miR-297 acts as an oncogene by targeting GPC5 in lung adenocarcinoma

Objectives Emerging studies have demonstrated that microRNAs (miRNAs) play crucial roles in carcinogenesis of many developing human tumours. However, the functions and mechanisms of miR‐297 in lung cancer have, up to now, been largely undefined. Materials and methods Here, miR‐297 expression was mea...

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Veröffentlicht in:Cell proliferation 2016-10, Vol.49 (5), p.636-643
Hauptverfasser: Sun, Yunchuan, Zhao, Jianyong, Yin, Xiaoming, Yuan, Xiangkun, Guo, Jianfei, Bi, Jianqiang
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container_end_page 643
container_issue 5
container_start_page 636
container_title Cell proliferation
container_volume 49
creator Sun, Yunchuan
Zhao, Jianyong
Yin, Xiaoming
Yuan, Xiangkun
Guo, Jianfei
Bi, Jianqiang
description Objectives Emerging studies have demonstrated that microRNAs (miRNAs) play crucial roles in carcinogenesis of many developing human tumours. However, the functions and mechanisms of miR‐297 in lung cancer have, up to now, been largely undefined. Materials and methods Here, miR‐297 expression was measured in lung adenocarcinoma tissues and cell lines, using qRT‐PCR. Lung adenocarcinoma cell line was treated with an miR‐297 mimic. MTT and colony analysis were performed to detect cell proliferation and colony formation. The direct target gene of miR‐297 was assessed by qRT‐PCR, Western blotting and luciferase assays. Results We demonstrated that miR‐297 expression was upregulated in lung adenocarcinomas compared to adjacent normal tissues. Expression of miR‐297 was also upregulated in tested lung adenocarcinoma cell lines. Ectopic expression of miR‐297 enhanced lung adenocarcinoma cell proliferation and colony formation. Furthermore, overexpression of miR‐297 promoted cell migration and invasion. In addition, we identified Glypican‐5 (GPC5) as a direct target gene of miR‐297 in lung adenocarcinoma cells. Expression of GPC5 was downregulated in both lung adenocarcinoma tissues and cell lines. Moreover, expression of GPC5 was inversely associated with expression of miR‐297 in lung adenocarcinoma tissues. Conclusions These results suggest that miR‐297 acted as an oncogenic miRNA, partly by targeting GPC5, adenocarcinoma of the lung.
doi_str_mv 10.1111/cpr.12288
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However, the functions and mechanisms of miR‐297 in lung cancer have, up to now, been largely undefined. Materials and methods Here, miR‐297 expression was measured in lung adenocarcinoma tissues and cell lines, using qRT‐PCR. Lung adenocarcinoma cell line was treated with an miR‐297 mimic. MTT and colony analysis were performed to detect cell proliferation and colony formation. The direct target gene of miR‐297 was assessed by qRT‐PCR, Western blotting and luciferase assays. Results We demonstrated that miR‐297 expression was upregulated in lung adenocarcinomas compared to adjacent normal tissues. Expression of miR‐297 was also upregulated in tested lung adenocarcinoma cell lines. Ectopic expression of miR‐297 enhanced lung adenocarcinoma cell proliferation and colony formation. Furthermore, overexpression of miR‐297 promoted cell migration and invasion. In addition, we identified Glypican‐5 (GPC5) as a direct target gene of miR‐297 in lung adenocarcinoma cells. Expression of GPC5 was downregulated in both lung adenocarcinoma tissues and cell lines. Moreover, expression of GPC5 was inversely associated with expression of miR‐297 in lung adenocarcinoma tissues. Conclusions These results suggest that miR‐297 acted as an oncogenic miRNA, partly by targeting GPC5, adenocarcinoma of the lung.</description><identifier>ISSN: 0960-7722</identifier><identifier>EISSN: 1365-2184</identifier><identifier>DOI: 10.1111/cpr.12288</identifier><identifier>PMID: 27554041</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>Adenocarcinoma - genetics ; Adenocarcinoma - pathology ; Adenocarcinoma of Lung ; Cell Line, Tumor ; Cell Movement ; Cell Proliferation ; Down-Regulation ; Gene Expression Regulation, Neoplastic ; Glypicans - genetics ; Humans ; Lung - metabolism ; Lung - pathology ; Lung Neoplasms - genetics ; Lung Neoplasms - pathology ; MicroRNAs - genetics ; Oncogenes ; Original ; Up-Regulation</subject><ispartof>Cell proliferation, 2016-10, Vol.49 (5), p.636-643</ispartof><rights>2016 John Wiley &amp; Sons Ltd</rights><rights>2016 John Wiley &amp; Sons Ltd.