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Antibodies to HSP70 and HSP90 in serum in non-small cell lung cancer patients
Heat shock proteins (HSPs) are components of a physiologic stress response that are also over-expressed in various cancers including non-small cell lung cancer (NSCLC). During NSCLC serum-antibody screening of a NSCLC cDNA T7 phage library for immunogenic proteins we isolated HSP70 and HSP90 protein...
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Published in: | Cancer detection and prevention 2003-01, Vol.27 (4), p.285-290 |
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creator | Zhong, Li Peng, Xuejun Hidalgo, Giovanna E Doherty, Dennis E Stromberg, Arnold J Hirschowitz, Edward A |
description | Heat shock proteins (HSPs) are components of a physiologic stress response that are also over-expressed in various cancers including non-small cell lung cancer (NSCLC). During NSCLC serum-antibody screening of a NSCLC cDNA T7 phage library for immunogenic proteins we isolated HSP70 and HSP90 proteins. Isolation of these proteins suggested that corresponding antibodies could be elevated in NSCLC patient sera, a novel finding that could pilot their use as markers of NSCLC. We showed histochemically that patient sera were more reactive with each phage-expressed protein than normal sera. Antibody affinity for each phage-expressed protein was confirmed by limiting the dilution of individual sera assayed by Ab enzyme-linked immunosorbent assay (ELISA). Sera from 49 NSCLC patients assayed by Ab ELISA and normalized to 40 controls showed that HSP70 antibodies were significantly greater in patient sera than in normals (
P=0.0002), while HSP90 antibodies were not significantly different (
P=0.11). Analysis of the results with logistic regression and receiver operating characteristics (ROC) curves showed that HSP70 antibodies were modest markers of NSCLC (sensitivity 0.74 and specificity 0.73; area under the curve or AUC=0.731), while HSP90 antibodies appeared to be poor in both criteria with an AUC of 0.602. Further evaluation of HSP70 antibodies as potential markers of disease may be rational. |
doi_str_mv | 10.1016/S0361-090X(03)00097-7 |
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P=0.0002), while HSP90 antibodies were not significantly different (
P=0.11). Analysis of the results with logistic regression and receiver operating characteristics (ROC) curves showed that HSP70 antibodies were modest markers of NSCLC (sensitivity 0.74 and specificity 0.73; area under the curve or AUC=0.731), while HSP90 antibodies appeared to be poor in both criteria with an AUC of 0.602. Further evaluation of HSP70 antibodies as potential markers of disease may be rational.</description><identifier>ISSN: 0361-090X</identifier><identifier>ISSN: 1877-7821</identifier><identifier>EISSN: 1873-443X</identifier><identifier>EISSN: 1877-783X</identifier><identifier>DOI: 10.1016/S0361-090X(03)00097-7</identifier><identifier>PMID: 12893076</identifier><identifier>CODEN: CDPRD4</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Antibodies ; Antibodies - analysis ; Biomarkers, Tumor - analysis ; Bone cancer ; Cancer ; Carcinoma, Non-Small-Cell Lung - immunology ; Carcinoma, Non-Small-Cell Lung - pathology ; Cardiovascular disease ; Dilution ; Enzyme-Linked Immunosorbent Assay ; Enzymes ; Epidemiology ; Heat shock proteins ; Histology ; HSP70 Heat-Shock Proteins - immunology ; HSP90 Heat-Shock Proteins - immunology ; Humans ; Lung cancer ; Lung Neoplasms - immunology ; Lung Neoplasms - pathology ; Markers ; Membranes ; Proteins ; Reference Values ; Regression Analysis ; Tumors</subject><ispartof>Cancer detection and prevention, 2003-01, Vol.27 (4), p.285-290</ispartof><rights>2003 International Society for Preventive Oncology</rights><rights>Copyright Elsevier Limited 2003</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c507t-fdd55d6724693b41f8311bd669c3da474f7543dd8cb79cbbbdc4552be4679e343</citedby><cites>FETCH-LOGICAL-c507t-fdd55d6724693b41f8311bd669c3da474f7543dd8cb79cbbbdc4552be4679e343</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12893076$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhong, Li</creatorcontrib><creatorcontrib>Peng, Xuejun</creatorcontrib><creatorcontrib>Hidalgo, Giovanna E</creatorcontrib><creatorcontrib>Doherty, Dennis E</creatorcontrib><creatorcontrib>Stromberg, Arnold J</creatorcontrib><creatorcontrib>Hirschowitz, Edward A</creatorcontrib><title>Antibodies to HSP70 and HSP90 in serum in non-small cell lung cancer patients</title><title>Cancer detection and prevention</title><addtitle>Cancer Detect Prev</addtitle><description>Heat shock proteins (HSPs) are components of a physiologic stress response that are also over-expressed in various cancers including non-small cell lung cancer (NSCLC). During NSCLC serum-antibody screening of a NSCLC cDNA T7 phage library for immunogenic proteins we isolated HSP70 and HSP90 proteins. Isolation of these proteins suggested that corresponding antibodies could be elevated in NSCLC patient sera, a novel finding that could pilot their use as markers of NSCLC. We showed histochemically that patient sera were more reactive with each phage-expressed protein than normal sera. Antibody affinity for each phage-expressed protein was confirmed by limiting the dilution of individual sera assayed by Ab enzyme-linked immunosorbent assay (ELISA). Sera from 49 NSCLC patients assayed by Ab ELISA and normalized to 40 controls showed that HSP70 antibodies were significantly greater in patient sera than in normals (
