Downregulation of astrocyte elevated gene-1 expression inhibits the development of vasculogenic mimicry in gliomas
Vasculogenic mimicry (VM) contributes to the resistance of anti-angiogenic therapies in glioma. Certain genes, including MMP-2 and VEGF may be associated with the development of VM. Astrocyte elevated gene-1 (AEG-1) is considered to be an oncogene that promotes autophagy, invasion, metastasis, angio...
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description | Vasculogenic mimicry (VM) contributes to the resistance of anti-angiogenic therapies in glioma. Certain genes, including MMP-2 and VEGF may be associated with the development of VM. Astrocyte elevated gene-1 (AEG-1) is considered to be an oncogene that promotes autophagy, invasion, metastasis, angiogenesis and drug resistance; however, the association between AEG-1 and VM formation is still unknown. The present study investigated the effects of AEG-1 downregulation on VM formation in the U87 glioma cell line in vitro and in xenograft models of glioma, and the potential underlying mechanisms of action. In the present study, U87 glioma cells were infected with the AEG-1 short hairpin RNA lentivirus. A Matrigel-based tube formation assay was performed to evaluate VM formation in vitro. Reverse transcription-quantitative PCR and western blot analysis were conducted to investigate the mRNA and protein expression levels of MMP-2 and VEGF. Glioma xenograft models were generated through the intracerebral implantation of U87 glioma cells into nude rats; CD34/Periodic Acid-Schiff double-staining was performed to detect VM channels in vivo. Following AEG-1 downregulation in U87 cells, the development of VM was significantly decreased in vitro and in vivo. In addition, the expression levels of MMP-2 and VEGF in glioma cells were decreased compared with the control group. These results suggested that downregulation of AEG-1 expression could significantly inhibit the development of VM in gliomas, both in vitro and in vivo, and may be partially related to the regulation of VEGF and MMP-2 expression. |
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Certain genes, including MMP-2 and VEGF may be associated with the development of VM. Astrocyte elevated gene-1 (AEG-1) is considered to be an oncogene that promotes autophagy, invasion, metastasis, angiogenesis and drug resistance; however, the association between AEG-1 and VM formation is still unknown. The present study investigated the effects of AEG-1 downregulation on VM formation in the U87 glioma cell line in vitro and in xenograft models of glioma, and the potential underlying mechanisms of action. In the present study, U87 glioma cells were infected with the AEG-1 short hairpin RNA lentivirus. A Matrigel-based tube formation assay was performed to evaluate VM formation in vitro. Reverse transcription-quantitative PCR and western blot analysis were conducted to investigate the mRNA and protein expression levels of MMP-2 and VEGF. Glioma xenograft models were generated through the intracerebral implantation of U87 glioma cells into nude rats; CD34/Periodic Acid-Schiff double-staining was performed to detect VM channels in vivo. Following AEG-1 downregulation in U87 cells, the development of VM was significantly decreased in vitro and in vivo. In addition, the expression levels of MMP-2 and VEGF in glioma cells were decreased compared with the control group. These results suggested that downregulation of AEG-1 expression could significantly inhibit the development of VM in gliomas, both in vitro and in vivo, and may be partially related to the regulation of VEGF and MMP-2 expression.</description><identifier>ISSN: 1792-0981</identifier><identifier>EISSN: 1792-1015</identifier><identifier>DOI: 10.3892/etm.2020.9454</identifier><identifier>PMID: 33235631</identifier><language>eng</language><publisher>ATHENS: Spandidos Publ Ltd</publisher><subject>Angiogenesis ; Antibodies ; Astrocytes ; Biotechnology ; Blood vessels ; Brain cancer ; Development and progression ; Drug resistance ; Fluorides ; Gene expression ; Genetic aspects ; Genetic research ; Glioma ; Gliomas ; Health aspects ; Infections ; Laboratory animals ; Life Sciences & Biomedicine ; Medicine, Research & Experimental ; Membranes ; Plasmids ; Research & Experimental Medicine ; Science & Technology ; Tumors</subject><ispartof>Experimental and therapeutic medicine, 2021-01, Vol.21 (1), p.1-1, Article 22</ispartof><rights>COPYRIGHT 2021 Spandidos Publications</rights><rights>Copyright Spandidos Publications UK Ltd. 2021</rights><rights>Copyright: © Liang et al. 