Molecular variants of the ATM gene in Hodgkin's disease in children
Ataxia telangiectasia is an autosomal recessive disease with a striking predisposition of lymphoid malignancies. ATM mutations have been reported in adult sporadic lymphoma and leukaemia. The aim of this study was to investigate the possible involvement of the ATM gene in the carcinogenesis of Hodgk...
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description | Ataxia telangiectasia is an autosomal recessive disease with a striking predisposition of lymphoid malignancies. ATM mutations have been reported in adult sporadic lymphoma and leukaemia. The aim of this study was to investigate the possible involvement of the ATM gene in the carcinogenesis of Hodgkin disease in children. Tumours were obtained from 23 patients and were subjected to mutation screening and loss of heterozygosity analysis. Eight base substitutions were identified in seven patients. Of them, Y54Y, a silent change, was observed in two patients and a known polymorphism, D1853N, in three patients. Of the other two patients, one harboured a combined genotype P604S/F1463C, identified previously in two patients with Hodgkin lymphoma, and the other a novel missense mutation, V595A. The alterations were present in the germ line, and both had a more aggressive disease. In all, 100 matched normal ethnic controls were screened for these mutations and P604S/F1463C was identified in one healthy control. Loss of heterozygosity was identified in four patients and in three of them it was located centromeric to the ATM gene, and, in one, it spanned a large region, indicating the involvement of other tumour-suppressor genes in this disease. Missense variants of the ATM gene are a rare event in childhood Hodgkin disease. |
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ATM mutations have been reported in adult sporadic lymphoma and leukaemia. The aim of this study was to investigate the possible involvement of the ATM gene in the carcinogenesis of Hodgkin disease in children. Tumours were obtained from 23 patients and were subjected to mutation screening and loss of heterozygosity analysis. Eight base substitutions were identified in seven patients. Of them, Y54Y, a silent change, was observed in two patients and a known polymorphism, D1853N, in three patients. Of the other two patients, one harboured a combined genotype P604S/F1463C, identified previously in two patients with Hodgkin lymphoma, and the other a novel missense mutation, V595A. The alterations were present in the germ line, and both had a more aggressive disease. In all, 100 matched normal ethnic controls were screened for these mutations and P604S/F1463C was identified in one healthy control. Loss of heterozygosity was identified in four patients and in three of them it was located centromeric to the ATM gene, and, in one, it spanned a large region, indicating the involvement of other tumour-suppressor genes in this disease. Missense variants of the ATM gene are a rare event in childhood Hodgkin disease.</description><identifier>ISSN: 0007-0920</identifier><identifier>EISSN: 1532-1827</identifier><identifier>DOI: 10.1038/sj.bjc.6601522</identifier><identifier>PMID: 14735203</identifier><identifier>CODEN: BJCAAI</identifier><language>eng</language><publisher>Basingstoke: Nature Publishing Group</publisher><subject>Adolescent ; Ataxia ; Ataxia Telangiectasia ; Ataxia Telangiectasia Mutated Proteins ; Biological and medical sciences ; Breast cancer ; Cancer research ; Cell Cycle Proteins ; Child ; Child, Preschool ; Cohort Studies ; DNA Mutational Analysis ; DNA-Binding Proteins ; Female ; Genes, Tumor Suppressor ; Genetic Predisposition to Disease ; Genetics and Genomics ; Genotype ; Hematologic and hematopoietic diseases ; Hematology ; Hodgkin Disease - genetics ; Hodgkin Disease - physiopathology ; Humans ; Kinases ; Leucine Zippers ; Leukemia ; Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis ; Loss of Heterozygosity ; Lymphoma ; Male ; Medical research ; Medical sciences ; Mutation ; Mutation, Missense ; Oncology ; Pediatrics ; Phosphatidylinositol 3-Kinases ; Polymorphism, Genetic ; Protein Serine-Threonine Kinases - genetics ; Tumor Suppressor Proteins ; Tumors</subject><ispartof>British journal of cancer, 2004-01, Vol.90 (2), p.522-525</ispartof><rights>2004 INIST-CNRS</rights><rights>Copyright Nature Publishing Group Jan 26, 2004</rights><rights>Copyright © 2003 Cancer Research UK 2003 Cancer Research UK</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c562t-a7f4a9ea2f7f383b29c2c410b02ac79a512d43125c53dcf7b1ce8558881952633</citedby><cites>FETCH-LOGICAL-c562t-a7f4a9ea2f7f383b29c2c410b02ac79a512d43125c53dcf7b1ce8558881952633</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2409549/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2409549/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,315,728,781,785,886,2728,27929,27930,53796,53798</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=15678394$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/14735203$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>LIBERZON, E</creatorcontrib><creatorcontrib>AVIGAD, S</creatorcontrib><creatorcontrib>YANIV, I</creatorcontrib><creatorcontrib>STARK, B</creatorcontrib><creatorcontrib>AVRAHAMI, G</creatorcontrib><creatorcontrib>GOSHEN, Y</creatorcontrib><creatorcontrib>ZAIZOV, R</creatorcontrib><title>Molecular