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LncRNA LOC653786 promotes growth of RCC cells via upregulating FOXM1
Renal cell carcinoma (RCC) is the most common kidney malignancy with poor prognosis. Recently, long noncoding RNAs (lncRNAs) have been demonstrated as important regulators in multiple cancers including RCC. LOC653786 is a lncRNA, but its role in cancer remains unclear. In this study, we for the firs...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5844731/ https://www.ncbi.nlm.nih.gov/pubmed/29552295 http://dx.doi.org/10.18632/oncotarget.24027 |
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author | Yang, Fan Wu, Qingjian Zhang, Yan Xiong, Haojun Li, Xinzhe Li, Bo Xie, Wei Zhang, Le Xu, Min Zhang, Kebin He, Fengtian |
author_facet | Yang, Fan Wu, Qingjian Zhang, Yan Xiong, Haojun Li, Xinzhe Li, Bo Xie, Wei Zhang, Le Xu, Min Zhang, Kebin He, Fengtian |
author_sort | Yang, Fan |
collection | PubMed |
description | Renal cell carcinoma (RCC) is the most common kidney malignancy with poor prognosis. Recently, long noncoding RNAs (lncRNAs) have been demonstrated as important regulators in multiple cancers including RCC. LOC653786 is a lncRNA, but its role in cancer remains unclear. In this study, we for the first time found that LOC653786 was upregulated in RCC tissues and cell lines, and this lncRNA promoted growth and cell cycle progression of RCC cells. Moreover, we showed that LOC653786 elevated the expression of forkhead box M1 (FOXM1) and its downstream target genes cyclin D1 and cyclin B1 in RCC cells. Reporter assay revealed that LOC653786 enhanced the transcriptional activity of FOXM1 gene promoter. Additionally, knockdown of FOXM1 attenuated the LOC653786-enhanced growth and cell cycle progression of RCC cells. Meanwhile, silencing of LOC653786 suppressed RCC cell growth and cell cycle progression, which was alleviated by overexpression of FOXM1. The in vivo experiments in nude mice showed knockdown of LOC653786 repressed xenograft tumor growth and FOXM1 expression. In conclusion, our results demonstrate that LOC653786 accelerates growth and cell cycle progression of RCC cells via upregulating FOXM1, suggesting that the ‘LOC653786/FOXM1’ pathway may serve as a novel target for RCC treatment. |
format | Online Article Text |
id | pubmed-5844731 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-58447312018-03-16 LncRNA LOC653786 promotes growth of RCC cells via upregulating FOXM1 Yang, Fan Wu, Qingjian Zhang, Yan Xiong, Haojun Li, Xinzhe Li, Bo Xie, Wei Zhang, Le Xu, Min Zhang, Kebin He, Fengtian Oncotarget Research Paper Renal cell carcinoma (RCC) is the most common kidney malignancy with poor prognosis. Recently, long noncoding RNAs (lncRNAs) have been demonstrated as important regulators in multiple cancers including RCC. LOC653786 is a lncRNA, but its role in cancer remains unclear. In this study, we for the first time found that LOC653786 was upregulated in RCC tissues and cell lines, and this lncRNA promoted growth and cell cycle progression of RCC cells. Moreover, we showed that LOC653786 elevated the expression of forkhead box M1 (FOXM1) and its downstream target genes cyclin D1 and cyclin B1 in RCC cells. Reporter assay revealed that LOC653786 enhanced the transcriptional activity of FOXM1 gene promoter. Additionally, knockdown of FOXM1 attenuated the LOC653786-enhanced growth and cell cycle progression of RCC cells. Meanwhile, silencing of LOC653786 suppressed RCC cell growth and cell cycle progression, which was alleviated by overexpression of FOXM1. The in vivo experiments in nude mice showed knockdown of LOC653786 repressed xenograft tumor growth and FOXM1 expression. In conclusion, our results demonstrate that LOC653786 accelerates growth and cell cycle progression of RCC cells via upregulating FOXM1, suggesting that the ‘LOC653786/FOXM1’ pathway may serve as a novel target for RCC treatment. Impact Journals LLC 2018-01-08 /pmc/articles/PMC5844731/ /pubmed/29552295 http://dx.doi.org/10.18632/oncotarget.24027 Text en Copyright: © 2018 Yang et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Yang, Fan Wu, Qingjian Zhang, Yan Xiong, Haojun Li, Xinzhe Li, Bo Xie, Wei Zhang, Le Xu, Min Zhang, Kebin He, Fengtian LncRNA LOC653786 promotes growth of RCC cells via upregulating FOXM1 |
title | LncRNA LOC653786 promotes growth of RCC cells via upregulating FOXM1 |
title_full | LncRNA LOC653786 promotes growth of RCC cells via upregulating FOXM1 |
title_fullStr | LncRNA LOC653786 promotes growth of RCC cells via upregulating FOXM1 |
title_full_unstemmed | LncRNA LOC653786 promotes growth of RCC cells via upregulating FOXM1 |
title_short | LncRNA LOC653786 promotes growth of RCC cells via upregulating FOXM1 |
title_sort | lncrna loc653786 promotes growth of rcc cells via upregulating foxm1 |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5844731/ https://www.ncbi.nlm.nih.gov/pubmed/29552295 http://dx.doi.org/10.18632/oncotarget.24027 |
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