Long non-coding RNA DNM3OS promotes tumor progression and EMT in gastric cancer by associating with Snail

Long non-coding RNAs (lncRNAs) act as tumor suppressors or oncogenes in tumor development and progression. In the present study, we explored the expression and biological role of the lncRNA DNM3OS in gastric cancer (GC). We observed that DNM3OS was upregulated in GC tissues and cell lines, and high...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Biochemical and biophysical research communications 2019-03, Vol.511 (1), p.57-62
Hauptverfasser: Wang, Shuchang, Ni, Bo, Zhang, Zizhen, Wang, Chaojie, Wo, Lulu, Zhou, Cixiang, Zhao, Qian, Zhao, Enhao
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 62
container_issue 1
container_start_page 57
container_title Biochemical and biophysical research communications
container_volume 511
creator Wang, Shuchang
Ni, Bo
Zhang, Zizhen
Wang, Chaojie
Wo, Lulu
Zhou, Cixiang
Zhao, Qian
Zhao, Enhao
description Long non-coding RNAs (lncRNAs) act as tumor suppressors or oncogenes in tumor development and progression. In the present study, we explored the expression and biological role of the lncRNA DNM3OS in gastric cancer (GC). We observed that DNM3OS was upregulated in GC tissues and cell lines, and high DNM3OS expression was correlated with malignant features and served as an indicator of a poor prognosis for GC patients. DNM3OS knockdown inhibited the proliferation of GC cells, and reduced DNM3OS suppressed tumor growth in vivo. Moreover, DNM3OS depletion inhibited the migration and invasion of GC cells through the suppression of the Snail-mediated epithelial-mesenchymal transition (EMT). In conclusion, we demonstrated that DNM3OS serves as an oncogenic lncRNA in GC, and we implicated DNM3OS as a promising prognostic factor and a potential therapeutic target for GC patients. •DNM3OS expression was elevated in GC patients tissues.•Higher expression of DNM3OS was associated with poor survival of GC patients.•DNM3OS promotes malignancy in GC cells.•DNM3OS depletion inhibited the invasion of GC cells through the suppression of the Snail-mediated EMT.
doi_str_mv 10.1016/j.bbrc.2019.02.030
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2186620190</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0006291X19302177</els_id><sourcerecordid>2186620190</sourcerecordid><originalsourceid>FETCH-LOGICAL-c356t-f0c11cf1d680ee9941271fec07ab8f22684e53448c0f7c637c3a41c92dc300323</originalsourceid><addsrcrecordid>eNp9kMFu1DAQhi0EokvLC3BAPnJJmLFTJ5G4VKUUpG0rtUXiZjmTyeLVxi52FtS3b6ItHDnNjPTNr5lPiHcIJQKaj9uy6xKVCrAtQZWg4YVYIbRQKITqpVgBgClUiz-OxJuctwCIlWlfiyMNdQ0IaiX8OoaNDDEUFHs_t7fXZ_Lz9ZW-uZMPKY5x4iyn_RjTMm4S5-xjkC708uLqXvogNy5PyZMkF4iT7B6lyzmSd9MS98dPP-VdcH53Il4Nbpf57XM9Ft-_XNyffy3WN5ffzs_WBelTMxUDECIN2JsGmNu2QlXjwAS165pBKdNUfKqrqiEYajK6Ju0qpFb1pAG00sfiwyF3vvfXnvNkR5-JdzsXOO6zVdgYsziDGVUHlFLMOfFgH5IfXXq0CHZRbLd2UWwX3IKys-J56f1z_r4buf-38tfpDHw6ADx_-dtzspk8z3J6n5gm20f_v_wnkaiL2Q</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2186620190</pqid></control><display><type>article</type><title>Long non-coding RNA DNM3OS promotes tumor progression and EMT in gastric cancer by associating with Snail</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><creator>Wang, Shuchang ; Ni, Bo ; Zhang, Zizhen ; Wang, Chaojie ; Wo, Lulu ; Zhou, Cixiang ; Zhao, Qian ; Zhao, Enhao</creator><creatorcontrib>Wang, Shuchang ; Ni, Bo ; Zhang, Zizhen ; Wang, Chaojie ; Wo, Lulu ; Zhou, Cixiang ; Zhao, Qian ; Zhao, Enhao</creatorcontrib><description>Long non-coding RNAs (lncRNAs) act as tumor suppressors or oncogenes in tumor development