variants of the ATM gene in Hodgkin's disease in children</title><title>British journal of cancer</title><addtitle>Br J Cancer</addtitle><description>Ataxia telangiectasia is an autosomal recessive disease with a striking predisposition of lymphoid malignancies. ATM mutations have been reported in adult sporadic lymphoma and leukaemia. The aim of this study was to investigate the possible involvement of the ATM gene in the carcinogenesis of Hodgkin disease in children. Tumours were obtained from 23 patients and were subjected to mutation screening and loss of heterozygosity analysis. Eight base substitutions were identified in seven patients. Of them, Y54Y, a silent change, was observed in two patients and a known polymorphism, D1853N, in three patients. Of the other two patients, one harboured a combined genotype P604S/F1463C, identified previously in two patients with Hodgkin lymphoma, and the other a novel missense mutation, V595A. The alterations were present in the germ line, and both had a more aggressive disease. In all, 100 matched normal ethnic controls were screened for these mutations and P604S/F1463C was identified in one healthy control. Loss of heterozygosity was identified in four patients and in three of them it was located centromeric to the ATM gene, and, in one, it spanned a large region, indicating the involvement of other tumour-suppressor genes in this disease. Missense variants of the ATM gene are a rare event in childhood Hodgkin disease.</description><subject>Adolescent</subject><subject>Ataxia</subject><subject>Ataxia Telangiectasia</subject><subject>Ataxia Telangiectasia Mutated Proteins</subject><subject>Biological and medical sciences</subject><subject>Breast cancer</subject><subject>Cancer research</subject><subject>Cell Cycle Proteins</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Cohort Studies</subject><subject>DNA Mutational Analysis</subject><subject>DNA-Binding Proteins</subject><subject>Female</subject><subject>Genes, Tumor Suppressor</subject><subject>Genetic Predisposition to Disease</subject><subject>Genetics and Genomics</subject><subject>Genotype</subject><subject>Hematologic and hematopoietic diseases</subject><subject>Hematology</subject><subject>Hodgkin Disease - genetics</subject><subject>Hodgkin Disease - physiopathology</subject><subject>Humans</subject><subject>Kinases</subject><subject>Leucine Zippers</subject><subject>Leukemia</subject><subject>Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis</subject><subject>Loss of Heterozygosity</subject><subject>Lymphoma</subject><subject>Male</subject><subject>Medical research</subject><subject>Medical sciences</subject><subject>Mutation</subject><subject>Mutation, Missense</subject><subject>Oncology</subject><subject>Pediatrics</subject><subject>Phosphatidylinositol 3-Kinases</subject><subject>Polymorphism, Genetic</subject><subject>Protein Serine-Threonine Kinases - genetics</subject><subject>Tumor Suppressor Proteins</subject><subject>Tumors</subject><issn>0007-0920</issn><issn>1532-1827</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNpd0UFvFCEUB3BiNHatXr1pJibqaVZ4DANcmjQbtU3a9FLP5A3D7DLOQoWZJn57p92x1Z4I8OO9R_6EvGV0zShXX3K_bnq7rmvKBMAzsmKCQ8kUyOdkRSmVJdVAj8irnPt5q6mSL8kRqyQXQPmKbC7j4Ow0YCpuMXkMYy5iV4w7V5xeXxZbF1zhQ3EW2-1PHz7novXZYb4_tDs_tMmF1-RFh0N2b5b1mPz49vV6c1ZeXH0_35xelFbUMJYouwq1Q-hkxxVvQFuwFaMNBbRSo2DQVpyBsIK3tpMNs04JoZRiWkDN-TE5OdS9mZq9a60LY8LB3CS_x_TbRPTm_5vgd2Ybbw1UVItKzwU-LQVS_DW5PJq9z9YNAwYXp2yYhFpJXc_wwxPYxymF-XMGQGvJKKtmtD4gm2LOyXUPkzBq7sIxuTdzOGYJZ37w_t_5H_mSxgw-LgCzxaFLGKzPj07UUnF91_ndwQUcp-QewN9GfwD3oaDW</recordid><startdate>20040126</startdate><enddate>20040126</enddate><creator>LIBERZON, E</creator><creator>AVIGAD, S</creator><creator>YANIV, I</creator><creator>STARK, B</creator><creator>AVRAHAMI, G</creator><creator>GOSHEN, Y</creator><creator>ZAIZOV, R</creator><general>Nature Publishing Group</general><scope>IQODW</scope><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>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AN0</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>5PM</scope></search><sort><creationdate>20040126</creationdate><title>Molecular variants of the ATM gene in Hodgkin's disease in children</title><author>LIBERZON, E ; AVIGAD, S ; YANIV, I ; STARK, B ; AVRAHAMI, G ; GOSHEN, Y ; ZAIZOV, R</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c562t-a7f4a9ea2f7f383b29c2c410b02ac79a512d43125c53dcf7b1ce8558881952633</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Adolescent</topic><topic>Ataxia</topic><topic>Ataxia