Stage-dependent expression of an angiogenic agent and vascular organization in experimental skin tumor development
Increased angiogenesis and expression of antibodies to vascular endothelial growth factor (VEGF), an angiogenic agent, have been shown in the tumor development of many tissues. Areas of skin expressing VEGF and total volume of vessels expressing laminin in the wall were measured in chemical carcinog...
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Veröffentlicht in: | Toxicologic pathology 2003-09, Vol.31 (5), p.539-548 |
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creator | NÄYHÄ, Veera LAITAKARI, Jaakko STENBÄCK, Frej |
description | Increased angiogenesis and expression of antibodies to vascular endothelial growth factor (VEGF), an angiogenic agent, have been shown in the tumor development of many tissues. Areas of skin expressing VEGF and total volume of vessels expressing laminin in the wall were measured in chemical carcinogen-exposed mice using CAS-200 morphometry apparatus having a sensitivity exceeding 99% and reproducibility exceeding 99%. The area of VEGF expression was increased in carcinogen-exposed skin, dysplasia and in well-differentiated squamous cell carcinomas, but decreased in squamous cell carcinomas with decreased degree of differentiation. The vessel volume increased prior to the formation of tumors in carcinogen-exposed skin as well as in highly malignant neoplasms. In well-differentiated squamous cell carcinomas with an expansive growth pattern, the vessels were parallel to the basal membrane, in moderately differentiated tumors the vessels were in the direction of tumor invasion, and in poorly differentiated tumors, active angiogenesis consisted of numerous, enlarged vessels within the tumor. This study showed increased VEGF expression and number of vessels occurring in early stages of skin tumor development, pointing to a role of angiogenesis in chemical risk assessment and in cancer prevention. Altered vessel structure and vessel arrangement were distinct in later stages of tumor growth and in malignant neoplasms, pointing to the utility of detailed vessel analysis in neoplasm characterization. |
doi_str_mv | 10.1080/01926230309791 |
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Areas of skin expressing VEGF and total volume of vessels expressing laminin in the wall were measured in chemical carcinogen-exposed mice using CAS-200 morphometry apparatus having a sensitivity exceeding 99% and reproducibility exceeding 99%. The area of VEGF expression was increased in carcinogen-exposed skin, dysplasia and in well-differentiated squamous cell carcinomas, but decreased in squamous cell carcinomas with decreased degree of differentiation. The vessel volume increased prior to the formation of tumors in carcinogen-exposed skin as well as in highly malignant neoplasms. In well-differentiated squamous cell carcinomas with an expansive growth pattern, the vessels were parallel to the basal membrane, in moderately differentiated tumors the vessels were in the direction of tumor invasion, and in poorly differentiated tumors, active angiogenesis consisted of numerous, enlarged vessels within the tumor. This study showed increased VEGF expression and number of vessels occurring in early stages of skin tumor development, pointing to a role of angiogenesis in chemical risk assessment and in cancer prevention. Altered vessel structure and vessel arrangement were distinct in later stages of tumor growth and in malignant neoplasms, pointing to the utility of detailed vessel analysis in neoplasm characterization.