MiR-205 functions as a tumor suppressor via targeting TGF-α in osteosarcoma

Osteosarcoma (OS) is the most common primary bone cancer, and it is most prevalent in children and young adults. The prognosis of OS remains poor, and survival of OS reached a plateau. The discovery of microRNAs (miRNAs) provides a new possibility for the early diagnosis and treatment of OS. In this...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Experimental and molecular pathology 2016-02, Vol.100 (1), p.160-166
Hauptverfasser: Yang, Guojin, Zhang, Peng, Lv, Aibin, Liu, Yulin, Wang, Guoxi
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 166
container_issue 1
container_start_page 160
container_title Experimental and molecular pathology
container_volume 100
creator Yang, Guojin
Zhang, Peng
Lv, Aibin
Liu, Yulin
Wang, Guoxi
description Osteosarcoma (OS) is the most common primary bone cancer, and it is most prevalent in children and young adults. The prognosis of OS remains poor, and survival of OS reached a plateau. The discovery of microRNAs (miRNAs) provides a new possibility for the early diagnosis and treatment of OS. In this study, we detected the expression level of miR-205 and Transforming growth factor-alpha (TGF-α) in 15 cases of clinical OS tissues and adjacent normal bone tissues. We found that the expression of miR-205 was significantly lower in OS tissues than in normal bone tissues; the expression of TGF-α mRNA was significantly increased in OS tissues than in normal bone tissues, the miR-205 was negatively correlated with TGF-α levels in both OS and normal bone tissues. Functional studies demonstrated that miR-205 significantly decreased the capability of cell proliferation, invasion and migration and induced G0/G1 growth arrest and apoptosis in OS cells. By using bioinformatics analytic tool (Targetscan), the 3'UTR of TGF-α gene was found to be a target of miR-205. Luciferase report assay further confirmed that TGF-α 3'UTR is a direct target of miR-205. We also found that the expression of TGF-α mRNA and protein was significantly down-regulated or up-regulated after miR-205 mimic or miR-205 inhibitor transfection. TGF-α knockdown study further showed that miR-205 regulated cell proliferation, invasion and migration by targeting TGF-α in OS. Enforced expression of TGF-α sufficiently restore the effects of miR-205 on cell proliferation, invasion and migration. In conclusion, our study suggested that miR-205 may function as a tumor suppressor via targeting TGF-α in OS, and the abnormal expression of miR-205 might be a key factor in OS progression. •Osteosarcoma (OS) is the most common primary bone cancer.•The discovery of microRNAs provides a new possibility for the early diagnosis and treatment of OS•MiR-205 may function as a tumor suppressor via targeting TGF-α in OS.•Abnormal expression of miR-205 might be a key factor in OS progression.
doi_str_mv 10.1016/j.yexmp.2015.12.010
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1762030383</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0014480015002609</els_id><sourcerecordid>1762030383</sourcerecordid><originalsourceid>FETCH-LOGICAL-c359t-9b847edca66b5751e52f9580a842e9657ab868782796f4f9fe6e3ac1a2c79243</originalsourceid><addsrcrecordid>eNp9kMFKAzEQhoMoWqtPIMgevew6yW6ym4MHKVaFiiC9hzSdLSndzZrsFn0sX8RnMrXqURiYYfhn_pmPkAsKGQUqrtfZO741XcaA8oyyDCgckBEFKVKQBT8kIwBapEUFcEJOQ1gDgATKjskJEyVUBeMjMnuyLykDntRDa3rr2pDoGEk_NM4nYeg6jyHEcmtjU_sV9rZdJfP7afr5kdg2caFHF7Q3rtFn5KjWm4DnP3lM5tO7-eQhnT3fP05uZ6nJuexTuaiKEpdGC7HgJafIWS15BTqehFLwUi8qUZUVK6Woi1rWKDDXhmpmSsmKfEyu9ms7714HDL1qbDC42egW3RAULQWDHPIqj9J8LzXeheCxVp23jfbvioLaUVRr9U1R7SgqylSkGKcufwyGRYPLv5lfbFFwsxdg_HJr0atgLLYGl9aj6dXS2X8NvgCy-YO_</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1762030383</pqid></control><display><type>article</type><title>MiR-205 functions as a tumor suppressor via targeting TGF-α in osteosarcoma</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><creator>Yang, Guojin ; Zhang, Peng ; Lv, Aibin ; Liu, Yulin ; Wang, Guoxi</creator><creatorcontrib>Yang, Guojin ; Zhang, Peng ; Lv, Aibin ; Liu, Yulin ; Wang, Guoxi</creatorcontrib><description>Osteosarcoma (OS) is