Clinical significance of urinary vascular endothelial growth factor and microvessel density in patients with renal cell carcinoma

Objectives. To investigate the urinary vascular endothelial growth factor (VEGF) levels from patients with renal cell carcinoma (RCC). Neovascularization, an essential event for the growth of solid tumors, is regulated by a number of angiogenic factors. VEGF is thought to exert potent angiogenic act...

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Veröffentlicht in:Urology (Ridgewood, N.J.) N.J.), 2001-12, Vol.58 (6), p.904-908
Hauptverfasser: Chang, Sung-Goo, Jeon, Sung-Hyun, Lee, Sun-Ju, Choi, Joong-Myung, Kim, Youn-Wha
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container_issue 6
container_start_page 904
container_title Urology (Ridgewood, N.J.)
container_volume 58
creator Chang, Sung-Goo
Jeon, Sung-Hyun
Lee, Sun-Ju
Choi, Joong-Myung
Kim, Youn-Wha
description Objectives. To investigate the urinary vascular endothelial growth factor (VEGF) levels from patients with renal cell carcinoma (RCC). Neovascularization, an essential event for the growth of solid tumors, is regulated by a number of angiogenic factors. VEGF is thought to exert potent angiogenic activity. Methods. Urine samples were obtained before radical nephrectomy from 27 patients with RCC and 10 control subjects with no evidence of cancer or inflammatory disease. VEGF was measured by enzyme-linked immunosorbent assay in the urine and corrected according to the 24-hour urine concentration of creatinine. The microvessel density was measured by immunohistochemical staining with CD31 monoclonal antibody. Nuclear morphometry was performed by photomicroscopy. Results. The corrected urinary VEGF levels in patients with RCC were much higher than those in the normal control group ( P = 0.039) and were more elevated in patients with higher stages of RCC (Stages III and IV versus Stages I and II; P = 0.024). A tendency was also noted for the VEGF levels to be higher according to cell grade. However, no statistical correlation was found between the corrected urinary VEGF and age, sex, tumor size, cell type, microvessel density, platelet count, or hemoglobin. The nuclear area was higher with more advanced-stage tumors ( P = 0.043) and tended to increase according to the tumor cell grade. Conclusions. The results of this study indicate that urinary VEGF levels are increased in patients with RCC. However, they may not reflect the underlying angiogenic activity, and it may be that other angiogenic factors play a more prominent role.
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To investigate the urinary vascular endothelial growth factor (VEGF) levels from patients with renal cell carcinoma (RCC). Neovascularization, an essential event for the growth of solid tumors, is regulated by a number of angiogenic factors. VEGF is thought to exert potent angiogenic activity. Methods. Urine samples were obtained before radical nephrectomy from 27 patients with RCC and 10 control subjects with no evidence of cancer or inflammatory disease. VEGF was measured by enzyme-linked immunosorbent assay in the urine and corrected according to the 24-hour urine concentration of creatinine. The microvessel density was measured by immunohistochemical staining with CD31 monoclonal antibody. Nuclear morphometry was performed by photomicroscopy. Results. The corrected urinary VEGF levels in patients with RCC were much higher than those in the normal control group ( P = 0.039) and were more elevated in patients with higher stages of RCC (Stages III and IV versus Stages I and II; P = 0.024). A tendency was also noted for the VEGF levels to be higher according to cell grade. However, no statistical correlation was found between the corrected urinary VEGF and age, sex, tumor size, cell type, microvessel density, platelet count, or hemoglobin. The nuclear area was higher with more advanced-stage tumors ( P = 0.043) and tended to increase according to the tumor cell grade. Conclusions. The results of this study indicate that urinary VEGF levels are increased in patients with RCC. However, they may not reflect the underlying angiogenic activity, and it may be that other angiogenic factors play a more prominent role.</description><identifier>ISSN: 0090-4295</identifier><identifier>EISSN: 1527-9995</identifier><identifier>DOI: 10.1016/S0090-4295(01)01375-9</identifier><identifier>PMID: 11744455</identifier><identifier>CODEN: URGYAZ</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Analysis of Variance ; Biological and medical sciences ; Carcinoma, Renal Cell - blood supply ; Carcinoma, Renal Cell - pathology ; Carcinoma, Renal Cell - urine ; Case-Control Studies ; Endothelial Growth Factors - urine ; Female ; Humans ; Kidney Neoplasms - blood supply ; Kidney Neoplasms - pathology ; Kidney Neoplasms - urine ; Kidneys ; Lymphokines - urine ; Male ; Medical sciences ; Microcirculation ; Middle Aged ; Neoplasm Proteins - urine ; Nephrology. Urinary tract diseases ; Tumors of the urinary system ; Vascular Endothelial Growth Factor A ; Vascular Endothelial Growth Factors</subject><ispartof>Urology (Ridgewood, N.J.), 2001-12, Vol.58 (6), p.904-908</ispartof><rights>2001 Elsevier Science Inc.