Coexpression of different antigenic markers on moieties that bear CA 125 determinants
CA 125 has been extensively evaluated as a serum marker for monitoring patients with epithelial ovarian carcinoma. Recently, consideration has been given to the use of CA 125 as one component in a strategy for early detection of this disease. A number of benign conditions can, however, increase CA 1...
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Veröffentlicht in: | Cancer research (Chicago, Ill.) Ill.), 1991-01, Vol.51 (2), p.468-475 |
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description | CA 125 has been extensively evaluated as a serum marker for monitoring patients with epithelial ovarian carcinoma. Recently, consideration has been given to the use of CA 125 as one component in a strategy for early detection of this disease. A number of benign conditions can, however, increase CA 125 in serum, limiting the utility of a single antigen determination for identifying ovarian cancer patients. Coexpression of different epitopes on the high molecular weight complexes that express CA 125 determinants might provide a more specific test for malignant disease, provided that adequate sensitivity were maintained. To determine how frequently determinants are coexpressed, macromolecular moieties containing CA 125 determinants have been isolated from ascites fluid of ovarian cancer patients by immunoaffinity chromatography. CA 125+ moieties have been probed on Western transfers with several murine monoclonal antibodies that recognize distinct tumor-associated epitopes. Marked heterogeneity was observed between patients with regard to antigenic determinants that could be coexpressed with CA 125. A fraction of ascites fluids from different ovarian cancer patients contained moieties which bound to OC 125 on a solid phase immmunoadsorbent and which also bound 125I-labeled monoclonal antibodies NS 19-9, B72.3, DF3, or the novel murine monoclonal antibody OC 3632 in a double determinant immunoradiometric assay. Serum samples were evaluated from patients with ovarian cancer and from apparently healthy individuals. Coexpression of TAG 72 and CA 125 was observed most frequently. When the double determinant assay for coexpression of TAG 72 and CA 125 was compared to assays for the individual antigens, the assay for coexpression was substantially less sensitive than those for the individual markers. |
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H ; SCHLOSSMAN, D. M ; HARRISON, C. L ; RHINEHARDT-CLARK, A ; SOPER, J. T ; KLUG, T. L ; ZURAWSKI, V. R ; BAST, R. C</creator><creatorcontrib>YU, Y. H ; SCHLOSSMAN, D. M ; HARRISON, C. L ; RHINEHARDT-CLARK, A ; SOPER, J. T ; KLUG, T. L ; ZURAWSKI, V. R ; BAST, R. C</creatorcontrib><description>CA 125 has been extensively evaluated as a serum marker for monitoring patients with epithelial ovarian carcinoma. Recently, consideration has been given to the use of CA 125 as one component in a strategy for early detection of this disease. A number of benign conditions can, however, increase CA 125 in serum, limiting the utility of a single antigen determination for identifying ovarian cancer patients. Coexpression of different epitopes on the high molecular weight complexes that express CA 125 determinants might provide a more specific test for malignant disease, provided that adequate sensitivity were maintained. To determine how frequently determinants are coexpressed, macromolecular moieties containing CA 125 determinants have been isolated from ascites fluid of ovarian cancer patients by immunoaffinity chromatography. CA 125+ moieties have been probed on Western transfers with several murine monoclonal antibodies that recognize distinct tumor-associated epitopes. Marked heterogeneity was observed between patients with regard to antigenic determinants that could be coexpressed with CA 125. A fraction of ascites fluids from different ovarian cancer patients contained moieties which bound to OC 125 on a solid phase immmunoadsorbent and which also bound 125I-labeled monoclonal antibodies NS 19-9, B72.3, DF3, or the novel murine monoclonal antibody OC 3632 in a double determinant immunoradiometric assay. Serum samples were evaluated from patients with ovarian cancer and from apparently healthy individuals. Coexpression of TAG 72 and CA 125 was observed most frequently. When the double determinant assay for coexpression of TAG 72 and CA 125 was compared to assays for the individual antigens, the assay for coexpression was substantially less sensitive than those for the individual markers.