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LncRNA TCONS_00004099-derived microRNA regulates oncogenesis through PTPRF in gliomas

BACKGROUND: Glioblastoma is the most common and aggressive primary tumor in the central nervous system (CNS). Patients with glioblastomas have poor prognosis due to its aggressive clinical behavior and resistance to the chemotherapeutic agent temozolomide (TMZ). Aberrant long non-coding RNAs (lncRNA...

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Autores principales: Wang, Yuhao, Shan, Aijun, Zhou, Zhiwei, Li, Wenpeng, Xie, Lin, Du, Bo, Lei, Bingxi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8267291/
https://www.ncbi.nlm.nih.gov/pubmed/34277823
http://dx.doi.org/10.21037/atm-21-2442
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author Wang, Yuhao
Shan, Aijun
Zhou, Zhiwei
Li, Wenpeng
Xie, Lin
Du, Bo
Lei, Bingxi
author_facet Wang, Yuhao
Shan, Aijun
Zhou, Zhiwei
Li, Wenpeng
Xie, Lin
Du, Bo
Lei, Bingxi
author_sort Wang, Yuhao
collection PubMed
description BACKGROUND: Glioblastoma is the most common and aggressive primary tumor in the central nervous system (CNS). Patients with glioblastomas have poor prognosis due to its aggressive clinical behavior and resistance to the chemotherapeutic agent temozolomide (TMZ). Aberrant long non-coding RNAs (lncRNAs) are involved in glioma progression and its regulatory mechanisms. Analysis of sequencing data identified a new lncRNA, named lncRNA TCONS_00004099, which could derive a new microRNA and was highly expressed in glioma. METHODS: To elucidate the role of lncRNA TCONS_00004099 in gliomas, Quantitative Real-time PCR (qPCR) was used to assess the differential expression of lncRNA TCONS_00004099 and its related miRNA in glioma tissues, normal brain tissues, glioma cell lines (U87 and U251 cells), and a normal human embryonic brain cell line (HEB). Cell Counting Kit-8 (CCK8) assays to assess cell proliferation, flow cytometry assays examining apoptosis and the cell cycle, colony formation assays, wound healing assay, transwell assays, and zebrafish xenograft models were performed to further clarify the effects of the lncRNA and the related miRNA. Finally, Western blots were carried out to verify the mechanisms related to PTPRF (Protein Tyrosine Phosphatase Receptor Type F). RESULTS: LncRNA TCONS_00004099 was significantly increased in glioma tissues and glioma cell lines. A novel miRNA (miRNA TCONS_00004099) derived from the lncRNA was identified by qPCR. Knockdown of this lncRNA suppressed cell proliferation, migration, invasion and enhanced TMZ-induced apoptosis in U87 and U251 cell lines in vitro and in vivo. The miRNA mimics or inhibitor of miRNA TCONS_00004099 was used to reverse the effects of knockdown or overexpression of lncRNA TCONS_00004099, respectively. Western Blot analyses verified that PTPRF is one of the downstream targets of lncRNA TCONS_00004099. CONCLUSIONS: These results demonstrated that lncRNA TCONS_00004099 promoted malignant behaviors in gliomas, including proliferation, metastasis, and anti-apoptosis. The effect of lncRNA TCONS_00004099 was mediated through miRNA TCONS_00004099 and its target PTPRF. Thus, the lncRNA TCONS_00004099/miRNA/PTPRF axis may be a potential therapeutic target for gliomas.
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spelling pubmed-82672912021-07-16 LncRNA TCONS_00004099-derived microRNA regulates oncogenesis through PTPRF in gliomas Wang, Yuhao Shan, Aijun Zhou, Zhiwei Li, Wenpeng Xie, Lin Du, Bo Lei, Bingxi Ann Transl Med Original Article BACKGROUND: Glioblastoma is the most common and aggressive primary tumor in the central nervous system (CNS). Patients with glioblastomas have poor prognosis due to its aggressive clinical behavior and resistance to the chemotherapeutic agent temozolomide (TMZ). Aberrant long non-coding RNAs (lncRNAs) are involved in glioma progression and its regulatory mechanisms. Analysis of sequencing data identified a new lncRNA, named lncRNA TCONS_00004099, which could derive a new microRNA and was highly expressed in glioma. METHODS: To elucidate the role of lncRNA TCONS_00004099 in gliomas, Quantitative Real-time PCR (qPCR) was used to assess the differential expression of lncRNA TCONS_00004099 and its related miRNA in glioma tissues, normal brain tissues, glioma cell lines (U87 and U251 cells), and a normal human embryonic brain cell line (HEB). Cell Counting Kit-8 (CCK8) assays to assess cell proliferation, flow cytometry assays examining apoptosis and the cell cycle, colony formation assays, wound healing assay, transwell assays, and zebrafish xenograft models were performed to further clarify the effects of the lncRNA and the related miRNA. Finally, Western blots were carried out to verify the mechanisms related to PTPRF (Protein Tyrosine Phosphatase Receptor Type F). RESULTS: LncRNA TCONS_00004099 was significantly increased in glioma tissues and glioma cell lines. A novel miRNA (miRNA TCONS_00004099) derived from the lncRNA was identified by qPCR. Knockdown of this lncRNA suppressed cell proliferation, migration, invasion and enhanced TMZ-induced apoptosis in U87 and U251 cell lines in vitro and in vivo. The miRNA mimics or inhibitor of miRNA TCONS_00004099 was used to reverse the effects of knockdown or overexpression of lncRNA TCONS_00004099, respectively. Western Blot analyses verified that PTPRF is one of the downstream targets of lncRNA TCONS_00004099. CONCLUSIONS: These results demonstrated that lncRNA TCONS_00004099 promoted malignant behaviors in gliomas, including proliferation, metastasis, and anti-apoptosis. The effect of lncRNA TCONS_00004099 was mediated through miRNA TCONS_00004099 and its target PTPRF. Thus, the lncRNA TCONS_00004099/miRNA/PTPRF axis may be a potential therapeutic target for gliomas. AME Publishing Company 2021-06 /pmc/articles/PMC8267291/ /pubmed/34277823 http://dx.doi.org/10.21037/atm-21-2442 Text en 2021 Annals of Translational Medicine. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Original Article
Wang, Yuhao
Shan, Aijun
Zhou, Zhiwei
Li, Wenpeng
Xie, Lin
Du, Bo
Lei, Bingxi
LncRNA TCONS_00004099-derived microRNA regulates oncogenesis through PTPRF in gliomas
title LncRNA TCONS_00004099-derived microRNA regulates oncogenesis through PTPRF in gliomas
title_full LncRNA TCONS_00004099-derived microRNA regulates oncogenesis through PTPRF in gliomas
title_fullStr LncRNA TCONS_00004099-derived microRNA regulates oncogenesis through PTPRF in gliomas
title_full_unstemmed LncRNA TCONS_00004099-derived microRNA regulates oncogenesis through PTPRF in gliomas
title_short LncRNA TCONS_00004099-derived microRNA regulates oncogenesis through PTPRF in gliomas
title_sort lncrna tcons_00004099-derived microrna regulates oncogenesis through ptprf in gliomas
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8267291/
https://www.ncbi.nlm.nih.gov/pubmed/34277823
http://dx.doi.org/10.21037/atm-21-2442
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