Correlation of N-cadherin expression in high grade gliomas with tissue invasion
Cadherins are Ca2+-dependent cell adhesion molecules that play an important role in tissue construction and morphogenesis in multicellular organisms. Over the last few years, reports have emerged in the literature describing the involvement of cadherins in tumor invasion and metastasis. Cadherins ty...
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description | Cadherins are Ca2+-dependent cell adhesion molecules that play an important role in tissue construction and morphogenesis in multicellular organisms. Over the last few years, reports have emerged in the literature describing the involvement of cadherins in tumor invasion and metastasis. Cadherins typically demonstrate up and down-regulation according to the biological needs of the tissue. Additionally, up-regulation of N-cadherin is thought to be important for tumor formation in early stages of tumor development. We studied N-cadherin in surgical specimens of patients with primary glioblastoma by microarray analysis and found that N-cadherin mRNA expression is up-regulated compared to normal brain. To study the effects of N-cadherin expression on invasion and metastasis in vitro and in vivo, we overexpressed N-cadherin in the rat C6 glioma cell line which normally has low levels of N-cadherin. We found that up-regulation of N-cadherin resulted in a slight decreased adhesion to type IV collagen, fibronectin, and laminin, but statistically significant decreased adhesion to type I collagen. Furthermore, increased expression of N-cadherin correlated with a dramatic decrease in invasive behavior in extracellular matrix invasion assays. We then proceeded to study these cell lines in vivo in a rat intracranial glioma model, and found that N-cadherin expression inversely correlated with invasion into surrounding tissues, irregular margins, and extracranial invasion. In summary, these data collectively demonstrate that N-cadherin levels are important in the malignant behavior of gliomas, and may serve as a prognostic indicator for patients with high-grade gliomas. |
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Over the last few years, reports have emerged in the literature describing the involvement of cadherins in tumor invasion and metastasis. Cadherins typically demonstrate up and down-regulation according to the biological needs of the tissue. Additionally, up-regulation of N-cadherin is thought to be important for tumor formation in early stages of tumor development. We studied N-cadherin in surgical specimens of patients with primary glioblastoma by microarray analysis and found that N-cadherin mRNA expression is up-regulated compared to normal brain. To study the effects of N-cadherin expression on invasion and metastasis in vitro and in vivo, we overexpressed N-cadherin in the rat C6 glioma cell line which normally has low levels of N-cadherin. We found that up-regulation of N-cadherin resulted in a slight decreased adhesion to type IV collagen, fibronectin, and laminin, but statistically significant decreased adhesion to type I collagen. Furthermore, increased expression of N-cadherin correlated with a dramatic decrease in invasive behavior in extracellular matrix invasion assays. We then proceeded to study these cell lines in vivo in a rat intracranial glioma model, and found that N-cadherin expression inversely correlated with invasion into surrounding tissues, irregular margins, and extracranial invasion. In summary, these data collectively demonstrate that N-cadherin levels are important in the malignant behavior of gliomas, and may serve as a prognostic indicator for patients with high-grade gliomas.</description><identifier>ISSN: 0167-594X</identifier><identifier>EISSN: 1573-7373</identifier><identifier>DOI: 10.1023/B:NEON.0000040811.14908.f2</identifier><identifier>PMID: 15527101</identifier><identifier>CODEN: JNODD2</identifier><language>eng</language><publisher>Dordrecht: Springer</publisher><subject>Adult ; Aged ; Aged, 80 and over ; Animals ; Antineoplastic agents ; Biological and medical sciences ; Brain Neoplasms - metabolism ; Brain Neoplasms - pathology ; Cadherins - genetics ; Cadherins - metabolism ; Cell Adhesion ; Cell Aggregation - drug effects ; Chemotherapy ; Collagen Type I - metabolism ; Collagen Type IV - metabolism ; Female ; Fibronectins - metabolism ; Gene Expression Profiling ; Gene Expression