MYC-Activated LncRNA MNX1-AS1 Promotes the Progression of Colorectal Cancer by Stabilizing YB1

Long noncoding RNAs (lncRNA) are involved in tumorigenesis and drug resistance. However, the roles and underlying mechanisms of lncRNAs in colorectal cancer are still unknown. In this work, through transcriptomic profiling analysis of 21 paired tumor and normal samples, we identified a novel colorec...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Cancer research (Chicago, Ill.) Ill.), 2021-05, Vol.81 (10), p.2636-2650
Hauptverfasser: Wu, Qi-Nian, Luo, Xiao-Jing, Liu, Jia, Lu, Yun-Xin, Wang, Yun, Qi, Jingjing, Liu, Ze-Xian, Huang, Qi-Tao, Liu, Ze-Kun, Lu, Jia-Bin, Jin, Ying, Pu, Heng-Ying, Hu, Pei-Shan, Zheng, Jia-Bo, Zeng, Zhao-Lei, Ju, Huai-Qiang, Xie, Dan, Zhao, Qi, Xu, Ruihua
Format: Artikel
Sprache:eng
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 2650
container_issue 10
container_start_page 2636
container_title Cancer research (Chicago, Ill.)
container_volume 81
creator Wu, Qi-Nian
Luo, Xiao-Jing
Liu, Jia
Lu, Yun-Xin
Wang, Yun
Qi, Jingjing
Liu, Ze-Xian
Huang, Qi-Tao
Liu, Ze-Kun
Lu, Jia-Bin
Jin, Ying
Pu, Heng-Ying
Hu, Pei-Shan
Zheng, Jia-Bo
Zeng, Zhao-Lei
Ju, Huai-Qiang
Xie, Dan
Zhao, Qi
Xu, Ruihua
description Long noncoding RNAs (lncRNA) are involved in tumorigenesis and drug resistance. However, the roles and underlying mechanisms of lncRNAs in colorectal cancer are still unknown. In this work, through transcriptomic profiling analysis of 21 paired tumor and normal samples, we identified a novel colorectal cancer-related lncRNA, . - expression was significantly upregulated in colorectal cancer and associated with poor prognosis. and gain- and loss-of-function experiments showed that - promotes the proliferation of colorectal cancer cells. - bound to and activated Y-box-binding protein 1 (YB1), a multifunctional RNA/DNA-binding protein, and prevented its ubiquitination and degradation. A marked overlap between genes that are differentially expressed in - knockdown cells and transcriptional targets of YB1 was observed. YB1 knockdown mimicked the loss of viability phenotype observed upon depletion of - . In addition, MYC bound the promoter of the - locus and activated its transcription. experiments showed that ASO inhibited - , which suppressed the proliferation of colorectal cancer cells in both cell-based and patient-derived xenograft models. Collectively, these findings suggest that the MYC- -YB1 axis might serve as a potential biomarker and therapeutic target in colorectal cancer. SIGNIFICANCE: This study highlights the discovery of a novel colorectal cancer biomarker and therapeutic target, - , a long noncoding RNA that drives proliferation via a MYC/ /YB1 signaling pathway. GRAPHICAL ABSTRACT: http://cancerres.aacrjournals.org/content/canres/81/10/2636/F1.large.jpg.