</description><identifier>ISSN: 0192-6233</identifier><identifier>EISSN: 1533-1601</identifier><identifier>DOI: 10.1080/01926230309791</identifier><identifier>PMID: 14692622</identifier><language>eng</language><publisher>Thousand Oaks, CA: Sage</publisher><subject>Animal tumors. Experimental tumors ; Animals ; Antibodies - metabolism ; Biological and medical sciences ; Carcinoma, Squamous Cell - blood supply ; Carcinoma, Squamous Cell - metabolism ; Disease Progression ; Experimental skin tumors ; Female ; Image Cytometry ; laminin ; Laminin - metabolism ; Medical sciences ; Mice ; Mice, Inbred Strains ; Neoplasm Staging ; Neovascularization, Pathologic - metabolism ; Reproducibility of Results ; Sensitivity and Specificity ; Skin Neoplasms - blood supply ; Skin Neoplasms - metabolism ; Tumors ; vascular endothelial growth factor ; Vascular Endothelial Growth Factor A - metabolism</subject><ispartof>Toxicologic pathology, 2003-09, Vol.31 (5), p.539-548</ispartof><rights>2004 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=15201812$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/14692622$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>NÄYHÄ, Veera</creatorcontrib><creatorcontrib>LAITAKARI, Jaakko</creatorcontrib><creatorcontrib>STENBÄCK, Frej</creatorcontrib><title>Stage-dependent expression of an angiogenic agent and vascular organization in experimental skin tumor development</title><title>Toxicologic pathology</title><addtitle>Toxicol Pathol</addtitle><description>Increased angiogenesis and expression of antibodies to vascular endothelial growth factor (VEGF), an angiogenic agent, have been shown in the tumor development of many tissues. Areas of skin expressing VEGF and total volume of vessels expressing laminin in the wall were measured in chemical carcinogen-exposed mice using CAS-200 morphometry apparatus having a sensitivity exceeding 99% and reproducibility exceeding 99%. The area of VEGF expression was increased in carcinogen-exposed skin, dysplasia and in well-differentiated squamous cell carcinomas, but decreased in squamous cell carcinomas with decreased degree of differentiation. The vessel volume increased prior to the formation of tumors in carcinogen-exposed skin as well as in highly malignant neoplasms. In well-differentiated squamous cell carcinomas with an expansive growth pattern, the vessels were parallel to the basal membrane, in moderately differentiated tumors the vessels were in the direction of tumor invasion, and in poorly differentiated tumors, active angiogenesis consisted of numerous, enlarged vessels within the tumor. This study showed increased VEGF expression and number of vessels occurring in early stages of skin tumor development, pointing to a role of angiogenesis in chemical risk assessment and in cancer prevention. Altered vessel structure and vessel arrangement were distinct in later stages of tumor growth and in malignant neoplasms, pointing to the utility of detailed vessel analysis in neoplasm characterization.</description><subject>Animal tumors. Experimental tumors</subject><subject>Animals</subject><subject>Antibodies - metabolism</subject><subject>Biological and medical sciences</subject><subject>Carcinoma, Squamous Cell - blood supply</subject><subject>Carcinoma, Squamous Cell - metabolism</subject><subject>Disease Progression</subject><subject>Experimental skin tumors</subject><subject>Female</subject><subject>Image Cytometry</subject><subject>laminin</subject><subject>Laminin - metabolism</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Inbred Strains</subject><subject>Neoplasm Staging</subject><subject>Neovascularization, Pathologic - metabolism</subject><subject>Reproducibility of Results</subject><subject>Sensitivity and Specificity</subject><subject>Skin Neoplasms - blood supply</subject><subject>Skin Neoplasms - metabolism</subject><subject>Tumors</subject><subject>vascular endothelial growth factor</subject><subject>Vascular Endothelial Growth Factor A - metabolism</subject><issn>0192-6233</issn><issn>1533-1601</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkUtLxDAUhYMozji6dSnd6K5jHn3NUgZfMODC2Zc77U2JtklN2kH99SZMYRAuBO75zoF7Qsg1o0tGC3pP2YpnXFBBV_mKnZA5S4WIWUbZKZkHMfaqmJEL5z4oZQVL6DmZsSQLNj4n9n2ABuMae9Q16iHC796ic8royMgItJ9GmQa1qiJPegJ0He3BVWMLNjK2Aa1-YQgGpYMdreo8B23kPv1mGDtjoxr32Jo-CJfkTELr8Gp6F2T79Lhdv8Sbt-fX9cMmrgTNh1hIyHJZcLkDIZDxhDK6y2ua8KxArEVe8EQIWIEsqtwfnfGkStNUFKJOcsrEgtwdYntrvkZ0Q9kpV2HbgkYzujIU50MyDy4PYGWNcxZl2fsLwP6UjJah5PJ_yd5wMyWPuw7rIz616oHbCfA1QSst6Eq5I5fy8BNc_AF8LIS4</recordid><startdate>20030901</startdate><enddate>20030901</enddate><creator>NÄYHÄ, Veera</creator><creator>LAITAKARI, Jaakko</creator><creator>STENBÄCK, Frej</creator><general>Sage</general><scope>IQODW</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>7U7</scope><scope>C1K</scope></search><sort><creationdate>20030901</creationdate><title>Stage-dependent