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Vascular endothelial growth factor and osteopontin in stage I lung adenocarcinoma
Tumor growth and metastasis are angiogenesis-dependent processes initiated and regulated by a number of cytokines. Vascular endothelial growth factor (VEGF) is a potent angiogenic protein with a selective mitogenic effect on vascular endothelial cells. Osteopontin (OPN) induces endothelial cell migr...
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Published in: | American journal of respiratory and critical care medicine 1999-10, Vol.160 (4), p.1269-1273 |
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container_title | American journal of respiratory and critical care medicine |
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creator | SHIJUBO, N UEDE, T KON, S MAEDA, M SEGAWA, T IMADA, A HIRASAWA, M ABE, S |
description | Tumor growth and metastasis are angiogenesis-dependent processes initiated and regulated by a number of cytokines. Vascular endothelial growth factor (VEGF) is a potent angiogenic protein with a selective mitogenic effect on vascular endothelial cells. Osteopontin (OPN) induces endothelial cell migration and upregulates endothelial cell migration induced by VEGF. To clarify the cooperative role of VEGF and OPN in tumor angiogenesis, we stained VEGF, OPN, and CD34 immunohistochemically in 87 cases of stage I non-small cell lung cancer (adenocarcinoma, 55, and squamous cell carcinoma, 32). Of the 87 patients studied, 27 patients had postoperative relapse and 60 patients did not. VEGF was found in 34 of 55 cases of adenocarcinomas and 14 of 32 squamous cell carcinomas, and OPN was found in 30 of 55 adenocarcinomas and 10 of 32 squamous cell carcinomas. In adenocarcinoma, microvessel counts of VEGF-positive and OPN-positive tumors were significantly higher than VEGF-negative and OPN-negative tumors, respectively, whereas in squamous cell carcinoma they were not. More importantly, patients with VEGF- and OPN-positive stage I lung adenocarcinoma had significantly worse prognosis as compared with other groups. Cooperation of OPN is important in VEGF-mediated tumor angiogenesis in stage I lung adenocarcinoma. |
doi_str_mv | 10.1164/ajrccm.160.4.9807094 |
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Vascular endothelial growth factor (VEGF) is a potent angiogenic protein with a selective mitogenic effect on vascular endothelial cells. Osteopontin (OPN) induces endothelial cell migration and upregulates endothelial cell migration induced by VEGF. To clarify the cooperative role of VEGF and OPN in tumor angiogenesis, we stained VEGF, OPN, and CD34 immunohistochemically in 87 cases of stage I non-small cell lung cancer (adenocarcinoma, 55, and squamous cell carcinoma, 32). Of the 87 patients studied, 27 patients had postoperative relapse and 60 patients did not. VEGF was found in 34 of 55 cases of adenocarcinomas and 14 of 32 squamous cell carcinomas, and OPN was found in 30 of 55 adenocarcinomas and 10 of 32 squamous cell carcinomas. In adenocarcinoma, microvessel counts of VEGF-positive and OPN-positive tumors were significantly higher than VEGF-negative and OPN-negative tumors, respectively, whereas in squamous cell carcinoma they were not. More importantly, patients with VEGF- and OPN-positive stage I lung adenocarcinoma had significantly worse prognosis as compared with other groups. 