2020</rights><oa>free_for_read</oa><woscitedreferencessubscribed>true</woscitedreferencessubscribed><woscitedreferencescount>5</woscitedreferencescount><woscitedreferencesoriginalsourcerecordid>wos000601205000001</woscitedreferencesoriginalsourcerecordid><cites>FETCH-LOGICAL-c345t-aa12273b39c7a1f7fe0a616bc8956db14e833d9f2bc2979534b0678103a8201e3</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/PMC7678608/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7678608/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,315,728,781,785,886,27929,27930,39263,53796,53798</link.rule.ids></links><search><creatorcontrib>Liang, Chen</creatorcontrib><creatorcontrib>Shangguan, Jian</creatorcontrib><creatorcontrib>Yang, Ling</creatorcontrib><creatorcontrib>Guo, Shiwen</creatorcontrib><title>Downregulation of astrocyte elevated gene-1 expression inhibits the development of vasculogenic mimicry in gliomas</title><title>Experimental and therapeutic medicine</title><addtitle>EXP THER MED</addtitle><description>Vasculogenic mimicry (VM) contributes to the resistance of anti-angiogenic therapies in glioma. Certain genes, including MMP-2 and VEGF may be associated with the development of VM. Astrocyte elevated gene-1 (AEG-1) is considered to be an oncogene that promotes autophagy, invasion, metastasis, angiogenesis and drug resistance; however, the association between AEG-1 and VM formation is still unknown. The present study investigated the effects of AEG-1 downregulation on VM formation in the U87 glioma cell line in vitro and in xenograft models of glioma, and the potential underlying mechanisms of action. In the present study, U87 glioma cells were infected with the AEG-1 short hairpin RNA lentivirus. A Matrigel-based tube formation assay was performed to evaluate VM formation in vitro. Reverse transcription-quantitative PCR and western blot analysis were conducted to investigate the mRNA and protein expression levels of MMP-2 and VEGF. Glioma xenograft models were generated through the intracerebral implantation of U87 glioma cells into nude rats; CD34/Periodic Acid-Schiff double-staining was performed to detect VM channels in vivo. Following AEG-1 downregulation in U87 cells, the development of VM was significantly decreased in vitro and in vivo. In addition, the expression levels of MMP-2 and VEGF in glioma cells were decreased compared with the control group. These results suggested that downregulation of AEG-1 expression could significantly inhibit the development of VM in gliomas, both in vitro and in vivo, and may be partially related to the regulation of VEGF and MMP-2 expression.</description><subject>Angiogenesis</subject><subject>Antibodies</subject><subject>Astrocytes</subject><subject>Biotechnology</subject><subject>Blood vessels</subject><subject>Brain cancer</subject><subject>Development and progression</subject><subject>Drug resistance</subject><subject>Fluorides</subject><subject>Gene expression</subject><subject>Genetic aspects</subject><subject>Genetic research</subject><subject>Glioma</subject><subject>Gliomas</subject><subject>Health aspects</subject><subject>Infections</subject><subject>Laboratory animals</subject><subject>Life Sciences & Biomedicine</subject><subject>Medicine, Research & Experimental</subject><subject>Membranes</subject><subject>Plasmids</subject><subject>Research & Experimental Medicine</subject><subject>Science & Technology</subject><subject>Tumors</subject><issn>1792-0981</issn><issn>1792-1015</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>HGBXW</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNqNks2L1DAYxoso7rLu0XvBiyAd89U0uQjL-AkLXvQc0vRtJ0uajEk66_z3ps6wsuLB5JCQ_J7nzRueqnqJ0YYKSd5CnjcEEbSRrGVPqkvcSdJghNun5z2SAl9U1yndoTJajoVon1cXlBLacoovq_g-3PsI0-J0tsHXYax1yjGYY4YaHBx0hqGewEODa_i5j5DSylm_s73Nqc47qAc4gAv7GXxeDQ46mcWFIrKmnu1sTTwWQT05G2adXlTPRu0SXJ_Xq-r7xw_ftp-b26-fvmxvbhtDWZsbrTEhHe2pNJ3GYzcC0hzz3gjZ8qHHDASlgxxJb4jsZEtZj3gnMKJaEISBXlXvTr77pZ9hMOV1UTu1j3bW8aiCturxjbc7NYWD6ooNR6IYvD4bxPBjgZTVbJMB57SHsCRFGGdYEiJZQV_9hd6FJfrSXqE61HacMvyHmrQDZf0YSl2zmqobzjrKBRFr2c0_qDIHKF8ZPIy2nD8SNCeBiSGlCONDjxipNSeq5EStOVFrTgovTvw99GFMxoI38KApOeEIE9SuiUF4a_PvZGzD4nORvvl_Kf0Ft-bQDQ</recordid><startdate>20210101</startdate><enddate>20210101</enddate><creator>Liang, Chen</creator><creator>Shangguan, Jian</creator><creator>Yang, Ling</creator><creator>Guo, Shiwen</creator><general>Spandidos Publ Ltd</general><general>Spandidos Publications</general><general>Spandidos Publications UK Ltd</general><general>D.A. Spandidos</general><scope>BLEPL</scope><scope>DTL</scope><scope>HGBXW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AN0</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20210101</creationdate><title>Downregulation of astrocyte elevated gene-1 expression inhibits