Long non-coding RNA NEAT1 promotes non-small cell lung cancer progression through regulation of miR-377-3p-E2F3 pathway
Recently, the long non-coding RNA (lncRNA) NEAT1 has been identified as an oncogenic gene in multiple cancer types and elevated expression of NEAT1 was tightly linked to tumorigenesis and cancer progression. However, the molecular basis for this observation has not been characterized in progression...
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description | Recently, the long non-coding RNA (lncRNA) NEAT1 has been identified as an oncogenic gene in multiple cancer types and elevated expression of NEAT1 was tightly linked to tumorigenesis and cancer progression. However, the molecular basis for this observation has not been characterized in progression of non-small cell lung cancer (NSCLC). In our studies, we identified NEAT1 was highly expressed in patients with NSCLC and was a novel regulator of NSCLC progression. Patients whose tumors had high NEAT1 expression had a shorter overall survival than patients whose tumors had low NEAT1 expression. Further, NEAT1 significantly accelerates NSCLC cell growth and metastasis in vitro and tumor growth in vivo. Additionally, by using bioinformatics study and RNA pull down combined with luciferase reporter assays, we demonstrated that NEAT1 functioned as a competing endogenous RNA (ceRNA) for hsa-miR-377-3p, antagonized its functions and led to the de-repression of its endogenous targets E2F3, which was a core oncogene in promoting NSCLC progression. Taken together, these observations imply that the NEAT1 modulated the expression of E2F3 gene by acting as a ceRNA, which may build up the missing link between the regulatory miRNA network and NSCLC progression. |
doi_str_mv | 10.18632/oncotarget.10108 |
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However, the molecular basis for this observation has not been characterized in progression of non-small cell lung cancer (NSCLC). In our studies, we identified NEAT1 was highly expressed in patients with NSCLC and was a novel regulator of NSCLC progression. Patients whose tumors had high NEAT1 expression had a shorter overall survival than patients whose tumors had low NEAT1 expression. Further, NEAT1 significantly accelerates NSCLC cell growth and metastasis in vitro and tumor growth in vivo. Additionally, by using bioinformatics study and RNA pull down combined with luciferase reporter assays, we demonstrated that NEAT1 functioned as a competing endogenous RNA (ceRNA) for hsa-miR-377-3p, antagonized its functions and led to the de-repression of its endogenous targets E2F3, which was a core oncogene in promoting NSCLC progression. Taken together, these observations imply that the NEAT1 modulated the expression of E2F3 gene by acting as a ceRNA, which may build up the missing link between the regulatory miRNA network and NSCLC progression.</description><identifier>ISSN: 1949-2553</identifier><identifier>EISSN: 1949-2553</identifier><identifier>DOI: 10.18632/oncotarget.10108</identifier><identifier>PMID: 27351135</identifier><language>eng</language><publisher>United States: Impact Journals LLC</publisher><subject>A549 Cells ; Adult ; Aged ; Aged, 80 and over ; Animals ; Carcinoma, Non-Small-Cell Lung - genetics ; Carcinoma, Non-Small-Cell Lung - pathology ; Cell Line, Tumor ; Disease Progression ; E2F3 Transcription Factor - genetics ; E2F3 Transcription Factor - metabolism ; Female ; Gene Expression Regulation, Neoplastic ; Humans ; Lung Neoplasms - genetics ; Lung Neoplasms - pathology ; Male ; Mice ; Mice, Inbred BALB C ; Mice, Nude ; MicroRNAs - genetics ; MicroRNAs - metabolism ; Middle Aged ; Research Paper ; RNA, Long Noncoding - physiology ; Signal Transduction - genetics</subject><ispartof>Oncotarget, 2016-08, Vol.7 (32), p.51784-51814</ispartof><rights>Copyright: © 2016 Sun et al. 