Tumor-associated proteolysis and prognosis: new functional risk factors in gastric cancer defined by the urokinase-type plasminogen activator system
The significance of tumor-associated proteolysis as reflected by parameters of the urokinase-type plasminogen activator (uPA) system for prognosis in cancer patients has been proposed because of evidence for its central role in basic mechanisms of invasion and metastasis. The aim of the present stud...
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Veröffentlicht in: | Journal of clinical oncology 1995-08, Vol.13 (8), p.2084-2093 |
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description | The significance of tumor-associated proteolysis as reflected by parameters of the urokinase-type plasminogen activator (uPA) system for prognosis in cancer patients has been proposed because of evidence for its central role in basic mechanisms of invasion and metastasis. The aim of the present study was to evaluate whether the expression of the uPA parameters might be of clinical value in gastric cancer as a tumor/biologically defined risk factor.
In a consecutive series of 203 patients resected for primary gastric cancer, the expression of uPA, uPA-receptor (uPA-R), plasminogen activator inhibitor (PAI)-1, and PAI-2 was determined immunohistochemically. The results were classified semiquantitatively (0 to 3). Patients were followed-up prospectively for a median of 31 months (range, 9 to 56 months). Disease-free and overall survival were analyzed according to Kaplan-Meier and with univariate and multivariate Cox analyses in relation to conventional prognostic factors.
Univariate analyses revealed a highly significant inverse correlation of uPA, uPA-R, and PAI-1 expression with survival time (P = .0008, P = .0002, and P = .0002, respectively), whereas PAI-2 demonstrated only a weak correlation. In multivariate analyses, PAI-1 was an independent and strong prognostic factor (P = .005; relative risk, 1.47 per staining degree; 95% confidence interval [CI], 1.31 to 1.64). In pT1/2 tumors and in Laurén's diffuse and mixed types, uPA, uPA-R, and PAI-1 added significant prognostic information. PAI-1 was also associated with survival in the subgroup of lymph node-positive patients.
PAI-1, uPA, and uPA-R are new functional risk factors reflecting clinical prognosis. In particular, PAI-1 is a new independent variable for the identification of patients at high risk after tumor resection. Our results support the hypothesis that the uPA system probably is of general importance for prognosis of patients with malignant disease, indicating an individual tumor's capacity for invasion and metastasis. |
doi_str_mv | 10.1200/JCO.1995.13.8.2084 |
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In a consecutive series of 203 patients resected for primary gastric cancer, the expression of uPA, uPA-receptor (uPA-R), plasminogen activator inhibitor (PAI)-1, and PAI-2 was determined immunohistochemically. The results were classified semiquantitatively (0 to 3). Patients were followed-up prospectively for a median of 31 months (range, 9 to 56 months). Disease-free and overall survival were analyzed according to Kaplan-Meier and with univariate and multivariate Cox analyses in relation to conventional prognostic factors.
Univariate analyses revealed a highly significant inverse correlation of uPA, uPA-R, and PAI-1 expression with survival time (P = .0008, P = .0002, and P = .0002, respectively), whereas PAI-2 demonstrated only a weak correlation. In multivariate analyses, PAI-1 was an independent and strong prognostic factor (P = .005; relative risk, 1.47 per staining degree; 95% confidence interval [CI], 1.31 to 1.64). In pT1/2 tumors and in Laurén's diffuse and mixed types, uPA, uPA-R, and PAI-1 added significant prognostic information. PAI-1 was also associated with survival in the subgroup of lymph node-positive patients.