</description><identifier>ISSN: 0008-5472</identifier><identifier>EISSN: 1538-7445</identifier><identifier>PMID: 1702359</identifier><identifier>CODEN: CNREA8</identifier><language>eng</language><publisher>Philadelphia, PA: American Association for Cancer Research</publisher><subject>Antibodies, Monoclonal - isolation & purification ; Antigen-Antibody Complex - analysis ; Antigens, Tumor-Associated, Carbohydrate - immunology ; Antigens, Tumor-Associated, Carbohydrate - isolation & purification ; Ascites - immunology ; Biological and medical sciences ; Blotting, Western ; Cell Line ; Chromatography, High Pressure Liquid ; Electrophoresis, Polyacrylamide Gel ; Epitopes - analysis ; Female ; Female genital diseases ; Gynecology. Andrology. Obstetrics ; Humans ; Medical sciences ; Molecular Weight ; Ovarian Neoplasms - immunology ; Radioimmunoassay ; Tumors</subject><ispartof>Cancer research (Chicago, Ill.), 1991-01, Vol.51 (2), p.468-475</ispartof><rights>1991 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&idt=19506185$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/1702359$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>YU, Y. H</creatorcontrib><creatorcontrib>SCHLOSSMAN, D. M</creatorcontrib><creatorcontrib>HARRISON, C. L</creatorcontrib><creatorcontrib>RHINEHARDT-CLARK, A</creatorcontrib><creatorcontrib>SOPER, J. T</creatorcontrib><creatorcontrib>KLUG, T. L</creatorcontrib><creatorcontrib>ZURAWSKI, V. R</creatorcontrib><creatorcontrib>BAST, R. C</creatorcontrib><title>Coexpression of different antigenic markers on moieties that bear CA 125 determinants</title><title>Cancer research (Chicago, Ill.)</title><addtitle>Cancer Res</addtitle><description>CA 125 has been extensively evaluated as a serum marker for monitoring patients with epithelial ovarian carcinoma. Recently, consideration has been given to the use of CA 125 as one component in a strategy for early detection of this disease. A number of benign conditions can, however, increase CA 125 in serum, limiting the utility of a single antigen determination for identifying ovarian cancer patients. Coexpression of different epitopes on the high molecular weight complexes that express CA 125 determinants might provide a more specific test for malignant disease, provided that adequate sensitivity were maintained. To determine how frequently determinants are coexpressed, macromolecular moieties containing CA 125 determinants have been isolated from ascites fluid of ovarian cancer patients by immunoaffinity chromatography. CA 125+ moieties have been probed on Western transfers with several murine monoclonal antibodies that recognize distinct tumor-associated epitopes. Marked heterogeneity was observed between patients with regard to antigenic determinants that could be coexpressed with CA 125. A fraction of ascites fluids from different ovarian cancer patients contained moieties which bound to OC 125 on a solid phase immmunoadsorbent and which also bound 125I-labeled monoclonal antibodies NS 19-9, B72.3, DF3, or the novel murine monoclonal antibody OC 3632 in a double determinant immunoradiometric assay. Serum samples were evaluated from patients with ovarian cancer and from apparently healthy individuals. Coexpression of TAG 72 and CA 125 was observed most frequently. When the double determinant assay for coexpression of TAG 72 and CA 125 was compared to assays for the individual antigens, the assay for coexpression was substantially less sensitive than those for the individual markers.</description><subject>Antibodies, Monoclonal - isolation & purification</subject><subject>Antigen-Antibody Complex - analysis</subject><subject>Antigens, Tumor-Associated, Carbohydrate - immunology</subject><subject>Antigens, Tumor-Associated, Carbohydrate - isolation & purification</subject><subject>Ascites - immunology</subject><subject>Biological and medical sciences</subject><subject>Blotting, Western</subject><subject>Cell Line</subject><subject>Chromatography, High Pressure Liquid</subject><subject>Electrophoresis, Polyacrylamide Gel</subject><subject>Epitopes - analysis</subject><subject>Female</subject><subject>Female genital diseases</subject><subject>Gynecology. Andrology. Obstetrics</subject><subject>Humans</subject><subject>Medical sciences</subject><subject>Molecular Weight</subject><subject>Ovarian Neoplasms - immunology</subject><subject>Radioimmunoassay</subject><subject>Tumors</subject><issn>0008-5472</issn><issn>1538-7445</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1991</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkEtLBDEQhIMo67r6E4Rc9DaQx2SSOS6DL1jw4p6HzkzHjc5jTbKg_96AA56Kpr5uquuMrLmSptBlqc7JmjFmClVqcUmuYvzIo-JMrciKayakqtdk38z4fQwYo58nOjvae-cw4JQoTMm_4-Q7OkL4xBBpJsbZY_IYaTpAohYh0GZLuVC0x4Rh9FNei9fkwsEQ8WbRDdk_Prw1z8Xu9eml2e6Kg6hMKgyIDpAh5DTKouBOmwqY5E5AKdBYyTVW3GrFLLclc6V2SkNvK4TO9ZXckPu_u8cwf50wpnb0scNhgAnnU2wNkxWrmcrg7QKe7Ih9eww-P_XTLj1k_27xIXYwuABT5-M_VitWcaPkL4ghZ4s</recordid><startdate>19910115</startdate><enddate>19910115</enddate><creator>YU, Y. H</creator><creator>SCHLOSSMAN, D. M</creator><creator>HARRISON, C. L</creator><creator>RHINEHARDT-CLARK, A</creator><creator>SOPER, J. T</creator><creator>KLUG, T. L</creator><creator>ZURAWSKI, V. R</creator><creator>BAST, R. C</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>19910115</creationdate><title>Coexpression of different antigenic markers on moieties that bear CA 125 