doi_str_mv 10.1158/0008-5472.CAN-20-3747
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2507146213</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2507146213</sourcerecordid><originalsourceid>FETCH-LOGICAL-c460t-6352375deb6a51d083d04fb1edffe24e634d5c4900871d910c79f51143248a283</originalsourceid><addsrcrecordid>eNo9kNtKxDAQhoMouq4-gpJLb6KZHJr2shZPsK7iAfTGkKapVrrNmnQFfXpb1L0afvj-GeZD6ADoMYBMTyilKZFCseMinxNGCVdCbaAJSJ4SJYTcRJM1s4N2Y3wfogQqt9EO5yplNMsm6OX6uSC57ZtP07sKzzp7N8_x9fwJSH4P-Db4he9dxP2bG8NrcDE2vsO-xoVvfXC2Ny0uTGddwOUXvu9N2bTNd9O94udT2ENbtWmj2_-bU_R4fvZQXJLZzcVVkc-IFQntScIl40pWrkyMhIqmvKKiLsFVde2YcAkXlbQiG_5RUGVArcpqCSA4E6lhKZ-io9-9y-A_Vi72etFE69rWdM6vomaSKhAJAz6g8he1wccYXK2XoVmY8KWB6lGtHrXpUZse1GpG9ah26B3-nViVC1etW_8u-Q8ueHHp</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2507146213</pqid></control><display><type>article</type><title>MYC-Activated LncRNA MNX1-AS1 Promotes the Progression of Colorectal Cancer by Stabilizing YB1</title><source>American Association for Cancer Research</source><source>EZB Electronic Journals Library</source><creator>Wu, Qi-Nian ; Luo, Xiao-Jing ; Liu, Jia ; Lu, Yun-Xin ; Wang, Yun ; Qi, Jingjing ; Liu, Ze-Xian ; Huang, Qi-Tao ; Liu, Ze-Kun ; Lu, Jia-Bin ; Jin, Ying ; Pu, Heng-Ying ; Hu, Pei-Shan ; Zheng, Jia-Bo ; Zeng, Zhao-Lei ; Ju, Huai-Qiang ; Xie, Dan ; Zhao, Qi ; Xu, Ruihua</creator><creatorcontrib>Wu, Qi-Nian ; Luo, Xiao-Jing ; Liu, Jia ; Lu, Yun-Xin ; Wang, Yun ; Qi, Jingjing ; Liu, Ze-Xian ; Huang, Qi-Tao ; Liu, Ze-Kun ; Lu, Jia-Bin ; Jin, Ying ; Pu, Heng-Ying ; Hu, Pei-Shan ; Zheng, Jia-Bo ; Zeng, Zhao-Lei ; Ju, Huai-Qiang ; Xie, Dan ; Zhao, Qi ; Xu, Ruihua</creatorcontrib><description>Long noncoding RNAs (lncRNA) are involved in tumorigenesis and drug resistance. However, the roles and underlying mechanisms of lncRNAs in colorectal cancer are still unknown. In this work, through transcriptomic profiling analysis of 21 paired tumor and normal samples, we identified a novel colorectal cancer-related lncRNA, . - expression was significantly upregulated in colorectal cancer and associated with poor prognosis. and gain- and loss-of-function experiments showed that - promotes the proliferation of colorectal cancer cells. - bound to and activated Y-box-binding protein 1 (YB1), a multifunctional RNA/DNA-binding protein, and prevented its ubiquitination and degradation. A marked overlap between genes that are differentially expressed in - knockdown cells and transcriptional targets of YB1 was observed. YB1 knockdown mimicked the loss of viability phenotype observed upon depletion of - . In addition, MYC bound the promoter of the - locus and activated its transcription. experiments showed that ASO inhibited - , which suppressed the proliferation of colorectal cancer cells in both cell-based and patient-derived xenograft models. Collectively, these findings suggest that the MYC- -YB1 axis might serve as a potential biomarker and therapeutic target in colorectal cancer. SIGNIFICANCE: This study highlights the discovery of a novel colorectal cancer biomarker and therapeutic target, - , a long noncoding RNA that drives proliferation via a MYC/ /YB1 signaling pathway. GRAPHICAL ABSTRACT: http://cancerres.aacrjournals.org/content/canres/81/10/2636/F1.large.jpg.