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The Prognostic Relevance of Apoptosis-related Proteins in Classical Hodgkin's Lymphomas
Neoplastic cells in classical Hodgkin's lymphomas (cHL) seem to correspond to defective germinal center B-cells, which escape from apoptosis. Epstein-Barr virus (EBV) may be implicated in this protective mechanism. The aim of the present study was to determine the expression of apoptosis-relate...
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Published in: | Leukemia & lymphoma 2003-01, Vol.44 (3), p.483-488 |
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description | Neoplastic cells in classical Hodgkin's lymphomas (cHL) seem to correspond to defective germinal center B-cells, which escape from apoptosis. Epstein-Barr virus (EBV) may be implicated in this protective mechanism. The aim of the present study was to determine the expression of apoptosis-related proteins in cHL among adult patients and correlate them with EBV expression, clinical findings and survival. EBV was detected by in situ hybridization (Epstein-Barr Encoded RNA, EBER, probe). Immunohistochemistry was used on paraffin sections to detect LMP-1/EBV, CD15 and the apoptosis-related proteins (bcl-2, bax, bcl-X, mcl-1 and CD95). Seventy-eight patients seen at our Institution were studied: 36 male and 42 female. Median age was 31 years (15-75 years). Histological types of cHL were: 61 nodular sclerosis (47 NS1 and 14 NS2), 15 mixed cellularity (MC), 1 lymphocyte depletion and 1 unclassified. In 50 cases there was EBV expression (64%). At least one apoptosis-associated protein was expressed in 92% and CD15 in 57.7% of the cases. In the univariate analysis, the following variables were related to a better overall survival: expression of CD15 (p =0.023), expression of mcl-1 protein (p =0.029), expression of bcl-2 protein (p =0.028, only in a Cox model after stratification for histology) and expression of LMP-1 (p =0.042). EBV expression presented a borderline inverse correlation with bcl-2. A prognostic index (PI) developed in the present study revealed that simultaneous expression of bcl-2, mcl-1 and LMP-1 was significant and independently correlated with an excellent survival. |
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Epstein-Barr virus (EBV) may be implicated in this protective mechanism. The aim of the present study was to determine the expression of apoptosis-related proteins in cHL among adult patients and correlate them with EBV expression, clinical findings and survival. EBV was detected by in situ hybridization (Epstein-Barr Encoded RNA, EBER, probe). Immunohistochemistry was used on paraffin sections to detect LMP-1/EBV, CD15 and the apoptosis-related proteins (bcl-2, bax, bcl-X, mcl-1 and CD95). Seventy-eight patients seen at our Institution were studied: 36 male and 42 female. Median age was 31 years (15-75 years). Histological types of cHL were: 61 nodular sclerosis (47 NS1 and 14 NS2), 15 mixed cellularity (MC), 1 lymphocyte depletion and 1 unclassified. In 50 cases there was EBV expression (64%). At least one apoptosis-associated protein was expressed in 92% and CD15 in 57.7% of the cases. In the univariate analysis, the following variables were related to a better overall survival: expression of CD15 (p =0.023), expression of mcl-1 protein (p =0.029), expression of bcl-2 protein (p =0.028, only in a Cox model after stratification for histology) and expression of LMP-1 (p =0.042). EBV expression presented a borderline inverse correlation with bcl-2. A prognostic index (PI) developed in the present study revealed that simultaneous expression of bcl-2, mcl-1 and LMP-1 was significant and independently correlated with an excellent survival.