c-KIT is frequently mutated in bilateral germ cell tumours and down-regulated during progression from intratubular germ cell neoplasia to seminoma
Testicular germ cell tumours (TGCTs) are the most frequent cancer type in young men; 5% of these patients develop a second TGCT in the contralateral testis. The pathogenesis of TGCT is closely linked to primordial germ cells (PGCs) or gonocytes. The receptor tyrosine kinase (c-KIT) is necessary for...
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description | Testicular germ cell tumours (TGCTs) are the most frequent cancer type in young men; 5% of these patients develop a second TGCT in the contralateral testis. The pathogenesis of TGCT is closely linked to primordial germ cells (PGCs) or gonocytes. The receptor tyrosine kinase (c-KIT) is necessary for migration and survival of PGCs and is expressed in intratubular neoplastic germ cells (IGCNUs) and seminomas. We studied the frequency of c-KIT exon 11 and 17 mutations in 155 unilateral (108 seminomas and 47 non-seminomas) and 22 bilateral (18 seminomas, two embryonal carcinomas, two IGCNU) cases. While no mutations were detected in exon 11, the mutation frequency in exon 17 was significantly higher in bilateral (14/22, 63.6%) compared to unilateral TGCT (10/155, 6.4%) (p < 0.001). Different activating mutations (Y823D, D816V, D816H and N822K) were detected in bilateral TGCT. Y823D mutation was identical in both testes in three cases and quantitative pyrosequencing showed that up to 76% of the cells analysed in tumour samples carried this mutation. One bilateral synchronous seminoma revealed a S821F mutation in one testis and a Y823D mutation contralaterally. To study the role of c-KIT in TGCT progression, we compared its expression in 41 seminomas and adjacent IGCNUs. Immunohistochemical analysis revealed that c-KIT expression was significantly reduced in seminomas compared to IGCNUs (p < 0.006) and that there were no significant changes in c-KIT mRNA copy numbers in progressed compared to low-stage seminomas. In summary, our study shows that patients with c-KIT mutations are more prone to develop a bilateral TGCT and suggests that in a portion of bilateral TGCTs, c-KIT mutations occur early during embryonal development, prior to the arrival of PGCs at the genital ridge. Furthermore, our findings show that c-KIT down-regulation occurs during the progression of IGCNU to seminoma. Copyright © 2007 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd. |
doi_str_mv | 10.1002/path.2225 |
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The pathogenesis of TGCT is closely linked to primordial germ cells (PGCs) or gonocytes. The receptor tyrosine kinase (c-KIT) is necessary for migration and survival of PGCs and is expressed in intratubular neoplastic germ cells (IGCNUs) and seminomas. We studied the frequency of c-KIT exon 11 and 17 mutations in 155 unilateral (108 seminomas and 47 non-seminomas) and 22 bilateral (18 seminomas, two embryonal carcinomas, two IGCNU) cases. While no mutations were detected in exon 11, the mutation frequency in exon 17 was significantly higher in bilateral (14/22, 63.6%) compared to unilateral TGCT (10/155, 6.4%) (p < 0.001). Different activating mutations (Y823D, D816V, D816H and N822K) were detected in bilateral TGCT. Y823D mutation was identical in both testes in three cases and quantitative pyrosequencing showed that up to 76% of the cells analysed in tumour samples carried this mutation. One bilateral synchronous seminoma revealed a S821F mutation in one testis and a Y823D mutation contralaterally. To study the role of c-KIT in TGCT progression, we compared its expression in 41 seminomas and adjacent IGCNUs. Immunohistochemical analysis revealed that c-KIT expression was significantly reduced in seminomas compared to IGCNUs (p < 0.006) and that there were no significant changes in c-KIT mRNA copy numbers in progressed compared to low-stage seminomas. In summary, our study shows that patients with c-KIT mutations are more prone to develop a bilateral TGCT and suggests that in a portion of bilateral TGCTs, c-KIT mutations occur early during embryonal development, prior to the arrival of PGCs at the genital ridge. Furthermore, our findings show that c-KIT down-regulation occurs during the progression of IGCNU to seminoma. Copyright © 2007 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.