the development of vasculogenic mimicry in gliomas</title><author>Liang, Chen ; Shangguan, Jian ; Yang, Ling ; Guo, Shiwen</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c345t-aa12273b39c7a1f7fe0a616bc8956db14e833d9f2bc2979534b0678103a8201e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Angiogenesis</topic><topic>Antibodies</topic><topic>Astrocytes</topic><topic>Biotechnology</topic><topic>Blood vessels</topic><topic>Brain cancer</topic><topic>Development and progression</topic><topic>Drug resistance</topic><topic>Fluorides</topic><topic>Gene expression</topic><topic>Genetic aspects</topic><topic>Genetic research</topic><topic>Glioma</topic><topic>Gliomas</topic><topic>Health aspects</topic><topic>Infections</topic><topic>Laboratory animals</topic><topic>Life Sciences & Biomedicine</topic><topic>Medicine, Research & Experimental</topic><topic>Membranes</topic><topic>Plasmids</topic><topic>Research & Experimental Medicine</topic><topic>Science & Technology</topic><topic>Tumors</topic><toplevel>online_resources</toplevel><creatorcontrib>Liang, Chen</creatorcontrib><creatorcontrib>Shangguan, Jian</creatorcontrib><creatorcontrib>Yang, Ling</creatorcontrib><creatorcontrib>Guo, Shiwen</creatorcontrib><collection>Web of Science Core Collection</collection><collection>Science Citation Index Expanded</collection><collection>Web of Science - Science Citation Index Expanded - 2021</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</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 Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>British Nursing Database</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Nursing & Allied Health Premium</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><jtitle>Experimental and therapeutic medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liang, Chen</au><au>Shangguan, Jian</au><au>Yang, Ling</au><au>Guo, Shiwen</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Downregulation of astrocyte elevated gene-1 expression inhibits the development of vasculogenic mimicry in gliomas</atitle><jtitle>Experimental and therapeutic medicine</jtitle><stitle>EXP THER MED</stitle><date>2021-01-01</date><risdate>2021</risdate><volume>21</volume><issue>1</issue><spage>1</spage><epage>1</epage><pages>1-1</pages><artnum>22</artnum><issn>1792-0981</issn><eissn>1792-1015</eissn><abstract>Vasculogenic mimicry (VM) contributes to the resistance of anti-angiogenic therapies in glioma. Certain genes, including MMP-2 and VEGF may be associated with the development of VM. Astrocyte elevated gene-1 (AEG-1) is considered to be an oncogene that promotes autophagy, invasion, metastasis, angiogenesis and drug resistance; however, the association between AEG-1 and VM formation is still unknown. The present study investigated the effects of AEG-1 downregulation on VM formation in the U87 glioma cell line in vitro and in xenograft models of glioma, and the potential underlying mechanisms of action. In the present study, U87 glioma cells were infected with the AEG-1 short hairpin RNA lentivirus. A Matrigel-based tube formation assay was performed to evaluate VM formation in vitro. Reverse transcription-quantitative PCR and western blot analysis were conducted to investigate the mRNA and protein expression levels of MMP-2 and VEGF. Glioma xenograft models were generated through the intracerebral implantation of U87 glioma cells into nude rats; CD34/Periodic Acid-Schiff double-staining was performed to detect VM channels in vivo. Following AEG-1 downregulation in U87 cells, the development of VM was significantly decreased in vitro and in vivo. In addition, the expression levels of MMP-2 and VEGF in glioma cells were decreased compared with the control group. These results suggested that downregulation of AEG-1 expression could significantly inhibit the development of VM in gliomas, both in vitro and in vivo, and may be partially related to the regulation of VEGF and MMP-2 expression.</abstract><cop>ATHENS</cop><pub>Spandidos Publ Ltd</pub><pmid>33235631</pmid><doi>10.3892/etm.2020.9454</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Angiogenesis Antibodies Astrocytes Biotechnology Blood vessels Brain cancer Development and progression Drug resistance Fluorides Gene expression Genetic aspects Genetic research Glioma Gliomas Health aspects Infections Laboratory animals Life Sciences & Biomedicine Medicine, Research & Experimental Membranes Plasmids Research & Experimental Medicine Science & Technology Tumors |
title | Downregulation of astrocyte elevated gene-1 expression inhibits the development of vasculogenic mimicry in gliomas |
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