CircRFX3 contributes to glioma progression through the circRFX3-miR-1179/miR-1229-VASP axis
Abstract Background Circular RNAs (circRNAs) are implicated in the carcinogenesis of human cancers. However, the functional roles of circRFX3 in glioma are not elucidated. Methods Quantitative real-time polymerase chain reaction (qRT-PCR) assay was performed for the levels of circRFX3, RFX3, miR-117...
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BMC
2021-11-01
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Series: | Cancer Cell International |
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Online Access: | https://doi.org/10.1186/s12935-021-02293-0 |
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author | Hongli Li Yiwei Zhang Huiqin Song Li Li |
author_facet | Hongli Li Yiwei Zhang Huiqin Song Li Li |
author_sort | Hongli Li |
collection | DOAJ |
description | Abstract Background Circular RNAs (circRNAs) are implicated in the carcinogenesis of human cancers. However, the functional roles of circRFX3 in glioma are not elucidated. Methods Quantitative 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. Results CircRFX3 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. Conclusion CircRFX3 served as a tumor promoter in glioma via modulating miR-1179/miR-1229-VASP axis, which might provide a novel target for glioma therapy. |
first_indexed | 2024-12-18T04:49:19Z |
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id | doaj.art-9c0c154b81e84b00b1b57dae2792e6e9 |
institution | Directory Open Access Journal |
issn | 1475-2867 |
language | English |
last_indexed | 2024-12-18T04:49:19Z |
publishDate | 2021-11-01 |
publisher | BMC |
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series | Cancer Cell International |
spelling | doaj.art-9c0c154b81e84b00b1b57dae2792e6e92022-12-21T21:20:28ZengBMCCancer Cell International1475-28672021-11-0121111310.1186/s12935-021-02293-0CircRFX3 contributes to glioma progression through the circRFX3-miR-1179/miR-1229-VASP axisHongli Li0Yiwei Zhang1Huiqin Song2Li Li3Department of Neurology, Huaihe Hospital, Henan UniversitySchool of Nursing and Health, North Section of Jinming Avenue, Henan UniversityDepartment of Pathology, The First Affiliated Hospital of Henan UniversitySchool of Nursing and Health, North Section of Jinming Avenue, Henan UniversityAbstract Background Circular RNAs (circRNAs) are implicated in the carcinogenesis of human cancers. However, the functional roles of circRFX3 in glioma are not elucidated. Methods Quantitative 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. Results CircRFX3 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. Conclusion CircRFX3 served as a tumor promoter in glioma via modulating miR-1179/miR-1229-VASP axis, which might provide a novel target for glioma therapy.https://doi.org/10.1186/s12935-021-02293-0GliomacircRFX3miR-1179miR-1229VASP |
spellingShingle | Hongli Li Yiwei Zhang Huiqin Song Li Li CircRFX3 contributes to glioma progression through the circRFX3-miR-1179/miR-1229-VASP axis Cancer Cell International Glioma circRFX3 miR-1179 miR-1229 VASP |
title | CircRFX3 contributes to glioma progression through the circRFX3-miR-1179/miR-1229-VASP axis |
title_full | CircRFX3 contributes to glioma progression through the circRFX3-miR-1179/miR-1229-VASP axis |
title_fullStr | CircRFX3 contributes to glioma progression through the circRFX3-miR-1179/miR-1229-VASP axis |
title_full_unstemmed | CircRFX3 contributes to glioma progression through the circRFX3-miR-1179/miR-1229-VASP axis |
title_short | CircRFX3 contributes to glioma progression through the circRFX3-miR-1179/miR-1229-VASP axis |
title_sort | circrfx3 contributes to glioma progression through the circrfx3 mir 1179 mir 1229 vasp axis |
topic | Glioma circRFX3 miR-1179 miR-1229 VASP |
url | https://doi.org/10.1186/s12935-021-02293-0 |
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