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Vascular endothelial growth factor (VEGF) is a potent angiogenic protein with a selective mitogenic effect on vascular endothelial cells. Osteopontin (OPN) induces endothelial cell migration and upregulates endothelial cell migration induced by VEGF. To clarify the cooperative role of VEGF and OPN in tumor angiogenesis, we stained VEGF, OPN, and CD34 immunohistochemically in 87 cases of stage I non-small cell lung cancer (adenocarcinoma, 55, and squamous cell carcinoma, 32). Of the 87 patients studied, 27 patients had postoperative relapse and 60 patients did not. VEGF was found in 34 of 55 cases of adenocarcinomas and 14 of 32 squamous cell carcinomas, and OPN was found in 30 of 55 adenocarcinomas and 10 of 32 squamous cell carcinomas. In adenocarcinoma, microvessel counts of VEGF-positive and OPN-positive tumors were significantly higher than VEGF-negative and OPN-negative tumors, respectively, whereas in squamous cell carcinoma they were not. More importantly, patients with VEGF- and OPN-positive stage I lung adenocarcinoma had significantly worse prognosis as compared with other groups. Cooperation of OPN is important in VEGF-mediated tumor angiogenesis in stage I lung adenocarcinoma.</description><subject>Adenocarcinoma - blood supply</subject><subject>Adenocarcinoma - chemistry</subject><subject>Adenocarcinoma - mortality</subject><subject>Adenocarcinoma - pathology</subject><subject>Biological and medical sciences</subject><subject>Carcinoma, Non-Small-Cell Lung - blood supply</subject><subject>Carcinoma, Non-Small-Cell Lung - chemistry</subject><subject>Carcinoma, Non-Small-Cell Lung - pathology</subject><subject>Carcinoma, Squamous Cell - chemistry</subject><subject>Carcinoma, Squamous Cell - pathology</subject><subject>Endothelial Growth Factors - analysis</subject><subject>Female</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Lung Neoplasms - blood supply</subject><subject>Lung Neoplasms - chemistry</subject><subject>Lung Neoplasms - mortality</subject><subject>Lung Neoplasms - pathology</subject><subject>Lymphokines - analysis</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Neovascularization, Pathologic</subject><subject>Osteopontin</subject><subject>Pneumology</subject><subject>Prognosis</subject><subject>Sialoglycoproteins - analysis</subject><subject>Survival Rate</subject><subject>Tumors of the respiratory system and mediastinum</subject><subject>Vascular Endothelial Growth Factor A</subject><subject>Vascular Endothelial Growth Factors</subject><issn>1073-449X</issn><issn>1535-4970</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><recordid>eNpNkF1LwzAUhoMobk7_gUguxLvOkyVNk0sZfgwGIqh4F9Ik3TraZCYt4r-3soLCgfdcPO978SB0SWBOCGe3eheNaeeEw5zNpYACJDtCU5LTPGOygOPhh4JmjMmPCTpLaQdAFoLAKZoQyEEIIqbo5V0n0zc6Yudt6LauqXWDNzF8dVtcadOFiLW3OKTOhX3wXe3xcKnTG4dXuOn9BmvrfDA6mtqHVp-jk0o3yV2MOUNvD_evy6ds_fy4Wt6tM0Ol6LKqlAUBkRelNUKSSltBnKQlsbktSgrUWleWwvKyoLnklHPOhGNSsNwxsITO0M1hdx_DZ-9Sp9o6Gdc02rvQJ1WAgJwzGEB2AE0MKUVXqX2sWx2_FQH1q1IdVKpBpWJqVDnUrsb9vmyd_Vc6uBuA6xEYFOqmitqbOv1xUiy4WNAfz7l-bA</recordid><startdate>19991001</startdate><enddate>19991001</enddate><creator>SHIJUBO, N</creator><creator>UEDE, T</creator><creator>KON, S</creator><creator>MAEDA, M</creator><creator>SEGAWA, T</creator><creator>IMADA, A</creator><creator>HIRASAWA, M</creator><creator>ABE, S</creator><general>American Lung Association</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>7X8</scope></search><sort><creationdate>19991001</creationdate><title>Vascular endothelial growth factor and osteopontin in stage I lung adenocarcinoma</title><author>SHIJUBO, N ; UEDE, T ; KON, S ; MAEDA, M ; SEGAWA, T ; IMADA, A ; HIRASAWA, M ; ABE, S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c398t-fb9710857bdc891fad81e93b1d5d7b303ddebb8d6b73596366648e49845e40d13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Adenocarcinoma - blood supply</topic><topic>Adenocarcinoma - chemistry</topic><topic>Adenocarcinoma - mortality</topic><topic>Adenocarcinoma - pathology</topic><topic>Biological and medical sciences</topic><topic>Carcinoma, Non-Small-Cell Lung - blood supply</topic><topic>Carcinoma, Non-Small-Cell Lung - chemistry</topic><topic>Carcinoma, Non-Small-Cell Lung - pathology</topic><topic>Carcinoma, Squamous Cell - chemistry</topic><topic>Carcinoma, Squamous Cell - pathology</topic><topic>Endothelial