expression of an angiogenic agent and vascular organization in experimental skin tumor development</title><author>NÄYHÄ, Veera ; LAITAKARI, Jaakko ; STENBÄCK, Frej</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c307t-3fa67f82fba33e124010b7d04268eed3782433a9af8c7533624c555383d47013</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Animal tumors. Experimental tumors</topic><topic>Animals</topic><topic>Antibodies - metabolism</topic><topic>Biological and medical sciences</topic><topic>Carcinoma, Squamous Cell - blood supply</topic><topic>Carcinoma, Squamous Cell - metabolism</topic><topic>Disease Progression</topic><topic>Experimental skin tumors</topic><topic>Female</topic><topic>Image Cytometry</topic><topic>laminin</topic><topic>Laminin - metabolism</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Mice, Inbred Strains</topic><topic>Neoplasm Staging</topic><topic>Neovascularization, Pathologic - metabolism</topic><topic>Reproducibility of Results</topic><topic>Sensitivity and Specificity</topic><topic>Skin Neoplasms - blood supply</topic><topic>Skin Neoplasms - metabolism</topic><topic>Tumors</topic><topic>vascular endothelial growth factor</topic><topic>Vascular Endothelial Growth Factor A - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>NÄYHÄ, Veera</creatorcontrib><creatorcontrib>LAITAKARI, Jaakko</creatorcontrib><creatorcontrib>STENBÄCK, Frej</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>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>Toxicologic pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>NÄYHÄ, Veera</au><au>LAITAKARI, Jaakko</au><au>STENBÄCK, Frej</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Stage-dependent expression of an angiogenic agent and vascular organization in experimental skin tumor development</atitle><jtitle>Toxicologic pathology</jtitle><addtitle>Toxicol Pathol</addtitle><date>2003-09-01</date><risdate>2003</risdate><volume>31</volume><issue>5</issue><spage>539</spage><epage>548</epage><pages>539-548</pages><issn>0192-6233</issn><eissn>1533-1601</eissn><abstract>Increased angiogenesis and expression of antibodies to vascular endothelial growth factor (VEGF), an angiogenic agent, have been shown in the tumor development of many tissues. Areas of skin expressing VEGF and total volume of vessels expressing laminin in the wall were measured in chemical carcinogen-exposed mice using CAS-200 morphometry apparatus having a sensitivity exceeding 99% and reproducibility exceeding 99%. The area of VEGF expression was increased in carcinogen-exposed skin, dysplasia and in well-differentiated squamous cell carcinomas, but decreased in squamous cell carcinomas with decreased degree of differentiation. The vessel volume increased prior to the formation of tumors in carcinogen-exposed skin as well as in highly malignant neoplasms. In well-differentiated squamous cell carcinomas with an expansive growth pattern, the vessels were parallel to the basal membrane, in moderately differentiated tumors the vessels were in the direction of tumor invasion, and in poorly differentiated tumors, active angiogenesis consisted of numerous, enlarged vessels within the tumor. 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subjects | Animal tumors. Experimental tumors Animals Antibodies - metabolism Biological and medical sciences Carcinoma, Squamous Cell - blood supply Carcinoma, Squamous Cell - metabolism Disease Progression Experimental skin tumors Female Image Cytometry laminin Laminin - metabolism Medical sciences Mice Mice, Inbred Strains Neoplasm Staging Neovascularization, Pathologic - metabolism Reproducibility of Results Sensitivity and Specificity Skin Neoplasms - blood supply Skin Neoplasms - metabolism Tumors vascular endothelial growth factor Vascular Endothelial Growth Factor A - metabolism |
title | Stage-dependent expression of an angiogenic agent and vascular organization in experimental skin tumor development |
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