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Overexpression of long non-coding RNA SOX2OT promotes esophageal squamous cell carcinoma growth
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. Quantitative PCR (qPC...
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Published in: | Cancer cell international 2018-05, Vol.18 (1), p.76-76, Article 76 |
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description | 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.
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.
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.
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. |
doi_str_mv | 10.1186/s12935-018-0570-7 |
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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.
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.
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.</description><identifier>ISSN: 1475-2867</identifier><identifier>EISSN: 1475-2867</identifier><identifier>DOI: 10.1186/s12935-018-0570-7</identifier><identifier>PMID: 29849506</identifier><language>eng</language><publisher>England: BioMed Central</publisher><subject>Breast cancer ; Cell culture ; Cell growth ; Cell proliferation ; Cholecystokinin ; Cloning ; Deoxyribonucleic acid ; DNA ; DNA methylation ; Ectopic expression ; ESCC ; Esophageal cancer ; Esophagus ; Isoforms ; LncRNA ; Medical prognosis ; Metastasis ; Non-coding RNA ; Primary Research ; RNA polymerase ; SOX2OT and SOX2 ; Squamous cell carcinoma ; Studies ; Tissues ; Transcription</subject><ispartof>Cancer cell international, 2018-05, Vol.18 (1), p.76-76, Article 76</ispartof><rights>Copyright © 2018. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and conditions, you may use this content in accordance with the terms of the License.</rights><rights>The Author(s) 2018</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c594t-f534ff3a80ff5a9e0d2fc35d992b35213a0179c50a50f3d8061d18b7843795f53</citedby><cites>FETCH-LOGICAL-c594t-f534ff3a80ff5a9e0d2fc35d992b35213a0179c50a50f3d8061d18b7843795f53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5970475/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2056986547?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29849506$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wu, Yuanyuan</creatorcontrib><creatorcontrib>Chen, Xuedan</creatorcontrib><creatorcontrib>Liang, Yan</creatorcontrib><creatorcontrib>Li, Juan</creatorcontrib><creatorcontrib>Zhang, Kun</creatorcontrib><creatorcontrib>Dai, Limeng</creatorcontrib><creatorcontrib>Guan, Xingying</creatorcontrib><creatorcontrib>Wang, Kai</creatorcontrib><creatorcontrib>Bai, Yun</creatorcontrib><title>Overexpression of long non-coding RNA SOX2OT promotes esophageal squamous cell carcinoma growth</title><title>Cancer cell international</title><addtitle>Cancer Cell Int</addtitle><description>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.
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.
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.
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.</description><subject>Breast cancer</subject><subject>Cell culture</subject><subject>Cell growth</subject><subject>Cell proliferation</subject><subject>Cholecystokinin</subject><subject>Cloning</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>DNA methylation</subject><subject>Ectopic expression</subject><subject>ESCC</subject><subject>Esophageal cancer</subject><subject>Esophagus</subject><subject>Isoforms</subject><subject>LncRNA</subject><subject>Medical prognosis</subject><subject>Metastasis</subject><subject>Non-coding RNA</subject><subject>Primary Research</subject><subject>RNA polymerase</subject><subject>SOX2OT and SOX2</subject><subject>Squamous cell