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circ_0030018 promotes glioma proliferation and metastasis

BACKGROUND: Circular RNA (circRNA) plays an essential role in tumor progression, including glioma. circ_0030018 is a newly discovered circRNA that is highly expressed in glioma. However, its role and mechanism in glioma need to be further elucidated. METHODS: The expression of circ_0030018, microRNA...

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Autores principales: Shao, Yun, Yang, Zhengxiang, Miao, Weifeng, Yu, Xiangrong, Wu, Yiping, Pu, Yi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: De Gruyter 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8190564/
https://www.ncbi.nlm.nih.gov/pubmed/34150336
http://dx.doi.org/10.1515/tnsci-2020-0175
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author Shao, Yun
Yang, Zhengxiang
Miao, Weifeng
Yu, Xiangrong
Wu, Yiping
Pu, Yi
author_facet Shao, Yun
Yang, Zhengxiang
Miao, Weifeng
Yu, Xiangrong
Wu, Yiping
Pu, Yi
author_sort Shao, Yun
collection PubMed
description BACKGROUND: Circular RNA (circRNA) plays an essential role in tumor progression, including glioma. circ_0030018 is a newly discovered circRNA that is highly expressed in glioma. However, its role and mechanism in glioma need to be further elucidated. METHODS: The expression of circ_0030018, microRNA (miR)-194-5p, and tripartite motif containing 44 (TRIM44) was examined using quantitative real-time PCR. Cell proliferation, migration, invasion, and apoptosis were determined using MTT assay, colony formation assay, transwell assay, and flow cytometry. Moreover, dual-luciferase reporter assay and RNA pull-down assay were used to verify the interactions among circ_0030018, miR-194-5p, and TRIM44. The protein expression of TRIM44 was assessed by western blot analysis. Animal experiments were conducted to explore the role of circ_0030018 in glioma tumor growth in vivo. RESULTS: circ_0030018 was overexpressed in glioma tissues and cells, and its silencing could inhibit glioma cell proliferation, migration, invasion, and accelerate apoptosis. miR-194-5p could be sponged by circ_0030018, and its overexpression could hinder the progression of glioma cells. Further experiments revealed that miR-194-5p inhibitor reversed the negative regulation of circ_0030018 knockdown on glioma cell progression. In addition, TRIM44 was a target of miR-194-5p, and its downregulation could repress glioma cell progression. Overexpressed TRIM44 reversed the inhibition effect of miR-194-5p on glioma cell progression. Animal experiments suggested that circ_0030018 knockdown could reduce glioma tumor growth through regulating miR-194-5p and TRIM44. CONCLUSION: Our 8data showed that circ_0030018 enhanced glioma progression by sponging miR-194-5p to regulate TRIM44, indicating that circ_0030018 might be a potential treatment target for glioma.
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spelling pubmed-81905642021-06-17 circ_0030018 promotes glioma proliferation and metastasis Shao, Yun Yang, Zhengxiang Miao, Weifeng Yu, Xiangrong Wu, Yiping Pu, Yi Transl Neurosci Research Article BACKGROUND: Circular RNA (circRNA) plays an essential role in tumor progression, including glioma. circ_0030018 is a newly discovered circRNA that is highly expressed in glioma. However, its role and mechanism in glioma need to be further elucidated. METHODS: The expression of circ_0030018, microRNA (miR)-194-5p, and tripartite motif containing 44 (TRIM44) was examined using quantitative real-time PCR. Cell proliferation, migration, invasion, and apoptosis were determined using MTT assay, colony formation assay, transwell assay, and flow cytometry. Moreover, dual-luciferase reporter assay and RNA pull-down assay were used to verify the interactions among circ_0030018, miR-194-5p, and TRIM44. The protein expression of TRIM44 was assessed by western blot analysis. Animal experiments were conducted to explore the role of circ_0030018 in glioma tumor growth in vivo. RESULTS: circ_0030018 was overexpressed in glioma tissues and cells, and its silencing could inhibit glioma cell proliferation, migration, invasion, and accelerate apoptosis. miR-194-5p could be sponged by circ_0030018, and its overexpression could hinder the progression of glioma cells. Further experiments revealed that miR-194-5p inhibitor reversed the negative regulation of circ_0030018 knockdown on glioma cell progression. In addition, TRIM44 was a target of miR-194-5p, and its downregulation could repress glioma cell progression. Overexpressed TRIM44 reversed the inhibition effect of miR-194-5p on glioma cell progression. Animal experiments suggested that circ_0030018 knockdown could reduce glioma tumor growth through regulating miR-194-5p and TRIM44. CONCLUSION: Our 8data showed that circ_0030018 enhanced glioma progression by sponging miR-194-5p to regulate TRIM44, indicating that circ_0030018 might be a potential treatment target for glioma. De Gruyter 2021-06-09 /pmc/articles/PMC8190564/ /pubmed/34150336 http://dx.doi.org/10.1515/tnsci-2020-0175 Text en © 2021 Yun Shao et al., published by De Gruyter https://creativecommons.org/licenses/by/4.0/This work is licensed under the Creative Commons Attribution 4.0 International License.
spellingShingle Research Article
Shao, Yun
Yang, Zhengxiang
Miao, Weifeng
Yu, Xiangrong
Wu, Yiping
Pu, Yi
circ_0030018 promotes glioma proliferation and metastasis
title circ_0030018 promotes glioma proliferation and metastasis
title_full circ_0030018 promotes glioma proliferation and metastasis
title_fullStr circ_0030018 promotes glioma proliferation and metastasis
title_full_unstemmed circ_0030018 promotes glioma proliferation and metastasis
title_short circ_0030018 promotes glioma proliferation and metastasis
title_sort circ_0030018 promotes glioma proliferation and metastasis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8190564/
https://www.ncbi.nlm.nih.gov/pubmed/34150336
http://dx.doi.org/10.1515/tnsci-2020-0175
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