</description><identifier>ISSN: 0008-5472</identifier><identifier>EISSN: 1538-7445</identifier><identifier>DOI: 10.1158/0008-5472.CAN-20-3747</identifier><identifier>PMID: 33782099</identifier><language>eng</language><publisher>United States</publisher><ispartof>Cancer research (Chicago, Ill.), 2021-05, Vol.81 (10), p.2636-2650</ispartof><rights>2021 American Association for Cancer Research.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c460t-6352375deb6a51d083d04fb1edffe24e634d5c4900871d910c79f51143248a283</citedby><cites>FETCH-LOGICAL-c460t-6352375deb6a51d083d04fb1edffe24e634d5c4900871d910c79f51143248a283</cites><orcidid>0000-0002-8683-6145 ; 0000-0001-9698-0610 ; 0000-0003-4420-5625 ; 0000-0003-1713-5465</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,3343,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33782099$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wu, Qi-Nian</creatorcontrib><creatorcontrib>Luo, Xiao-Jing</creatorcontrib><creatorcontrib>Liu, Jia</creatorcontrib><creatorcontrib>Lu, Yun-Xin</creatorcontrib><creatorcontrib>Wang, Yun</creatorcontrib><creatorcontrib>Qi, Jingjing</creatorcontrib><creatorcontrib>Liu, Ze-Xian</creatorcontrib><creatorcontrib>Huang, Qi-Tao</creatorcontrib><creatorcontrib>Liu, Ze-Kun</creatorcontrib><creatorcontrib>Lu, Jia-Bin</creatorcontrib><creatorcontrib>Jin, Ying</creatorcontrib><creatorcontrib>Pu, Heng-Ying</creatorcontrib><creatorcontrib>Hu, Pei-Shan</creatorcontrib><creatorcontrib>Zheng, Jia-Bo</creatorcontrib><creatorcontrib>Zeng, Zhao-Lei</creatorcontrib><creatorcontrib>Ju, Huai-Qiang</creatorcontrib><creatorcontrib>Xie, Dan</creatorcontrib><creatorcontrib>Zhao, Qi</creatorcontrib><creatorcontrib>Xu, Ruihua</creatorcontrib><title>MYC-Activated LncRNA MNX1-AS1 Promotes the Progression of Colorectal Cancer by Stabilizing YB1</title><title>Cancer research (Chicago, Ill.)</title><addtitle>Cancer Res</addtitle><description>Long noncoding RNAs (lncRNA) are involved in tumorigenesis and drug resistance. However, the roles and underlying mechanisms of lncRNAs in colorectal cancer are still unknown. In this work, through transcriptomic profiling analysis of 21 paired tumor and normal samples, we identified a novel colorectal cancer-related lncRNA, . - expression was significantly upregulated in colorectal cancer and associated with poor prognosis. and gain- and loss-of-function experiments showed that - promotes the proliferation of colorectal cancer cells. - bound to and activated Y-box-binding protein 1 (YB1), a multifunctional RNA/DNA-binding protein, and prevented its ubiquitination and degradation. A marked overlap between genes that are differentially expressed in - knockdown cells and transcriptional targets of YB1 was observed. YB1 knockdown mimicked the loss of viability phenotype observed upon depletion of - . In addition, MYC bound the promoter of the - locus and activated its transcription. experiments showed that ASO inhibited - , which suppressed the proliferation of colorectal cancer cells in both cell-based and patient-derived xenograft models. Collectively, these findings suggest that the MYC- -YB1 axis might serve as a potential biomarker and therapeutic target in colorectal cancer. SIGNIFICANCE: This study highlights the discovery of a novel colorectal cancer biomarker and therapeutic target, - , a long noncoding RNA that drives proliferation via a MYC/ /YB1 signaling pathway. GRAPHICAL ABSTRACT: http://cancerres.aacrjournals.org/content/canres/81/10/2636/F1.large.jpg.