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Long noncoding RNA DANCR promotes colorectal cancer proliferation and metastasis via miR-577 sponging
Long non-coding RNAs (lncRNAs) play key roles in various malignant tumors, including colorectal cancer (CRC). Long non-coding RNA differentiation antagonizing non-protein coding RNA (DANCR) is overexpressed in CRC patients, but whether it affects CRC proliferation and metastasis via regulation of he...
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Published in: | Experimental & molecular medicine 2018, 50(0), , pp.1-17 |
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description | Long non-coding RNAs (lncRNAs) play key roles in various malignant tumors, including colorectal cancer (CRC). Long non-coding RNA differentiation antagonizing non-protein coding RNA (DANCR) is overexpressed in CRC patients, but whether it affects CRC proliferation and metastasis via regulation of heat shock protein 27 (HSP27) remains unclear. In the present study, we found that DANCR was highly expressed and correlated with proliferation and metastasis in CRC. In addition, we demonstrated that DANCR and HSP27 were both targets of microRNA-577 (miR-577) and shared the same binding site. Furthermore, we revealed that DANCR promoted HSP27 expression and its mediation of proliferation/metastasis via miR-577 sponging. Finally, using an in vivo study, we confirmed that overexpression of DANCR promoted CRC tumor growth and liver metastasis. The present study demonstrated the function of DANCR in CRC and might provide a new target in the treatment of CRC.
Colorectal cancer: Long non-coding RNA offers new drug target
A long non-coding RNA linked to colorectal cancer causes tumor progression by unleashing the activity of a protein involved in cell proliferation and spread. Researchers in China led by Xiandong Zeng from Shenyang Medical College explain why the expression of a long non-coding RNA molecule known as DANCR correlates with poor prognosis in patients and mouse models carrying colorectal cancer tissue. They showed that DANCR displaces a small regulatory microRNA from its normal binding spot on the gene transcript that encodes HSP27, a protein involved in the growth and metastasis of colorectal cancer cells. This microRNA normally suppresses HSP27 activity, whereas DANCR, by outcompeting the microRNA, promotes HSP27 expression, leading to cell proliferation and metastasis. Drugs that block DANCR could thus help treat the disease. |
doi_str_mv | 10.1038/s12276-018-0082-5 |
format | article |
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Colorectal cancer: Long non-coding RNA offers new drug target
A long non-coding RNA linked to colorectal cancer causes tumor progression by unleashing the activity of a protein involved in cell proliferation and spread. Researchers in China led by Xiandong Zeng from Shenyang Medical College explain why the expression of a long non-coding RNA molecule known as DANCR correlates with poor prognosis in patients and mouse models carrying colorectal cancer tissue. They showed that DANCR displaces a small regulatory microRNA from its normal binding spot on the gene transcript that encodes HSP27, a protein involved in the growth and metastasis of colorectal cancer cells. This microRNA normally suppresses HSP27 activity, whereas DANCR, by outcompeting the microRNA, promotes HSP27 expression, leading to cell proliferation and metastasis. Drugs that block DANCR could thus help treat the disease.</description><identifier>ISSN: 1226-3613</identifier><identifier>EISSN: 2092-6413</identifier><identifier>DOI: 10.1038/s12276-018-0082-5</identifier><identifier>PMID: 29717105</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>42/41 ; 631/337/384/2568 ; 631/67/395 ; Animals ; Base Sequence ; Binding sites ; Biomedical and Life Sciences ; Biomedicine ; Cell Line, Tumor ; Cell Proliferation - genetics ; Colorectal cancer ; Colorectal carcinoma ; Colorectal Neoplasms - genetics ; Colorectal Neoplasms - pathology ; Female ; Gene Expression Regulation, Neoplastic ; Heat shock proteins ; HSP27 Heat-Shock Proteins - metabolism ; Hsp27 protein ; Humans ; Liver ; Male ; Medical Biochemistry ; Metastases ; Metastasis ; Mice, Inbred NOD ; Mice, SCID ; MicroRNAs - genetics ; MicroRNAs - metabolism ; Middle Aged ; miRNA ; Models, Biological ; Molecular Chaperones ; Molecular Medicine ; Neoplasm Metastasis ; Non-coding RNA ; Prognosis ; RNA, Long Noncoding - genetics ; RNA, Long Noncoding - metabolism ; Stem Cells ; Tumors ; Up-Regulation - genetics ; 생화학</subject><ispartof>Experimental and Molecular Medicine, 2018, 50(0), , pp.1-17</ispartof><rights>The Author(s) 2018</rights><rights>2018. This work is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c570t-82766f575e97bacf02e2fb06c806bb3aaf5ce79a057419849029da1921aa5b793</citedby><cites>FETCH-LOGICAL-c570t-82766f575e97bacf02e2fb06c806bb3aaf5ce79a057419849029da1921aa5b793</cites><orcidid>0000-0003-0593-4147</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2036413772/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2036413772?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29717105$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://www.kci.go.kr/kciportal/ci/sereArticleSearch/ciSereArtiView.kci?sereArticleSearchBean.artiId=ART002347994$$DAccess content in National Research Foundation of Korea (NRF)$$Hfree_for_read</backlink></links><search><creatorcontrib>Wang, Yong</creatorcontrib><creatorcontrib>Lu, Zhi</creatorcontrib><creatorcontrib>Wang, Ningnin</creatorcontrib><creatorcontrib>Feng, Jianzhou</creatorcontrib><creatorcontrib>Zhang, Junjie</creatorcontrib><creatorcontrib>Luan, Lan</creatorcontrib><creatorcontrib>Zhao, Wei</creatorcontrib><creatorcontrib>Zeng, Xiandong</creatorcontrib><title>Long noncoding RNA DANCR promotes colorectal cancer proliferation and metastasis via miR-577 sponging</title><title>Experimental & molecular medicine</title><addtitle>Exp Mol Med</addtitle><addtitle>Exp Mol Med</addtitle><description>Long non-coding RNAs (lncRNAs) play key roles in various malignant tumors, including colorectal cancer (CRC). Long non-coding RNA differentiation antagonizing non-protein coding RNA (DANCR) is overexpressed in CRC patients, but whether it affects CRC proliferation and metastasis via regulation of heat shock protein 27 (HSP27) remains unclear. In the present study, we found that DANCR was highly expressed and correlated with proliferation and metastasis in CRC. In addition, we demonstrated that DANCR and HSP27 were both targets of microRNA-577 (miR-577) and shared the same binding site. Furthermore, we revealed that DANCR promoted HSP27 expression and its mediation of proliferation/metastasis via miR-577 sponging. Finally, using an in vivo study, we confirmed that overexpression of DANCR promoted CRC tumor growth and liver metastasis. The present study demonstrated the function of DANCR in CRC and might provide a new target in the treatment of CRC.
Colorectal cancer: Long non-coding RNA offers new drug target
A long non-coding RNA linked to colorectal cancer causes tumor progression by unleashing the activity of a protein involved in cell proliferation and spread. Researchers in China led by Xiandong Zeng from Shenyang Medical College explain why the expression of a long non-coding RNA molecule known as DANCR correlates with poor prognosis in patients and mouse models carrying colorectal cancer tissue. They showed that DANCR displaces a small regulatory microRNA from its normal binding spot on the gene transcript that encodes HSP27, a protein involved in the growth and metastasis of colorectal cancer cells. This microRNA normally suppresses HSP27 activity, whereas DANCR, by outcompeting the microRNA, promotes HSP27 expression, leading to cell proliferation and metastasis. Drugs that block DANCR could thus help treat the disease.</description><subject>42/41</subject><subject>631/337/384/2568</subject><subject>631/67/395</subject><subject>Animals</subject><subject>Base Sequence</subject><subject>Binding sites</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Cell Line, Tumor</subject><subject>Cell Proliferation - genetics</subject><subject>Colorectal cancer</subject><subject>Colorectal carcinoma</subject><subject>Colorectal Neoplasms - genetics</subject><subject>Colorectal Neoplasms - pathology</subject><subject>Female</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>Heat shock proteins</subject><subject>HSP27 Heat-Shock Proteins - metabolism</subject><subject>Hsp27 