Regulation, Neoplastic ; Glioma - metabolism ; Glioma - pathology ; Humans ; Laminin - metabolism ; Male ; Medical sciences ; Middle Aged ; Neoplasm Invasiveness ; Neoplasm Staging ; Neurology ; Oligonucleotide Array Sequence Analysis ; Pharmacology. Drug treatments ; Rats ; Rats, Sprague-Dawley ; RNA, Messenger - metabolism ; Tumor Cells, Cultured ; Tumors of the nervous system. Phacomatoses</subject><ispartof>Journal of neuro-oncology, 2004-10, Vol.70 (1), p.3-15</ispartof><rights>2004 INIST-CNRS</rights><rights>Copyright (c) 2004 Kluwer Academic Publishers</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c429t-7d46eb068be0af18830f642d49607e8b2fc3170acba7487f5b5e3d5feb1c1b643</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=16171043$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15527101$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>ASANO, Kenichiro</creatorcontrib><creatorcontrib>DUNTSCH, Christopher D</creatorcontrib><creatorcontrib>QIHONG ZHOU</creatorcontrib><creatorcontrib>WEIMAR, James D</creatorcontrib><creatorcontrib>BORDELON, Dwight</creatorcontrib><creatorcontrib>ROBERTSON, Jon H</creatorcontrib><creatorcontrib>POURMOTABBED, Tayebeh</creatorcontrib><title>Correlation of N-cadherin expression in high grade gliomas with tissue invasion</title><title>Journal of neuro-oncology</title><addtitle>J Neurooncol</addtitle><description>Cadherins are Ca2+-dependent cell adhesion molecules that play an important role in tissue construction and morphogenesis in multicellular organisms. Over the last few years, reports have emerged in the literature describing the involvement of cadherins in tumor invasion and metastasis. Cadherins typically demonstrate up and down-regulation according to the biological needs of the tissue. Additionally, up-regulation of N-cadherin is thought to be important for tumor formation in early stages of tumor development. We studied N-cadherin in surgical specimens of patients with primary glioblastoma by microarray analysis and found that N-cadherin mRNA expression is up-regulated compared to normal brain. To study the effects of N-cadherin expression on invasion and metastasis in vitro and in vivo, we overexpressed N-cadherin in the rat C6 glioma cell line which normally has low levels of N-cadherin. We found that up-regulation of N-cadherin resulted in a slight decreased adhesion to type IV collagen, fibronectin, and laminin, but statistically significant decreased adhesion to type I collagen. Furthermore, increased expression of N-cadherin correlated with a dramatic decrease in invasive behavior in extracellular matrix invasion assays. We then proceeded to study these cell lines in vivo in a rat intracranial glioma model, and found that N-cadherin expression inversely correlated with invasion into surrounding tissues, irregular margins, and extracranial invasion. In summary, these data collectively demonstrate that N-cadherin levels are important in the malignant behavior of gliomas, and may serve as a prognostic indicator for patients with high-grade gliomas.</description><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Animals</subject><subject>Antineoplastic agents</subject><subject>Biological and medical sciences</subject><subject>Brain Neoplasms - metabolism</subject><subject>Brain Neoplasms - pathology</subject><subject>Cadherins - genetics</subject><subject>Cadherins - metabolism</subject><subject>Cell Adhesion</subject><subject>Cell Aggregation - drug effects</subject><subject>Chemotherapy</subject><subject>Collagen Type I - metabolism</subject><subject>Collagen Type IV - metabolism</subject><subject>Female</subject><subject>Fibronectins - metabolism</subject><subject>Gene Expression Profiling</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>Glioma - metabolism</subject><subject>Glioma - pathology</subject><subject>Humans</subject><subject>Laminin - metabolism</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Neoplasm Invasiveness</subject><subject>Neoplasm Staging</subject><subject>Neurology</subject><subject>Oligonucleotide Array Sequence Analysis</subject><subject>Pharmacology. Drug treatments</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>RNA, Messenger - metabolism</subject><subject>Tumor Cells, Cultured</subject><subject>Tumors of the nervous system. 