</description><issn>0008-5472</issn><issn>1538-7445</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNo9kNtKxDAQhoMouq4-gpJLb6KZHJr2shZPsK7iAfTGkKapVrrNmnQFfXpb1L0afvj-GeZD6ADoMYBMTyilKZFCseMinxNGCVdCbaAJSJ4SJYTcRJM1s4N2Y3wfogQqt9EO5yplNMsm6OX6uSC57ZtP07sKzzp7N8_x9fwJSH4P-Db4he9dxP2bG8NrcDE2vsO-xoVvfXC2Ny0uTGddwOUXvu9N2bTNd9O94udT2ENbtWmj2_-bU_R4fvZQXJLZzcVVkc-IFQntScIl40pWrkyMhIqmvKKiLsFVde2YcAkXlbQiG_5RUGVArcpqCSA4E6lhKZ-io9-9y-A_Vi72etFE69rWdM6vomaSKhAJAz6g8he1wccYXK2XoVmY8KWB6lGtHrXpUZse1GpG9ah26B3-nViVC1etW_8u-Q8ueHHp</recordid><startdate>20210515</startdate><enddate>20210515</enddate><creator>Wu, Qi-Nian</creator><creator>Luo, Xiao-Jing</creator><creator>Liu, Jia</creator><creator>Lu, Yun-Xin</creator><creator>Wang, Yun</creator><creator>Qi, Jingjing</creator><creator>Liu, Ze-Xian</creator><creator>Huang, Qi-Tao</creator><creator>Liu, Ze-Kun</creator><creator>Lu, Jia-Bin</creator><creator>Jin, Ying</creator><creator>Pu, Heng-Ying</creator><creator>Hu, Pei-Shan</creator><creator>Zheng, Jia-Bo</creator><creator>Zeng, Zhao-Lei</creator><creator>Ju, Huai-Qiang</creator><creator>Xie, Dan</creator><creator>Zhao, Qi</creator><creator>Xu, Ruihua</creator><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-8683-6145</orcidid><orcidid>https://orcid.org/0000-0001-9698-0610</orcidid><orcidid>https://orcid.org/0000-0003-4420-5625</orcidid><orcidid>https://orcid.org/0000-0003-1713-5465</orcidid></search><sort><creationdate>20210515</creationdate><title>MYC-Activated LncRNA MNX1-AS1 Promotes the Progression of Colorectal Cancer by Stabilizing YB1</title><author>Wu, Qi-Nian ; Luo, Xiao-Jing ; Liu, Jia ; Lu, Yun-Xin ; Wang, Yun ; Qi, Jingjing ; Liu, Ze-Xian ; Huang, Qi-Tao ; Liu, Ze-Kun ; Lu, Jia-Bin ; Jin, Ying ; Pu, Heng-Ying ; Hu, Pei-Shan ; Zheng, Jia-Bo ; Zeng, Zhao-Lei ; Ju, Huai-Qiang ; Xie, Dan ; Zhao, Qi ; Xu, Ruihua</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c460t-6352375deb6a51d083d04fb1edffe24e634d5c4900871d910c79f51143248a283</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wu, Qi-Nian</creatorcontrib><creatorcontrib>Luo, Xiao-Jing</creatorcontrib><creatorcontrib>Liu, Jia</creatorcontrib><creatorcontrib>Lu, Yun-Xin</creatorcontrib><creatorcontrib>Wang, Yun</creatorcontrib><creatorcontrib>Qi, Jingjing</creatorcontrib><creatorcontrib>Liu, Ze-Xian</creatorcontrib><creatorcontrib>Huang, Qi-Tao</creatorcontrib><creatorcontrib>Liu, Ze-Kun</creatorcontrib><creatorcontrib>Lu, Jia-Bin</creatorcontrib><creatorcontrib>Jin, Ying</creatorcontrib><creatorcontrib>Pu, Heng-Ying</creatorcontrib><creatorcontrib>Hu, Pei-Shan</creatorcontrib><creatorcontrib>Zheng, Jia-Bo</creatorcontrib><creatorcontrib>Zeng, Zhao-Lei</creatorcontrib><creatorcontrib>Ju, Huai-Qiang</creatorcontrib><creatorcontrib>Xie, Dan</creatorcontrib><creatorcontrib>Zhao, Qi</creatorcontrib><creatorcontrib>Xu, Ruihua</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Cancer research (Chicago, Ill.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wu, Qi-Nian</au><au>Luo, Xiao-Jing</au><au>Liu, Jia</au><au>Lu, Yun-Xin</au><au>Wang, Yun</au><au>Qi, Jingjing</au><au>Liu, Ze-Xian</au><au>Huang, Qi-Tao</au><au>Liu, Ze-Kun</au><au>Lu, Jia-Bin</au><au>Jin, Ying</au><au>Pu, Heng-Ying</au><au>Hu, Pei-Shan</au><au>Zheng, Jia-Bo</au><au>Zeng, Zhao-Lei</au><au>Ju, Huai-Qiang</au><au>Xie, Dan</au><au>Zhao, Qi</au><au>Xu, Ruihua</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>MYC-Activated LncRNA MNX1-AS1 Promotes the Progression of Colorectal Cancer by Stabilizing YB1</atitle><jtitle>Cancer research (Chicago, Ill.)