determinants</title><author>YU, Y. H ; SCHLOSSMAN, D. M ; HARRISON, C. L ; RHINEHARDT-CLARK, A ; SOPER, J. T ; KLUG, T. L ; ZURAWSKI, V. R ; BAST, R. C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-h268t-8a2cae0ea7025be21f786a031f2a42e8b317e61b750b1b40f47f57adb6eacfd63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1991</creationdate><topic>Antibodies, Monoclonal - isolation & purification</topic><topic>Antigen-Antibody Complex - analysis</topic><topic>Antigens, Tumor-Associated, Carbohydrate - immunology</topic><topic>Antigens, Tumor-Associated, Carbohydrate - isolation & purification</topic><topic>Ascites - immunology</topic><topic>Biological and medical sciences</topic><topic>Blotting, Western</topic><topic>Cell Line</topic><topic>Chromatography, High Pressure Liquid</topic><topic>Electrophoresis, Polyacrylamide Gel</topic><topic>Epitopes - analysis</topic><topic>Female</topic><topic>Female genital diseases</topic><topic>Gynecology. Andrology. Obstetrics</topic><topic>Humans</topic><topic>Medical sciences</topic><topic>Molecular Weight</topic><topic>Ovarian Neoplasms - immunology</topic><topic>Radioimmunoassay</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>YU, Y. H</creatorcontrib><creatorcontrib>SCHLOSSMAN, D. M</creatorcontrib><creatorcontrib>HARRISON, C. L</creatorcontrib><creatorcontrib>RHINEHARDT-CLARK, A</creatorcontrib><creatorcontrib>SOPER, J. T</creatorcontrib><creatorcontrib>KLUG, T. L</creatorcontrib><creatorcontrib>ZURAWSKI, V. R</creatorcontrib><creatorcontrib>BAST, R. C</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>Cancer research (Chicago, Ill.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>YU, Y. H</au><au>SCHLOSSMAN, D. M</au><au>HARRISON, C. L</au><au>RHINEHARDT-CLARK, A</au><au>SOPER, J. T</au><au>KLUG, T. L</au><au>ZURAWSKI, V. R</au><au>BAST, R. C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Coexpression of different antigenic markers on moieties that bear CA 125 determinants</atitle><jtitle>Cancer research (Chicago, Ill.)</jtitle><addtitle>Cancer Res</addtitle><date>1991-01-15</date><risdate>1991</risdate><volume>51</volume><issue>2</issue><spage>468</spage><epage>475</epage><pages>468-475</pages><issn>0008-5472</issn><eissn>1538-7445</eissn><coden>CNREA8</coden><abstract>CA 125 has been extensively evaluated as a serum marker for monitoring patients with epithelial ovarian carcinoma. Recently, consideration has been given to the use of CA 125 as one component in a strategy for early detection of this disease. A number of benign conditions can, however, increase CA 125 in serum, limiting the utility of a single antigen determination for identifying ovarian cancer patients. Coexpression of different epitopes on the high molecular weight complexes that express CA 125 determinants might provide a more specific test for malignant disease, provided that adequate sensitivity were maintained. To determine how frequently determinants are coexpressed, macromolecular moieties containing CA 125 determinants have been isolated from ascites fluid of ovarian cancer patients by immunoaffinity chromatography. CA 125+ moieties have been probed on Western transfers with several murine monoclonal antibodies that recognize distinct tumor-associated epitopes. Marked heterogeneity was observed between patients with regard to antigenic determinants that could be coexpressed with CA 125. A fraction of ascites fluids from different ovarian cancer patients contained moieties which bound to OC 125 on a solid phase immmunoadsorbent and which also bound 125I-labeled monoclonal antibodies NS 19-9, B72.3, DF3, or the novel murine monoclonal antibody OC 3632 in a double determinant immunoradiometric assay. Serum samples were evaluated from patients with ovarian cancer and from apparently healthy individuals. Coexpression of TAG 72 and CA 125 was observed most frequently. When the double determinant assay for coexpression of TAG 72 and CA 125 was compared to assays for the individual antigens, the assay for coexpression was substantially less sensitive than those for the individual markers.</abstract><cop>Philadelphia, PA</cop><pub>American Association for Cancer Research</pub><pmid>1702359</pmid><tpages>8</tpages></addata></record> |
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subjects | Antibodies, Monoclonal - isolation & purification Antigen-Antibody Complex - analysis Antigens, Tumor-Associated, Carbohydrate - immunology Antigens, Tumor-Associated, Carbohydrate - isolation & purification Ascites - immunology Biological and medical sciences Blotting, Western Cell Line Chromatography, High Pressure Liquid Electrophoresis, Polyacrylamide Gel Epitopes - analysis Female Female genital diseases Gynecology. Andrology. Obstetrics Humans Medical sciences Molecular Weight Ovarian Neoplasms - immunology Radioimmunoassay Tumors |
title | Coexpression of different antigenic markers on moieties that bear CA 125 determinants |
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