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MYC Targeted Long Noncoding RNA DANCR Promotes Cancer in Part by Reducing p21 Levels
The MYC oncogene broadly promotes transcription mediated by all nuclear RNA polymerases, thereby acting as a positive modifier of global gene expression. Here, we report that MYC stimulates the transcription of DANCR, a long noncoding RNA (lncRNA) that is widely overexpressed in human cancer. We ide...
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Published in: | Cancer research (Chicago, Ill.) Ill.), 2018-01, Vol.78 (1), p.64-74 |
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creator | Lu, Yunqi Hu, Zhongyi Mangala, Lingegowda S Stine, Zachary E Hu, Xiaowen Jiang, Dahai Xiang, Yan Zhang, Youyou Pradeep, Sunila Rodriguez-Aguayo, Cristian Lopez-Berestein, Gabriel DeMarzo, Angelo M Sood, Anil K Zhang, Lin Dang, Chi V |
description | The MYC oncogene broadly promotes transcription mediated by all nuclear RNA polymerases, thereby acting as a positive modifier of global gene expression. Here, we report that MYC stimulates the transcription of DANCR, a long noncoding RNA (lncRNA) that is widely overexpressed in human cancer. We identified DANCR through its overexpression in a transgenic model of MYC-induced lymphoma, but found that it was broadly upregulated in many human cancer cell lines and cancers, including most notably in prostate and ovarian cancers. Mechanistic investigations indicated that DANCR limited the expression of cell-cycle inhibitor p21 (CDKN1A) and that the inhibitory effects of DANCR loss on cell proliferation could be partially rescued by p21 silencing. In a xenograft model of human ovarian cancer, a nanoparticle-mediated siRNA strategy to target DANCR
was sufficient to strongly inhibit tumor growth. Our observations expand knowledge of how MYC drives cancer cell proliferation by identifying DANCR as a critical lncRNA widely overexpressed in human cancers.
These findings expand knowledge of how MYC drives cancer cell proliferation by identifying an oncogenic long noncoding RNA that is widely overexpressed in human cancers.
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doi_str_mv | 10.1158/0008-5472.can-17-0815 |
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was sufficient to strongly inhibit tumor growth. Our observations expand knowledge of how MYC drives cancer cell proliferation by identifying DANCR as a critical lncRNA widely overexpressed in human cancers.
These findings expand knowledge of how MYC drives cancer cell proliferation by identifying an oncogenic long noncoding RNA that is widely overexpressed in human cancers.
.</description><identifier>ISSN: 0008-5472</identifier><identifier>EISSN: 1538-7445</identifier><identifier>DOI: 10.1158/0008-5472.can-17-0815</identifier><identifier>PMID: 29180471</identifier><language>eng</language><publisher>United States: American Association for Cancer Research, Inc</publisher><subject>Animals ; Cell growth ; Cell Line, Tumor ; Cell proliferation ; Cyclin-dependent kinase inhibitor p21 ; Cyclin-Dependent Kinase Inhibitor p21 - genetics ; Cyclin-Dependent Kinase Inhibitor p21 - metabolism ; Female ; Gene expression ; Gene Expression Regulation, Neoplastic ; Genes, myc ; Humans ; Lymphoma ; Lymphoma, B-Cell - genetics ; Lymphoma, B-Cell - pathology ; Male ; Mice, Nude ; Myc protein ; Nanoparticles ; Ovarian cancer ; Ovarian carcinoma ; Ovarian Neoplasms - genetics ; Ovarian Neoplasms - pathology ; Prostate ; Prostatic Neoplasms - genetics ; Prostatic Neoplasms - pathology ; RNA, Long Noncoding - genetics ; siRNA ; Transcription ; Tumor cell lines ; Xenograft Model Antitumor Assays ; Xenografts</subject><ispartof>Cancer research (Chicago, Ill.), 2018-01, Vol.78 (1), p.64-74</ispartof><rights>2017 American Association for Cancer Research.