the most common primary bone cancer, and it is most prevalent in children and young adults. The prognosis of OS remains poor, and survival of OS reached a plateau. The discovery of microRNAs (miRNAs) provides a new possibility for the early diagnosis and treatment of OS. In this study, we detected the expression level of miR-205 and Transforming growth factor-alpha (TGF-α) in 15 cases of clinical OS tissues and adjacent normal bone tissues. We found that the expression of miR-205 was significantly lower in OS tissues than in normal bone tissues; the expression of TGF-α mRNA was significantly increased in OS tissues than in normal bone tissues, the miR-205 was negatively correlated with TGF-α levels in both OS and normal bone tissues. Functional studies demonstrated that miR-205 significantly decreased the capability of cell proliferation, invasion and migration and induced G0/G1 growth arrest and apoptosis in OS cells. By using bioinformatics analytic tool (Targetscan), the 3'UTR of TGF-α gene was found to be a target of miR-205. Luciferase report assay further confirmed that TGF-α 3'UTR is a direct target of miR-205. We also found that the expression of TGF-α mRNA and protein was significantly down-regulated or up-regulated after miR-205 mimic or miR-205 inhibitor transfection. TGF-α knockdown study further showed that miR-205 regulated cell proliferation, invasion and migration by targeting TGF-α in OS. Enforced expression of TGF-α sufficiently restore the effects of miR-205 on cell proliferation, invasion and migration. In conclusion, our study suggested that miR-205 may function as a tumor suppressor via targeting TGF-α in OS, and the abnormal expression of miR-205 might be a key factor in OS progression. •Osteosarcoma (OS) is the most common primary bone cancer.•The discovery of microRNAs provides a new possibility for the early diagnosis and treatment of OS•MiR-205 may function as a tumor suppressor via targeting TGF-α in OS.•Abnormal expression of miR-205 might be a key factor in OS progression.</description><identifier>ISSN: 0014-4800</identifier><identifier>EISSN: 1096-0945</identifier><identifier>DOI: 10.1016/j.yexmp.2015.12.010</identifier><identifier>PMID: 26708425</identifier><language>eng</language><publisher>Netherlands: Elsevier Inc</publisher><subject>Apoptosis - genetics ; Bone Neoplasms - genetics ; Cell Line, Tumor ; Cell proliferation ; Cell Proliferation - genetics ; Gene Expression Regulation, Neoplastic - genetics ; Genes, Tumor Suppressor - physiology ; Humans ; Invasion ; MicroRNAs - genetics ; Migration ; miR-205 ; miRNA ; Osteosarcoma - genetics ; TGF-α ; Transforming Growth Factor alpha - genetics</subject><ispartof>Experimental and molecular pathology, 2016-02, Vol.100 (1), p.160-166</ispartof><rights>2015 Elsevier Inc.</rights><rights>Copyright © 2015 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c359t-9b847edca66b5751e52f9580a842e9657ab868782796f4f9fe6e3ac1a2c79243</citedby><cites>FETCH-LOGICAL-c359t-9b847edca66b5751e52f9580a842e9657ab868782796f4f9fe6e3ac1a2c79243</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0014480015002609$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26708425$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yang, Guojin</creatorcontrib><creatorcontrib>Zhang, Peng</creatorcontrib><creatorcontrib>Lv, Aibin</creatorcontrib><creatorcontrib>Liu, Yulin</creatorcontrib><creatorcontrib>Wang, Guoxi</creatorcontrib><title>MiR-205 functions as a tumor suppressor via targeting TGF-α in osteosarcoma</title><title>Experimental and molecular pathology</title><addtitle>Exp Mol Pathol</addtitle><description>Osteosarcoma (OS) is the most common primary bone cancer, and it is most prevalent in children and young adults. The prognosis of OS remains poor, and survival of OS reached a plateau. The discovery of microRNAs (miRNAs) provides a new possibility for the early diagnosis and treatment of OS. In this study, we detected the expression level of miR-205 and Transforming growth factor-alpha (TGF-α) in 15 cases of clinical OS tissues and adjacent normal bone tissues. We found that the expression of miR-205 was significantly lower in