protein</subject><subject>Humans</subject><subject>Liver</subject><subject>Male</subject><subject>Medical Biochemistry</subject><subject>Metastases</subject><subject>Metastasis</subject><subject>Mice, Inbred NOD</subject><subject>Mice, SCID</subject><subject>MicroRNAs - genetics</subject><subject>MicroRNAs - metabolism</subject><subject>Middle Aged</subject><subject>miRNA</subject><subject>Models, Biological</subject><subject>Molecular Chaperones</subject><subject>Molecular Medicine</subject><subject>Neoplasm Metastasis</subject><subject>Non-coding RNA</subject><subject>Prognosis</subject><subject>RNA, Long Noncoding - genetics</subject><subject>RNA, Long Noncoding - metabolism</subject><subject>Stem Cells</subject><subject>Tumors</subject><subject>Up-Regulation - genetics</subject><subject>생화학</subject><issn>1226-3613</issn><issn>2092-6413</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNp1kl1rFDEUhgdR7Fr9Ad5IwJt6MZrPyeRGWFZbF5YKS70OZzKZNduZZE1mC_57Mzu1WkEInJDznDfnJG9RvCb4PcGs_pAIpbIqMalLjGtaiifFgmJFy4oT9rRY5HRVsoqws-JFSnuMqeCSPy_OqJJEEiwWhd0Ev0M-eBNal3fb6yX6tLxebdEhhiGMNiET-hCtGaFHBryxcUr1rrMRRhc8At-iwY6Q8nIJ3TlAg9uWQkqUDlk9y74snnXQJ_vqPp4X3y4_36y-lJuvV-vVclMaIfFY1nmaqhNSWCUbMB2mlnYNrkyNq6ZhAJ0wVirAQnKiaq4wVS0QRQmAaKRi58W7WdfHTt8apwO4U9wFfRv1cnuz1pyTqhZ1Ztcz2wbY60N0A8Sfp4LTQYg7DXF0preaEiFJC9Rw6LhocVNNXVVM5Rk5Jm3W-jhrHY7NYFtj_RihfyT6OOPd99zTnRaK1ZhMjV_cC8Tw42jTqAeXjO178DYck6aYMSYVxzSjb_9B9-EYfX7WiZp-XsqJIjNlYkgp2u6hGYL1ZB49m0dn8-jJPFrkmjd_T_FQ8dstGaAzkHLK72z8c_X_VX8BhSTNpA</recordid><startdate>20180501</startdate><enddate>20180501</enddate><creator>Wang, Yong</creator><creator>Lu, Zhi</creator><creator>Wang, Ningnin</creator><creator>Feng, Jianzhou</creator><creator>Zhang, Junjie</creator><creator>Luan, Lan</creator><creator>Zhao, Wei</creator><creator>Zeng, Xiandong</creator><general>Nature Publishing Group UK</general><general>Springer Nature B.V</general><general>Nature Publishing Group</general><general>생화학분자생물학회</general><scope>C6C</scope><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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</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><scope>ACYCR</scope><orcidid>https://orcid.org/0000-0003-0593-4147</orcidid></search><sort><creationdate>20180501</creationdate><title>Long noncoding RNA DANCR promotes colorectal cancer proliferation and metastasis via miR-577 sponging</title><author>Wang, Yong ; Lu, Zhi ; Wang, Ningnin ; Feng, Jianzhou ; Zhang, Junjie ; Luan, Lan ; Zhao, Wei ; Zeng, Xiandong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c570t-82766f575e97bacf02e2fb06c806bb3aaf5ce79a057419849029da1921aa5b793</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>42/41</topic><topic>631/337/384/2568</topic><topic>631/67/395</topic><topic>Animals</topic><topic>Base Sequence</topic><topic>Binding sites</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Cell Line, Tumor</topic><topic>Cell Proliferation - genetics</topic><topic>Colorectal cancer</topic><topic>Colorectal carcinoma</topic><topic>Colorectal Neoplasms - genetics</topic><topic>Colorectal Neoplasms - pathology</topic><topic>Female</topic><topic>Gene Expression Regulation, Neoplastic</topic><topic>Heat shock proteins</topic><topic>HSP27 Heat-Shock Proteins - metabolism</topic><topic>Hsp27 protein</topic><topic>Humans</topic><topic>Liver</topic><topic>Male</topic><topic>Medical Biochemistry</topic><topic>Metastases</topic><topic>Metastasis</topic><topic>Mice, Inbred NOD</topic><topic>Mice, SCID</topic><topic>MicroRNAs - genetics</topic><topic>MicroRNAs - metabolism</topic><topic>Middle Aged</topic><topic>miRNA</topic><topic>Models, Biological</topic><topic>Molecular Chaperones</topic><topic>Molecular Medicine</topic><topic>Neoplasm Metastasis</topic><topic>Non-coding RNA</topic><topic>Prognosis</topic><topic>RNA, Long Noncoding - genetics</topic><topic>RNA, Long Noncoding - metabolism</topic><topic>Stem Cells</topic><topic>Tumors</topic><topic>Up-Regulation - genetics</topic><topic>생화학</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Yong</creatorcontrib><creatorcontrib>Lu, Zhi</creatorcontrib><creatorcontrib>Wang, Ningnin</creatorcontrib><creatorcontrib>Feng, Jianzhou</creatorcontrib><creatorcontrib>Zhang, Junjie</creatorcontrib><creatorcontrib>Luan, Lan</creatorcontrib><creatorcontrib>Zhao, Wei</creatorcontrib><creatorcontrib>Zeng, Xiandong</creatorcontrib><collection>SpringerOpen</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</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>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>ProQuest