</description><identifier>ISSN: 0022-3417</identifier><identifier>EISSN: 1096-9896</identifier><identifier>DOI: 10.1002/path.2225</identifier><identifier>PMID: 17768701</identifier><identifier>CODEN: JPTLAS</identifier><language>eng</language><publisher>Chichester, UK: John Wiley & Sons, Ltd</publisher><subject>Adult ; Biological and medical sciences ; c-KIT ; Chi-Square Distribution ; Disease Progression ; DNA Mutational Analysis ; Gene Expression Regulation, Neoplastic ; germ ; Humans ; IGCNU ; Immunohistochemistry ; Investigative techniques, diagnostic techniques (general aspects) ; Male ; Medical sciences ; Middle Aged ; Mutation ; Neoplasms, Germ Cell and Embryonal - metabolism ; Neoplasms, Germ Cell and Embryonal - pathology ; Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques ; Proto-Oncogene Proteins c-kit - analysis ; Proto-Oncogene Proteins c-kit - genetics ; Proto-Oncogene Proteins c-kit - metabolism ; Reverse Transcriptase Polymerase Chain Reaction ; seminoma ; Seminoma - metabolism ; Seminoma - pathology ; Statistics, Nonparametric ; testicular ; Testicular Neoplasms - metabolism ; Testicular Neoplasms - pathology</subject><ispartof>The Journal of pathology, 2007-11, Vol.213 (3), p.311-318</ispartof><rights>Copyright © 2007 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.</rights><rights>2007 INIST-CNRS</rights><rights>Copyright 2007 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4155-edb8280fba22864116244d7c65e998be31707bf57de898325ef80c75fe8ce4453</citedby><cites>FETCH-LOGICAL-c4155-edb8280fba22864116244d7c65e998be31707bf57de898325ef80c75fe8ce4453</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fpath.2225$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fpath.2225$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=19189434$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17768701$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Biermann, K</creatorcontrib><creatorcontrib>Göke, F</creatorcontrib><creatorcontrib>Nettersheim, D</creatorcontrib><creatorcontrib>Eckert, D</creatorcontrib><creatorcontrib>Zhou, H</creatorcontrib><creatorcontrib>Kahl, P</creatorcontrib><creatorcontrib>Gashaw, I</creatorcontrib><creatorcontrib>Schorle, H</creatorcontrib><creatorcontrib>Büttner, R</creatorcontrib><title>c-KIT is frequently mutated in bilateral germ cell tumours and down-regulated during progression from intratubular germ cell neoplasia to seminoma</title><title>The Journal of pathology</title><addtitle>J. Pathol</addtitle><description>Testicular germ cell tumours (TGCTs) are the most frequent cancer type in young men; 5% of these patients develop a second TGCT in the contralateral testis. The pathogenesis of TGCT is closely linked to primordial germ cells (PGCs) or gonocytes. The receptor tyrosine kinase (c-KIT) is necessary for migration and survival of PGCs and is expressed in intratubular neoplastic germ cells (IGCNUs) and seminomas. We studied the frequency of c-KIT exon 11 and 17 mutations in 155 unilateral (108 seminomas and 47 non-seminomas) and 22 bilateral (18 seminomas, two embryonal carcinomas, two IGCNU) cases. While no mutations were detected in exon 11, the mutation frequency in exon 17 was significantly higher in bilateral (14/22, 63.6%) compared to unilateral TGCT (10/155, 6.4%) (p < 0.001). Different activating mutations (Y823D, D816V, D816H and N822K) were detected in bilateral TGCT. Y823D mutation was identical in both testes in three cases and quantitative pyrosequencing showed that up to 76% of the cells analysed in tumour samples carried this mutation. One bilateral synchronous seminoma revealed a S821F mutation in one testis and a Y823D mutation contralaterally. To study the role of c-KIT in TGCT progression, we compared its expression in 41 seminomas and adjacent IGCNUs. Immunohistochemical analysis revealed that c-KIT expression was significantly reduced in seminomas compared to IGCNUs (p < 0.006) and that there were no significant changes in c-KIT mRNA copy numbers in progressed compared to low-stage seminomas. In summary, our study shows that patients with c-KIT mutations are more prone to develop a bilateral TGCT and suggests that in a portion of bilateral TGCTs, c-KIT mutations occur early during embryonal development, prior to the arrival of PGCs at the genital ridge. Furthermore, our findings show that c-KIT down-regulation occurs during the progression of IGCNU to seminoma. Copyright © 2007 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.