2016</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c422t-1d5c3c9ce5812140ff977b1f09d2db3e815bb0166f9ab79bdd82064afb03216d3</citedby><cites>FETCH-LOGICAL-c422t-1d5c3c9ce5812140ff977b1f09d2db3e815bb0166f9ab79bdd82064afb03216d3</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/PMC5239515/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5239515/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27351135$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sun, Chengcao</creatorcontrib><creatorcontrib>Li, Shujun</creatorcontrib><creatorcontrib>Zhang, Feng</creatorcontrib><creatorcontrib>Xi, Yongyong</creatorcontrib><creatorcontrib>Wang, Liang</creatorcontrib><creatorcontrib>Bi, Yongyi</creatorcontrib><creatorcontrib>Li, Dejia</creatorcontrib><title>Long non-coding RNA NEAT1 promotes non-small cell lung cancer progression through regulation of miR-377-3p-E2F3 pathway</title><title>Oncotarget</title><addtitle>Oncotarget</addtitle><description>Recently, the long non-coding RNA (lncRNA) NEAT1 has been identified as an oncogenic gene in multiple cancer types and elevated expression of NEAT1 was tightly linked to tumorigenesis and cancer progression. However, the molecular basis for this observation has not been characterized in progression of non-small cell lung cancer (NSCLC). In our studies, we identified NEAT1 was highly expressed in patients with NSCLC and was a novel regulator of NSCLC progression. Patients whose tumors had high NEAT1 expression had a shorter overall survival than patients whose tumors had low NEAT1 expression. Further, NEAT1 significantly accelerates NSCLC cell growth and metastasis in vitro and tumor growth in vivo. Additionally, by using bioinformatics study and RNA pull down combined with luciferase reporter assays, we demonstrated that NEAT1 functioned as a competing endogenous RNA (ceRNA) for hsa-miR-377-3p, antagonized its functions and led to the de-repression of its endogenous targets E2F3, which was a core oncogene in promoting NSCLC progression. Taken together, these observations imply that the NEAT1 modulated the expression of E2F3 gene by acting as a ceRNA, which may build up the missing link between the regulatory miRNA network and NSCLC progression.</description><subject>A549 Cells</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Animals</subject><subject>Carcinoma, Non-Small-Cell Lung - genetics</subject><subject>Carcinoma, Non-Small-Cell Lung - pathology</subject><subject>Cell Line, Tumor</subject><subject>Disease Progression</subject><subject>E2F3 Transcription Factor - genetics</subject><subject>E2F3 Transcription Factor - metabolism</subject><subject>Female</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>Humans</subject><subject>Lung Neoplasms - genetics</subject><subject>Lung Neoplasms - pathology</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Mice, Nude</subject><subject>MicroRNAs - genetics</subject><subject>MicroRNAs - metabolism</subject><subject>Middle Aged</subject><subject>Research Paper</subject><subject>RNA, Long Noncoding - physiology</subject><subject>Signal Transduction - genetics</subject><issn>1949-2553</issn><issn>1949-2553</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVUW1LwzAQDqI4mfsBfpH-gc5c0rTNF2GMTYUxYczPJU3TF2mTkrSO_Xu7Tee8D3cPd_c8B_cg9AB4CnFIyZPR0nTCFqqbAgYcX6E74AH3CWP0-gKP0MS5TzwEC6KY8Fs0IhFlAJTdod3K6MLTRvvSZNUAN-uZt17MtuC11jSmU-44dY2oa0-qIdX9sCaFlsoedgqrnKuM9rrSmr4oPauKvhbdoWVyr6k2Po0in7b-giyp14qu3In9PbrJRe3U5KeO0cdysZ2_-qv3l7f5bOXLgJDOh4xJKrlULAYCAc5zHkUp5JhnJEupioGlKYYwzLlII55mWUxwGIg8xZRAmNExej7ptn3aqEwq3VlRJ62tGmH3iRFV8n-iqzIpzFfCCOUM2CAAJwFpjXNW5Wcu4ORoRPJnRHI0YuA8Xh49M37fTr8BnlGIRg</recordid><startdate>20160809</startdate><enddate>20160809</enddate><creator>Sun, Chengcao</creator><creator>Li, Shujun</creator><creator>Zhang, Feng</creator><creator>Xi, Yongyong</creator><creator>Wang, Liang</creator><creator>Bi, Yongyi</creator><creator>Li, Dejia</creator><general>Impact Journals LLC</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>5PM</scope></search><sort><creationdate>20160809</creationdate><title>Long non-coding RNA NEAT1 promotes non-small cell lung cancer progression through regulation of miR-377-3p-E2F3 pathway</title><author>Sun, Chengcao ; Li, Shujun ; Zhang, Feng ; Xi, Yongyong ; Wang, Liang ; Bi, Yongyi ; Li, Dejia</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c422t-1d5c3c9ce5812140ff977b1f09d2db3e815bb0166f9ab79bdd82064afb03216d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>A549 