PAI-1, uPA, and uPA-R are new functional risk factors reflecting clinical prognosis. In particular, PAI-1 is a new independent variable for the identification of patients at high risk after tumor resection. Our results support the hypothesis that the uPA system probably is of general importance for prognosis of patients with malignant disease, indicating an individual tumor's capacity for invasion and metastasis.</description><identifier>ISSN: 0732-183X</identifier><identifier>EISSN: 1527-7755</identifier><identifier>DOI: 10.1200/JCO.1995.13.8.2084</identifier><identifier>PMID: 7636552</identifier><language>eng</language><publisher>Baltimore, MD: American Society of Clinical Oncology</publisher><subject>Adult ; Aged ; Biological and medical sciences ; Disease-Free Survival ; Female ; Follow-Up Studies ; Gastroenterology. Liver. Pancreas. Abdomen ; Humans ; Immunohistochemistry ; Male ; Medical sciences ; Middle Aged ; Multivariate Analysis ; Plasminogen Activator Inhibitor 1 - metabolism ; Plasminogen Activator Inhibitor 2 - metabolism ; Prognosis ; Prospective Studies ; Proteins - metabolism ; Receptors, Cell Surface - metabolism ; Receptors, Urokinase Plasminogen Activator ; Regression Analysis ; Risk Factors ; Stomach Neoplasms - metabolism ; Stomach Neoplasms - mortality ; Stomach Neoplasms - physiopathology ; Stomach. Duodenum. Small intestine. Colon. Rectum. Anus ; Survival Rate ; Tumors ; Urokinase-Type Plasminogen Activator - metabolism</subject><ispartof>Journal of clinical oncology, 1995-08, Vol.13 (8), p.2084-2093</ispartof><rights>1995 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c358t-d0e1b0aac6c7a28b7d5951aaf9773edb4dbda29c4a3215dbc611cb3015db43873</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,3716,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=3618822$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7636552$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>HEISS, M. M</creatorcontrib><creatorcontrib>BABIC, R</creatorcontrib><creatorcontrib>ALLGAYER, H</creatorcontrib><creatorcontrib>GRUETZNER, K. U</creatorcontrib><creatorcontrib>JAUCH, K.-W</creatorcontrib><creatorcontrib>LOEHRS, U</creatorcontrib><creatorcontrib>SCHILDBERG, F. W</creatorcontrib><title>Tumor-associated proteolysis and prognosis: new functional risk factors in gastric cancer defined by the urokinase-type plasminogen activator system</title><title>Journal of clinical oncology</title><addtitle>J Clin Oncol</addtitle><description>The significance of tumor-associated proteolysis as reflected by parameters of the urokinase-type plasminogen activator (uPA) system for prognosis in cancer patients has been proposed because of evidence for its central role in basic mechanisms of invasion and metastasis. The aim of the present study was to evaluate whether the expression of the uPA parameters might be of clinical value in gastric cancer as a tumor/biologically defined risk factor.
In a consecutive series of 203 patients resected for primary gastric cancer, the expression of uPA, uPA-receptor (uPA-R), plasminogen activator inhibitor (PAI)-1, and PAI-2 was determined immunohistochemically. The results were classified semiquantitatively (0 to 3). Patients were followed-up prospectively for a median of 31 months (range, 9 to 56 months). Disease-free and overall survival were analyzed according to Kaplan-Meier and with univariate and multivariate Cox analyses in relation to conventional prognostic factors.
Univariate analyses revealed a highly significant inverse correlation of uPA, uPA-R, and PAI-1 expression with survival time (P = .0008, P = .0002, and P = .0002, respectively), whereas PAI-2 demonstrated only a weak correlation. In multivariate analyses, PAI-1 was an independent and strong prognostic factor (P = .005; relative risk, 1.47 per staining degree; 95% confidence interval [CI], 1.31 to 1.64). In pT1/2 tumors and in Laurén's diffuse and mixed types, uPA, uPA-R, and PAI-1 added significant prognostic information. PAI-1 was also associated with survival in the subgroup of lymph node-positive patients.
PAI-1, uPA, and uPA-R are new functional risk factors reflecting clinical prognosis. In particular, PAI-1 is a new independent variable for the identification of patients at high risk after tumor resection. Our results support the hypothesis that the uPA system probably is of general importance for prognosis of patients with malignant disease, indicating an individual tumor's capacity for invasion and metastasis.