carcinoma</subject><subject>Studies</subject><subject>Tissues</subject><subject>Transcription</subject><issn>1475-2867</issn><issn>1475-2867</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNpdkk1rFTEUhoMotlZ_gBsJuHEzmu-PjVCK1ULxglZwFzKZZO5cZpJpMlPtvzfXW0vrKoec9zycvHkBeI3Re4yV-FAw0ZQ3CKsGcYka-QQcYyZ5Q5SQTx_UR-BFKTuEsFQCPQdHRCumORLHwGxufPa_5-xLGVKEKcAxxR7GFBuXuqGW376ewu-bn2RzBeecprT4An1J89b23o6wXK92SmuBzo8jdDa7IabJwj6nX8v2JXgW7Fj8q7vzBPw4_3R19qW53Hy-ODu9bBzXbGkCpywEahUKgVvtUUeCo7zTmrSUE0xt3V07jixHgXYKCdxh1UrFqNS8Tp-AiwO3S3Zn5jxMNt-aZAfz9yLl3ti8DG70htHWE28rRigWuGp95zSzuNOeM4VUZX08sOa1nWrTxyXb8RH0cScOW9OnG8O1RNXyCnh3B8jpevVlMdNQ9vbY6KtThlSVZkIiUaVv_5Pu0ppjtaqquNBKcCarCh9ULqdSsg_3y2Bk9lEwhyiYGgWzj4LZz7x5-Ir7iX9_T_8A85Cvpg</recordid><startdate>20180525</startdate><enddate>20180525</enddate><creator>Wu, Yuanyuan</creator><creator>Chen, Xuedan</creator><creator>Liang, Yan</creator><creator>Li, Juan</creator><creator>Zhang, Kun</creator><creator>Dai, Limeng</creator><creator>Guan, Xingying</creator><creator>Wang, Kai</creator><creator>Bai, Yun</creator><general>BioMed Central</general><general>BMC</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7TM</scope><scope>7TO</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20180525</creationdate><title>Overexpression of long non-coding RNA SOX2OT promotes esophageal squamous cell carcinoma growth</title><author>Wu, Yuanyuan ; Chen, Xuedan ; Liang, Yan ; Li, Juan ; Zhang, Kun ; Dai, Limeng ; Guan, Xingying ; Wang, Kai ; Bai, Yun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c594t-f534ff3a80ff5a9e0d2fc35d992b35213a0179c50a50f3d8061d18b7843795f53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Breast cancer</topic><topic>Cell culture</topic><topic>Cell growth</topic><topic>Cell proliferation</topic><topic>Cholecystokinin</topic><topic>Cloning</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>DNA methylation</topic><topic>Ectopic expression</topic><topic>ESCC</topic><topic>Esophageal cancer</topic><topic>Esophagus</topic><topic>Isoforms</topic><topic>LncRNA</topic><topic>Medical prognosis</topic><topic>Metastasis</topic><topic>Non-coding RNA</topic><topic>Primary Research</topic><topic>RNA polymerase</topic><topic>SOX2OT and SOX2</topic><topic>Squamous cell carcinoma</topic><topic>Studies</topic><topic>Tissues</topic><topic>Transcription</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wu, Yuanyuan</creatorcontrib><creatorcontrib>Chen, Xuedan</creatorcontrib><creatorcontrib>Liang, Yan</creatorcontrib><creatorcontrib>Li, Juan</creatorcontrib><creatorcontrib>Zhang, Kun</creatorcontrib><creatorcontrib>Dai, Limeng</creatorcontrib><creatorcontrib>Guan, Xingying</creatorcontrib><creatorcontrib>Wang, Kai</creatorcontrib><creatorcontrib>Bai, Yun</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Publicly Available Content Database (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Cancer cell international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wu, Yuanyuan</au><au>Chen, Xuedan</au><au>Liang, Yan</au><au>Li, Juan</au><au>Zhang, Kun</au><au>Dai, Limeng</au><au>Guan, Xingying</au><au>Wang, Kai</au><au>Bai, Yun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Overexpression of long non-coding RNA SOX2OT promotes esophageal squamous cell carcinoma growth</atitle><jtitle>Cancer cell international</jtitle><addtitle>Cancer Cell Int</addtitle><date>2018-05-25</date><risdate>2018</risdate><volume>18</volume><issue>1</issue><spage>76</spage><epage>76</epage><pages>76-76</pages><artnum>76</artnum><issn>1475-2867</issn><eissn>1475-2867</eissn><abstract>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.
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.
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.
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.</abstract><cop>England</cop><pub>BioMed Central</pub><pmid>29849506</pmid><doi>10.1186/s12935-018-0570-7</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Breast cancer Cell culture Cell growth Cell proliferation Cholecystokinin Cloning Deoxyribonucleic acid DNA DNA methylation Ectopic expression ESCC Esophageal cancer Esophagus Isoforms LncRNA Medical prognosis Metastasis Non-coding RNA Primary Research RNA polymerase SOX2OT and SOX2 Squamous cell carcinoma Studies Tissues Transcription |
title | Overexpression of long non-coding RNA SOX2OT promotes esophageal squamous cell carcinoma growth |
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