Cathepsins B, H, and L and their inhibitors stefin A and cystatin C in sera of melanoma patients

The levels of cathepsins (Cats) B, H, and L and their inhibitors stefin A and cystatin C were determined in the sera of 43 patients with metastatic melanoma, in 54 patients with treated cutaneous melanoma with no evidence of metastatic disease, and in 30 healthy blood donors, using quantitative ELIS...

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Veröffentlicht in:Clinical cancer research 1997-10, Vol.3 (10), p.1815-1822
Hauptverfasser: KOS, J, STABUC, B, SCHWEIGER, A, KRASOVEC, M, CIMERMAN, N, KOPITAR-JERALA, N, VRHOVEC, I
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container_end_page 1822
container_issue 10
container_start_page 1815
container_title Clinical cancer research
container_volume 3
creator KOS, J
STABUC, B
SCHWEIGER, A
KRASOVEC, M
CIMERMAN, N
KOPITAR-JERALA, N
VRHOVEC, I
description The levels of cathepsins (Cats) B, H, and L and their inhibitors stefin A and cystatin C were determined in the sera of 43 patients with metastatic melanoma, in 54 patients with treated cutaneous melanoma with no evidence of metastatic disease, and in 30 healthy blood donors, using quantitative ELISAs. The levels of Cats B and H and cystatin C were significantly higher within the group of metastatic melanoma patients compared with the healthy controls. The median Cat B was 4.8 versus 3.6 ng/ml (P < 0.013), the median Cat H was 13.7 versus 4.9 ng/ml (P < 0.0001), and the median cystatin C was 470 versus 320 ng/ml (P < 0.02). Cat H was also significantly increased within the group of melanoma patients with no metastasis, with a median of 9.6 ng/ml. Cat B was found to correlate with Cat L (r = 0.36; P < 0.02) and cystatin C (r = 0.41; P < 0.008). The serum level of Cat H was significantly increased in patients showing no response to the chemoimmunotherapy as compared to the level in responders. Metastatic melanoma patients with high contents of Cat B and Cat H experienced significantly shorter overall survival rates than the patients with low levels of each enzyme (Cat B: P < 0.003 and relative risk, 2.5; Cat H: P < 0.006 and relative risk, 2.4, using medians as cutoff values). The other potential factors for prognosis for this group of patients revealed moderate (histological type and age) or no (tumor thickness, sex, and lymph node metastasis) prognostic significance. Similarly, no difference in survival was found for stefin A, cystatin C, and Cat L. These results suggest that the serum levels of Cats B and H could serve as prognostic factors for patients with advanced melanoma.
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The levels of Cats B and H and cystatin C were significantly higher within the group of metastatic melanoma patients compared with the healthy controls. The median Cat B was 4.8 versus 3.6 ng/ml (P < 0.013), the median Cat H was 13.7 versus 4.9 ng/ml (P < 0.0001), and the median cystatin C was 470 versus 320 ng/ml (P < 0.02). Cat H was also significantly increased within the group of melanoma patients with no metastasis, with a median of 9.6 ng/ml. Cat B was found to correlate with Cat L (r = 0.36; P < 0.02) and cystatin C (r = 0.41; P < 0.008). The serum level of Cat H was significantly increased in patients showing no response to the chemoimmunotherapy as compared to the level in responders. Metastatic melanoma patients with high contents of Cat B and Cat H experienced significantly shorter overall survival rates than the patients with low levels of each enzyme (Cat B: P < 0.003 and relative risk, 2.5; Cat H: P < 0.006 and relative risk, 2.4, using medians as cutoff values). The other potential factors for prognosis for this group of patients revealed moderate (histological type and age) or no (tumor thickness, sex, and lymph node metastasis) prognostic significance. Similarly, no difference in survival was found for stefin A, cystatin C, and Cat L. These results suggest that the serum levels of Cats B and H could serve as prognostic factors for patients with advanced melanoma.]]