P=0.0002), while HSP90 antibodies were not significantly different (
P=0.11). Analysis of the results with logistic regression and receiver operating characteristics (ROC) curves showed that HSP70 antibodies were modest markers of NSCLC (sensitivity 0.74 and specificity 0.73; area under the curve or AUC=0.731), while HSP90 antibodies appeared to be poor in both criteria with an AUC of 0.602. Further evaluation of HSP70 antibodies as potential markers of disease may be rational.</description><subject>Antibodies</subject><subject>Antibodies - analysis</subject><subject>Biomarkers, Tumor - analysis</subject><subject>Bone cancer</subject><subject>Cancer</subject><subject>Carcinoma, Non-Small-Cell Lung - immunology</subject><subject>Carcinoma, Non-Small-Cell Lung - pathology</subject><subject>Cardiovascular disease</subject><subject>Dilution</subject><subject>Enzyme-Linked Immunosorbent Assay</subject><subject>Enzymes</subject><subject>Epidemiology</subject><subject>Heat shock proteins</subject><subject>Histology</subject><subject>HSP70 Heat-Shock Proteins - immunology</subject><subject>HSP90 Heat-Shock Proteins - immunology</subject><subject>Humans</subject><subject>Lung cancer</subject><subject>Lung Neoplasms - immunology</subject><subject>Lung Neoplasms - pathology</subject><subject>Markers</subject><subject>Membranes</subject><subject>Proteins</subject><subject>Reference Values</subject><subject>Regression Analysis</subject><subject>Tumors</subject><issn>0361-090X</issn><issn>1877-7821</issn><issn>1873-443X</issn><issn>1877-783X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><recordid>eNqFkE1LxDAQhoMouq7-BKUgiB6qk02aNCdZxC9QFFbBW2g-KpFtuiat4L833V0UvHiZmcMzMy8PQgcYzjBgdj4DwnAOAl5PgJwCgOA530AjXHKSU0peN9HoB9lBuzG-Q9oThG2jHTwpBQHORuhh6junWuNszLo2u509ccgqb4ZJQOZ8Fm3om2Hwrc9jU83nmbapzHv_lunKaxuyRdU567u4h7bqah7t_rqP0cv11fPlbX7_eHN3Ob3PdQG8y2tjisIwPqEpj6K4LgnGyjAmNDEV5bTmBSXGlFpxoZVSRtOimChLGReWUDJGx6u7i9B-9DZ2snFxSFV52_ZRckIZsIIk8OgP-N72wadsElNcMiowF4kqVpQObYzB1nIRXFOFL4lBDrbl0rYcVEogcmk7PRmjw_X1XjXW_G6t9SbgYgXYJOPT2SCjTqK0NS5Y3UnTun9efAMgL4zS</recordid><startdate>20030101</startdate><enddate>20030101</enddate><creator>Zhong, Li</creator><creator>Peng, Xuejun</creator><creator>Hidalgo, Giovanna E</creator><creator>Doherty, Dennis E</creator><creator>Stromberg, Arnold J</creator><creator>Hirschowitz, Edward A</creator><general>Elsevier Ltd</general><general>Elsevier Limited</general><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>3V.</scope><scope>7RV</scope><scope>7TO</scope><scope>7X7</scope><scope>7XB</scope><scope>88C</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M0T</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>20030101</creationdate><title>Antibodies to HSP70 and HSP90 in serum in non-small cell lung cancer patients</title><author>Zhong, Li ; 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During NSCLC serum-antibody screening of a NSCLC cDNA T7 phage library for immunogenic proteins we isolated HSP70 and HSP90 proteins. Isolation of these proteins suggested that corresponding antibodies could be elevated in NSCLC patient sera, a novel finding that could pilot their use as markers of NSCLC. We showed histochemically that patient sera were more reactive with each phage-expressed protein than normal sera. Antibody affinity for each phage-expressed protein was confirmed by limiting the dilution of individual sera assayed by Ab enzyme-linked immunosorbent assay (ELISA). Sera from 49 NSCLC patients assayed by Ab ELISA and normalized to 40 controls showed that HSP70 antibodies were significantly greater in patient sera than in normals (
P=0.0002), while HSP90 antibodies were not significantly different (
P=0.11). Analysis of the results with logistic regression and receiver operating characteristics (ROC) curves showed that HSP70 antibodies were modest markers of NSCLC (sensitivity 0.74 and specificity 0.73; area under the curve or AUC=0.731), while HSP90 antibodies appeared to be poor in both criteria with an AUC of 0.602. Further evaluation of HSP70 antibodies as potential markers of disease may be rational.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>12893076</pmid><doi>10.1016/S0361-090X(03)00097-7</doi><tpages>6</tpages></addata></record> |
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subjects | Antibodies Antibodies - analysis Biomarkers, Tumor - analysis Bone cancer Cancer Carcinoma, Non-Small-Cell Lung - immunology Carcinoma, Non-Small-Cell Lung - pathology Cardiovascular disease Dilution Enzyme-Linked Immunosorbent Assay Enzymes Epidemiology Heat shock proteins Histology HSP70 Heat-Shock Proteins - immunology HSP90 Heat-Shock Proteins - immunology Humans Lung cancer Lung Neoplasms - immunology Lung Neoplasms - pathology Markers Membranes Proteins Reference Values Regression Analysis Tumors |
title | Antibodies to HSP70 and HSP90 in serum in non-small cell lung cancer patients |
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