Comparison of ZAP-70/Syk mRNA levels with immunoglobulin heavy-chain gene mutation status and disease progression in chronic lymphocytic leukemia
Department of Hematology, Catholic University Hospial A. Gemelli, Rome, Italy. laurenti@rm.unicatt.it BACKGROUND AND OBJECTIVES: The protein tyrosine kinase ZAP-70 has recently emerged as a major prognostic indicator in chronic lymphocytic leukemia (CLL). ZAP-70 is structurally and functionally homo...
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Veröffentlicht in: | Haematologica (Roma) 2005-11, Vol.90 (11), p.1533-1540 |
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creator | Laurenti, L Petlickovski, A Rumi, C Gobessi, S Piccioni, P Tarnani, M Puggioni, P Marietti, S Sica, S Leone, G Efremov, DG |
description | Department of Hematology, Catholic University Hospial A. Gemelli, Rome, Italy. laurenti@rm.unicatt.it
BACKGROUND AND OBJECTIVES: The protein tyrosine kinase ZAP-70 has recently emerged as a major prognostic indicator in chronic lymphocytic leukemia (CLL). ZAP-70 is structurally and functionally homologous to Syk, a key mediator of B-cell receptor signaling. We therefore evaluated ZAP-70 expression in CLL B cells using Syk as an intracellular standard. DESIGN AND METHODS: The relative amounts of ZAP-70 and Syk were determined in purified B cells from 92 CLL patients using a novel reverse transcriptase/polymerase chain reaction (RT-PCR) procedure that co-amplifies both transcripts with equal efficiency. The ZAP-70/Syk mRNA ratio was correlated with VH gene mutation status, median treatment-free survival and FACS analysis of ZAP-70 expression. RESULTS: ZAP-70 was expressed in the majority of cases with unmutated VH genes (88%), but also at lower levels in a substantial fraction of cases with mutated VH genes (44%). High levels of ZAP-70, defined as ZAP-70/Syk mRNA ratios above 0.25, were observed mainly in cases with unmutated VH genes and correlated with short treatment-free survival. In contrast, no difference was observed in the median treatment-free survival between patients with low ZAP-70/Syk ratios (0.05-0.25) and patients with no or negligible ZAP-70 expression (ZAP-70/Syk |
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BACKGROUND AND OBJECTIVES: The protein tyrosine kinase ZAP-70 has recently emerged as a major prognostic indicator in chronic lymphocytic leukemia (CLL). ZAP-70 is structurally and functionally homologous to Syk, a key mediator of B-cell receptor signaling. We therefore evaluated ZAP-70 expression in CLL B cells using Syk as an intracellular standard. DESIGN AND METHODS: The relative amounts of ZAP-70 and Syk were determined in purified B cells from 92 CLL patients using a novel reverse transcriptase/polymerase chain reaction (RT-PCR) procedure that co-amplifies both transcripts with equal efficiency. The ZAP-70/Syk mRNA ratio was correlated with VH gene mutation status, median treatment-free survival and FACS analysis of ZAP-70 expression. RESULTS: ZAP-70 was expressed in the majority of cases with unmutated VH genes (88%), but also at lower levels in a substantial fraction of cases with mutated VH genes (44%). High levels of ZAP-70, defined as ZAP-70/Syk mRNA ratios above 0.25, were observed mainly in cases with unmutated VH genes and correlated with short treatment-free survival. In contrast, no difference was observed in the median treatment-free survival between patients with low ZAP-70/Syk ratios (0.05-0.25) and patients with no or negligible ZAP-70 expression (ZAP-70/Syk</description><identifier>ISSN: 0390-6078</identifier><identifier>EISSN: 1592-8721</identifier><identifier>PMID: 16266901</identifier><language>eng</language><publisher>Pavia: Haematologica</publisher><subject>Adult ; Aged ; Aged, 80 and over ; Base Sequence ; Biological and medical sciences ; Disease Progression ; Female ; Genes, Immunoglobulin Heavy Chain - genetics ; Hematologic and hematopoietic diseases ; Humans ; Intracellular Signaling Peptides and Proteins - genetics ; Leukemia, Lymphocytic, Chronic, B-Cell - enzymology ; Leukemia, Lymphocytic, Chronic, B-Cell - genetics ; Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis ; Male ; Medical sciences ; Middle Aged ; Molecular Sequence Data ; Mutation ; Protein-Tyrosine Kinases - genetics ; RNA, Messenger - genetics ; Syk Kinase ; ZAP-70 Protein-Tyrosine Kinase - genetics</subject><ispartof>Haematologica (Roma), 2005-11, Vol.90 (11), p.1533-1540</ispartof><rights>2006 