</rights><rights>Copyright American Association for Cancer Research, Inc. Jan 1, 2018</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c450t-dfd02b21f61b27a9acdf28cb8d6ef9544150e77c61184a789391de12438e396c3</citedby><cites>FETCH-LOGICAL-c450t-dfd02b21f61b27a9acdf28cb8d6ef9544150e77c61184a789391de12438e396c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29180471$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lu, Yunqi</creatorcontrib><creatorcontrib>Hu, Zhongyi</creatorcontrib><creatorcontrib>Mangala, Lingegowda S</creatorcontrib><creatorcontrib>Stine, Zachary E</creatorcontrib><creatorcontrib>Hu, Xiaowen</creatorcontrib><creatorcontrib>Jiang, Dahai</creatorcontrib><creatorcontrib>Xiang, Yan</creatorcontrib><creatorcontrib>Zhang, Youyou</creatorcontrib><creatorcontrib>Pradeep, Sunila</creatorcontrib><creatorcontrib>Rodriguez-Aguayo, Cristian</creatorcontrib><creatorcontrib>Lopez-Berestein, Gabriel</creatorcontrib><creatorcontrib>DeMarzo, Angelo M</creatorcontrib><creatorcontrib>Sood, Anil K</creatorcontrib><creatorcontrib>Zhang, Lin</creatorcontrib><creatorcontrib>Dang, Chi V</creatorcontrib><title>MYC Targeted Long Noncoding RNA DANCR Promotes Cancer in Part by Reducing p21 Levels</title><title>Cancer research (Chicago, Ill.)</title><addtitle>Cancer Res</addtitle><description>The MYC oncogene broadly promotes transcription mediated by all nuclear RNA polymerases, thereby acting as a positive modifier of global gene expression. Here, we report that MYC stimulates the transcription of DANCR, a long noncoding RNA (lncRNA) that is widely overexpressed in human cancer. We identified DANCR through its overexpression in a transgenic model of MYC-induced lymphoma, but found that it was broadly upregulated in many human cancer cell lines and cancers, including most notably in prostate and ovarian cancers. Mechanistic investigations indicated that DANCR limited the expression of cell-cycle inhibitor p21 (CDKN1A) and that the inhibitory effects of DANCR loss on cell proliferation could be partially rescued by p21 silencing. In a xenograft model of human ovarian cancer, a nanoparticle-mediated siRNA strategy to target DANCR
was sufficient to strongly inhibit tumor growth. Our observations expand knowledge of how MYC drives cancer cell proliferation by identifying DANCR as a critical lncRNA widely overexpressed in human cancers.
These findings expand knowledge of how MYC drives cancer cell proliferation by identifying an oncogenic long noncoding RNA that is widely overexpressed in human cancers.
.</description><subject>Animals</subject><subject>Cell growth</subject><subject>Cell Line, Tumor</subject><subject>Cell proliferation</subject><subject>Cyclin-dependent kinase inhibitor p21</subject><subject>Cyclin-Dependent Kinase Inhibitor p21 - genetics</subject><subject>Cyclin-Dependent Kinase Inhibitor p21 - metabolism</subject><subject>Female</subject><subject>Gene expression</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>Genes, myc</subject><subject>Humans</subject><subject>Lymphoma</subject><subject>Lymphoma, B-Cell - genetics</subject><subject>Lymphoma, B-Cell - pathology</subject><subject>Male</subject><subject>Mice, Nude</subject><subject>Myc protein</subject><subject>Nanoparticles</subject><subject>Ovarian cancer</subject><subject>Ovarian carcinoma</subject><subject>Ovarian Neoplasms - genetics</subject><subject>Ovarian