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LOXL1‐AS1 communicating with TIAR modulates vasculogenic mimicry in glioma via regulation of the miR‐374b‐5p/MMP14 axis
At present, growing evidence indicates that long non‐coding RNAs (lncRNAs) participate in the progression of glioma. The function of LOXL1‐AS1 in vasculogenic mimicry (VM) in glioma remains unclear. First, the expressions of TIAR, the lncRNA LOXL1‐AS1, miR‐374b‐5p and MMP14 were examined by qRT‐PCR...
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Published in: | Journal of cellular and molecular medicine 2022-01, Vol.26 (2), p.475-490 |
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description | At present, growing evidence indicates that long non‐coding RNAs (lncRNAs) participate in the progression of glioma. The function of LOXL1‐AS1 in vasculogenic mimicry (VM) in glioma remains unclear. First, the expressions of TIAR, the lncRNA LOXL1‐AS1, miR‐374b‐5p and MMP14 were examined by qRT‐PCR and Western blot in both, glioma tissues and glioma cell lines. Proliferation, migration, invasion and tube formation assays were conducted to evaluate the roles of TIAR, LOXL1‐AS1, miR‐374b‐5p and MMP14 in malignant cellular behaviours in glioma cells. A nude mouse xenograft model and dual staining for CD34 and PAS were used to assess whether VM was affected by TIAR, LOXL1‐AS1 or miR‐374b‐5p in vivo. In this study, low levels of TIAR and high levels of LOXL1‐AS1 were found in glioma cells and tissues. TIAR downregulated the expression of LOXL1‐AS1 by destabilizing it. LOXL1‐AS1 acted like a miRNA sponge towards miR‐374b‐5p so that downregulation of the former greatly inhibited cell proliferation, migration, invasion and VM. Additionally, miR‐374b‐5p overexpression repressed malignant biological behaviours and VM in glioma by modifying MMP14. In summary, we demonstrated that TIAR combined with LOXL1‐AS1 modulates VM in glioma via the miR‐374b‐5p/MMP14 axis, revealing novel targets for glioma therapy. |
doi_str_mv | 10.1111/jcmm.17106 |
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The function of LOXL1‐AS1 in vasculogenic mimicry (VM) in glioma remains unclear. First, the expressions of TIAR, the lncRNA LOXL1‐AS1, miR‐374b‐5p and MMP14 were examined by qRT‐PCR and Western blot in both, glioma tissues and glioma cell lines. Proliferation, migration, invasion and tube formation assays were conducted to evaluate the roles of TIAR, LOXL1‐AS1, miR‐374b‐5p and MMP14 in malignant cellular behaviours in glioma cells. A nude mouse xenograft model and dual staining for CD34 and PAS were used to assess whether VM was affected by TIAR, LOXL1‐AS1 or miR‐374b‐5p in vivo. In this study, low levels of TIAR and high levels of LOXL1‐AS1 were found in glioma cells and tissues. TIAR downregulated the expression of LOXL1‐AS1 by destabilizing it. LOXL1‐AS1 acted like a miRNA sponge towards miR‐374b‐5p so that downregulation of the former greatly inhibited cell proliferation, migration, invasion and VM. Additionally, miR‐374b‐5p overexpression repressed malignant biological behaviours and VM in glioma by modifying MMP14. In summary, we demonstrated that TIAR combined with LOXL1‐AS1 modulates VM in glioma via the miR‐374b‐5p/MMP14 axis, revealing novel targets for glioma therapy.</description><identifier>ISSN: 1582-1838</identifier><identifier>EISSN: 1582-4934</identifier><identifier>DOI: 10.1111/jcmm.17106</identifier><identifier>PMID: 34890108</identifier><language>eng</language><publisher>England: John Wiley & Sons, Inc</publisher><subject>Amino Acid Oxidoreductases - metabolism ; Angiogenesis ; Animals ; Antibodies ; Behavior ; CD34 antigen ; Cell Line, Tumor ; Cell lines ; Cell migration ; Cell Movement - genetics ; Cell proliferation ; Cell Proliferation - genetics ; Colorectal cancer ; Gene Expression Regulation, Neoplastic ; Glioma ; Glioma - genetics ; Glioma - pathology ; Glioma cells ; Humans ; Liver cancer ; LOXL1‐AS1 ; Lung cancer ; Matrix Metalloproteinase 14 - genetics ; Matrix Metalloproteinase 14 - metabolism ; Medical prognosis ; Membranes ; Metastasis ; Mice ; MicroRNAs ; MicroRNAs - genetics ; MicroRNAs - metabolism ; Mimicry ; miRNA ; miR‐374b‐5p ; MMP14 ; Nervous system ; Non-coding RNA ; Original ; Proteins ; RNA, Long Noncoding - genetics ; RNA-Binding Proteins - metabolism ; TIAR ; Tumors ; vasculogenic mimicry ; Xenografts</subject><ispartof>Journal of cellular and molecular medicine, 2022-01, Vol.26 (2), p.475-490</ispartof><rights>2021 The Authors. published by Foundation for Cellular and Molecular Medicine and John Wiley & Sons Ltd.</rights><rights>2021 The Authors. Journal of Cellular and Molecular Medicine published by Foundation for Cellular and Molecular Medicine and John Wiley & Sons Ltd.</rights><rights>2022. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4486-9367566159385f690b7b4e55a6bbf2e44859a8019f3168b05242ba55f83574393</citedby><cites>FETCH-LOGICAL-c4486-9367566159385f690b7b4e55a6bbf2e44859a8019f3168b05242ba55f83574393</cites><orcidid>0000-0003-1760-7741</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2618154742/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2618154742?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,11562,25753,27924,27925,37012,37013,44590,46052,46476,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34890108$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yi, Bolong</creatorcontrib><creatorcontrib>Li, Hao</creatorcontrib><creatorcontrib>Cai, Heng</creatorcontrib><creatorcontrib>Lou, Xin</creatorcontrib><creatorcontrib>Yu, Mingjun</creatorcontrib><creatorcontrib>Li, Zhen</creatorcontrib><title>LOXL1‐AS1 communicating with TIAR modulates vasculogenic mimicry in glioma via regulation of the miR‐374b‐5p/MMP14 axis</title><title>Journal of cellular and molecular medicine</title><addtitle>J Cell Mol Med</addtitle><description>At present, growing evidence indicates that long non‐coding RNAs (lncRNAs) participate in the progression of glioma. The function of LOXL1‐AS1 in vasculogenic mimicry (VM) in glioma remains unclear. First, the expressions of TIAR, the lncRNA LOXL1‐AS1, miR‐374b‐5p and MMP14 were examined by qRT‐PCR and Western blot in both, glioma tissues and glioma cell lines. Proliferation, migration, invasion and tube formation assays were conducted to evaluate the roles of TIAR, LOXL1‐AS1, miR‐374b‐5p and MMP14 in malignant cellular behaviours in glioma cells. A nude mouse xenograft model and dual staining for CD34 and PAS were used to assess whether VM was affected by TIAR, LOXL1‐AS1 or miR‐374b‐5p in vivo. In this study, low levels of TIAR and high levels of LOXL1‐AS1 were found in glioma cells and tissues. TIAR downregulated the expression of LOXL1‐AS1 by destabilizing it. LOXL1‐AS1 acted like a miRNA sponge towards miR‐374b‐5p so that downregulation of the former greatly inhibited cell proliferation, migration, invasion and VM. Additionally, miR‐374b‐5p overexpression repressed malignant biological behaviours and VM in glioma by modifying MMP14. In summary, we demonstrated that TIAR combined with LOXL1‐AS1 modulates VM in glioma via the miR‐374b‐5p/MMP14 axis, revealing novel targets for glioma therapy.</description><subject>Amino Acid Oxidoreductases - metabolism</subject><subject>Angiogenesis</subject><subject>Animals</subject><subject>Antibodies</subject><subject>Behavior</subject><subject>CD34 antigen</subject><subject>Cell Line, Tumor</subject><subject>Cell lines</subject><subject>Cell migration</subject><subject>Cell Movement - genetics</subject><subject>Cell proliferation</subject><subject>Cell Proliferation - genetics</subject><subject>Colorectal cancer</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>Glioma</subject><subject>Glioma - genetics</subject><subject>Glioma - pathology</subject><subject>Glioma cells</subject><subject>Humans</subject><subject>Liver