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6496124/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6496124/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,1417,27924,27925,45574,45575,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27554041$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sun, Yunchuan</creatorcontrib><creatorcontrib>Zhao, Jianyong</creatorcontrib><creatorcontrib>Yin, Xiaoming</creatorcontrib><creatorcontrib>Yuan, Xiangkun</creatorcontrib><creatorcontrib>Guo, Jianfei</creatorcontrib><creatorcontrib>Bi, Jianqiang</creatorcontrib><title>miR-297 acts as an oncogene by targeting GPC5 in lung adenocarcinoma</title><title>Cell proliferation</title><addtitle>Cell Prolif</addtitle><description>Objectives Emerging studies have demonstrated that microRNAs (miRNAs) play crucial roles in carcinogenesis of many developing human tumours. However, the functions and mechanisms of miR‐297 in lung cancer have, up to now, been largely undefined. Materials and methods Here, miR‐297 expression was measured in lung adenocarcinoma tissues and cell lines, using qRT‐PCR. Lung adenocarcinoma cell line was treated with an miR‐297 mimic. MTT and colony analysis were performed to detect cell proliferation and colony formation. The direct target gene of miR‐297 was assessed by qRT‐PCR, Western blotting and luciferase assays. Results We demonstrated that miR‐297 expression was upregulated in lung adenocarcinomas compared to adjacent normal tissues. Expression of miR‐297 was also upregulated in tested lung adenocarcinoma cell lines. Ectopic expression of miR‐297 enhanced lung adenocarcinoma cell proliferation and colony formation. Furthermore, overexpression of miR‐297 promoted cell migration and invasion. In addition, we identified Glypican‐5 (GPC5) as a direct target gene of miR‐297 in lung adenocarcinoma cells. Expression of GPC5 was downregulated in both lung adenocarcinoma tissues and cell lines. Moreover, expression of GPC5 was inversely associated with expression of miR‐297 in lung adenocarcinoma tissues. Conclusions These results suggest that miR‐297 acted as an oncogenic miRNA, partly by targeting GPC5, adenocarcinoma of the lung.</description><subject>Adenocarcinoma - genetics</subject><subject>Adenocarcinoma - pathology</subject><subject>Adenocarcinoma of Lung</subject><subject>Cell Line, Tumor</subject><subject>Cell Movement</subject><subject>Cell Proliferation</subject><subject>Down-Regulation</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>Glypicans - genetics</subject><subject>Humans</subject><subject>Lung - metabolism</subject><subject>Lung - pathology</subject><subject>Lung Neoplasms - genetics</subject><subject>Lung Neoplasms - pathology</subject><subject>MicroRNAs - genetics</subject><subject>Oncogenes</subject><subject>Original</subject><subject>Up-Regulation</subject><issn>0960-7722</issn><issn>1365-2184</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVUctOwzAQtBCIlsKBH0A5cknrV2LnggQBAlIFVQUUcbEcxy2GxClxAvTvSR9UYK3kXe3OzGoHgGME-6h9AzWv-ghjzndAF5Ew8DHidBd0YRRCnzGMO-DAuTcIEUEs3AcdzIKAQoq64LIwYx9HzJOqdp5sw3qlVeVMW-2lC6-W1UzXxs68ZBQHnrFe3rSFzLQtlayUsWUhD8HeVOZOH23-Hni8vnqIb_zhfXIbnw99E1DOfUw0y6JMY5KGjCGop0pySmgUYZQpTmTQ7qXwlNCUIKkpiQgnEGMCWcozGJIeOFvzzpu00JnStq5kLuaVKWS1EKU04n_HmlcxKz9FSKMQYdoSnG4IqvKj0a4WhXFK57m0umycQByzCAUcL7VO_mptRX5P1w4M1gNfJteLbR9BsfREtJ6IlSciHo1XSYvw1wjjav29RcjqXYSMsEBM7hJBnydPyQWPxQv5ASzRi6U</recordid><startdate>201610</startdate><enddate>201610</enddate><creator>Sun, Yunchuan</creator><creator>Zhao, Jianyong</creator><creator>Yin, Xiaoming</creator><creator>Yuan, Xiangkun</creator><creator>Guo, Jianfei</creator><creator>Bi, Jianqiang</creator><general>Blackwell Publishing Ltd</general><general>John Wiley and Sons Inc</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7QO</scope><scope>7TO</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>5PM</scope></search><sort><creationdate>201610</creationdate><title>miR-297 