</description><subject>Adult</subject><subject>Biological and medical sciences</subject><subject>c-KIT</subject><subject>Chi-Square Distribution</subject><subject>Disease Progression</subject><subject>DNA Mutational Analysis</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>germ</subject><subject>Humans</subject><subject>IGCNU</subject><subject>Immunohistochemistry</subject><subject>Investigative techniques, diagnostic techniques (general aspects)</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Mutation</subject><subject>Neoplasms, Germ Cell and Embryonal - metabolism</subject><subject>Neoplasms, Germ Cell and Embryonal - pathology</subject><subject>Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques</subject><subject>Proto-Oncogene Proteins c-kit - analysis</subject><subject>Proto-Oncogene Proteins c-kit - genetics</subject><subject>Proto-Oncogene Proteins c-kit - metabolism</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>seminoma</subject><subject>Seminoma - metabolism</subject><subject>Seminoma - pathology</subject><subject>Statistics, Nonparametric</subject><subject>testicular</subject><subject>Testicular Neoplasms - metabolism</subject><subject>Testicular Neoplasms - pathology</subject><issn>0022-3417</issn><issn>1096-9896</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kUtv1DAUhS0EokNhwR8Ab6jEIq2fsb2sSumDCpCYiqXlJDeDIY-p7ajM3-AX4yERZcPKlvydc8_1QeglJceUEHaydenbMWNMPkIrSkxZGG3Kx2iV31jBBVUH6FmM3wkhxkj5FB1QpUqtCF2hX3Xx4WqNfcRtgLsJhtTtcD8ll6DBfsCV7_I1uA5vIPS4hq7DaerHKUTshgY34_1QBNhM3R9FMwU_bPA2jJsAMfpxyL5jn51ScGmqMhb-cRpg3HYueofTiCP0fhh79xw9aV0X4cVyHqLb9-frs8vi5tPF1dnpTVELKmUBTaWZJm3lGNOloLRkQjSqLiUYoyvgVBFVtVI1oI3mTEKrSa1kC7oGISQ_REezb06bN4_J9j7uY7kca4q21IIKrlgG385gHcYYA7R2G3zvws5SYvcF2H0Bdl9AZl8tplPVQ_NALj-egTcL4GLtuja4ofbxgTNUG8FF5k5m7t53sPv_RPv5dH25jC5mhY8Jfv5VuPDDloorab9-vLDacHpN5LV9l_nXM9-60bpNyCluv7AckRDNKOGc_waTj7fM</recordid><startdate>200711</startdate><enddate>200711</enddate><creator>Biermann, K</creator><creator>Göke, F</creator><creator>Nettersheim, D</creator><creator>Eckert, D</creator><creator>Zhou, H</creator><creator>Kahl, P</creator><creator>Gashaw, I</creator><creator>Schorle, H</creator><creator>Büttner, R</creator><general>John Wiley & Sons, Ltd</general><general>Wiley</general><scope>FBQ</scope><scope>BSCLL</scope><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>7X8</scope></search><sort><creationdate>200711</creationdate><title>c-KIT is frequently mutated in bilateral germ cell tumours and down-regulated during progression from intratubular germ cell neoplasia to seminoma</title><author>Biermann, K ; Göke, F ; Nettersheim, D ; Eckert, D ; Zhou, H ; Kahl, P ; Gashaw, I ; Schorle, H ; Büttner, R</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4155-edb8280fba22864116244d7c65e998be31707bf57de898325ef80c75fe8ce4453</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Adult</topic><topic>Biological and medical sciences</topic><topic>c-KIT</topic><topic>Chi-Square Distribution</topic><topic>Disease Progression</topic><topic>DNA Mutational Analysis</topic><topic>Gene Expression Regulation, Neoplastic</topic><topic>germ</topic><topic>Humans</topic><topic>IGCNU</topic><topic>Immunohistochemistry</topic><topic>Investigative techniques, diagnostic techniques (general aspects)</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Mutation</topic><topic>Neoplasms, Germ Cell and Embryonal - metabolism</topic><topic>Neoplasms, Germ Cell and Embryonal - pathology</topic><topic>Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques</topic><topic>Proto-Oncogene Proteins c-kit - analysis</topic><topic>Proto-Oncogene Proteins c-kit - genetics</topic><topic>Proto-Oncogene Proteins c-kit - metabolism</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><topic>seminoma</topic><topic>Seminoma - metabolism</topic><topic>Seminoma - pathology</topic><topic>Statistics, Nonparametric</topic><topic>testicular</topic><topic>Testicular Neoplasms - metabolism</topic><topic>Testicular Neoplasms - pathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Biermann, K</creatorcontrib><creatorcontrib>Göke, F</creatorcontrib><creatorcontrib>Nettersheim, D</creatorcontrib><creatorcontrib>Eckert, D</creatorcontrib><creatorcontrib>Zhou, H</creatorcontrib><creatorcontrib>Kahl, P</creatorcontrib><creatorcontrib>Gashaw, I</creatorcontrib><creatorcontrib>Schorle, H</creatorcontrib><creatorcontrib>Büttner, R</creatorcontrib><collection>AGRIS</collection><collection>Istex</collection><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>MEDLINE - Academic</collection><jtitle>The Journal of pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Biermann, K</au><au>Göke, F</au><au>Nettersheim, D</au><au>Eckert, D</au><au>Zhou, H</au><au>Kahl, P</au><au>Gashaw, I</au><au>Schorle, H</au><au>Büttner, R</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>c-KIT is frequently mutated in bilateral germ cell tumours and down-regulated during progression from intratubular germ cell neoplasia to seminoma</atitle><jtitle>The Journal of pathology</jtitle><addtitle>J. Pathol</addtitle><date>2007-11</date><risdate>2007</risdate><volume>213</volume><issue>3</issue><spage>311</spage><epage>318</epage><pages>311-318</pages><issn>0022-3417</issn><eissn>1096-9896</eissn><coden>JPTLAS</coden><abstract>Testicular germ cell tumours (TGCTs) are the most frequent cancer type in young men; 5% of these patients develop a second TGCT in the contralateral testis. The pathogenesis of TGCT is closely linked to primordial germ cells (PGCs) or gonocytes. The receptor tyrosine kinase (c-KIT) is necessary for migration and survival of PGCs and is expressed in intratubular neoplastic germ cells (IGCNUs) and seminomas. We studied the frequency of c-KIT exon 11 and 17 mutations in 155 unilateral (108 seminomas and 47 non-seminomas) and 22 bilateral (18 seminomas, two embryonal carcinomas, two IGCNU) cases. While no mutations were detected in exon 11, the mutation frequency in exon 17 was significantly higher in bilateral (14/22, 63.6%) compared to unilateral TGCT (10/155, 6.4%) (p < 0.001). Different activating mutations (Y823D, D816V, D816H and N822K) were detected in bilateral TGCT. Y823D mutation was identical in both testes in three cases and quantitative pyrosequencing showed that up to 76% of the cells analysed in tumour samples carried this mutation. One bilateral synchronous seminoma revealed a S821F mutation in one testis and a Y823D mutation contralaterally. To study the role of c-KIT in TGCT progression, we compared its expression in 41 seminomas and adjacent IGCNUs. Immunohistochemical analysis revealed that c-KIT expression was significantly reduced in seminomas compared to IGCNUs (p < 0.006) and that there were no significant changes in c-KIT mRNA copy numbers in progressed compared to low-stage seminomas. In summary, our study shows that patients with c-KIT mutations are more prone to develop a bilateral TGCT and suggests that in a portion of bilateral TGCTs, c-KIT mutations occur early during embryonal development, prior to the arrival of PGCs at the genital ridge. Furthermore, our findings show that c-KIT down-regulation occurs during the progression of IGCNU to seminoma. Copyright © 2007 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.</abstract><cop>Chichester, UK</cop><pub>John Wiley & Sons, Ltd</pub><pmid>17768701</pmid><doi>10.1002/path.2225</doi><tpages>8</tpages></addata></record> |
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subjects | Adult Biological and medical sciences c-KIT Chi-Square Distribution Disease Progression DNA Mutational Analysis Gene Expression Regulation, Neoplastic germ Humans IGCNU Immunohistochemistry Investigative techniques, diagnostic techniques (general aspects) Male Medical sciences Middle Aged Mutation Neoplasms, Germ Cell and Embryonal - metabolism Neoplasms, Germ Cell and Embryonal - pathology Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques Proto-Oncogene Proteins c-kit - analysis Proto-Oncogene Proteins c-kit - genetics Proto-Oncogene Proteins c-kit - metabolism Reverse Transcriptase Polymerase Chain Reaction seminoma Seminoma - metabolism Seminoma - pathology Statistics, Nonparametric testicular Testicular Neoplasms - metabolism Testicular Neoplasms - pathology |
title | c-KIT is frequently mutated in bilateral germ cell tumours and down-regulated during progression from intratubular germ cell neoplasia to seminoma |
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