Telangiectasia</topic><topic>Ataxia Telangiectasia Mutated Proteins</topic><topic>Biological and medical sciences</topic><topic>Breast cancer</topic><topic>Cancer research</topic><topic>Cell Cycle Proteins</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Cohort Studies</topic><topic>DNA Mutational Analysis</topic><topic>DNA-Binding Proteins</topic><topic>Female</topic><topic>Genes, Tumor Suppressor</topic><topic>Genetic Predisposition to Disease</topic><topic>Genetics and Genomics</topic><topic>Genotype</topic><topic>Hematologic and hematopoietic diseases</topic><topic>Hematology</topic><topic>Hodgkin Disease - genetics</topic><topic>Hodgkin Disease - physiopathology</topic><topic>Humans</topic><topic>Kinases</topic><topic>Leucine Zippers</topic><topic>Leukemia</topic><topic>Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis</topic><topic>Loss of Heterozygosity</topic><topic>Lymphoma</topic><topic>Male</topic><topic>Medical research</topic><topic>Medical sciences</topic><topic>Mutation</topic><topic>Mutation, Missense</topic><topic>Oncology</topic><topic>Pediatrics</topic><topic>Phosphatidylinositol 3-Kinases</topic><topic>Polymorphism, Genetic</topic><topic>Protein Serine-Threonine Kinases - genetics</topic><topic>Tumor Suppressor Proteins</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>LIBERZON, E</creatorcontrib><creatorcontrib>AVIGAD, S</creatorcontrib><creatorcontrib>YANIV, I</creatorcontrib><creatorcontrib>STARK, B</creatorcontrib><creatorcontrib>AVRAHAMI, G</creatorcontrib><creatorcontrib>GOSHEN, Y</creatorcontrib><creatorcontrib>ZAIZOV, R</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>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>British Nursing Database</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection (ProQuest)</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>British journal of cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>LIBERZON, E</au><au>AVIGAD, S</au><au>YANIV, I</au><au>STARK, B</au><au>AVRAHAMI, G</au><au>GOSHEN, Y</au><au>ZAIZOV, R</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Molecular variants of the ATM gene in Hodgkin's disease in children</atitle><jtitle>British journal of cancer</jtitle><addtitle>Br J Cancer</addtitle><date>2004-01-26</date><risdate>2004</risdate><volume>90</volume><issue>2</issue><spage>522</spage><epage>525</epage><pages>522-525</pages><issn>0007-0920</issn><eissn>1532-1827</eissn><coden>BJCAAI</coden><abstract>Ataxia telangiectasia is an autosomal recessive disease with a striking predisposition of lymphoid malignancies. ATM mutations have been reported in adult sporadic lymphoma and leukaemia. The aim of this study was to investigate the possible involvement of the ATM gene in the carcinogenesis of Hodgkin disease in children. Tumours were obtained from 23 patients and were subjected to mutation screening and loss of heterozygosity analysis. Eight base substitutions were identified in seven patients. Of them, Y54Y, a silent change, was observed in two patients and a known polymorphism, D1853N, in three patients. Of the other two patients, one harboured a combined genotype P604S/F1463C, identified previously in two patients with Hodgkin lymphoma, and the other a novel missense mutation, V595A. The alterations were present in the germ line, and both had a more aggressive disease. In all, 100 matched normal ethnic controls were screened for these mutations and P604S/F1463C was identified in one healthy control. Loss of heterozygosity was identified in four patients and in three of them it was located centromeric to the ATM gene, and, in one, it spanned a large region, indicating the involvement of other tumour-suppressor genes in this disease. Missense variants of the ATM gene are a rare event in childhood Hodgkin disease.</abstract><cop>Basingstoke</cop><pub>Nature Publishing Group</pub><pmid>14735203</pmid><doi>10.1038/sj.bjc.6601522</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adolescent Ataxia Ataxia Telangiectasia Ataxia Telangiectasia Mutated Proteins Biological and medical sciences Breast cancer Cancer research Cell Cycle Proteins Child Child, Preschool Cohort Studies DNA Mutational Analysis DNA-Binding Proteins Female Genes, Tumor Suppressor Genetic Predisposition to Disease Genetics and Genomics Genotype Hematologic and hematopoietic diseases Hematology Hodgkin Disease - genetics Hodgkin Disease - physiopathology Humans Kinases Leucine Zippers Leukemia Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis Loss of Heterozygosity Lymphoma Male Medical research Medical sciences Mutation Mutation, Missense Oncology Pediatrics Phosphatidylinositol 3-Kinases Polymorphism, Genetic Protein Serine-Threonine Kinases - genetics Tumor Suppressor Proteins Tumors |
title | Molecular variants of the ATM gene in Hodgkin's disease in children |
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