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The long non-coding RNA LOC441204 enhances cell growth in human glioma
Glioma is the most common and aggressive type of brain tumor. While long non-coding RNAs (lncRNAs) are clearly more abundant in human brain than protein-coding genes, the specific roles of lncRNAs and mechanisms underlying their dysregulation in glioma remain unclear. Here, we focused on lncRNAs tha...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5514141/ https://www.ncbi.nlm.nih.gov/pubmed/28717243 http://dx.doi.org/10.1038/s41598-017-05688-0 |
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author | Lin, Tzu-Kang Chang, Chang-Nen Tsai, Cheng-Shian Huang, Yin-Cheng Lu, Yu-Jen Chen, Wei-Jan Lin, Yang-Hsiang Chung, I.-Hsiao Lin, Kwang-Huei |
author_facet | Lin, Tzu-Kang Chang, Chang-Nen Tsai, Cheng-Shian Huang, Yin-Cheng Lu, Yu-Jen Chen, Wei-Jan Lin, Yang-Hsiang Chung, I.-Hsiao Lin, Kwang-Huei |
author_sort | Lin, Tzu-Kang |
collection | PubMed |
description | Glioma is the most common and aggressive type of brain tumor. While long non-coding RNAs (lncRNAs) are clearly more abundant in human brain than protein-coding genes, the specific roles of lncRNAs and mechanisms underlying their dysregulation in glioma remain unclear. Here, we focused on lncRNAs that are differentially expressed in brain tumor and their potential biological functions. LOC441204, a novel non-coding RNA gene displaying high expression in clinical specimens of brain tumor and significant upregulation in glioma cell lines in microarray analyses, was selected for further study. Notably, knockdown of LOC441204 suppressed tumor cell proliferation in two glioma cell lines. Moreover, LOC441204-induced tumor cell growth was mediated the stabilization of β-catenin pathway. Briefly, LOC441204 bound to β-catenin preventing its degradation, resulting in downstream p21 repression and cdk4 activation to enhance glioma cell proliferation. Collectively, our findings indicate a pro-oncogenic role of LOC441204 in tumor cell growth through activation of the β-catenin/p21/cdk4 cascade to act as a potential diagnostic marker or therapeutic target in brain tumor. |
format | Online Article Text |
id | pubmed-5514141 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55141412017-07-19 The long non-coding RNA LOC441204 enhances cell growth in human glioma Lin, Tzu-Kang Chang, Chang-Nen Tsai, Cheng-Shian Huang, Yin-Cheng Lu, Yu-Jen Chen, Wei-Jan Lin, Yang-Hsiang Chung, I.-Hsiao Lin, Kwang-Huei Sci Rep Article Glioma is the most common and aggressive type of brain tumor. While long non-coding RNAs (lncRNAs) are clearly more abundant in human brain than protein-coding genes, the specific roles of lncRNAs and mechanisms underlying their dysregulation in glioma remain unclear. Here, we focused on lncRNAs that are differentially expressed in brain tumor and their potential biological functions. LOC441204, a novel non-coding RNA gene displaying high expression in clinical specimens of brain tumor and significant upregulation in glioma cell lines in microarray analyses, was selected for further study. Notably, knockdown of LOC441204 suppressed tumor cell proliferation in two glioma cell lines. Moreover, LOC441204-induced tumor cell growth was mediated the stabilization of β-catenin pathway. Briefly, LOC441204 bound to β-catenin preventing its degradation, resulting in downstream p21 repression and cdk4 activation to enhance glioma cell proliferation. Collectively, our findings indicate a pro-oncogenic role of LOC441204 in tumor cell growth through activation of the β-catenin/p21/cdk4 cascade to act as a potential diagnostic marker or therapeutic target in brain tumor. Nature Publishing Group UK 2017-07-17 /pmc/articles/PMC5514141/ /pubmed/28717243 http://dx.doi.org/10.1038/s41598-017-05688-0 Text en © The Author(s) 2017 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Lin, Tzu-Kang Chang, Chang-Nen Tsai, Cheng-Shian Huang, Yin-Cheng Lu, Yu-Jen Chen, Wei-Jan Lin, Yang-Hsiang Chung, I.-Hsiao Lin, Kwang-Huei The long non-coding RNA LOC441204 enhances cell growth in human glioma |
title | The long non-coding RNA LOC441204 enhances cell growth in human glioma |
title_full | The long non-coding RNA LOC441204 enhances cell growth in human glioma |
title_fullStr | The long non-coding RNA LOC441204 enhances cell growth in human glioma |
title_full_unstemmed | The long non-coding RNA LOC441204 enhances cell growth in human glioma |
title_short | The long non-coding RNA LOC441204 enhances cell growth in human glioma |
title_sort | long non-coding rna loc441204 enhances cell growth in human glioma |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5514141/ https://www.ncbi.nlm.nih.gov/pubmed/28717243 http://dx.doi.org/10.1038/s41598-017-05688-0 |
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