</description><identifier>ISSN: 1042-8194</identifier><identifier>EISSN: 1029-2403</identifier><identifier>DOI: 10.1080/1042819021000037958</identifier><identifier>PMID: 12688319</identifier><language>eng</language><publisher>United States: Informa UK Ltd</publisher><subject>Adolescent ; Adult ; Aged ; Apoptosis ; Apoptosis, Immunohistochemistry ; bcl-2-Associated X Protein ; bcl-X Protein ; Biomarkers ; Epstein-Barr Virus ; Epstein-Barr Virus Infections - metabolism ; fas Receptor - analysis ; Female ; Hodgkin Disease - metabolism ; Hodgkin Disease - mortality ; Hodgkin Disease - pathology ; Hodgkin Disease - virology ; Hodgkin's Lymphoma ; Humans ; In Situ Hybridization ; Lewis X Antigen - analysis ; Life Tables ; Male ; Middle Aged ; Myeloid Cell Leukemia Sequence 1 Protein ; Neoplasm Proteins - analysis ; Prognosis ; Proportional Hazards Models ; Proto-Oncogene Proteins - analysis ; Proto-Oncogene Proteins c-bcl-2 - analysis ; Retrospective Studies ; RNA, Viral - analysis ; Survival Analysis ; Tumor Virus Infections - metabolism ; Viral Matrix Proteins - analysis</subject><ispartof>Leukemia & lymphoma, 2003-01, Vol.44 (3), p.483-488</ispartof><rights>2003 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted 2003</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c441t-ee424b3b380d35953c6fd5041a69cc3c078f8e6cf0e8bb9ebcd99cec2ba45d63</citedby><cites>FETCH-LOGICAL-c441t-ee424b3b380d35953c6fd5041a69cc3c078f8e6cf0e8bb9ebcd99cec2ba45d63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12688319$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Vassallo, José</creatorcontrib><creatorcontrib>Metze, Konradin</creatorcontrib><creatorcontrib>Traina, Fabíola</creatorcontrib><creatorcontrib>A. de Souza, Cármino</creatorcontrib><creatorcontrib>Lorand-Metze, Irene</creatorcontrib><title>The Prognostic Relevance of Apoptosis-related Proteins in Classical Hodgkin's Lymphomas</title><title>Leukemia & lymphoma</title><addtitle>Leuk Lymphoma</addtitle><description>Neoplastic cells in classical Hodgkin's lymphomas (cHL) seem to correspond to defective germinal center B-cells, which escape from apoptosis. Epstein-Barr virus (EBV) may be implicated in this protective mechanism. The aim of the present study was to determine the expression of apoptosis-related proteins in cHL among adult patients and correlate them with EBV expression, clinical findings and survival. EBV was detected by in situ hybridization (Epstein-Barr Encoded RNA, EBER, probe). Immunohistochemistry was used on paraffin sections to detect LMP-1/EBV, CD15 and the apoptosis-related proteins (bcl-2, bax, bcl-X, mcl-1 and CD95). Seventy-eight patients seen at our Institution were studied: 36 male and 42 female. Median age was 31 years (15-75 years). Histological types of cHL were: 61 nodular sclerosis (47 NS1 and 14 NS2), 15 mixed cellularity (MC), 1 lymphocyte depletion and 1 unclassified. In 50 cases there was EBV expression (64%). At least one apoptosis-associated protein was expressed in 92% and CD15 in 57.7% of the cases. In the univariate analysis, the following variables were related to a better overall survival: expression of CD15 (p =0.023), expression of mcl-1 protein (p =0.029), expression of bcl-2 protein (p =0.028, only in a Cox model after stratification for histology) and expression of LMP-1 (p =0.042). EBV expression presented a borderline inverse correlation with bcl-2. A prognostic index (PI) developed in the present study revealed that simultaneous expression of bcl-2, mcl-1 and LMP-1 was significant and independently correlated with an excellent survival.