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=17262672$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16266901$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Laurenti, L</creatorcontrib><creatorcontrib>Petlickovski, A</creatorcontrib><creatorcontrib>Rumi, C</creatorcontrib><creatorcontrib>Gobessi, S</creatorcontrib><creatorcontrib>Piccioni, P</creatorcontrib><creatorcontrib>Tarnani, M</creatorcontrib><creatorcontrib>Puggioni, P</creatorcontrib><creatorcontrib>Marietti, S</creatorcontrib><creatorcontrib>Sica, S</creatorcontrib><creatorcontrib>Leone, G</creatorcontrib><creatorcontrib>Efremov, DG</creatorcontrib><title>Comparison of ZAP-70/Syk mRNA levels with immunoglobulin heavy-chain gene mutation status and disease progression in chronic lymphocytic leukemia</title><title>Haematologica (Roma)</title><addtitle>Haematologica</addtitle><description>Department of Hematology, Catholic University Hospial A. Gemelli, Rome, Italy. laurenti@rm.unicatt.it
BACKGROUND AND OBJECTIVES: The protein tyrosine kinase ZAP-70 has recently emerged as a major prognostic indicator in chronic lymphocytic leukemia (CLL). ZAP-70 is structurally and functionally homologous to Syk, a key mediator of B-cell receptor signaling. We therefore evaluated ZAP-70 expression in CLL B cells using Syk as an intracellular standard. DESIGN AND METHODS: The relative amounts of ZAP-70 and Syk were determined in purified B cells from 92 CLL patients using a novel reverse transcriptase/polymerase chain reaction (RT-PCR) procedure that co-amplifies both transcripts with equal efficiency. The ZAP-70/Syk mRNA ratio was correlated with VH gene mutation status, median treatment-free survival and FACS analysis of ZAP-70 expression. RESULTS: ZAP-70 was expressed in the majority of cases with unmutated VH genes (88%), but also at lower levels in a substantial fraction of cases with mutated VH genes (44%). High levels of ZAP-70, defined as ZAP-70/Syk mRNA ratios above 0.25, were observed mainly in cases with unmutated VH genes and correlated with short treatment-free survival. In contrast, no difference was observed in the median treatment-free survival between patients with low ZAP-70/Syk ratios (0.05-0.25) and patients with no or negligible ZAP-70 expression (ZAP-70/Syk</description><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Base Sequence</subject><subject>Biological and medical sciences</subject><subject>Disease Progression</subject><subject>Female</subject><subject>Genes, Immunoglobulin Heavy Chain - genetics</subject><subject>Hematologic and hematopoietic diseases</subject><subject>Humans</subject><subject>Intracellular Signaling Peptides and Proteins - genetics</subject><subject>Leukemia, Lymphocytic, Chronic, B-Cell - enzymology</subject><subject>Leukemia, Lymphocytic, Chronic, B-Cell - genetics</subject><subject>Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Molecular Sequence Data</subject><subject>Mutation</subject><subject>Protein-Tyrosine Kinases - genetics</subject><subject>RNA, Messenger - genetics</subject><subject>Syk Kinase</subject><subject>ZAP-70 Protein-Tyrosine Kinase - genetics</subject><issn>0390-6078</issn><issn>1592-8721</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpF0MlO5DAQBuAIDYJmeQXkC8MpGi-dOD62WsMioRnEcuESOU6lY7DjJpUQ5TF4Y4zo0Zzql-rTr1LtJQuWKZ4WkrMfyYIKRdOcyuIwOUJ8oZRTpeRBcshynueKskXysQ5-q3uLoSOhIc-ru1TSXw_zK_H3f1bEwTs4JJMdWmK9H7uwcaEane1IC_p9Tk2rY95AB8SPgx5s7ME4RyS6q0ltETQC2fZh0wPi1zp60_ahs4a42W_bYObhK8P4Ct7qk2S_0Q7hdDePk6fL34_r6_T279XNenWbtlyyIV7JmGmqqjIFpUyrmlMQjIoG6kbIJRjeUGpMwXhhWC1EpvJGGVFUS6Z0pmpxnPz87o23vY2AQ-ktGnBOdxBGLPNCZlm-zCI828Gx8lCX29563c_lvydGcL4DGo12Ta87Y_G_kzxKyaO7-Hat3bST7aFEr52LtbycpknRkrGSZUKIT0zli-I</recordid><startdate>20051101</startdate><enddate>20051101</enddate><creator>Laurenti, L</creator><creator>Petlickovski, A</creator><creator>Rumi, C</creator><creator>Gobessi, S</creator><creator>Piccioni, P</creator><creator>Tarnani, M</creator><creator>Puggioni, P</creator><creator>Marietti, S</creator><creator>Sica, S</creator><creator>Leone, G</creator><creator>Efremov, DG</creator><general>Haematologica</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>20051101</creationdate><title>Comparison of ZAP-70/Syk mRNA levels with immunoglobulin heavy-chain gene mutation status and disease progression in chronic lymphocytic leukemia</title><author>Laurenti, L ; Petlickovski, A ; Rumi, C ; Gobessi, S ; Piccioni, P ; Tarnani, M ; Puggioni, P ; Marietti, S ; Sica, S ; Leone, G ; Efremov, DG</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-h271t-7011cfbbbc8001a9d20e3103fedf374ec2f00cc8128c1d33596f9c38b419a59d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Base Sequence</topic><topic>Biological and medical sciences</topic><topic>Disease Progression</topic><topic>Female</topic><topic>Genes, Immunoglobulin Heavy Chain - genetics</topic><topic>Hematologic and hematopoietic diseases</topic><topic>Humans</topic><topic>Intracellular Signaling Peptides and Proteins - genetics</topic><topic>Leukemia, Lymphocytic, Chronic, B-Cell - enzymology</topic><topic>Leukemia, Lymphocytic, Chronic, B-Cell - genetics</topic><topic>Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Molecular Sequence Data</topic><topic>Mutation</topic><topic>Protein-Tyrosine Kinases - genetics</topic><topic>RNA, Messenger - genetics</topic><topic>Syk Kinase</topic><topic>ZAP-70 Protein-Tyrosine Kinase - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Laurenti, L</creatorcontrib><creatorcontrib>Petlickovski, A</creatorcontrib><creatorcontrib>Rumi, C</creatorcontrib><creatorcontrib>Gobessi, S</creatorcontrib><creatorcontrib>Piccioni, P</creatorcontrib><creatorcontrib>Tarnani, M</creatorcontrib><creatorcontrib>Puggioni, P</creatorcontrib><creatorcontrib>Marietti, S</creatorcontrib><creatorcontrib>Sica, S</creatorcontrib><creatorcontrib>Leone, G</creatorcontrib><creatorcontrib>Efremov, DG</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>Haematologica (Roma)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Laurenti, L</au><au>Petlickovski, A</au><au>Rumi, C</au><au>Gobessi, S</au><au>Piccioni, P</au><au>Tarnani, M</au><au>Puggioni, P</au><au>Marietti, S</au><au>Sica, S</au><au>Leone, G</au><au>Efremov, DG</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Comparison of ZAP-70/Syk mRNA levels with immunoglobulin heavy-chain gene mutation status and disease progression in chronic lymphocytic leukemia</atitle><jtitle>Haematologica (Roma)</jtitle><addtitle>Haematologica</addtitle><date>2005-11-01</date><risdate>2005</risdate><volume>90</volume><issue>11</issue><spage>1533</spage><epage>1540</epage><pages>1533-1540</pages><issn>0390-6078</issn><eissn>1592-8721</eissn><abstract>Department of Hematology, Catholic University Hospial A. Gemelli, Rome, Italy. laurenti@rm.unicatt.it
BACKGROUND AND OBJECTIVES: The protein tyrosine kinase ZAP-70 has recently emerged as a major prognostic indicator in chronic lymphocytic leukemia (CLL). ZAP-70 is structurally and functionally homologous to Syk, a key mediator of B-cell receptor signaling. We therefore evaluated ZAP-70 expression in CLL B cells using Syk as an intracellular standard. DESIGN AND METHODS: The relative amounts of ZAP-70 and Syk were determined in purified B cells from 92 CLL patients using a novel reverse transcriptase/polymerase chain reaction (RT-PCR) procedure that co-amplifies both transcripts with equal efficiency. The ZAP-70/Syk mRNA ratio was correlated with VH gene mutation status, median treatment-free survival and FACS analysis of ZAP-70 expression. RESULTS: ZAP-70 was expressed in the majority of cases with unmutated VH genes (88%), but also at lower levels in a substantial fraction of cases with mutated VH genes (44%). High levels of ZAP-70, defined as ZAP-70/Syk mRNA ratios above 0.25, were observed mainly in cases with unmutated VH genes and correlated with short treatment-free survival. In contrast, no difference was observed in the median treatment-free survival between patients with low ZAP-70/Syk ratios (0.05-0.25) and patients with no or negligible ZAP-70 expression (ZAP-70/Syk</abstract><cop>Pavia</cop><pub>Haematologica</pub><pmid>16266901</pmid><tpages>8</tpages></addata></record> |
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subjects | Adult Aged Aged, 80 and over Base Sequence Biological and medical sciences Disease Progression Female Genes, Immunoglobulin Heavy Chain - genetics Hematologic and hematopoietic diseases Humans Intracellular Signaling Peptides and Proteins - genetics Leukemia, Lymphocytic, Chronic, B-Cell - enzymology Leukemia, Lymphocytic, Chronic, B-Cell - genetics Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis Male Medical sciences Middle Aged Molecular Sequence Data Mutation Protein-Tyrosine Kinases - genetics RNA, Messenger - genetics Syk Kinase ZAP-70 Protein-Tyrosine Kinase - genetics |
title | Comparison of ZAP-70/Syk mRNA levels with immunoglobulin heavy-chain gene mutation status and disease progression in chronic lymphocytic leukemia |
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