</rights><rights>2002 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c391t-d2ebfe2460ee722b44d6e4e9a09405c8d619a8e7050333ec052829d61920f7683</citedby><cites>FETCH-LOGICAL-c391t-d2ebfe2460ee722b44d6e4e9a09405c8d619a8e7050333ec052829d61920f7683</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/S0090-4295(01)01375-9$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=13383413$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11744455$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chang, Sung-Goo</creatorcontrib><creatorcontrib>Jeon, Sung-Hyun</creatorcontrib><creatorcontrib>Lee, Sun-Ju</creatorcontrib><creatorcontrib>Choi, Joong-Myung</creatorcontrib><creatorcontrib>Kim, Youn-Wha</creatorcontrib><title>Clinical significance of urinary vascular endothelial growth factor and microvessel density in patients with renal cell carcinoma</title><title>Urology (Ridgewood, N.J.)</title><addtitle>Urology</addtitle><description>Objectives. To investigate the urinary vascular endothelial growth factor (VEGF) levels from patients with renal cell carcinoma (RCC). Neovascularization, an essential event for the growth of solid tumors, is regulated by a number of angiogenic factors. VEGF is thought to exert potent angiogenic activity. Methods. Urine samples were obtained before radical nephrectomy from 27 patients with RCC and 10 control subjects with no evidence of cancer or inflammatory disease. VEGF was measured by enzyme-linked immunosorbent assay in the urine and corrected according to the 24-hour urine concentration of creatinine. The microvessel density was measured by immunohistochemical staining with CD31 monoclonal antibody. Nuclear morphometry was performed by photomicroscopy. Results. The corrected urinary VEGF levels in patients with RCC were much higher than those in the normal control group ( P = 0.039) and were more elevated in patients with higher stages of RCC (Stages III and IV versus Stages I and II; P = 0.024). A tendency was also noted for the VEGF levels to be higher according to cell grade. However, no statistical correlation was found between the corrected urinary VEGF and age, sex, tumor size, cell type, microvessel density, platelet count, or hemoglobin. The nuclear area was higher with more advanced-stage tumors ( P = 0.043) and tended to increase according to the tumor cell grade. Conclusions. The results of this study indicate that urinary VEGF levels are increased in patients with RCC. However, they may not reflect the underlying angiogenic activity, and it may be that other angiogenic factors play a more prominent role.</description><subject>Analysis of Variance</subject><subject>Biological and medical sciences</subject><subject>Carcinoma, Renal Cell - blood supply</subject><subject>Carcinoma, Renal Cell - pathology</subject><subject>Carcinoma, Renal Cell - urine</subject><subject>Case-Control Studies</subject><subject>Endothelial Growth Factors - urine</subject><subject>Female</subject><subject>Humans</subject><subject>Kidney Neoplasms - blood supply</subject><subject>Kidney Neoplasms - pathology</subject><subject>Kidney Neoplasms - urine</subject><subject>Kidneys</subject><subject>Lymphokines - urine</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Microcirculation</subject><subject>Middle Aged</subject><subject>Neoplasm Proteins - urine</subject><subject>Nephrology. Urinary tract diseases</subject><subject>Tumors of the urinary system</subject><subject>Vascular Endothelial Growth Factor A</subject><subject>Vascular Endothelial Growth Factors</subject><issn>0090-4295</issn><issn>1527-9995</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE1v1DAQhi0EosvCTwD5AoJDYPyVxCeEVnxJlTgAZ8vrTFqjxF5sZ6se-ec43RU9cpmxrOe1Zx5CnjN4y4C1774DaGgk1-o1sDfARKca_YBsmOJdo7VWD8nmH3JBnuT8CwDatu0ekwvGOimlUhvyZzf54J2daPZXwY_1GBzSONIl-WDTLT3a7JbJJophiOUaJ1_hqxRvyjUdrSsxURsGOnuX4hFzxokOGLIvt9QHerDFYyiZ3vjKJww17HCqxSbnQ5ztU_JotFPGZ-e-JT8_ffyx-9Jcfvv8dffhsnFCs9IMHPcjctkCYsf5XsqhRYnagpagXD-0TNseO1AghEAHivdcr7ccxq7txZa8Or17SPH3grmY2ed1FBswLtl0XKiewwqqE1gXyjnhaA7Jz1WFYWBW9-bOvVnFGmDmzr3RNffi_MGyn3G4T51lV-DlGahK7TSmqtrne06IXshat-T9icOq4-gxmeyqRIeDT-iKGaL_zyh_AfYEorI</recordid><startdate>20011201</startdate><enddate>20011201</enddate><creator>Chang, Sung-Goo</creator><creator>Jeon, Sung-Hyun</creator><creator>Lee, Sun-Ju</creator><creator>Choi, Joong-Myung</creator><creator>Kim, Youn-Wha</creator><general>Elsevier Inc</general><general>Elsevier