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Long Noncoding RNA LINC00173 Promotes NUTF2 Expression Through Sponging miR-765 and Facilitates Tumorigenesis in Glioma
BACKGROUND: Glioma is one of the leading causes of cancer-related deaths. This study aimed to investigate the function and mechanism of long noncoding RNA (lncRNA) LINC00173 in the regulation of glioma progression. METHODS: LINC00173 expression was measured using qRT-PCR. Survival rate was analyzed...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7429190/ https://www.ncbi.nlm.nih.gov/pubmed/32848473 http://dx.doi.org/10.2147/CMAR.S262279 |
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author | Du, Qinghua Liu, Jin Tian, Da Zhang, Xuelei Zhu, Jinwei Qiu, Weiwen Wu, Jun |
author_facet | Du, Qinghua Liu, Jin Tian, Da Zhang, Xuelei Zhu, Jinwei Qiu, Weiwen Wu, Jun |
author_sort | Du, Qinghua |
collection | PubMed |
description | BACKGROUND: Glioma is one of the leading causes of cancer-related deaths. This study aimed to investigate the function and mechanism of long noncoding RNA (lncRNA) LINC00173 in the regulation of glioma progression. METHODS: LINC00173 expression was measured using qRT-PCR. Survival rate was analyzed through Kaplan–Meier method. CCK8, colony formation and EdU assays were performed to measure cell proliferation while transwell was used to determine cell migration and invasion. Luciferase reporter assay was conducted to test RNA interaction. RESULTS: LINC00173 expression was elevated in glioma tissues and cells. LINC00173 high expression predicted poor prognosis. Loss of LINC00173 inhibited proliferation, migration and invasion. LINC00173 interacted with miR-765 to enhance NUTF2 expression. MiR-765 expression was negatively correlated with LINC00173 and NUTF2 in glioma tissues. NUTF2 level was increased in glioma tissues. NUTF2 overexpression rescued the potential of proliferation, migration and invasion in LINC00173-silenced cells. CONCLUSION: Our research demonstrated that LINC00173 promotes glioma progression through targeting miR-765/NUTF2 axis. |
format | Online Article Text |
id | pubmed-7429190 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-74291902020-08-25 Long Noncoding RNA LINC00173 Promotes NUTF2 Expression Through Sponging miR-765 and Facilitates Tumorigenesis in Glioma Du, Qinghua Liu, Jin Tian, Da Zhang, Xuelei Zhu, Jinwei Qiu, Weiwen Wu, Jun Cancer Manag Res Original Research BACKGROUND: Glioma is one of the leading causes of cancer-related deaths. This study aimed to investigate the function and mechanism of long noncoding RNA (lncRNA) LINC00173 in the regulation of glioma progression. METHODS: LINC00173 expression was measured using qRT-PCR. Survival rate was analyzed through Kaplan–Meier method. CCK8, colony formation and EdU assays were performed to measure cell proliferation while transwell was used to determine cell migration and invasion. Luciferase reporter assay was conducted to test RNA interaction. RESULTS: LINC00173 expression was elevated in glioma tissues and cells. LINC00173 high expression predicted poor prognosis. Loss of LINC00173 inhibited proliferation, migration and invasion. LINC00173 interacted with miR-765 to enhance NUTF2 expression. MiR-765 expression was negatively correlated with LINC00173 and NUTF2 in glioma tissues. NUTF2 level was increased in glioma tissues. NUTF2 overexpression rescued the potential of proliferation, migration and invasion in LINC00173-silenced cells. CONCLUSION: Our research demonstrated that LINC00173 promotes glioma progression through targeting miR-765/NUTF2 axis. Dove 2020-08-12 /pmc/articles/PMC7429190/ /pubmed/32848473 http://dx.doi.org/10.2147/CMAR.S262279 Text en © 2020 Du et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Original Research Du, Qinghua Liu, Jin Tian, Da Zhang, Xuelei Zhu, Jinwei Qiu, Weiwen Wu, Jun Long Noncoding RNA LINC00173 Promotes NUTF2 Expression Through Sponging miR-765 and Facilitates Tumorigenesis in Glioma |
title | Long Noncoding RNA LINC00173 Promotes NUTF2 Expression Through Sponging miR-765 and Facilitates Tumorigenesis in Glioma |
title_full | Long Noncoding RNA LINC00173 Promotes NUTF2 Expression Through Sponging miR-765 and Facilitates Tumorigenesis in Glioma |
title_fullStr | Long Noncoding RNA LINC00173 Promotes NUTF2 Expression Through Sponging miR-765 and Facilitates Tumorigenesis in Glioma |
title_full_unstemmed | Long Noncoding RNA LINC00173 Promotes NUTF2 Expression Through Sponging miR-765 and Facilitates Tumorigenesis in Glioma |
title_short | Long Noncoding RNA LINC00173 Promotes NUTF2 Expression Through Sponging miR-765 and Facilitates Tumorigenesis in Glioma |
title_sort | long noncoding rna linc00173 promotes nutf2 expression through sponging mir-765 and facilitates tumorigenesis in glioma |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7429190/ https://www.ncbi.nlm.nih.gov/pubmed/32848473 http://dx.doi.org/10.2147/CMAR.S262279 |
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