Natural Science Collection</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>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biological Sciences</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest Biological Science Journals</collection><collection>Publicly Available Content Database</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><collection>Korean Citation Index</collection><jtitle>Experimental & molecular medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Yong</au><au>Lu, Zhi</au><au>Wang, Ningnin</au><au>Feng, Jianzhou</au><au>Zhang, Junjie</au><au>Luan, Lan</au><au>Zhao, Wei</au><au>Zeng, Xiandong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Long noncoding RNA DANCR promotes colorectal cancer proliferation and metastasis via miR-577 sponging</atitle><jtitle>Experimental & molecular medicine</jtitle><stitle>Exp Mol Med</stitle><addtitle>Exp Mol Med</addtitle><date>2018-05-01</date><risdate>2018</risdate><volume>50</volume><issue>5</issue><spage>1</spage><epage>17</epage><pages>1-17</pages><issn>1226-3613</issn><eissn>2092-6413</eissn><abstract>Long non-coding RNAs (lncRNAs) play key roles in various malignant tumors, including colorectal cancer (CRC). Long non-coding RNA differentiation antagonizing non-protein coding RNA (DANCR) is overexpressed in CRC patients, but whether it affects CRC proliferation and metastasis via regulation of heat shock protein 27 (HSP27) remains unclear. In the present study, we found that DANCR was highly expressed and correlated with proliferation and metastasis in CRC. In addition, we demonstrated that DANCR and HSP27 were both targets of microRNA-577 (miR-577) and shared the same binding site. Furthermore, we revealed that DANCR promoted HSP27 expression and its mediation of proliferation/metastasis via miR-577 sponging. Finally, using an in vivo study, we confirmed that overexpression of DANCR promoted CRC tumor growth and liver metastasis. The present study demonstrated the function of DANCR in CRC and might provide a new target in the treatment of CRC.
Colorectal cancer: Long non-coding RNA offers new drug target
A long non-coding RNA linked to colorectal cancer causes tumor progression by unleashing the activity of a protein involved in cell proliferation and spread. Researchers in China led by Xiandong Zeng from Shenyang Medical College explain why the expression of a long non-coding RNA molecule known as DANCR correlates with poor prognosis in patients and mouse models carrying colorectal cancer tissue. They showed that DANCR displaces a small regulatory microRNA from its normal binding spot on the gene transcript that encodes HSP27, a protein involved in the growth and metastasis of colorectal cancer cells. This microRNA normally suppresses HSP27 activity, whereas DANCR, by outcompeting the microRNA, promotes HSP27 expression, leading to cell proliferation and metastasis. Drugs that block DANCR could thus help treat the disease.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>29717105</pmid><doi>10.1038/s12276-018-0082-5</doi><tpages>17</tpages><orcidid>https://orcid.org/0000-0003-0593-4147</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | 42/41 631/337/384/2568 631/67/395 Animals Base Sequence Binding sites Biomedical and Life Sciences Biomedicine Cell Line, Tumor Cell Proliferation - genetics Colorectal cancer Colorectal carcinoma Colorectal Neoplasms - genetics Colorectal Neoplasms - pathology Female Gene Expression Regulation, Neoplastic Heat shock proteins HSP27 Heat-Shock Proteins - metabolism Hsp27 protein Humans Liver Male Medical Biochemistry Metastases Metastasis Mice, Inbred NOD Mice, SCID MicroRNAs - genetics MicroRNAs - metabolism Middle Aged miRNA Models, Biological Molecular Chaperones Molecular Medicine Neoplasm Metastasis Non-coding RNA Prognosis RNA, Long Noncoding - genetics RNA, Long Noncoding - metabolism Stem Cells Tumors Up-Regulation - genetics 생화학 |
title | Long noncoding RNA DANCR promotes colorectal cancer proliferation and metastasis via miR-577 sponging |
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