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Published in: Cancer Cell International 1/2018

Open Access 01-12-2018 | Primary research

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

Authors: Yuanyuan Wu, Xuedan Chen, Yan Liang, Juan Li, Kun Zhang, Limeng Dai, Xingying Guan, Kai Wang, Yun Bai

Published in: Cancer Cell International | Issue 1/2018

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Abstract

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.
Appendix
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Metadata
Title
Overexpression of long non-coding RNA SOX2OT promotes esophageal squamous cell carcinoma growth
Authors
Yuanyuan Wu
Xuedan Chen
Yan Liang
Juan Li
Kun Zhang
Limeng Dai
Xingying Guan
Kai Wang
Yun Bai
Publication date
01-12-2018
Publisher
BioMed Central
Published in
Cancer Cell International / Issue 1/2018
Electronic ISSN: 1475-2867
DOI
https://doi.org/10.1186/s12935-018-0570-7

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