and progression. In the present study, we explored the expression and biological role of the lncRNA DNM3OS in gastric cancer (GC). We observed that DNM3OS was upregulated in GC tissues and cell lines, and high DNM3OS expression was correlated with malignant features and served as an indicator of a poor prognosis for GC patients. DNM3OS knockdown inhibited the proliferation of GC cells, and reduced DNM3OS suppressed tumor growth in vivo. Moreover, DNM3OS depletion inhibited the migration and invasion of GC cells through the suppression of the Snail-mediated epithelial-mesenchymal transition (EMT). In conclusion, we demonstrated that DNM3OS serves as an oncogenic lncRNA in GC, and we implicated DNM3OS as a promising prognostic factor and a potential therapeutic target for GC patients. •DNM3OS expression was elevated in GC patients tissues.•Higher expression of DNM3OS was associated with poor survival of GC patients.•DNM3OS promotes malignancy in GC cells.•DNM3OS depletion inhibited the invasion of GC cells through the suppression of the Snail-mediated EMT.</description><identifier>ISSN: 0006-291X</identifier><identifier>EISSN: 1090-2104</identifier><identifier>DOI: 10.1016/j.bbrc.2019.02.030</identifier><identifier>PMID: 30770102</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Animals ; Cell Line, Tumor ; Disease Progression ; DNM3OS ; EMT ; Epithelial-Mesenchymal Transition ; Gastric cancer ; Gene Expression Regulation, Neoplastic ; Humans ; Mice, Nude ; Neoplasm Invasiveness - genetics ; Neoplasm Invasiveness - pathology ; RNA, Long Noncoding - genetics ; Snail ; Snail Family Transcription Factors - genetics ; Stomach Neoplasms - genetics ; Stomach Neoplasms - pathology</subject><ispartof>Biochemical and biophysical research communications, 2019-03, Vol.511 (1), p.57-62</ispartof><rights>2019 Elsevier Inc.</rights><rights>Copyright © 2019 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c356t-f0c11cf1d680ee9941271fec07ab8f22684e53448c0f7c637c3a41c92dc300323</citedby><cites>FETCH-LOGICAL-c356t-f0c11cf1d680ee9941271fec07ab8f22684e53448c0f7c637c3a41c92dc300323</cites><orcidid>0000-0003-1112-0043 ; 0000-0001-6731-2891</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0006291X19302177$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30770102$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wang, Shuchang</creatorcontrib><creatorcontrib>Ni, Bo</creatorcontrib><creatorcontrib>Zhang, Zizhen</creatorcontrib><creatorcontrib>Wang, Chaojie</creatorcontrib><creatorcontrib>Wo, Lulu</creatorcontrib><creatorcontrib>Zhou, Cixiang</creatorcontrib><creatorcontrib>Zhao, Qian</creatorcontrib><creatorcontrib>Zhao, Enhao</creatorcontrib><title>Long non-coding RNA DNM3OS promotes tumor progression and EMT in gastric cancer by associating with Snail</title><title>Biochemical and biophysical research communications</title><addtitle>Biochem Biophys Res Commun</addtitle><description>Long non-coding RNAs (lncRNAs) act as tumor suppressors or oncogenes in tumor development and progression. In the present study, we explored the expression and biological role of the lncRNA DNM3OS in gastric cancer (GC). We observed that DNM3OS was upregulated in GC tissues and cell lines, and high DNM3OS expression was correlated with malignant features and served as an indicator of a poor prognosis for GC patients. DNM3OS knockdown inhibited the proliferation of GC cells, and reduced DNM3OS suppressed tumor growth in vivo. Moreover, DNM3OS depletion inhibited the migration and invasion of GC cells through the suppression of the Snail-mediated epithelial-mesenchymal transition (EMT). In conclusion, we demonstrated that DNM3OS serves as an oncogenic lncRNA in GC, and we implicated DNM3OS as a promising prognostic factor and a potential therapeutic target for GC patients. •DNM3OS expression was elevated in GC patients tissues.