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LINC01158 works as an oncogene in glioma via sponging miR-6734-3p to boost CENPK expression
BACKGROUND: Long non-coding RNAs (lncRNAs) have been certified to play vital biological functions in glioma and have received considerable attention in the recent literature. Nonetheless, the role of LINC01158 in glioma remains to be elucidated. METHODS: qRT-PCR, western blot and GEPIA database were...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8161569/ https://www.ncbi.nlm.nih.gov/pubmed/34044826 http://dx.doi.org/10.1186/s12935-021-01931-x |
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author | Sun, Zhenxing Wei, Naili Yao, Shenglian Wang, Guihuai Sun, Yaxing Wang, Zhenze Yuan, Dan |
author_facet | Sun, Zhenxing Wei, Naili Yao, Shenglian Wang, Guihuai Sun, Yaxing Wang, Zhenze Yuan, Dan |
author_sort | Sun, Zhenxing |
collection | PubMed |
description | BACKGROUND: Long non-coding RNAs (lncRNAs) have been certified to play vital biological functions in glioma and have received considerable attention in the recent literature. Nonetheless, the role of LINC01158 in glioma remains to be elucidated. METHODS: qRT-PCR, western blot and GEPIA database were applied for reporting the expression of CENPK and LINC01158 in glioma and the correlation between LINC01158 and CENPK expression. EdU, colony formation, CCK-8, caspase-3 activity and TUNEL assays probed the impacts of LINC01158 on glioma cell growth. Subcellular fractionation and FISH assays revealed the cellular distribution of LINC01158. Luciferase reporter and RIP assays examined ceRNA network of LINC01158, CENPK and miR-6734-3p. RESULTS: LINC01158 and CENPK were both overexpressed in glioma and a positive regulation of LINC01158 on CENPK was corroborated. LINC01158 served a pro-proliferative and anti-apoptotic part in glioma by sponging miR-6734-3p to augment CENPK. CONCLUSION: LINC01158 enhances CENPK by serving as sponge for miR-6734-3p to facilitate glioma development, proposing LINC01158 as a new player in glioma. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12935-021-01931-x. |
format | Online Article Text |
id | pubmed-8161569 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-81615692021-06-01 LINC01158 works as an oncogene in glioma via sponging miR-6734-3p to boost CENPK expression Sun, Zhenxing Wei, Naili Yao, Shenglian Wang, Guihuai Sun, Yaxing Wang, Zhenze Yuan, Dan Cancer Cell Int Primary Research BACKGROUND: Long non-coding RNAs (lncRNAs) have been certified to play vital biological functions in glioma and have received considerable attention in the recent literature. Nonetheless, the role of LINC01158 in glioma remains to be elucidated. METHODS: qRT-PCR, western blot and GEPIA database were applied for reporting the expression of CENPK and LINC01158 in glioma and the correlation between LINC01158 and CENPK expression. EdU, colony formation, CCK-8, caspase-3 activity and TUNEL assays probed the impacts of LINC01158 on glioma cell growth. Subcellular fractionation and FISH assays revealed the cellular distribution of LINC01158. Luciferase reporter and RIP assays examined ceRNA network of LINC01158, CENPK and miR-6734-3p. RESULTS: LINC01158 and CENPK were both overexpressed in glioma and a positive regulation of LINC01158 on CENPK was corroborated. LINC01158 served a pro-proliferative and anti-apoptotic part in glioma by sponging miR-6734-3p to augment CENPK. CONCLUSION: LINC01158 enhances CENPK by serving as sponge for miR-6734-3p to facilitate glioma development, proposing LINC01158 as a new player in glioma. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12935-021-01931-x. BioMed Central 2021-05-27 /pmc/articles/PMC8161569/ /pubmed/34044826 http://dx.doi.org/10.1186/s12935-021-01931-x Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Primary Research Sun, Zhenxing Wei, Naili Yao, Shenglian Wang, Guihuai Sun, Yaxing Wang, Zhenze Yuan, Dan LINC01158 works as an oncogene in glioma via sponging miR-6734-3p to boost CENPK expression |
title | LINC01158 works as an oncogene in glioma via sponging miR-6734-3p to boost CENPK expression |
title_full | LINC01158 works as an oncogene in glioma via sponging miR-6734-3p to boost CENPK expression |
title_fullStr | LINC01158 works as an oncogene in glioma via sponging miR-6734-3p to boost CENPK expression |
title_full_unstemmed | LINC01158 works as an oncogene in glioma via sponging miR-6734-3p to boost CENPK expression |
title_short | LINC01158 works as an oncogene in glioma via sponging miR-6734-3p to boost CENPK expression |
title_sort | linc01158 works as an oncogene in glioma via sponging mir-6734-3p to boost cenpk expression |
topic | Primary Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8161569/ https://www.ncbi.nlm.nih.gov/pubmed/34044826 http://dx.doi.org/10.1186/s12935-021-01931-x |
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