OS tissues than in normal bone tissues; the expression of TGF-α mRNA was significantly increased in OS tissues than in normal bone tissues, the miR-205 was negatively correlated with TGF-α levels in both OS and normal bone tissues. Functional studies demonstrated that miR-205 significantly decreased the capability of cell proliferation, invasion and migration and induced G0/G1 growth arrest and apoptosis in OS cells. By using bioinformatics analytic tool (Targetscan), the 3'UTR of TGF-α gene was found to be a target of miR-205. Luciferase report assay further confirmed that TGF-α 3'UTR is a direct target of miR-205. We also found that the expression of TGF-α mRNA and protein was significantly down-regulated or up-regulated after miR-205 mimic or miR-205 inhibitor transfection. TGF-α knockdown study further showed that miR-205 regulated cell proliferation, invasion and migration by targeting TGF-α in OS. Enforced expression of TGF-α sufficiently restore the effects of miR-205 on cell proliferation, invasion and migration. In conclusion, our study suggested that miR-205 may function as a tumor suppressor via targeting TGF-α in OS, and the abnormal expression of miR-205 might be a key factor in OS progression. •Osteosarcoma (OS) is the most common primary bone cancer.•The discovery of microRNAs provides a new possibility for the early diagnosis and treatment of OS•MiR-205 may function as a tumor suppressor via targeting TGF-α in OS.•Abnormal expression of miR-205 might be a key factor in OS progression.</description><subject>Apoptosis - genetics</subject><subject>Bone Neoplasms - genetics</subject><subject>Cell Line, Tumor</subject><subject>Cell proliferation</subject><subject>Cell Proliferation - genetics</subject><subject>Gene Expression Regulation, Neoplastic - genetics</subject><subject>Genes, Tumor Suppressor - physiology</subject><subject>Humans</subject><subject>Invasion</subject><subject>MicroRNAs - genetics</subject><subject>Migration</subject><subject>miR-205</subject><subject>miRNA</subject><subject>Osteosarcoma - genetics</subject><subject>TGF-α</subject><subject>Transforming Growth Factor alpha - genetics</subject><issn>0014-4800</issn><issn>1096-0945</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kMFKAzEQhoMoWqtPIMgevew6yW6ym4MHKVaFiiC9hzSdLSndzZrsFn0sX8RnMrXqURiYYfhn_pmPkAsKGQUqrtfZO741XcaA8oyyDCgckBEFKVKQBT8kIwBapEUFcEJOQ1gDgATKjskJEyVUBeMjMnuyLykDntRDa3rr2pDoGEk_NM4nYeg6jyHEcmtjU_sV9rZdJfP7afr5kdg2caFHF7Q3rtFn5KjWm4DnP3lM5tO7-eQhnT3fP05uZ6nJuexTuaiKEpdGC7HgJafIWS15BTqehFLwUi8qUZUVK6Woi1rWKDDXhmpmSsmKfEyu9ms7714HDL1qbDC42egW3RAULQWDHPIqj9J8LzXeheCxVp23jfbvioLaUVRr9U1R7SgqylSkGKcufwyGRYPLv5lfbFFwsxdg_HJr0atgLLYGl9aj6dXS2X8NvgCy-YO_</recordid><startdate>201602</startdate><enddate>201602</enddate><creator>Yang, Guojin</creator><creator>Zhang, Peng</creator><creator>Lv, Aibin</creator><creator>Liu, Yulin</creator><creator>Wang, Guoxi</creator><general>Elsevier 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>7X8</scope></search><sort><creationdate>201602</creationdate><title>MiR-205 functions as a tumor suppressor via targeting TGF-α in osteosarcoma</title><author>Yang, Guojin ; Zhang, Peng ; Lv, Aibin ; Liu, Yulin ; Wang, Guoxi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c359t-9b847edca66b5751e52f9580a842e9657ab868782796f4f9fe6e3ac1a2c79243</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Apoptosis - genetics</topic><topic>Bone Neoplasms - genetics</topic><topic>Cell Line, Tumor</topic><topic>Cell proliferation</topic><topic>Cell Proliferation - genetics</topic><topic>Gene Expression Regulation, Neoplastic - genetics</topic><topic>Genes, Tumor Suppressor - physiology</topic><topic>Humans</topic><topic>Invasion</topic><topic>MicroRNAs - genetics</topic><topic>Migration</topic><topic>miR-205</topic><topic>miRNA</topic><topic>Osteosarcoma - genetics</topic><topic>TGF-α</topic><topic>Transforming Growth Factor alpha - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yang, Guojin</creatorcontrib><creatorcontrib>Zhang, Peng</creatorcontrib><creatorcontrib>Lv, Aibin</creatorcontrib><creatorcontrib>Liu, Yulin</creatorcontrib><creatorcontrib>Wang, Guoxi</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Experimental