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Drug treatments</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>RNA, Messenger - metabolism</topic><topic>Tumor Cells, Cultured</topic><topic>Tumors of the nervous system. Phacomatoses</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>ASANO, Kenichiro</creatorcontrib><creatorcontrib>DUNTSCH, Christopher D</creatorcontrib><creatorcontrib>QIHONG ZHOU</creatorcontrib><creatorcontrib>WEIMAR, James D</creatorcontrib><creatorcontrib>BORDELON, Dwight</creatorcontrib><creatorcontrib>ROBERTSON, Jon H</creatorcontrib><creatorcontrib>POURMOTABBED, Tayebeh</creatorcontrib><collection>Pascal-Francis</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>Neurosciences Abstracts</collection><collection>Health & Medical Collection (Proquest)</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database (Proquest)</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 UK/Ireland</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>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</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><jtitle>Journal of neuro-oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>ASANO, Kenichiro</au><au>DUNTSCH, Christopher D</au><au>QIHONG ZHOU</au><au>WEIMAR, James D</au><au>BORDELON, Dwight</au><au>ROBERTSON, Jon H</au><au>POURMOTABBED, Tayebeh</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Correlation of N-cadherin expression in high grade gliomas with tissue invasion</atitle><jtitle>Journal of neuro-oncology</jtitle><addtitle>J Neurooncol</addtitle><date>2004-10-01</date><risdate>2004</risdate><volume>70</volume><issue>1</issue><spage>3</spage><epage>15</epage><pages>3-15</pages><issn>0167-594X</issn><eissn>1573-7373</eissn><coden>JNODD2</coden><abstract>Cadherins are Ca2+-dependent cell adhesion molecules that play an important role in tissue construction and morphogenesis in multicellular organisms. Over the last few years, reports have emerged in the literature describing the involvement of cadherins in tumor invasion and metastasis. Cadherins typically demonstrate up and down-regulation according to the biological needs of the tissue. Additionally, up-regulation of N-cadherin is thought to be important for tumor formation in early stages of tumor development. We studied N-cadherin in surgical specimens of patients with primary glioblastoma by microarray analysis and found that N-cadherin mRNA expression is up-regulated compared to normal brain. To study the effects of N-cadherin expression on invasion and metastasis in vitro and in vivo, we overexpressed N-cadherin in the rat C6 glioma cell line which normally has low levels of N-cadherin. We found that up-regulation of N-cadherin resulted in a slight decreased adhesion to type IV collagen, fibronectin, and laminin, but statistically significant decreased adhesion to type I collagen. Furthermore, increased expression of N-cadherin correlated with a dramatic decrease in invasive behavior in extracellular matrix invasion assays. We then proceeded to study these cell lines in vivo in a rat intracranial glioma model, and found that N-cadherin expression inversely correlated with invasion into surrounding tissues, irregular margins, and extracranial invasion. In summary, these data collectively demonstrate that N-cadherin levels are important in the malignant behavior of gliomas, and may serve as a prognostic indicator for patients with high-grade gliomas.</abstract><cop>Dordrecht</cop><pub>Springer</pub><pmid>15527101</pmid><doi>10.1023/B:NEON.0000040811.14908.f2</doi><tpages>13</tpages></addata></record> |
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subjects | Adult Aged Aged, 80 and over Animals Antineoplastic agents Biological and medical sciences Brain Neoplasms - metabolism Brain Neoplasms - pathology Cadherins - genetics Cadherins - metabolism Cell Adhesion Cell Aggregation - drug effects Chemotherapy Collagen Type I - metabolism Collagen Type IV - metabolism Female Fibronectins - metabolism Gene Expression Profiling Gene Expression Regulation, Neoplastic Glioma - metabolism Glioma - pathology Humans Laminin - metabolism Male Medical sciences Middle Aged Neoplasm Invasiveness Neoplasm Staging Neurology Oligonucleotide Array Sequence Analysis Pharmacology. Drug treatments Rats Rats, Sprague-Dawley RNA, Messenger - metabolism Tumor Cells, Cultured Tumors of the nervous system. Phacomatoses |
title | Correlation of N-cadherin expression in high grade gliomas with tissue invasion |
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