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Overexpression of long non-coding RNA SOX2OT promotes esophageal squamous cell carcinoma growth

BACKGROUND: SOX2 overlapping transcript (SOX2OT) has been reported to be an important lncRNA in various cancers. SOX2 is embedded in an intron of the SOX2OT gene. But the role of SOX2OT in esophageal squamous cell carcinoma (ESCC) and the association between SOX2OT and SOX2 remain unclear. METHODS:...

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Autores principales: Wu, Yuanyuan, Chen, Xuedan, Liang, Yan, Li, Juan, Zhang, Kun, Dai, Limeng, Guan, Xingying, Wang, Kai, Bai, Yun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5970475/
https://www.ncbi.nlm.nih.gov/pubmed/29849506
http://dx.doi.org/10.1186/s12935-018-0570-7
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author Wu, Yuanyuan
Chen, Xuedan
Liang, Yan
Li, Juan
Zhang, Kun
Dai, Limeng
Guan, Xingying
Wang, Kai
Bai, Yun
author_facet Wu, Yuanyuan
Chen, Xuedan
Liang, Yan
Li, Juan
Zhang, Kun
Dai, Limeng
Guan, Xingying
Wang, Kai
Bai, Yun
author_sort Wu, Yuanyuan
collection PubMed
description BACKGROUND: SOX2 overlapping transcript (SOX2OT) has been reported to be an important lncRNA in various cancers. SOX2 is embedded in an intron of the SOX2OT gene. But the role of SOX2OT in esophageal squamous cell carcinoma (ESCC) and the association between SOX2OT and SOX2 remain unclear. METHODS: Quantitative PCR (qPCR) was used to detect the expression of SOX2OT and SOX2 in ESCC tissues and cells. The isoforms of SOX2OT were identified by PCR and confirmed by sequencing. CCK-8 and Edu assays were performed to investigate the effects of SOX2OT on cell growth. The relationship between SOX2OT and SOX2 was explored by luciferase reporter assay. RESULTS: Both SOX2OT and SOX2 were upregulated in ESCC tissues and cells. SOX2OT expression was positively associated with SOX2 expression in ESCC tissues. NR_004053 was one of the major SOX2OT transcripts aberrantly expressed in ESCC tissues and cells. Overexpression of SOX2OT (NR_004053) promoted ESCC cell growth, antagonized the effect of DDP and increased cell proliferation ratio. Ectopic expression of SOX2 could increase the luciferase activity of SOX2OT-pGL3/Basic and SOX2OT expression, while overexpression of SOX2OT (NR_004053) had no effect on SOX2 expression. CONCLUSION: Our study demonstrates that the major isoform of SOX2OT in ESCC, SOX2OT (NR_004053) contributes to cell growth. SOX2 promotes SOX2OT expression at transcriptional level. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12935-018-0570-7) contains supplementary material, which is available to authorized users.
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spelling pubmed-59704752018-05-30 Overexpression of long non-coding RNA SOX2OT promotes esophageal squamous cell carcinoma growth Wu, Yuanyuan Chen, Xuedan Liang, Yan Li, Juan Zhang, Kun Dai, Limeng Guan, Xingying Wang, Kai Bai, Yun Cancer Cell Int Primary Research BACKGROUND: SOX2 overlapping transcript (SOX2OT) has been reported to be an important lncRNA in various cancers. SOX2 is embedded in an intron of the SOX2OT gene. But the role of SOX2OT in esophageal squamous cell carcinoma (ESCC) and the association between SOX2OT and SOX2 remain unclear. METHODS: Quantitative PCR (qPCR) was used to detect the expression of SOX2OT and SOX2 in ESCC tissues and cells. The isoforms of SOX2OT were identified by PCR and confirmed by sequencing. CCK-8 and Edu assays were performed to investigate the effects of SOX2OT on cell growth. The relationship between SOX2OT and SOX2 was explored by luciferase reporter assay. RESULTS: Both SOX2OT and SOX2 were upregulated in ESCC tissues and cells. SOX2OT expression was positively associated with SOX2 expression in ESCC tissues. NR_004053 was one of the major SOX2OT transcripts aberrantly expressed in ESCC tissues and cells. Overexpression of SOX2OT (NR_004053) promoted ESCC cell growth, antagonized the effect of DDP and increased cell proliferation ratio. Ectopic expression of SOX2 could increase the luciferase activity of SOX2OT-pGL3/Basic and SOX2OT expression, while overexpression of SOX2OT (NR_004053) had no effect on SOX2 expression. CONCLUSION: Our study demonstrates that the major isoform of SOX2OT in ESCC, SOX2OT (NR_004053) contributes to cell growth. SOX2 promotes SOX2OT expression at transcriptional level. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12935-018-0570-7) contains supplementary material, which is available to authorized users. BioMed Central 2018-05-25 /pmc/articles/PMC5970475/ /pubmed/29849506 http://dx.doi.org/10.1186/s12935-018-0570-7 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Primary Research
Wu, Yuanyuan
Chen, Xuedan
Liang, Yan
Li, Juan
Zhang, Kun
Dai, Limeng
Guan, Xingying
Wang, Kai
Bai, Yun
Overexpression of long non-coding RNA SOX2OT promotes esophageal squamous cell carcinoma growth
title Overexpression of long non-coding RNA SOX2OT promotes esophageal squamous cell carcinoma growth
title_full Overexpression of long non-coding RNA SOX2OT promotes esophageal squamous cell carcinoma growth
title_fullStr Overexpression of long non-coding RNA SOX2OT promotes esophageal squamous cell carcinoma growth
title_full_unstemmed Overexpression of long non-coding RNA SOX2OT promotes esophageal squamous cell carcinoma growth
title_short Overexpression of long non-coding RNA SOX2OT promotes esophageal squamous cell carcinoma growth
title_sort overexpression of long non-coding rna sox2ot promotes esophageal squamous cell carcinoma growth
topic Primary Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5970475/
https://www.ncbi.nlm.nih.gov/pubmed/29849506
http://dx.doi.org/10.1186/s12935-018-0570-7
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