BCL6: somatic mutations and expression in early-stage chronic lymphocytic leukemia
BCL6 somatic mutations affect normal and tumoral post germinal center B-lymphocytes. Our objective was to analyse expression, mutations and polymorphisms in the BCL6 gene and to correlate those variables with the clinical outcome in early-stage chronic lymphocytic leukemia (CLL). CLL samples were us...
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Veröffentlicht in: | Leukemia & lymphoma 2009-01, Vol.50 (5), p.773-780 |
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description | BCL6 somatic mutations affect normal and tumoral post germinal center B-lymphocytes. Our objective was to analyse expression, mutations and polymorphisms in the BCL6 gene and to correlate those variables with the clinical outcome in early-stage chronic lymphocytic leukemia (CLL). CLL samples were used for characterisation of the mutational status of BCL6 immunoglobulin variable heavy chain (IGHV) genes, and expression of BCL6 was determined by real time PCR and immunoblot. Out of 68 cases, 29% show somatic mutations on BCL6 which occur exclusively in IGHV mutated cases. They are single nucleotide substitutions located mainly in two short mutational hot spots. CLL cells express different levels of BCL6 regardless of the mutational status, the number of mutations and polymorphisms. CLL cases expressing high levels of BCL6 have significantly shorter treatment-free interval. In conclusion, in early-stage patients with CLL, we found no correlation between expression and the mutations or polymorphism in BCL6, but high levels of BCL6 can discriminate patients with a worse prognosis. |
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Our objective was to analyse expression, mutations and polymorphisms in the BCL6 gene and to correlate those variables with the clinical outcome in early-stage chronic lymphocytic leukemia (CLL). CLL samples were used for characterisation of the mutational status of BCL6 immunoglobulin variable heavy chain (IGHV) genes, and expression of BCL6 was determined by real time PCR and immunoblot. Out of 68 cases, 29% show somatic mutations on BCL6 which occur exclusively in IGHV mutated cases. They are single nucleotide substitutions located mainly in two short mutational hot spots. CLL cells express different levels of BCL6 regardless of the mutational status, the number of mutations and polymorphisms. CLL cases expressing high levels of BCL6 have significantly shorter treatment-free interval. In conclusion, in early-stage patients with CLL, we found no correlation between expression and the mutations or polymorphism in BCL6, but high levels of BCL6 can discriminate patients with a worse prognosis.</description><identifier>ISSN: 1042-8194</identifier><identifier>EISSN: 1029-2403</identifier><identifier>DOI: 10.1080/10428190902842626</identifier><identifier>PMID: 19367498</identifier><language>eng</language><publisher>United States: Informa UK Ltd</publisher><subject>Adult ; Aged ; Aged, 80 and over ; BCL6 ; CLL ; DNA-Binding Proteins - analysis ; DNA-Binding Proteins - genetics ; expression ; Female ; Genes, Immunoglobulin ; Humans ; IGHV ; Immunoglobulin Heavy Chains - genetics ; Leukemia, Lymphocytic, Chronic, B-Cell - diagnosis ; Leukemia, Lymphocytic, Chronic, B-Cell - genetics ; Male ; Middle Aged ; Mutation ; Point Mutation ; Polymorphism, Genetic ; polymorphisms ; Predictive Value of Tests ; Prognosis ; Proto-Oncogene Proteins c-bcl-6 ; somatic mutations ; Treatment Outcome</subject><ispartof>Leukemia & lymphoma, 2009-01, Vol.50 (5), p.773-780</ispartof><rights>2009 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted 2009</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c470t-1b3d0612fc0a4d8efffded289e5ae180067d4a1664d0ff11bff128368524400f3</citedby><cites>FETCH-LOGICAL-c470t-1b3d0612fc0a4d8efffded289e5ae180067d4a1664d0ff11bff128368524400f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.tandfonline.com/doi/pdf/10.1080/10428190902842626$$EPDF$$P50$$Ginformahealthcare$$H</linktopdf><linktohtml>$$Uhttps://www.tandfonline.com/doi/full/10.1080/10428190902842626$$EHTML$$P50$$Ginformahealthcare$$H</linktohtml><link.rule.ids>314,777,781,27905,27906,59626,59732,60415,60521,61200,61235,61381,61416</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19367498$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jantus