</description><subject>Adult</subject><subject>Aged</subject><subject>Biological and medical sciences</subject><subject>Disease-Free Survival</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Multivariate Analysis</subject><subject>Plasminogen Activator Inhibitor 1 - metabolism</subject><subject>Plasminogen Activator Inhibitor 2 - metabolism</subject><subject>Prognosis</subject><subject>Prospective Studies</subject><subject>Proteins - metabolism</subject><subject>Receptors, Cell Surface - metabolism</subject><subject>Receptors, Urokinase Plasminogen Activator</subject><subject>Regression Analysis</subject><subject>Risk Factors</subject><subject>Stomach Neoplasms - metabolism</subject><subject>Stomach Neoplasms - mortality</subject><subject>Stomach Neoplasms - physiopathology</subject><subject>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</subject><subject>Survival Rate</subject><subject>Tumors</subject><subject>Urokinase-Type Plasminogen Activator - metabolism</subject><issn>0732-183X</issn><issn>1527-7755</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1995</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkc9u1DAQxi0EKtvCCyAh-YC4JfhPHCfc0AoKqFIvReJmTRxn121iL56kVd6DB8ZLV-1pZjTf_Maej5B3nJVcMPbp5_a65G2rSi7LphSsqV6QDVdCF1or9ZJsmJai4I38_ZqcI94yxqtGqjNypmtZKyU25O_NMsVUAGK0HmbX00OKs4vjih4phP_1LsRcfabBPdBhCXb2McBIk8c7OoCdY0LqA90BzslbaiFYl2jvBh8ysFvpvHd0SfHOB0BXzOvB0cMIOPkQdy7QjPD3kDEUV5zd9Ia8GmBE9_YUL8ivb19vtt-Lq-vLH9svV4WVqpmLnjneMQBbWw2i6XSvWsUBhlZr6fqu6rseRGsrkIKrvrM157aT7JhXstHygnx85OY__lkczmbyaN04QnBxQaN1JVUreRaKR6FNETG5wRySnyCthjNztMJkK8zRCsOlaczRijz0_kRfusn1TyOn2-f-h1Mf0MI4pHw2j08yWfOmEeL5kXu_2z_45AxOMI4ZKsytjc_7_gFQLaOT</recordid><startdate>19950801</startdate><enddate>19950801</enddate><creator>HEISS, M. 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M</creatorcontrib><creatorcontrib>BABIC, R</creatorcontrib><creatorcontrib>ALLGAYER, H</creatorcontrib><creatorcontrib>GRUETZNER, K. U</creatorcontrib><creatorcontrib>JAUCH, K.-W</creatorcontrib><creatorcontrib>LOEHRS, U</creatorcontrib><creatorcontrib>SCHILDBERG, F. W</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>Journal of clinical oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>HEISS, M. M</au><au>BABIC, R</au><au>ALLGAYER, H</au><au>GRUETZNER, K. U</au><au>JAUCH, K.-W</au><au>LOEHRS, U</au><au>SCHILDBERG, F. W</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Tumor-associated proteolysis and prognosis: new functional risk factors in gastric cancer defined by the urokinase-type plasminogen activator system</atitle><jtitle>Journal of clinical oncology</jtitle><addtitle>J Clin Oncol</addtitle><date>1995-08-01</date><risdate>1995</risdate><volume>13</volume><issue>8</issue><spage>2084</spage><epage>2093</epage><pages>2084-2093</pages><issn>0732-183X</issn><eissn>1527-7755</eissn><abstract>The significance of tumor-associated proteolysis as reflected by parameters of the urokinase-type plasminogen activator (uPA) system for prognosis in cancer patients has been proposed because of evidence for its central role in basic mechanisms of invasion and metastasis. The aim of the present study was to evaluate whether the expression of the uPA parameters might be of clinical value in gastric cancer as a tumor/biologically defined risk factor.
In a consecutive series of 203 patients resected for primary gastric cancer, the expression of uPA, uPA-receptor (uPA-R), plasminogen activator inhibitor (PAI)-1, and PAI-2 was determined immunohistochemically. The results were classified semiquantitatively (0 to 3). Patients were followed-up prospectively for a median of 31 months (range, 9 to 56 months). Disease-free and overall survival were analyzed according to Kaplan-Meier and with univariate and multivariate Cox analyses in relation to conventional prognostic factors.
Univariate analyses revealed a highly significant inverse correlation of uPA, uPA-R, and PAI-1 expression with survival time (P = .0008, P = .0002, and P = .0002, respectively), whereas PAI-2 demonstrated only a weak correlation. In multivariate analyses, PAI-1 was an independent and strong prognostic factor (P = .005; relative risk, 1.47 per staining degree; 95% confidence interval [CI], 1.31 to 1.64). In pT1/2 tumors and in Laurén's diffuse and mixed types, uPA, uPA-R, and PAI-1 added significant prognostic information. PAI-1 was also associated with survival in the subgroup of lymph node-positive patients.
PAI-1, uPA, and uPA-R are new functional risk factors reflecting clinical prognosis. In particular, PAI-1 is a new independent variable for the identification of patients at high risk after tumor resection. Our results support the hypothesis that the uPA system probably is of general importance for prognosis of patients with malignant disease, indicating an individual tumor's capacity for invasion and metastasis.</abstract><cop>Baltimore, MD</cop><pub>American Society of Clinical Oncology</pub><pmid>7636552</pmid><doi>10.1200/JCO.1995.13.8.2084</doi><tpages>10</tpages></addata></record> |
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subjects | Adult Aged Biological and medical sciences Disease-Free Survival Female Follow-Up Studies Gastroenterology. Liver. Pancreas. Abdomen Humans Immunohistochemistry Male Medical sciences Middle Aged Multivariate Analysis Plasminogen Activator Inhibitor 1 - metabolism Plasminogen Activator Inhibitor 2 - metabolism Prognosis Prospective Studies Proteins - metabolism Receptors, Cell Surface - metabolism Receptors, Urokinase Plasminogen Activator Regression Analysis Risk Factors Stomach Neoplasms - metabolism Stomach Neoplasms - mortality Stomach Neoplasms - physiopathology Stomach. Duodenum. Small intestine. Colon. Rectum. Anus Survival Rate Tumors Urokinase-Type Plasminogen Activator - metabolism |
title | Tumor-associated proteolysis and prognosis: new functional risk factors in gastric cancer defined by the urokinase-type plasminogen activator system |
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