Neoplasms - pathology</subject><subject>Prostate</subject><subject>Prostatic Neoplasms - genetics</subject><subject>Prostatic Neoplasms - pathology</subject><subject>RNA, Long Noncoding - genetics</subject><subject>siRNA</subject><subject>Transcription</subject><subject>Tumor cell lines</subject><subject>Xenograft Model Antitumor Assays</subject><subject>Xenografts</subject><issn>0008-5472</issn><issn>1538-7445</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNpdkE1rGzEQhkVpSJyPn9Ai6KWXdTRaaSUdzaZtAo4TjHvoSWil2eBgr1xpt5B_n12c5pDTzMDzvgwPIV-AzQGkvmaM6UIKxefedQWogmmQn8gMZKkLJYT8TGbvzBk5z_l5PCUweUrOuAHNhIIZ2dz_qenGpSfsMdBl7J7oKnY-hu24rVcLerNY1Wv6mOI-9php7TqPiW47-uhST5sXusYw-Ik-cKBL_Ie7fElOWrfLePU2L8jvnz829W2xfPh1Vy-WhReS9UVoA-MNh7aChitnnA8t177RocLWSCFAMlTKVwBaOKVNaSAgcFFqLE3lywvy_dh7SPHvgLm3-232uNu5DuOQLZjKmLJkWo_otw_ocxxSN35nOWOV1hqqaqTkkfIp5pywtYe03bv0YoHZSbudlNpJqa0XKwvKTtrH3Ne39qHZY3hP_fdcvgIcqnqD</recordid><startdate>20180101</startdate><enddate>20180101</enddate><creator>Lu, Yunqi</creator><creator>Hu, Zhongyi</creator><creator>Mangala, Lingegowda S</creator><creator>Stine, Zachary E</creator><creator>Hu, Xiaowen</creator><creator>Jiang, Dahai</creator><creator>Xiang, Yan</creator><creator>Zhang, Youyou</creator><creator>Pradeep, Sunila</creator><creator>Rodriguez-Aguayo, Cristian</creator><creator>Lopez-Berestein, Gabriel</creator><creator>DeMarzo, Angelo M</creator><creator>Sood, Anil K</creator><creator>Zhang, Lin</creator><creator>Dang, Chi V</creator><general>American Association for Cancer Research, 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>7T5</scope><scope>7TM</scope><scope>7TO</scope><scope>7U9</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>20180101</creationdate><title>MYC Targeted Long Noncoding RNA DANCR Promotes Cancer in Part by Reducing p21 Levels</title><author>Lu, Yunqi ; Hu, Zhongyi ; Mangala, Lingegowda S ; Stine, Zachary E ; Hu, Xiaowen ; Jiang, Dahai ; Xiang, Yan ; Zhang, Youyou ; Pradeep, Sunila ; Rodriguez-Aguayo, Cristian ; Lopez-Berestein, Gabriel ; DeMarzo, Angelo M ; Sood, Anil K ; Zhang, Lin ; Dang, Chi V</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c450t-dfd02b21f61b27a9acdf28cb8d6ef9544150e77c61184a789391de12438e396c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Animals</topic><topic>Cell growth</topic><topic>Cell Line, Tumor</topic><topic>Cell proliferation</topic><topic>Cyclin-dependent kinase inhibitor p21</topic><topic>Cyclin-Dependent Kinase Inhibitor p21 - genetics</topic><topic>Cyclin-Dependent Kinase Inhibitor p21 - metabolism</topic><topic>Female</topic><topic>Gene expression</topic><topic>Gene Expression Regulation, Neoplastic</topic><topic>Genes, myc</topic><topic>Humans</topic><topic>Lymphoma</topic><topic>Lymphoma, B-Cell - genetics</topic><topic>Lymphoma, B-Cell - pathology</topic><topic>Male</topic><topic>Mice, Nude</topic><topic>Myc protein</topic><topic>Nanoparticles</topic><topic>Ovarian cancer</topic><topic>Ovarian carcinoma</topic><topic>Ovarian Neoplasms - genetics</topic><topic>Ovarian Neoplasms - pathology</topic><topic>Prostate</topic><topic>Prostatic Neoplasms - genetics</topic><topic>Prostatic Neoplasms - pathology</topic><topic>RNA, Long Noncoding - genetics</topic><topic>siRNA</topic><topic>Transcription</topic><topic>Tumor cell lines</topic><topic>Xenograft Model Antitumor Assays</topic><topic>Xenografts</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lu, Yunqi</creatorcontrib><creatorcontrib>Hu, Zhongyi</creatorcontrib><creatorcontrib>Mangala, Lingegowda S</creatorcontrib><creatorcontrib>Stine, Zachary