</jtitle><addtitle>Cancer Res</addtitle><date>2021-05-15</date><risdate>2021</risdate><volume>81</volume><issue>10</issue><spage>2636</spage><epage>2650</epage><pages>2636-2650</pages><issn>0008-5472</issn><eissn>1538-7445</eissn><abstract>Long noncoding RNAs (lncRNA) are involved in tumorigenesis and drug resistance. However, the roles and underlying mechanisms of lncRNAs in colorectal cancer are still unknown. In this work, through transcriptomic profiling analysis of 21 paired tumor and normal samples, we identified a novel colorectal cancer-related lncRNA, . - expression was significantly upregulated in colorectal cancer and associated with poor prognosis. and gain- and loss-of-function experiments showed that - promotes the proliferation of colorectal cancer cells. - bound to and activated Y-box-binding protein 1 (YB1), a multifunctional RNA/DNA-binding protein, and prevented its ubiquitination and degradation. A marked overlap between genes that are differentially expressed in - knockdown cells and transcriptional targets of YB1 was observed. YB1 knockdown mimicked the loss of viability phenotype observed upon depletion of - . In addition, MYC bound the promoter of the - locus and activated its transcription. experiments showed that ASO inhibited - , which suppressed the proliferation of colorectal cancer cells in both cell-based and patient-derived xenograft models. Collectively, these findings suggest that the MYC- -YB1 axis might serve as a potential biomarker and therapeutic target in colorectal cancer. SIGNIFICANCE: This study highlights the discovery of a novel colorectal cancer biomarker and therapeutic target, - , a long noncoding RNA that drives proliferation via a MYC/ /YB1 signaling pathway. GRAPHICAL ABSTRACT: http://cancerres.aacrjournals.org/content/canres/81/10/2636/F1.large.jpg.</abstract><cop>United States</cop><pmid>33782099</pmid><doi>10.1158/0008-5472.CAN-20-3747</doi><tpages>15</tpages><orcidid>https://orcid.org/0000-0002-8683-6145</orcidid><orcidid>https://orcid.org/0000-0001-9698-0610</orcidid><orcidid>https://orcid.org/0000-0003-4420-5625</orcidid><orcidid>https://orcid.org/0000-0003-1713-5465</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0008-5472
ispartof Cancer research (Chicago, Ill.), 2021-05, Vol.81 (10), p.2636-2650
issn 0008-5472
1538-7445
language eng
recordid cdi_proquest_miscellaneous_2507146213
source American Association for Cancer Research; EZB Electronic Journals Library
title MYC-Activated LncRNA MNX1-AS1 Promotes the Progression of Colorectal Cancer by Stabilizing YB1
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-07T18%3A46%3A22IST&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=MYC-Activated%20LncRNA%20MNX1-AS1%20Promotes%20the%20Progression%20of%20Colorectal%20Cancer%20by%20Stabilizing%20YB1&rft.jtitle=Cancer%20research%20(Chicago,%20Ill.)&rft.au=Wu,%20Qi-Nian&rft.date=2021-05-15&rft.volume=81&rft.issue=10&rft.spage=2636&rft.epage=2650&rft.pages=2636-2650&rft.issn=0008-5472&rft.eissn=1538-7445&rft_id=info:doi/10.1158/0008-5472.CAN-20-3747&rft_dat=%3Cproquest_cross%3E2507146213%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=2507146213&rft_id=info:pmid/33782099&rfr_iscdi=true