acts as an oncogene by targeting GPC5 in lung adenocarcinoma</title><author>Sun, Yunchuan ; Zhao, Jianyong ; Yin, Xiaoming ; Yuan, Xiangkun ; Guo, Jianfei ; Bi, Jianqiang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-i5488-23e7d9de23b67710efca84349921dc83a5275c2f34b31ae439383022307b8d063</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Adenocarcinoma - genetics</topic><topic>Adenocarcinoma - pathology</topic><topic>Adenocarcinoma of Lung</topic><topic>Cell Line, Tumor</topic><topic>Cell Movement</topic><topic>Cell Proliferation</topic><topic>Down-Regulation</topic><topic>Gene Expression Regulation, Neoplastic</topic><topic>Glypicans - genetics</topic><topic>Humans</topic><topic>Lung - metabolism</topic><topic>Lung - pathology</topic><topic>Lung Neoplasms - genetics</topic><topic>Lung Neoplasms - pathology</topic><topic>MicroRNAs - genetics</topic><topic>Oncogenes</topic><topic>Original</topic><topic>Up-Regulation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sun, Yunchuan</creatorcontrib><creatorcontrib>Zhao, Jianyong</creatorcontrib><creatorcontrib>Yin, Xiaoming</creatorcontrib><creatorcontrib>Yuan, Xiangkun</creatorcontrib><creatorcontrib>Guo, Jianfei</creatorcontrib><creatorcontrib>Bi, Jianqiang</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>Biotechnology Research Abstracts</collection><collection>Oncogenes and Growth Factors 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>PubMed Central (Full Participant titles)</collection><jtitle>Cell proliferation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sun, Yunchuan</au><au>Zhao, Jianyong</au><au>Yin, Xiaoming</au><au>Yuan, Xiangkun</au><au>Guo, Jianfei</au><au>Bi, Jianqiang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>miR-297 acts as an oncogene by targeting GPC5 in lung adenocarcinoma</atitle><jtitle>Cell proliferation</jtitle><addtitle>Cell Prolif</addtitle><date>2016-10</date><risdate>2016</risdate><volume>49</volume><issue>5</issue><spage>636</spage><epage>643</epage><pages>636-643</pages><issn>0960-7722</issn><eissn>1365-2184</eissn><abstract>Objectives Emerging studies have demonstrated that microRNAs (miRNAs) play crucial roles in carcinogenesis of many developing human tumours. However, the functions and mechanisms of miR‐297 in lung cancer have, up to now, been largely undefined. Materials and methods Here, miR‐297 expression was measured in lung adenocarcinoma tissues and cell lines, using qRT‐PCR. Lung adenocarcinoma cell line was treated with an miR‐297 mimic. MTT and colony analysis were performed to detect cell proliferation and colony formation. The direct target gene of miR‐297 was assessed by qRT‐PCR, Western blotting and luciferase assays. Results We demonstrated that miR‐297 expression was upregulated in lung adenocarcinomas compared to adjacent normal tissues. Expression of miR‐297 was also upregulated in tested lung adenocarcinoma cell lines. Ectopic expression of miR‐297 enhanced lung adenocarcinoma cell proliferation and colony formation. Furthermore, overexpression of miR‐297 promoted cell migration and invasion. In addition, we identified Glypican‐5 (GPC5) as a direct target gene of miR‐297 in lung adenocarcinoma cells. Expression of GPC5 was downregulated in both lung adenocarcinoma tissues and cell lines. Moreover, expression of GPC5 was inversely associated with expression of miR‐297 in lung adenocarcinoma tissues. Conclusions These results suggest that miR‐297 acted as an oncogenic miRNA, partly by targeting GPC5, adenocarcinoma of the lung.</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>27554041</pmid><doi>10.1111/cpr.12288</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
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subjects Adenocarcinoma - genetics
Adenocarcinoma - pathology
Adenocarcinoma of Lung
Cell Line, Tumor
Cell Movement
Cell Proliferation
Down-Regulation
Gene Expression Regulation, Neoplastic
Glypicans - genetics
Humans
Lung - metabolism
Lung - pathology
Lung Neoplasms - genetics
Lung Neoplasms - pathology
MicroRNAs - genetics
Oncogenes
Original
Up-Regulation
title miR-297 acts as an oncogene by targeting GPC5 in lung adenocarcinoma
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