Growth Factors - analysis</topic><topic>Female</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Lung Neoplasms - blood supply</topic><topic>Lung Neoplasms - chemistry</topic><topic>Lung Neoplasms - mortality</topic><topic>Lung Neoplasms - pathology</topic><topic>Lymphokines - analysis</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Neovascularization, Pathologic</topic><topic>Osteopontin</topic><topic>Pneumology</topic><topic>Prognosis</topic><topic>Sialoglycoproteins - analysis</topic><topic>Survival Rate</topic><topic>Tumors of the respiratory system and mediastinum</topic><topic>Vascular Endothelial Growth Factor A</topic><topic>Vascular Endothelial Growth Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>SHIJUBO, N</creatorcontrib><creatorcontrib>UEDE, T</creatorcontrib><creatorcontrib>KON, S</creatorcontrib><creatorcontrib>MAEDA, M</creatorcontrib><creatorcontrib>SEGAWA, T</creatorcontrib><creatorcontrib>IMADA, A</creatorcontrib><creatorcontrib>HIRASAWA, M</creatorcontrib><creatorcontrib>ABE, S</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>MEDLINE - Academic</collection><jtitle>American journal of respiratory and critical care medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>SHIJUBO, N</au><au>UEDE, T</au><au>KON, S</au><au>MAEDA, M</au><au>SEGAWA, T</au><au>IMADA, A</au><au>HIRASAWA, M</au><au>ABE, S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Vascular endothelial growth factor and osteopontin in stage I lung adenocarcinoma</atitle><jtitle>American journal of respiratory and critical care medicine</jtitle><addtitle>Am J Respir Crit Care Med</addtitle><date>1999-10-01</date><risdate>1999</risdate><volume>160</volume><issue>4</issue><spage>1269</spage><epage>1273</epage><pages>1269-1273</pages><issn>1073-449X</issn><eissn>1535-4970</eissn><abstract>Tumor growth and metastasis are angiogenesis-dependent processes initiated and regulated by a number of cytokines. Vascular endothelial growth factor (VEGF) is a potent angiogenic protein with a selective mitogenic effect on vascular endothelial cells. Osteopontin (OPN) induces endothelial cell migration and upregulates endothelial cell migration induced by VEGF. To clarify the cooperative role of VEGF and OPN in tumor angiogenesis, we stained VEGF, OPN, and CD34 immunohistochemically in 87 cases of stage I non-small cell lung cancer (adenocarcinoma, 55, and squamous cell carcinoma, 32). Of the 87 patients studied, 27 patients had postoperative relapse and 60 patients did not. VEGF was found in 34 of 55 cases of adenocarcinomas and 14 of 32 squamous cell carcinomas, and OPN was found in 30 of 55 adenocarcinomas and 10 of 32 squamous cell carcinomas. In adenocarcinoma, microvessel counts of VEGF-positive and OPN-positive tumors were significantly higher than VEGF-negative and OPN-negative tumors, respectively, whereas in squamous cell carcinoma they were not. 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subjects | Adenocarcinoma - blood supply Adenocarcinoma - chemistry Adenocarcinoma - mortality Adenocarcinoma - pathology Biological and medical sciences Carcinoma, Non-Small-Cell Lung - blood supply Carcinoma, Non-Small-Cell Lung - chemistry Carcinoma, Non-Small-Cell Lung - pathology Carcinoma, Squamous Cell - chemistry Carcinoma, Squamous Cell - pathology Endothelial Growth Factors - analysis Female Humans Immunohistochemistry Lung Neoplasms - blood supply Lung Neoplasms - chemistry Lung Neoplasms - mortality Lung Neoplasms - pathology Lymphokines - analysis Male Medical sciences Neovascularization, Pathologic Osteopontin Pneumology Prognosis Sialoglycoproteins - analysis Survival Rate Tumors of the respiratory system and mediastinum Vascular Endothelial Growth Factor A Vascular Endothelial Growth Factors |
title | Vascular endothelial growth factor and osteopontin in stage I lung adenocarcinoma |
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