Lewintre, Eloisa</creatorcontrib><creatorcontrib>Reinoso Martín, Cristina</creatorcontrib><creatorcontrib>García Ballesteros, Carlos</creatorcontrib><creatorcontrib>Pendas, Jehzabel</creatorcontrib><creatorcontrib>Benet Campos, Carmen</creatorcontrib><creatorcontrib>Mayans Ferrer, José Ramón</creatorcontrib><creatorcontrib>García-Conde, Javier</creatorcontrib><title>BCL6: somatic mutations and expression in early-stage chronic lymphocytic leukemia</title><title>Leukemia & lymphoma</title><addtitle>Leuk Lymphoma</addtitle><description>BCL6 somatic mutations affect normal and tumoral post germinal center B-lymphocytes. Our objective was to analyse expression, mutations and polymorphisms in the BCL6 gene and to correlate those variables with the clinical outcome in early-stage chronic lymphocytic leukemia (CLL). CLL samples were used for characterisation of the mutational status of BCL6 immunoglobulin variable heavy chain (IGHV) genes, and expression of BCL6 was determined by real time PCR and immunoblot. Out of 68 cases, 29% show somatic mutations on BCL6 which occur exclusively in IGHV mutated cases. They are single nucleotide substitutions located mainly in two short mutational hot spots. CLL cells express different levels of BCL6 regardless of the mutational status, the number of mutations and polymorphisms. CLL cases expressing high levels of BCL6 have significantly shorter treatment-free interval. In conclusion, in early-stage patients with CLL, we found no correlation between expression and the mutations or polymorphism in BCL6, but high levels of BCL6 can discriminate patients with a worse prognosis.</description><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>BCL6</subject><subject>CLL</subject><subject>DNA-Binding Proteins - analysis</subject><subject>DNA-Binding Proteins - genetics</subject><subject>expression</subject><subject>Female</subject><subject>Genes, Immunoglobulin</subject><subject>Humans</subject><subject>IGHV</subject><subject>Immunoglobulin Heavy Chains - genetics</subject><subject>Leukemia, Lymphocytic, Chronic, B-Cell - diagnosis</subject><subject>Leukemia, Lymphocytic, Chronic, B-Cell - genetics</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Mutation</subject><subject>Point Mutation</subject><subject>Polymorphism, Genetic</subject><subject>polymorphisms</subject><subject>Predictive Value of Tests</subject><subject>Prognosis</subject><subject>Proto-Oncogene Proteins c-bcl-6</subject><subject>somatic mutations</subject><subject>Treatment Outcome</subject><issn>1042-8194</issn><issn>1029-2403</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kEFrGzEQhUVJqRO3PyCXsKfcNhlpZVmb5JKaJi0YCqU9C1kaxetoV460S7v_vjI2hBDwZd4MfO8xPELOKVxRkHBNgTNJa6iBSc4EEx_IKQVWl4xDdbLbOSszwCfkLKUNAMxqwT6RCa0rMee1PCW_vi6W4qZIodV9Y4p26LOGLhW6swX-20ZMKd9F0xWoox_L1OsnLMw6hi7zfmy362DGndfj8Ixtoz-Tj077hF8OOiV_Hr79Xnwvlz8ffyzul6Xhc-hLuqosCMqcAc2tROecRctkjTONVAKIueWaCsEtOEfpKg8mKyFnjHMAV03J5T53G8PLgKlXbZMMeq87DENSYs64FDXNIN2DJoaUIjq1jU2r46goqF2R6l2R2XNxCB9WLdpXx6G5DNztgaZzIbb6b4jeql6PPkQXdWeapKpj-bdv7GvUvl8bHVFtwhC7XNyR7_4DkVWTfQ</recordid><startdate>20090101</startdate><enddate>20090101</enddate><creator>Jantus Lewintre, Eloisa</creator><creator>Reinoso Martín, Cristina</creator><creator>García Ballesteros, Carlos</creator><creator>Pendas, Jehzabel</creator><creator>Benet Campos, Carmen</creator><creator>Mayans Ferrer, José Ramón</creator><creator>García-Conde, Javier</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>7X8</scope></search><sort><creationdate>20090101</creationdate><title>BCL6: somatic mutations and expression in early-stage chronic lymphocytic leukemia</title><author>Jantus Lewintre, Eloisa ; Reinoso Martín, Cristina ; García Ballesteros, Carlos ; Pendas, Jehzabel ; Benet Campos, Carmen ; Mayans Ferrer, José Ramón ; García-Conde, Javier</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c470t-1b3d0612fc0a4d8efffded289e5ae180067d4a1664d0ff11bff128368524400f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>BCL6</topic><topic>CLL</topic><topic>DNA-Binding Proteins - analysis</topic><topic>DNA-Binding Proteins - genetics</topic><topic>expression</topic><topic>Female</topic><topic>Genes, Immunoglobulin</topic><topic>Humans</topic><topic>IGHV</topic><topic>Immunoglobulin Heavy Chains - genetics</topic><topic>Leukemia, Lymphocytic, Chronic, B-Cell - diagnosis</topic><topic>Leukemia, Lymphocytic, Chronic, B-Cell - genetics</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Mutation</topic><topic>Point Mutation</topic><topic>Polymorphism, Genetic</topic><topic>polymorphisms</topic><topic>Predictive Value of Tests</topic><topic>Prognosis</topic><topic>Proto-Oncogene Proteins c-bcl-6</topic><topic>somatic mutations</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jantus Lewintre, Eloisa</creatorcontrib><creatorcontrib>Reinoso Martín, Cristina</creatorcontrib><creatorcontrib>García Ballesteros, Carlos</creatorcontrib><creatorcontrib>Pendas, Jehzabel</creatorcontrib><creatorcontrib>Benet Campos, Carmen</creatorcontrib><creatorcontrib>Mayans Ferrer, José Ramón</creatorcontrib><creatorcontrib>García-Conde, Javier</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Leukemia & lymphoma</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jantus Lewintre, Eloisa</au><au>Reinoso Martín, Cristina</au><au>García Ballesteros, Carlos</au><au>Pendas, Jehzabel</au><au>Benet Campos, Carmen</au><au>Mayans Ferrer, José Ramón</au><au>García-Conde, Javier</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>BCL6: somatic mutations and expression in early-stage chronic lymphocytic leukemia</atitle><jtitle>Leukemia & lymphoma</jtitle><addtitle>Leuk Lymphoma</addtitle><date>2009-01-01</date><risdate>2009</risdate><volume>50</volume><issue>5</issue><spage>773</spage><epage>780</epage><pages>773-780</pages><issn>1042-8194</issn><eissn>1029-2403</eissn><abstract>BCL6 somatic mutations affect normal and tumoral post germinal center B-lymphocytes. Our objective was to analyse expression, mutations and polymorphisms in the BCL6 gene and to correlate those variables with the clinical outcome in early-stage chronic lymphocytic leukemia (CLL). CLL samples were used for characterisation of the mutational status of BCL6 immunoglobulin variable heavy chain (IGHV) genes, and expression of BCL6 was determined by real time PCR and immunoblot. Out of 68 cases, 29% show somatic mutations on BCL6 which occur exclusively in IGHV mutated cases. They are single nucleotide substitutions located mainly in two short mutational hot spots. CLL cells express different levels of BCL6 regardless of the mutational status, the number of mutations and polymorphisms. CLL cases expressing high levels of BCL6 have significantly shorter treatment-free interval. In conclusion, in early-stage patients with CLL, we found no correlation between expression and the mutations or polymorphism in BCL6, but high levels of BCL6 can discriminate patients with a worse prognosis.</abstract><cop>United States</cop><pub>Informa UK Ltd</pub><pmid>19367498</pmid><doi>10.1080/10428190902842626</doi><tpages>8</tpages></addata></record> |
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subjects | Adult Aged Aged, 80 and over BCL6 CLL DNA-Binding Proteins - analysis DNA-Binding Proteins - genetics expression Female Genes, Immunoglobulin Humans IGHV Immunoglobulin Heavy Chains - genetics Leukemia, Lymphocytic, Chronic, B-Cell - diagnosis Leukemia, Lymphocytic, Chronic, B-Cell - genetics Male Middle Aged Mutation Point Mutation Polymorphism, Genetic polymorphisms Predictive Value of Tests Prognosis Proto-Oncogene Proteins c-bcl-6 somatic mutations Treatment Outcome |
title | BCL6: somatic mutations and expression in early-stage chronic lymphocytic leukemia |
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