E</creatorcontrib><creatorcontrib>Hu, Xiaowen</creatorcontrib><creatorcontrib>Jiang, Dahai</creatorcontrib><creatorcontrib>Xiang, Yan</creatorcontrib><creatorcontrib>Zhang, Youyou</creatorcontrib><creatorcontrib>Pradeep, Sunila</creatorcontrib><creatorcontrib>Rodriguez-Aguayo, Cristian</creatorcontrib><creatorcontrib>Lopez-Berestein, Gabriel</creatorcontrib><creatorcontrib>DeMarzo, Angelo M</creatorcontrib><creatorcontrib>Sood, Anil K</creatorcontrib><creatorcontrib>Zhang, Lin</creatorcontrib><creatorcontrib>Dang, Chi V</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Cancer research (Chicago, Ill.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lu, Yunqi</au><au>Hu, Zhongyi</au><au>Mangala, Lingegowda S</au><au>Stine, Zachary E</au><au>Hu, Xiaowen</au><au>Jiang, Dahai</au><au>Xiang, Yan</au><au>Zhang, Youyou</au><au>Pradeep, Sunila</au><au>Rodriguez-Aguayo, Cristian</au><au>Lopez-Berestein, Gabriel</au><au>DeMarzo, Angelo M</au><au>Sood, Anil K</au><au>Zhang, Lin</au><au>Dang, Chi V</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>MYC Targeted Long Noncoding RNA DANCR Promotes Cancer in Part by Reducing p21 Levels</atitle><jtitle>Cancer research (Chicago, Ill.)</jtitle><addtitle>Cancer Res</addtitle><date>2018-01-01</date><risdate>2018</risdate><volume>78</volume><issue>1</issue><spage>64</spage><epage>74</epage><pages>64-74</pages><issn>0008-5472</issn><eissn>1538-7445</eissn><abstract>The MYC oncogene broadly promotes transcription mediated by all nuclear RNA polymerases, thereby acting as a positive modifier of global gene expression. Here, we report that MYC stimulates the transcription of DANCR, a long noncoding RNA (lncRNA) that is widely overexpressed in human cancer. We identified DANCR through its overexpression in a transgenic model of MYC-induced lymphoma, but found that it was broadly upregulated in many human cancer cell lines and cancers, including most notably in prostate and ovarian cancers. Mechanistic investigations indicated that DANCR limited the expression of cell-cycle inhibitor p21 (CDKN1A) and that the inhibitory effects of DANCR loss on cell proliferation could be partially rescued by p21 silencing. In a xenograft model of human ovarian cancer, a nanoparticle-mediated siRNA strategy to target DANCR
was sufficient to strongly inhibit tumor growth. Our observations expand knowledge of how MYC drives cancer cell proliferation by identifying DANCR as a critical lncRNA widely overexpressed in human cancers.
These findings expand knowledge of how MYC drives cancer cell proliferation by identifying an oncogenic long noncoding RNA that is widely overexpressed in human cancers.
.</abstract><cop>United States</cop><pub>American Association for Cancer Research, Inc</pub><pmid>29180471</pmid><doi>10.1158/0008-5472.can-17-0815</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Cell growth Cell Line, Tumor Cell proliferation Cyclin-dependent kinase inhibitor p21 Cyclin-Dependent Kinase Inhibitor p21 - genetics Cyclin-Dependent Kinase Inhibitor p21 - metabolism Female Gene expression Gene Expression Regulation, Neoplastic Genes, myc Humans Lymphoma Lymphoma, B-Cell - genetics Lymphoma, B-Cell - pathology Male Mice, Nude Myc protein Nanoparticles Ovarian cancer Ovarian carcinoma Ovarian Neoplasms - genetics Ovarian Neoplasms - pathology Prostate Prostatic Neoplasms - genetics Prostatic Neoplasms - pathology RNA, Long Noncoding - genetics siRNA Transcription Tumor cell lines Xenograft Model Antitumor Assays Xenografts |
title | MYC Targeted Long Noncoding RNA DANCR Promotes Cancer in Part by Reducing p21 Levels |
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