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Apoptosis</subject><subject>Apoptosis, Immunohistochemistry</subject><subject>bcl-2-Associated X Protein</subject><subject>bcl-X Protein</subject><subject>Biomarkers</subject><subject>Epstein-Barr Virus</subject><subject>Epstein-Barr Virus Infections - metabolism</subject><subject>fas Receptor - analysis</subject><subject>Female</subject><subject>Hodgkin Disease - metabolism</subject><subject>Hodgkin Disease - mortality</subject><subject>Hodgkin Disease - pathology</subject><subject>Hodgkin Disease - virology</subject><subject>Hodgkin's Lymphoma</subject><subject>Humans</subject><subject>In Situ Hybridization</subject><subject>Lewis X Antigen - analysis</subject><subject>Life Tables</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Myeloid Cell Leukemia Sequence 1 Protein</subject><subject>Neoplasm Proteins - analysis</subject><subject>Prognosis</subject><subject>Proportional Hazards Models</subject><subject>Proto-Oncogene Proteins - analysis</subject><subject>Proto-Oncogene Proteins c-bcl-2 - analysis</subject><subject>Retrospective Studies</subject><subject>RNA, Viral - analysis</subject><subject>Survival Analysis</subject><subject>Tumor Virus Infections - metabolism</subject><subject>Viral Matrix Proteins - analysis</subject><issn>1042-8194</issn><issn>1029-2403</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><recordid>eNqFkM1q3DAUhUVpaX6aJygUr5qVU_3ZIy1aCEPSBAYSykCWQpavM0pky9X1JMzbR8MMlEBJ7kZ38Z0j6SPkK6NnjCr6g1HJFdOUM5pHzHSlPpBDRrkuuaTi43aXvMyIPCBHiA-ZqnTNP5MDxmulBNOH5G65guI2xfsh4uRd8QcCPNnBQRG74nyM4xTRY5kg2AnaLTmBH7DwQzEPFtE7G4qr2N4_-uEUi8WmH1ext_iFfOpsQDjZn8dkeXmxnF-Vi5vf1_PzRemkZFMJILlsRCMUbUWlK-Hqrq2oZLbWzglHZ6pTULuOgmoaDY1rtXbgeGNl1dbimHzf1Y4p_l0DTqb36CAEO0Bco5nlT84qyd4Fma5lrbXOoNiBLkXEBJ0Zk-9t2hhGzda7-Y_3nPq2r183PbT_MnvRGfi1A_zQxdTb55hCaya7CTF1KQv3aMTbN_x8VbACG6aVswnMQ1ynIUt-84UvmdakiQ</recordid><startdate>20030101</startdate><enddate>20030101</enddate><creator>Vassallo, José</creator><creator>Metze, Konradin</creator><creator>Traina, Fabíola</creator><creator>A. de Souza, Cármino</creator><creator>Lorand-Metze, Irene</creator><general>Informa UK Ltd</general><general>Taylor & Francis</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>7T5</scope><scope>7U9</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>20030101</creationdate><title>The Prognostic Relevance of Apoptosis-related Proteins in Classical Hodgkin's Lymphomas</title><author>Vassallo, José ; Metze, Konradin ; Traina, Fabíola ; A. de Souza, Cármino ; Lorand-Metze, Irene</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c441t-ee424b3b380d35953c6fd5041a69cc3c078f8e6cf0e8bb9ebcd99cec2ba45d63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Apoptosis</topic><topic>Apoptosis, Immunohistochemistry</topic><topic>bcl-2-Associated X Protein</topic><topic>bcl-X Protein</topic><topic>Biomarkers</topic><topic>Epstein-Barr Virus</topic><topic>Epstein-Barr Virus Infections - metabolism</topic><topic>fas Receptor - analysis</topic><topic>Female</topic><topic>Hodgkin Disease - metabolism</topic><topic>Hodgkin Disease - mortality</topic><topic>Hodgkin Disease - pathology</topic><topic>Hodgkin Disease - virology</topic><topic>Hodgkin's Lymphoma</topic><topic>Humans</topic><topic>In Situ Hybridization</topic><topic>Lewis X Antigen - analysis</topic><topic>Life Tables</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Myeloid Cell Leukemia Sequence 1 Protein</topic><topic>Neoplasm Proteins - analysis</topic><topic>Prognosis</topic><topic>Proportional Hazards Models</topic><topic>Proto-Oncogene Proteins - analysis</topic><topic>Proto-Oncogene Proteins c-bcl-2 - analysis</topic><topic>Retrospective Studies</topic><topic>RNA, Viral - analysis</topic><topic>Survival Analysis</topic><topic>Tumor Virus