Cells</topic><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Animals</topic><topic>Carcinoma, Non-Small-Cell Lung - genetics</topic><topic>Carcinoma, Non-Small-Cell Lung - pathology</topic><topic>Cell Line, Tumor</topic><topic>Disease Progression</topic><topic>E2F3 Transcription Factor - genetics</topic><topic>E2F3 Transcription Factor - metabolism</topic><topic>Female</topic><topic>Gene Expression Regulation, Neoplastic</topic><topic>Humans</topic><topic>Lung Neoplasms - genetics</topic><topic>Lung Neoplasms - pathology</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Mice, Nude</topic><topic>MicroRNAs - genetics</topic><topic>MicroRNAs - metabolism</topic><topic>Middle Aged</topic><topic>Research Paper</topic><topic>RNA, Long Noncoding - physiology</topic><topic>Signal Transduction - genetics</topic><toplevel>online_resources</toplevel><creatorcontrib>Sun, Chengcao</creatorcontrib><creatorcontrib>Li, Shujun</creatorcontrib><creatorcontrib>Zhang, Feng</creatorcontrib><creatorcontrib>Xi, Yongyong</creatorcontrib><creatorcontrib>Wang, Liang</creatorcontrib><creatorcontrib>Bi, Yongyi</creatorcontrib><creatorcontrib>Li, Dejia</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Oncotarget</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sun, Chengcao</au><au>Li, Shujun</au><au>Zhang, Feng</au><au>Xi, Yongyong</au><au>Wang, Liang</au><au>Bi, Yongyi</au><au>Li, Dejia</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Long non-coding RNA NEAT1 promotes non-small cell lung cancer progression through regulation of miR-377-3p-E2F3 pathway</atitle><jtitle>Oncotarget</jtitle><addtitle>Oncotarget</addtitle><date>2016-08-09</date><risdate>2016</risdate><volume>7</volume><issue>32</issue><spage>51784</spage><epage>51814</epage><pages>51784-51814</pages><issn>1949-2553</issn><eissn>1949-2553</eissn><abstract>Recently, the long non-coding RNA (lncRNA) NEAT1 has been identified as an oncogenic gene in multiple cancer types and elevated expression of NEAT1 was tightly linked to tumorigenesis and cancer progression. However, the molecular basis for this observation has not been characterized in progression of non-small cell lung cancer (NSCLC). In our studies, we identified NEAT1 was highly expressed in patients with NSCLC and was a novel regulator of NSCLC progression. Patients whose tumors had high NEAT1 expression had a shorter overall survival than patients whose tumors had low NEAT1 expression. Further, NEAT1 significantly accelerates NSCLC cell growth and metastasis in vitro and tumor growth in vivo. Additionally, by using bioinformatics study and RNA pull down combined with luciferase reporter assays, we demonstrated that NEAT1 functioned as a competing endogenous RNA (ceRNA) for hsa-miR-377-3p, antagonized its functions and led to the de-repression of its endogenous targets E2F3, which was a core oncogene in promoting NSCLC progression. Taken together, these observations imply that the NEAT1 modulated the expression of E2F3 gene by acting as a ceRNA, which may build up the missing link between the regulatory miRNA network and NSCLC progression.</abstract><cop>United States</cop><pub>Impact Journals LLC</pub><pmid>27351135</pmid><doi>10.18632/oncotarget.10108</doi><tpages>31</tpages><oa>free_for_read</oa></addata></record> |
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subjects | A549 Cells Adult Aged Aged, 80 and over Animals Carcinoma, Non-Small-Cell Lung - genetics Carcinoma, Non-Small-Cell Lung - pathology Cell Line, Tumor Disease Progression E2F3 Transcription Factor - genetics E2F3 Transcription Factor - metabolism Female Gene Expression Regulation, Neoplastic Humans Lung Neoplasms - genetics Lung Neoplasms - pathology Male Mice Mice, Inbred BALB C Mice, Nude MicroRNAs - genetics MicroRNAs - metabolism Middle Aged Research Paper RNA, Long Noncoding - physiology Signal Transduction - genetics |
title | Long non-coding RNA NEAT1 promotes non-small cell lung cancer progression through regulation of miR-377-3p-E2F3 pathway |
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