></description><identifier>ISSN: 1078-0432</identifier><identifier>EISSN: 1557-3265</identifier><identifier>PMID: 9815568</identifier><language>eng</language><publisher>Philadelphia, PA: American Association for Cancer Research</publisher><subject>Adult ; Aged ; Biological and medical sciences ; Biomarkers, Tumor - blood ; Cathepsin B - antagonists &amp; inhibitors ; Cathepsin B - blood ; Cathepsin H ; Cathepsin L ; Cathepsins - analysis ; Cathepsins - antagonists &amp; inhibitors ; Cathepsins - blood ; Cystatin A ; Cystatin C ; Cystatins - blood ; Cysteine Endopeptidases - analysis ; Cysteine Endopeptidases - blood ; Dermatology ; Endopeptidases ; Enzyme Inhibitors - blood ; Enzyme-Linked Immunosorbent Assay ; Female ; Host-tumor relations. Immunology. Biological markers ; Humans ; Life Tables ; Lymphatic Metastasis ; Male ; Medical sciences ; Melanoma - blood ; Melanoma - enzymology ; Melanoma - mortality ; Melanoma - pathology ; Middle Aged ; Neoplasm Metastasis ; Neoplasm Proteins - antagonists &amp; inhibitors ; Neoplasm Proteins - blood ; Prognosis ; Proportional Hazards Models ; Skin Neoplasms - blood ; Skin Neoplasms - enzymology ; Skin Neoplasms - mortality ; Survival Analysis ; Survival Rate ; Tumors ; Tumors of the skin and soft tissue. Premalignant lesions</subject><ispartof>Clinical cancer research, 1997-10, Vol.3 (10), p.1815-1822</ispartof><rights>1997 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=2851648$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9815568$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>KOS, J</creatorcontrib><creatorcontrib>STABUC, B</creatorcontrib><creatorcontrib>SCHWEIGER, A</creatorcontrib><creatorcontrib>KRASOVEC, M</creatorcontrib><creatorcontrib>CIMERMAN, N</creatorcontrib><creatorcontrib>KOPITAR-JERALA, N</creatorcontrib><creatorcontrib>VRHOVEC, I</creatorcontrib><title>Cathepsins B, H, and L and their inhibitors stefin A and cystatin C in sera of melanoma patients</title><title>Clinical cancer research</title><addtitle>Clin Cancer Res</addtitle><description><![CDATA[The levels of cathepsins (Cats) B, H, and L and their inhibitors stefin A and cystatin C were determined in the sera of 43 patients with metastatic melanoma, in 54 patients with treated cutaneous melanoma with no evidence of metastatic disease, and in 30 healthy blood donors, using quantitative ELISAs. The levels of Cats B and H and cystatin C were significantly higher within the group of metastatic melanoma patients compared with the healthy controls. The median Cat B was 4.8 versus 3.6 ng/ml (P < 0.013), the median Cat H was 13.7 versus 4.9 ng/ml (P < 0.0001), and the median cystatin C was 470 versus 320 ng/ml (P < 0.02). Cat H was also significantly increased within the group of melanoma patients with no metastasis, with a median of 9.6 ng/ml. Cat B was found to correlate with Cat L (r = 0.36; P < 0.02) and cystatin C (r = 0.41; P < 0.008). The serum level of Cat H was significantly increased in patients showing no response to the chemoimmunotherapy as compared to the level in responders. Metastatic melanoma patients with high contents of Cat B and Cat H experienced significantly shorter overall survival rates than the patients with low levels of each enzyme (Cat B: P < 0.003 and relative risk, 2.5; Cat H: P < 0.006 and relative risk, 2.4, using medians as cutoff values). The other potential factors for prognosis for this group of patients revealed moderate (histological type and age) or no (tumor thickness, sex, and lymph node metastasis) prognostic significance. Similarly, no difference in survival was found for stefin A, cystatin C, and Cat L. These results suggest that the serum levels of Cats B and H could serve as prognostic factors for patients with advanced melanoma.]]