•Higher expression of DNM3OS was associated with poor survival of GC patients.•DNM3OS promotes malignancy in GC cells.•DNM3OS depletion inhibited the invasion of GC cells through the suppression of the Snail-mediated EMT.</description><subject>Animals</subject><subject>Cell Line, Tumor</subject><subject>Disease Progression</subject><subject>DNM3OS</subject><subject>EMT</subject><subject>Epithelial-Mesenchymal Transition</subject><subject>Gastric cancer</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>Humans</subject><subject>Mice, Nude</subject><subject>Neoplasm Invasiveness - genetics</subject><subject>Neoplasm Invasiveness - pathology</subject><subject>RNA, Long Noncoding - genetics</subject><subject>Snail</subject><subject>Snail Family Transcription Factors - genetics</subject><subject>Stomach Neoplasms - genetics</subject><subject>Stomach Neoplasms - pathology</subject><issn>0006-291X</issn><issn>1090-2104</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kMFu1DAQhi0EokvLC3BAPnJJmLFTJ5G4VKUUpG0rtUXiZjmTyeLVxi52FtS3b6ItHDnNjPTNr5lPiHcIJQKaj9uy6xKVCrAtQZWg4YVYIbRQKITqpVgBgClUiz-OxJuctwCIlWlfiyMNdQ0IaiX8OoaNDDEUFHs_t7fXZ_Lz9ZW-uZMPKY5x4iyn_RjTMm4S5-xjkC708uLqXvogNy5PyZMkF4iT7B6lyzmSd9MS98dPP-VdcH53Il4Nbpf57XM9Ft-_XNyffy3WN5ffzs_WBelTMxUDECIN2JsGmNu2QlXjwAS165pBKdNUfKqrqiEYajK6Ju0qpFb1pAG00sfiwyF3vvfXnvNkR5-JdzsXOO6zVdgYsziDGVUHlFLMOfFgH5IfXXq0CHZRbLd2UWwX3IKys-J56f1z_r4buf-38tfpDHw6ADx_-dtzspk8z3J6n5gm20f_v_wnkaiL2Q</recordid><startdate>20190326</startdate><enddate>20190326</enddate><creator>Wang, Shuchang</creator><creator>Ni, Bo</creator><creator>Zhang, Zizhen</creator><creator>Wang, Chaojie</creator><creator>Wo, Lulu</creator><creator>Zhou, Cixiang</creator><creator>Zhao, Qian</creator><creator>Zhao, Enhao</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-1112-0043</orcidid><orcidid>https://orcid.org/0000-0001-6731-2891</orcidid></search><sort><creationdate>20190326</creationdate><title>Long non-coding RNA DNM3OS promotes tumor progression and EMT in gastric cancer by associating with Snail</title><author>Wang, Shuchang ; Ni, Bo ; Zhang, Zizhen ; Wang, Chaojie ; Wo, Lulu ; Zhou, Cixiang ; Zhao, Qian ; Zhao, Enhao</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c356t-f0c11cf1d680ee9941271fec07ab8f22684e53448c0f7c637c3a41c92dc300323</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Animals</topic><topic>Cell Line, Tumor</topic><topic>Disease Progression</topic><topic>DNM3OS</topic><topic>EMT</topic><topic>Epithelial-Mesenchymal Transition</topic><topic>Gastric cancer</topic><topic>Gene Expression Regulation, Neoplastic</topic><topic>Humans</topic><topic>Mice, Nude</topic><topic>Neoplasm Invasiveness - genetics</topic><topic>Neoplasm Invasiveness - pathology</topic><topic>RNA, Long Noncoding - genetics</topic><topic>Snail</topic><topic>Snail Family Transcription Factors - genetics</topic><topic>Stomach Neoplasms - genetics</topic><topic>Stomach Neoplasms - pathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Shuchang</creatorcontrib><creatorcontrib>Ni, Bo</creatorcontrib><creatorcontrib>Zhang, Zizhen</creatorcontrib><creatorcontrib>Wang, Chaojie</creatorcontrib><creatorcontrib>Wo, Lulu</creatorcontrib><creatorcontrib>Zhou, Cixiang</creatorcontrib><creatorcontrib>Zhao, Qian</creatorcontrib><creatorcontrib>Zhao, Enhao</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Biochemical