX3, RFX3, miR-1179, miR-1229 and vasodilator stimulated phosphoprotein (VASP). Actinomycin D assay and RNase R assay were employed to analyze the characteristics of circRFX3. Cell Counting Kit-8 (CCK-8) assay and colony formation assay were conducted for cell proliferation. Transwell assay was used for cell migration and invasion. Flow cytometry analysis was adopted for cell apoptosis. RNA pull-down assay, dual-luciferase reporter assay and RNA immunoprecipitation (RIP) assay were employed to analyze the interaction between miR-1179/miR-1229 and circRFX3 or VASP. Western blot assay was conducted for VASP protein level. Murine xenograft model assay was used to investigate the role of circRFX3 in vivo.ResultsCircRFX3 level was increased in glioma tissues and cells. Knockdown of circRFX3 suppressed glioma cell proliferation, migration and invasion and promoted apoptosis in vitro and repressed tumorigenesis of glioma in vivo. MiR-1179 and miR-1229 were identified to be the targets of circRFX3. MiR-1179 or miR-1229 inhibition reversed the impacts of circRFX3 knockdown on glioma cell malignant behaviors. Additionally, VASP was demonstrated to be the target gene of miR-1179 and miR-1229, and VASP overexpression abolished the effect of circRFX3 knockdown on glioma cell progression.ConclusionCircRFX3 served as a tumor promoter in glioma via modulating miR-1179/miR-1229-VASP axis, which might provide a novel target for glioma therapy.

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