></description><subject>Adult</subject><subject>Aged</subject><subject>Biological and medical sciences</subject><subject>Biomarkers, Tumor - blood</subject><subject>Cathepsin B - antagonists &amp; inhibitors</subject><subject>Cathepsin B - blood</subject><subject>Cathepsin H</subject><subject>Cathepsin L</subject><subject>Cathepsins - analysis</subject><subject>Cathepsins - antagonists &amp; inhibitors</subject><subject>Cathepsins - blood</subject><subject>Cystatin A</subject><subject>Cystatin C</subject><subject>Cystatins - blood</subject><subject>Cysteine Endopeptidases - analysis</subject><subject>Cysteine Endopeptidases - blood</subject><subject>Dermatology</subject><subject>Endopeptidases</subject><subject>Enzyme Inhibitors - blood</subject><subject>Enzyme-Linked Immunosorbent Assay</subject><subject>Female</subject><subject>Host-tumor relations. Immunology. Biological markers</subject><subject>Humans</subject><subject>Life Tables</subject><subject>Lymphatic Metastasis</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Melanoma - blood</subject><subject>Melanoma - enzymology</subject><subject>Melanoma - mortality</subject><subject>Melanoma - pathology</subject><subject>Middle Aged</subject><subject>Neoplasm Metastasis</subject><subject>Neoplasm Proteins - antagonists &amp; inhibitors</subject><subject>Neoplasm Proteins - blood</subject><subject>Prognosis</subject><subject>Proportional Hazards Models</subject><subject>Skin Neoplasms - blood</subject><subject>Skin Neoplasms - enzymology</subject><subject>Skin Neoplasms - mortality</subject><subject>Survival Analysis</subject><subject>Survival Rate</subject><subject>Tumors</subject><subject>Tumors of the skin and soft tissue. Premalignant lesions</subject><issn>1078-0432</issn><issn>1557-3265</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9kMtKxDAUhoMo4zj6CEIWIi6mkGuTLMfiDQbc6DqmbWojvZlkkHl740xxcy58Hz-HcwKWmHORUZLz0zQjITPEKDkHFyF8IYQZRmwBFkomLZdL8FGY2NopuCHA-zV8XkMz1HB7qAk4D93QutLF0QcYom3cADcHWu1DNDGtRVJgsN7AsYG97cww9gZOidkhhktw1pgu2Ku5r8D748Nb8ZxtX59eis02a0kuY1YLzLhtiBKkJLVClGImGWoqY7jCmAjUIIlRulkSUxpOMCclVUIxKbGyiq7A7TF38uP3zoaoexcq26Vz7LgLWqicCppyV-B6Fndlb2s9edcbv9fzSxK_mbkJlekab4bKhX-NSI5z9qfdHbXWfbY_zltdJdF6b4M1vmo11RhpnELpLwHGdbE</recordid><startdate>19971001</startdate><enddate>19971001</enddate><creator>KOS, J</creator><creator>STABUC, B</creator><creator>SCHWEIGER, A</creator><creator>KRASOVEC, M</creator><creator>CIMERMAN, N</creator><creator>KOPITAR-JERALA, N</creator><creator>VRHOVEC, I</creator><general>American Association for Cancer Research</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>19971001</creationdate><title>Cathepsins B, H, and L and their inhibitors stefin A and cystatin C in sera of melanoma patients</title><author>KOS, J ; STABUC, B ; SCHWEIGER, A ; KRASOVEC, M ; CIMERMAN, N ; KOPITAR-JERALA, N ; VRHOVEC, I</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-h268t-d7145ef2972b2d903314840fcaa5911270f081056882aba52152b397948819e93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Biological and medical sciences</topic><topic>Biomarkers, Tumor - blood</topic><topic>Cathepsin B - antagonists &amp; inhibitors</topic><topic>Cathepsin B - blood</topic><topic>Cathepsin H</topic><topic>Cathepsin L</topic><topic>Cathepsins - analysis</topic><topic>Cathepsins - antagonists &amp; inhibitors</topic><topic>Cathepsins - blood</topic><topic>Cystatin A</topic><topic>Cystatin C</topic><topic>Cystatins - blood</topic><topic>Cysteine Endopeptidases - analysis</topic><topic>Cysteine Endopeptidases - blood</topic><topic>Dermatology</topic><topic>Endopeptidases</topic><topic>Enzyme Inhibitors - blood</topic><topic>Enzyme-Linked Immunosorbent Assay</topic><topic>Female</topic><topic>Host-tumor relations. Immunology. Biological markers</topic><topic>Humans</topic><topic>Life Tables</topic><topic>Lymphatic Metastasis</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Melanoma - blood</topic><topic>Melanoma - enzymology</topic><topic>Melanoma - mortality</topic><topic>Melanoma - pathology</topic><topic>Middle Aged</topic><topic>Neoplasm Metastasis</topic><topic>Neoplasm Proteins - antagonists &amp; inhibitors</topic><topic>Neoplasm Proteins - blood</topic><topic>Prognosis</topic><topic>Proportional Hazards Models</topic><topic>Skin Neoplasms - blood</topic><topic>Skin Neoplasms - enzymology</topic><topic>Skin Neoplasms - mortality</topic><topic>Survival Analysis</topic><topic>Survival Rate</topic><topic>Tumors</topic><topic>Tumors of the skin and soft