and biophysical research communications</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Shuchang</au><au>Ni, Bo</au><au>Zhang, Zizhen</au><au>Wang, Chaojie</au><au>Wo, Lulu</au><au>Zhou, Cixiang</au><au>Zhao, Qian</au><au>Zhao, Enhao</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Long non-coding RNA DNM3OS promotes tumor progression and EMT in gastric cancer by associating with Snail</atitle><jtitle>Biochemical and biophysical research communications</jtitle><addtitle>Biochem Biophys Res Commun</addtitle><date>2019-03-26</date><risdate>2019</risdate><volume>511</volume><issue>1</issue><spage>57</spage><epage>62</epage><pages>57-62</pages><issn>0006-291X</issn><eissn>1090-2104</eissn><abstract>Long non-coding RNAs (lncRNAs) act as tumor suppressors or oncogenes in tumor development and progression. In the present study, we explored the expression and biological role of the lncRNA DNM3OS in gastric cancer (GC). We observed that DNM3OS was upregulated in GC tissues and cell lines, and high DNM3OS expression was correlated with malignant features and served as an indicator of a poor prognosis for GC patients. DNM3OS knockdown inhibited the proliferation of GC cells, and reduced DNM3OS suppressed tumor growth in vivo. Moreover, DNM3OS depletion inhibited the migration and invasion of GC cells through the suppression of the Snail-mediated epithelial-mesenchymal transition (EMT). In conclusion, we demonstrated that DNM3OS serves as an oncogenic lncRNA in GC, and we implicated DNM3OS as a promising prognostic factor and a potential therapeutic target for GC patients. •DNM3OS expression was elevated in GC patients tissues.•Higher expression of DNM3OS was associated with poor survival of GC patients.•DNM3OS promotes malignancy in GC cells.•DNM3OS depletion inhibited the invasion of GC cells through the suppression of the Snail-mediated EMT.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>30770102</pmid><doi>10.1016/j.bbrc.2019.02.030</doi><tpages>6</tpages><orcidid>https://orcid.org/0000-0003-1112-0043</orcidid><orcidid>https://orcid.org/0000-0001-6731-2891</orcidid></addata></record>
fulltext fulltext
identifier ISSN: 0006-291X
ispartof Biochemical and biophysical research communications, 2019-03, Vol.511 (1), p.57-62
issn 0006-291X
1090-2104
language eng
recordid cdi_proquest_miscellaneous_2186620190
source MEDLINE; Elsevier ScienceDirect Journals
subjects Animals
Cell Line, Tumor
Disease Progression
DNM3OS
EMT
Epithelial-Mesenchymal Transition
Gastric cancer
Gene Expression Regulation, Neoplastic
Humans
Mice, Nude
Neoplasm Invasiveness - genetics
Neoplasm Invasiveness - pathology
RNA, Long Noncoding - genetics
Snail
Snail Family Transcription Factors - genetics
Stomach Neoplasms - genetics
Stomach Neoplasms - pathology
title Long non-coding RNA DNM3OS promotes tumor progression and EMT in gastric cancer by associating with Snail
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-31T05%3A48%3A41IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Long%20non-coding%20RNA%20DNM3OS%20promotes%20tumor%20progression%20and%20EMT%20in%20gastric%20cancer%20by%20associating%20with%20Snail&rft.jtitle=Biochemical%20and%20biophysical%20research%20communications&rft.au=Wang,%20Shuchang&rft.date=2019-03-26&rft.volume=511&rft.issue=1&rft.spage=57&rft.epage=62&rft.pages=57-62&rft.issn=0006-291X&rft.eissn=1090-2104&rft_id=info:doi/10.1016/j.bbrc.2019.02.030&rft_dat=%3Cproquest_cross%3E2186620190%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2186620190&rft_id=info:pmid/30770102&rft_els_id=S0006291X19302177&rfr_iscdi=true