Infections - metabolism</topic><topic>Viral Matrix Proteins - analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Vassallo, José</creatorcontrib><creatorcontrib>Metze, Konradin</creatorcontrib><creatorcontrib>Traina, Fabíola</creatorcontrib><creatorcontrib>A. de Souza, Cármino</creatorcontrib><creatorcontrib>Lorand-Metze, Irene</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Leukemia & lymphoma</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Vassallo, José</au><au>Metze, Konradin</au><au>Traina, Fabíola</au><au>A. de Souza, Cármino</au><au>Lorand-Metze, Irene</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Prognostic Relevance of Apoptosis-related Proteins in Classical Hodgkin's Lymphomas</atitle><jtitle>Leukemia & lymphoma</jtitle><addtitle>Leuk Lymphoma</addtitle><date>2003-01-01</date><risdate>2003</risdate><volume>44</volume><issue>3</issue><spage>483</spage><epage>488</epage><pages>483-488</pages><issn>1042-8194</issn><eissn>1029-2403</eissn><abstract>Neoplastic cells in classical Hodgkin's lymphomas (cHL) seem to correspond to defective germinal center B-cells, which escape from apoptosis. Epstein-Barr virus (EBV) may be implicated in this protective mechanism. The aim of the present study was to determine the expression of apoptosis-related proteins in cHL among adult patients and correlate them with EBV expression, clinical findings and survival. EBV was detected by in situ hybridization (Epstein-Barr Encoded RNA, EBER, probe). Immunohistochemistry was used on paraffin sections to detect LMP-1/EBV, CD15 and the apoptosis-related proteins (bcl-2, bax, bcl-X, mcl-1 and CD95). Seventy-eight patients seen at our Institution were studied: 36 male and 42 female. Median age was 31 years (15-75 years). Histological types of cHL were: 61 nodular sclerosis (47 NS1 and 14 NS2), 15 mixed cellularity (MC), 1 lymphocyte depletion and 1 unclassified. In 50 cases there was EBV expression (64%). At least one apoptosis-associated protein was expressed in 92% and CD15 in 57.7% of the cases. In the univariate analysis, the following variables were related to a better overall survival: expression of CD15 (p =0.023), expression of mcl-1 protein (p =0.029), expression of bcl-2 protein (p =0.028, only in a Cox model after stratification for histology) and expression of LMP-1 (p =0.042). EBV expression presented a borderline inverse correlation with bcl-2. A prognostic index (PI) developed in the present study revealed that simultaneous expression of bcl-2, mcl-1 and LMP-1 was significant and independently correlated with an excellent survival.</abstract><cop>United States</cop><pub>Informa UK Ltd</pub><pmid>12688319</pmid><doi>10.1080/1042819021000037958</doi><tpages>6</tpages></addata></record> |
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subjects | Adolescent Adult Aged Apoptosis Apoptosis, Immunohistochemistry bcl-2-Associated X Protein bcl-X Protein Biomarkers Epstein-Barr Virus Epstein-Barr Virus Infections - metabolism fas Receptor - analysis Female Hodgkin Disease - metabolism Hodgkin Disease - mortality Hodgkin Disease - pathology Hodgkin Disease - virology Hodgkin's Lymphoma Humans In Situ Hybridization Lewis X Antigen - analysis Life Tables Male Middle Aged Myeloid Cell Leukemia Sequence 1 Protein Neoplasm Proteins - analysis Prognosis Proportional Hazards Models Proto-Oncogene Proteins - analysis Proto-Oncogene Proteins c-bcl-2 - analysis Retrospective Studies RNA, Viral - analysis Survival Analysis Tumor Virus Infections - metabolism Viral Matrix Proteins - analysis |
title | The Prognostic Relevance of Apoptosis-related Proteins in Classical Hodgkin's Lymphomas |
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