and molecular pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yang, Guojin</au><au>Zhang, Peng</au><au>Lv, Aibin</au><au>Liu, Yulin</au><au>Wang, Guoxi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>MiR-205 functions as a tumor suppressor via targeting TGF-α in osteosarcoma</atitle><jtitle>Experimental and molecular pathology</jtitle><addtitle>Exp Mol Pathol</addtitle><date>2016-02</date><risdate>2016</risdate><volume>100</volume><issue>1</issue><spage>160</spage><epage>166</epage><pages>160-166</pages><issn>0014-4800</issn><eissn>1096-0945</eissn><abstract>Osteosarcoma (OS) is the most common primary bone cancer, and it is most prevalent in children and young adults. The prognosis of OS remains poor, and survival of OS reached a plateau. The discovery of microRNAs (miRNAs) provides a new possibility for the early diagnosis and treatment of OS. In this study, we detected the expression level of miR-205 and Transforming growth factor-alpha (TGF-α) in 15 cases of clinical OS tissues and adjacent normal bone tissues. We found that the expression of miR-205 was significantly lower in OS tissues than in normal bone tissues; the expression of TGF-α mRNA was significantly increased in OS tissues than in normal bone tissues, the miR-205 was negatively correlated with TGF-α levels in both OS and normal bone tissues. Functional studies demonstrated that miR-205 significantly decreased the capability of cell proliferation, invasion and migration and induced G0/G1 growth arrest and apoptosis in OS cells. By using bioinformatics analytic tool (Targetscan), the 3'UTR of TGF-α gene was found to be a target of miR-205. Luciferase report assay further confirmed that TGF-α 3'UTR is a direct target of miR-205. We also found that the expression of TGF-α mRNA and protein was significantly down-regulated or up-regulated after miR-205 mimic or miR-205 inhibitor transfection. TGF-α knockdown study further showed that miR-205 regulated cell proliferation, invasion and migration by targeting TGF-α in OS. Enforced expression of TGF-α sufficiently restore the effects of miR-205 on cell proliferation, invasion and migration. In conclusion, our study suggested that miR-205 may function as a tumor suppressor via targeting TGF-α in OS, and the abnormal expression of miR-205 might be a key factor in OS progression. •Osteosarcoma (OS) is the most common primary bone cancer.•The discovery of microRNAs provides a new possibility for the early diagnosis and treatment of OS•MiR-205 may function as a tumor suppressor via targeting TGF-α in OS.•Abnormal expression of miR-205 might be a key factor in OS progression.</abstract><cop>Netherlands</cop><pub>Elsevier Inc</pub><pmid>26708425</pmid><doi>10.1016/j.yexmp.2015.12.010</doi><tpages>7</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0014-4800
ispartof Experimental and molecular pathology, 2016-02, Vol.100 (1), p.160-166
issn 0014-4800
1096-0945
language eng
recordid cdi_proquest_miscellaneous_1762030383
source MEDLINE; Elsevier ScienceDirect Journals
subjects Apoptosis - genetics
Bone Neoplasms - genetics
Cell Line, Tumor
Cell proliferation
Cell Proliferation - genetics
Gene Expression Regulation, Neoplastic - genetics
Genes, Tumor Suppressor - physiology
Humans
Invasion
MicroRNAs - genetics
Migration
miR-205
miRNA
Osteosarcoma - genetics
TGF-α
Transforming Growth Factor alpha - genetics
title MiR-205 functions as a tumor suppressor via targeting TGF-α in osteosarcoma
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-05T12%3A07%3A14IST&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=MiR-205%20functions%20as%20a%20tumor%20suppressor%20via%20targeting%20TGF-%CE%B1%20in%20osteosarcoma&rft.jtitle=Experimental%20and%20molecular%20pathology&rft.au=Yang,%20Guojin&rft.date=2016-02&rft.volume=100&rft.issue=1&rft.spage=160&rft.epage=166&rft.pages=160-166&rft.issn=0014-4800&rft.eissn=1096-0945&rft_id=info:doi/10.1016/j.yexmp.2015.12.010&rft_dat=%3Cproquest_cross%3E1762030383%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=1762030383&rft_id=info:pmid/26708425&rft_els_id=S0014480015002609&rfr_iscdi=true