tissue. Premalignant lesions</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>KOS, J</creatorcontrib><creatorcontrib>STABUC, B</creatorcontrib><creatorcontrib>SCHWEIGER, A</creatorcontrib><creatorcontrib>KRASOVEC, M</creatorcontrib><creatorcontrib>CIMERMAN, N</creatorcontrib><creatorcontrib>KOPITAR-JERALA, N</creatorcontrib><creatorcontrib>VRHOVEC, I</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>MEDLINE - Academic</collection><jtitle>Clinical cancer research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>KOS, J</au><au>STABUC, B</au><au>SCHWEIGER, A</au><au>KRASOVEC, M</au><au>CIMERMAN, N</au><au>KOPITAR-JERALA, N</au><au>VRHOVEC, I</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cathepsins B, H, and L and their inhibitors stefin A and cystatin C in sera of melanoma patients</atitle><jtitle>Clinical cancer research</jtitle><addtitle>Clin Cancer Res</addtitle><date>1997-10-01</date><risdate>1997</risdate><volume>3</volume><issue>10</issue><spage>1815</spage><epage>1822</epage><pages>1815-1822</pages><issn>1078-0432</issn><eissn>1557-3265</eissn><abstract><![CDATA[The levels of cathepsins (Cats) B, H, and L and their inhibitors stefin A and cystatin C were determined in the sera of 43 patients with metastatic melanoma, in 54 patients with treated cutaneous melanoma with no evidence of metastatic disease, and in 30 healthy blood donors, using quantitative ELISAs. The levels of Cats B and H and cystatin C were significantly higher within the group of metastatic melanoma patients compared with the healthy controls. The median Cat B was 4.8 versus 3.6 ng/ml (P < 0.013), the median Cat H was 13.7 versus 4.9 ng/ml (P < 0.0001), and the median cystatin C was 470 versus 320 ng/ml (P < 0.02). Cat H was also significantly increased within the group of melanoma patients with no metastasis, with a median of 9.6 ng/ml. Cat B was found to correlate with Cat L (r = 0.36; P < 0.02) and cystatin C (r = 0.41; P < 0.008). The serum level of Cat H was significantly increased in patients showing no response to the chemoimmunotherapy as compared to the level in responders. Metastatic melanoma patients with high contents of Cat B and Cat H experienced significantly shorter overall survival rates than the patients with low levels of each enzyme (Cat B: P < 0.003 and relative risk, 2.5; Cat H: P < 0.006 and relative risk, 2.4, using medians as cutoff values). The other potential factors for prognosis for this group of patients revealed moderate (histological type and age) or no (tumor thickness, sex, and lymph node metastasis) prognostic significance. Similarly, no difference in survival was found for stefin A, cystatin C, and Cat L. These results suggest that the serum levels of Cats B and H could serve as prognostic factors for patients with advanced melanoma.]]></abstract><cop>Philadelphia, PA</cop><pub>American Association for Cancer Research</pub><pmid>9815568</pmid><tpages>8</tpages></addata></record>
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subjects Adult
Aged
Biological and medical sciences
Biomarkers, Tumor - blood
Cathepsin B - antagonists & inhibitors
Cathepsin B - blood
Cathepsin H
Cathepsin L
Cathepsins - analysis
Cathepsins - antagonists & inhibitors
Cathepsins - blood
Cystatin A
Cystatin C
Cystatins - blood
Cysteine Endopeptidases - analysis
Cysteine Endopeptidases - blood
Dermatology
Endopeptidases
Enzyme Inhibitors - blood
Enzyme-Linked Immunosorbent Assay
Female
Host-tumor relations. Immunology. Biological markers
Humans
Life Tables
Lymphatic Metastasis
Male
Medical sciences
Melanoma - blood
Melanoma - enzymology
Melanoma - mortality
Melanoma - pathology
Middle Aged
Neoplasm Metastasis
Neoplasm Proteins - antagonists & inhibitors
Neoplasm Proteins - blood
Prognosis
Proportional Hazards Models
Skin Neoplasms - blood
Skin Neoplasms - enzymology
Skin Neoplasms - mortality
Survival Analysis
Survival Rate
Tumors
Tumors of the skin and soft tissue. Premalignant lesions
title Cathepsins B, H, and L and their inhibitors stefin A and cystatin C in sera of melanoma patients
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