cancer</subject><subject>LOXL1‐AS1</subject><subject>Lung cancer</subject><subject>Matrix Metalloproteinase 14 - genetics</subject><subject>Matrix Metalloproteinase 14 - metabolism</subject><subject>Medical prognosis</subject><subject>Membranes</subject><subject>Metastasis</subject><subject>Mice</subject><subject>MicroRNAs</subject><subject>MicroRNAs - genetics</subject><subject>MicroRNAs - metabolism</subject><subject>Mimicry</subject><subject>miRNA</subject><subject>miR‐374b‐5p</subject><subject>MMP14</subject><subject>Nervous system</subject><subject>Non-coding RNA</subject><subject>Original</subject><subject>Proteins</subject><subject>RNA, Long Noncoding - genetics</subject><subject>RNA-Binding Proteins - metabolism</subject><subject>TIAR</subject><subject>Tumors</subject><subject>vasculogenic mimicry</subject><subject>Xenografts</subject><issn>1582-1838</issn><issn>1582-4934</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>PIMPY</sourceid><recordid>eNp90d1qFDEUB_Agiq3VGx9AAt6IsG3O5GOSG2FZ_KjsUqkVvAuZaWY2y2SyTWa27oXgI_iMPolZdy3qhbk5gfzyzwkHoadATiGvs1Xt_SmUQMQ9dAxcFhOmKLt_2IOk8gg9SmlFCBVA1UN0RJlUBIg8Rl_nF5_n8OPb9-lHwHXwfuxdbQbXt_jWDUt8dT69xD5cj50ZbMIbk-qxC63NCnvnXR232PW47VzwBm-cwdG2O-xCj0ODh6XN7jI_QEtW5cLXZ4vFB2DYfHHpMXrQmC7ZJ4d6gj69eX01ezeZX7w9n03nk5oxKSaKipILAVxRyRuhSFVWzHJuRFU1hc2GKyMJqIaCkBXhBSsqw3kjKS8ZVfQEvdrnrsfK2-va9kM0nV5H503c6mCc_vukd0vdho2W-brgLAe8OATEcDPaNGjvUm27zvQ2jEkXgkief8jLTJ__Q1dhjH3-XlYggbOSFVm93Ks6hpSibe6aAaJ3U9W7qepfU8342Z_t39HfY8wA9uDWdXb7nyj9frZY7EN_ApORreA</recordid><startdate>202201</startdate><enddate>202201</enddate><creator>Yi, Bolong</creator><creator>Li, Hao</creator><creator>Cai, Heng</creator><creator>Lou, Xin</creator><creator>Yu, Mingjun</creator><creator>Li, Zhen</creator><general>John Wiley & Sons, Inc</general><general>John Wiley and Sons Inc</general><scope>24P</scope><scope>WIN</scope><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>3V.</scope><scope>7QP</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>P64</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-1760-7741</orcidid></search><sort><creationdate>202201</creationdate><title>LOXL1‐AS1 communicating with TIAR modulates vasculogenic mimicry in glioma via regulation of the miR‐374b‐5p/MMP14 axis</title><author>Yi, Bolong ; Li, Hao ; Cai, Heng ; Lou, Xin ; Yu, Mingjun ; Li, Zhen</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4486-9367566159385f690b7b4e55a6bbf2e44859a8019f3168b05242ba55f83574393</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Amino Acid Oxidoreductases - metabolism</topic><topic>Angiogenesis</topic><topic>Animals</topic><topic>Antibodies</topic><topic>Behavior</topic><topic>CD34 antigen</topic><topic>Cell Line, Tumor</topic><topic>Cell lines</topic><topic>Cell migration</topic><topic>Cell Movement - genetics</topic><topic>Cell proliferation</topic><topic>Cell Proliferation - genetics</topic><topic>Colorectal cancer</topic><topic>Gene Expression Regulation, Neoplastic</topic><topic>Glioma</topic><topic>Glioma - genetics</topic><topic>Glioma - pathology</topic><topic>Glioma cells</topic><topic>Humans</topic><topic>Liver cancer</topic><topic>LOXL1‐AS1</topic><topic>Lung cancer</topic><topic>Matrix Metalloproteinase 14 - genetics</topic><topic>Matrix Metalloproteinase 14 - metabolism</topic><topic>Medical prognosis</topic><topic>Membranes</topic><topic>Metastasis</topic><topic>Mice</topic><topic>MicroRNAs</topic><topic>MicroRNAs - genetics</topic><topic>MicroRNAs - metabolism</topic><topic>Mimicry</topic><topic>miRNA</topic><topic>miR‐374b‐5p</topic><topic>MMP14</topic><topic>Nervous system</topic><topic>Non-coding RNA</topic><topic>Original</topic><topic>Proteins</topic><topic>RNA, Long Noncoding - genetics</topic><topic>RNA-Binding Proteins - metabolism</topic><topic>TIAR</topic><topic>Tumors</topic><topic>vasculogenic