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LncRNA LOC105369504 inhibits tumor proliferation and metastasis in colorectal cancer by regulating PSPC1
There is growing evidence that long non-coding RNAs (lncRNAs) are significant contributors to the epigenetic mechanisms implicated in the emergence, progression and metastasis of the colorectal cancer (CRC), but many remain underexplored. A novel lncRNA LOC105369504, was identified to be a potential...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9998613/ https://www.ncbi.nlm.nih.gov/pubmed/36894530 http://dx.doi.org/10.1038/s41420-023-01384-3 |
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author | Zhan, Ting Cheng, Xueting Zhu, Qingxi Han, Zheng Zhu, Kejing Tan, Jie Liu, Men Chen, Wei Chen, Xiaoli Chen, Xiaohong Tian, Xia Huang, Xiaodong |
author_facet | Zhan, Ting Cheng, Xueting Zhu, Qingxi Han, Zheng Zhu, Kejing Tan, Jie Liu, Men Chen, Wei Chen, Xiaoli Chen, Xiaohong Tian, Xia Huang, Xiaodong |
author_sort | Zhan, Ting |
collection | PubMed |
description | There is growing evidence that long non-coding RNAs (lncRNAs) are significant contributors to the epigenetic mechanisms implicated in the emergence, progression and metastasis of the colorectal cancer (CRC), but many remain underexplored. A novel lncRNA LOC105369504, was identified to be a potential functional lncRNA by microarray analysis. In CRC, the expression of LOC105369504 was markedly decreased and resulted in distinct variations in proliferation, invasion, migration and epithelial-mesenchymal transition (EMT) in vivo and in vitro. This study showed that LOC105369504 bound to the protein of paraspeckles compound 1 (PSPC1) directly and regulated its stability using the ubiquitin-proteasome pathway in CRC cells. The suppression of CRC by LOC105369504 could be reversed through PSPC1 overexpression.This study showed that in CRC, LOC105369504 was under-regulated and as a novel lncRNA, LOC105369504 exerted tumor suppressive activity to suppress the proliferation together with metastasis in CRC cells through the regulation of PSPC1. These results offer new perspectives on the lncRNA effect on the progression of CRC. |
format | Online Article Text |
id | pubmed-9998613 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-99986132023-03-11 LncRNA LOC105369504 inhibits tumor proliferation and metastasis in colorectal cancer by regulating PSPC1 Zhan, Ting Cheng, Xueting Zhu, Qingxi Han, Zheng Zhu, Kejing Tan, Jie Liu, Men Chen, Wei Chen, Xiaoli Chen, Xiaohong Tian, Xia Huang, Xiaodong Cell Death Discov Article There is growing evidence that long non-coding RNAs (lncRNAs) are significant contributors to the epigenetic mechanisms implicated in the emergence, progression and metastasis of the colorectal cancer (CRC), but many remain underexplored. A novel lncRNA LOC105369504, was identified to be a potential functional lncRNA by microarray analysis. In CRC, the expression of LOC105369504 was markedly decreased and resulted in distinct variations in proliferation, invasion, migration and epithelial-mesenchymal transition (EMT) in vivo and in vitro. This study showed that LOC105369504 bound to the protein of paraspeckles compound 1 (PSPC1) directly and regulated its stability using the ubiquitin-proteasome pathway in CRC cells. The suppression of CRC by LOC105369504 could be reversed through PSPC1 overexpression.This study showed that in CRC, LOC105369504 was under-regulated and as a novel lncRNA, LOC105369504 exerted tumor suppressive activity to suppress the proliferation together with metastasis in CRC cells through the regulation of PSPC1. These results offer new perspectives on the lncRNA effect on the progression of CRC. Nature Publishing Group UK 2023-03-10 /pmc/articles/PMC9998613/ /pubmed/36894530 http://dx.doi.org/10.1038/s41420-023-01384-3 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Zhan, Ting Cheng, Xueting Zhu, Qingxi Han, Zheng Zhu, Kejing Tan, Jie Liu, Men Chen, Wei Chen, Xiaoli Chen, Xiaohong Tian, Xia Huang, Xiaodong LncRNA LOC105369504 inhibits tumor proliferation and metastasis in colorectal cancer by regulating PSPC1 |
title | LncRNA LOC105369504 inhibits tumor proliferation and metastasis in colorectal cancer by regulating PSPC1 |
title_full | LncRNA LOC105369504 inhibits tumor proliferation and metastasis in colorectal cancer by regulating PSPC1 |
title_fullStr | LncRNA LOC105369504 inhibits tumor proliferation and metastasis in colorectal cancer by regulating PSPC1 |
title_full_unstemmed | LncRNA LOC105369504 inhibits tumor proliferation and metastasis in colorectal cancer by regulating PSPC1 |
title_short | LncRNA LOC105369504 inhibits tumor proliferation and metastasis in colorectal cancer by regulating PSPC1 |
title_sort | lncrna loc105369504 inhibits tumor proliferation and metastasis in colorectal cancer by regulating pspc1 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9998613/ https://www.ncbi.nlm.nih.gov/pubmed/36894530 http://dx.doi.org/10.1038/s41420-023-01384-3 |
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