Science</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>20011201</creationdate><title>Clinical significance of urinary vascular endothelial growth factor and microvessel density in patients with renal cell carcinoma</title><author>Chang, Sung-Goo ; Jeon, Sung-Hyun ; Lee, Sun-Ju ; Choi, Joong-Myung ; Kim, Youn-Wha</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c391t-d2ebfe2460ee722b44d6e4e9a09405c8d619a8e7050333ec052829d61920f7683</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Analysis of Variance</topic><topic>Biological and medical sciences</topic><topic>Carcinoma, Renal Cell - blood supply</topic><topic>Carcinoma, Renal Cell - pathology</topic><topic>Carcinoma, Renal Cell - urine</topic><topic>Case-Control Studies</topic><topic>Endothelial Growth Factors - urine</topic><topic>Female</topic><topic>Humans</topic><topic>Kidney Neoplasms - blood supply</topic><topic>Kidney Neoplasms - pathology</topic><topic>Kidney Neoplasms - urine</topic><topic>Kidneys</topic><topic>Lymphokines - urine</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Microcirculation</topic><topic>Middle Aged</topic><topic>Neoplasm Proteins - urine</topic><topic>Nephrology. Urinary tract diseases</topic><topic>Tumors of the urinary system</topic><topic>Vascular Endothelial Growth Factor A</topic><topic>Vascular Endothelial Growth Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chang, Sung-Goo</creatorcontrib><creatorcontrib>Jeon, Sung-Hyun</creatorcontrib><creatorcontrib>Lee, Sun-Ju</creatorcontrib><creatorcontrib>Choi, Joong-Myung</creatorcontrib><creatorcontrib>Kim, Youn-Wha</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>Urology (Ridgewood, N.J.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chang, Sung-Goo</au><au>Jeon, Sung-Hyun</au><au>Lee, Sun-Ju</au><au>Choi, Joong-Myung</au><au>Kim, Youn-Wha</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Clinical significance of urinary vascular endothelial growth factor and microvessel density in patients with renal cell carcinoma</atitle><jtitle>Urology (Ridgewood, N.J.)</jtitle><addtitle>Urology</addtitle><date>2001-12-01</date><risdate>2001</risdate><volume>58</volume><issue>6</issue><spage>904</spage><epage>908</epage><pages>904-908</pages><issn>0090-4295</issn><eissn>1527-9995</eissn><coden>URGYAZ</coden><abstract>Objectives. To investigate the urinary vascular endothelial growth factor (VEGF) levels from patients with renal cell carcinoma (RCC). Neovascularization, an essential event for the growth of solid tumors, is regulated by a number of angiogenic factors. VEGF is thought to exert potent angiogenic activity. Methods. Urine samples were obtained before radical nephrectomy from 27 patients with RCC and 10 control subjects with no evidence of cancer or inflammatory disease. VEGF was measured by enzyme-linked immunosorbent assay in the urine and corrected according to the 24-hour urine concentration of creatinine. The microvessel density was measured by immunohistochemical staining with CD31 monoclonal antibody. Nuclear morphometry was performed by photomicroscopy. Results. The corrected urinary VEGF levels in patients with RCC were much higher than those in the normal control group ( P = 0.039) and were more elevated in patients with higher stages of RCC (Stages III and IV versus Stages I and II; P = 0.024). A tendency was also noted for the VEGF levels to be higher according to cell grade. However, no statistical correlation was found between the corrected urinary VEGF and age, sex, tumor size, cell type, microvessel density, platelet count, or hemoglobin. The nuclear area was higher with more advanced-stage tumors ( P = 0.043) and tended to increase according to the tumor cell grade. Conclusions. The results of this study indicate that urinary VEGF levels are increased in patients with RCC. However, they may not reflect the underlying angiogenic activity, and it may be that other angiogenic factors play a more prominent role.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>11744455</pmid><doi>10.1016/S0090-4295(01)01375-9</doi><tpages>5</tpages></addata></record>
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subjects Analysis of Variance
Biological and medical sciences
Carcinoma, Renal Cell - blood supply
Carcinoma, Renal Cell - pathology
Carcinoma, Renal Cell - urine
Case-Control Studies
Endothelial Growth Factors - urine
Female
Humans
Kidney Neoplasms - blood supply
Kidney Neoplasms - pathology
Kidney Neoplasms - urine
Kidneys
Lymphokines - urine
Male
Medical sciences
Microcirculation
Middle Aged
Neoplasm Proteins - urine
Nephrology. Urinary tract diseases
Tumors of the urinary system
Vascular Endothelial Growth Factor A
Vascular Endothelial Growth Factors
title Clinical significance of urinary vascular endothelial growth factor and microvessel density in patients with renal cell carcinoma
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