mimicry</topic><topic>Xenografts</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yi, Bolong</creatorcontrib><creatorcontrib>Li, Hao</creatorcontrib><creatorcontrib>Cai, Heng</creatorcontrib><creatorcontrib>Lou, Xin</creatorcontrib><creatorcontrib>Yu, Mingjun</creatorcontrib><creatorcontrib>Li, Zhen</creatorcontrib><collection>Wiley Online Library Open Access</collection><collection>Wiley Online Library Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</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)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biological Sciences</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Science Database (ProQuest)</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Publicly Available Content Database</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>ProQuest Central Basic</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of cellular and molecular medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yi, Bolong</au><au>Li, Hao</au><au>Cai, Heng</au><au>Lou, Xin</au><au>Yu, Mingjun</au><au>Li, Zhen</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>LOXL1‐AS1 communicating with TIAR modulates vasculogenic mimicry in glioma via regulation of the miR‐374b‐5p/MMP14 axis</atitle><jtitle>Journal of cellular and molecular medicine</jtitle><addtitle>J Cell Mol Med</addtitle><date>2022-01</date><risdate>2022</risdate><volume>26</volume><issue>2</issue><spage>475</spage><epage>490</epage><pages>475-490</pages><issn>1582-1838</issn><eissn>1582-4934</eissn><abstract>At present, growing evidence indicates that long non‐coding RNAs (lncRNAs) participate in the progression of glioma. The function of LOXL1‐AS1 in vasculogenic mimicry (VM) in glioma remains unclear. First, the expressions of TIAR, the lncRNA LOXL1‐AS1, miR‐374b‐5p and MMP14 were examined by qRT‐PCR and Western blot in both, glioma tissues and glioma cell lines. Proliferation, migration, invasion and tube formation assays were conducted to evaluate the roles of TIAR, LOXL1‐AS1, miR‐374b‐5p and MMP14 in malignant cellular behaviours in glioma cells. A nude mouse xenograft model and dual staining for CD34 and PAS were used to assess whether VM was affected by TIAR, LOXL1‐AS1 or miR‐374b‐5p in vivo. In this study, low levels of TIAR and high levels of LOXL1‐AS1 were found in glioma cells and tissues. TIAR downregulated the expression of LOXL1‐AS1 by destabilizing it. LOXL1‐AS1 acted like a miRNA sponge towards miR‐374b‐5p so that downregulation of the former greatly inhibited cell proliferation, migration, invasion and VM. Additionally, miR‐374b‐5p overexpression repressed malignant biological behaviours and VM in glioma by modifying MMP14. In summary, we demonstrated that TIAR combined with LOXL1‐AS1 modulates VM in glioma via the miR‐374b‐5p/MMP14 axis, revealing novel targets for glioma therapy.</abstract><cop>England</cop><pub>John Wiley & Sons, Inc</pub><pmid>34890108</pmid><doi>10.1111/jcmm.17106</doi><tpages>16</tpages><orcidid>https://orcid.org/0000-0003-1760-7741</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Amino Acid Oxidoreductases - metabolism Angiogenesis Animals Antibodies Behavior CD34 antigen Cell Line, Tumor Cell lines Cell migration Cell Movement - genetics Cell proliferation Cell Proliferation - genetics Colorectal cancer Gene Expression Regulation, Neoplastic Glioma Glioma - genetics Glioma - pathology Glioma cells Humans Liver cancer LOXL1‐AS1 Lung cancer Matrix Metalloproteinase 14 - genetics Matrix Metalloproteinase 14 - metabolism Medical prognosis Membranes Metastasis Mice MicroRNAs MicroRNAs - genetics MicroRNAs - metabolism Mimicry miRNA miR‐374b‐5p MMP14 Nervous system Non-coding RNA Original Proteins RNA, Long Noncoding - genetics RNA-Binding Proteins - metabolism TIAR Tumors vasculogenic mimicry Xenografts |
title | LOXL1‐AS1 communicating with TIAR modulates vasculogenic mimicry in glioma via regulation of the miR‐374b‐5p/MMP14 axis |
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