Merkel cell carcinoma of the skin: pathological and molecular evidence for a causative role of MCV in oncogenesis
Merkel cell carcinoma (MCC), a skin tumour with neuroendocrine features, was recently found to be associated with a new type of human polyomavirus, called Merkel cell virus (MCV). We investigated the specificity of this association as well as a causal role of MCV in oncogenesis. DNA and RNA from ten...
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Veröffentlicht in: | The Journal of pathology 2009-05, Vol.218 (1), p.48-56 |
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creator | Sastre-Garau, Xavier Peter, Martine Avril, Marie-Françoise Laude, Hélène Couturier, Jérôme Rozenberg, Flore Almeida, Anna Boitier, Françoise Carlotti, Agnès Couturaud, Benoıt Dupin, Nicolas |
description | Merkel cell carcinoma (MCC), a skin tumour with neuroendocrine features, was recently found to be associated with a new type of human polyomavirus, called Merkel cell virus (MCV). We investigated the specificity of this association as well as a causal role of MCV in oncogenesis. DNA and RNA from ten cases of MCC were analysed using PCR and RT-PCR. DNA from 1241 specimens of a wide range of human tumours was also analysed. The DIPS technique was used to identify the integration locus of viral DNA sequences. Array CGH was performed to analyse structural alterations of the cell genome. MCV DNA sequences were found in all ten cases of MCC and in none of the 1241 specimens of other tumour types. Clonal integration of MCV into the host genome was seen in all MCC cases and was checked by FISH in one case. A recurrent pattern of conserved viral sequences which encompassed the replication origin, the small tumour (ST), and the 5' part of the large tumour (LT) antigen DNA sequences was observed. Both ST and LT viral sequences were found to be significantly expressed in all MCCs. Neither recurrent site of integration nor alteration of cellular genes located near the viral sequences was observed. The tight association of MCV with MCC, the clonal pattern of MCV integration, and the expression of the viral oncoproteins strongly support a causative role for MCV in the tumour process. This information will help the development of novel approaches for the assessment and therapy of MCC and biologically related tumours. Copyright © 2009 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd. |
doi_str_mv | 10.1002/path.2532 |
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We investigated the specificity of this association as well as a causal role of MCV in oncogenesis. DNA and RNA from ten cases of MCC were analysed using PCR and RT-PCR. DNA from 1241 specimens of a wide range of human tumours was also analysed. The DIPS technique was used to identify the integration locus of viral DNA sequences. Array CGH was performed to analyse structural alterations of the cell genome. MCV DNA sequences were found in all ten cases of MCC and in none of the 1241 specimens of other tumour types. Clonal integration of MCV into the host genome was seen in all MCC cases and was checked by FISH in one case. A recurrent pattern of conserved viral sequences which encompassed the replication origin, the small tumour (ST), and the 5' part of the large tumour (LT) antigen DNA sequences was observed. Both ST and LT viral sequences were found to be significantly expressed in all MCCs. Neither recurrent site of integration nor alteration of cellular genes located near the viral sequences was observed. The tight association of MCV with MCC, the clonal pattern of MCV integration, and the expression of the viral oncoproteins strongly support a causative role for MCV in the tumour process. This information will help the development of novel approaches for the assessment and therapy of MCC and biologically related tumours. Copyright © 2009 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.2532</identifier><identifier>PMID: 19291712</identifier><identifier>CODEN: JPTLAS</identifier><language>eng</language><publisher>Chichester, UK: John Wiley & Sons, Ltd</publisher><subject>Aged ; Aged, 80 and over ; Biological and medical sciences ; Carcinoma, Merkel Cell - pathology ; Carcinoma, Merkel Cell - virology ; Comparative Genomic Hybridization ; Dermatology ; DNA, Viral - analysis ; Female ; Gene Expression Regulation, Neoplastic ; human polyomavirus ; Humans ; In Situ Hybridization, Fluorescence ; Investigative techniques, diagnostic techniques (general aspects) ; Male ; Medical sciences ; Merkel cell carcinoma ; Merkel cell virus ; Merkel Cells - pathology ; Merkel Cells - virology ; Middle Aged ; Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques ; Polyomavirus ; Polyomavirus - pathogenicity ; Polyomavirus Infections - complications ; RNA, Viral - analysis ; Skin Neoplasms - pathology ; Skin Neoplasms - virology ; small T oncogene ; Tumors of the skin and soft tissue. Premalignant lesions ; viral integration ; viral oncogenesis ; Virus Integration ; Virus Replication</subject><ispartof>The Journal of pathology, 2009-05, Vol.218 (1), p.48-56</ispartof><rights>Copyright © 2009 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.</rights><rights>2009 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5122-d42af370d3c394a50cc1751768d6d02b7402ffd009e4b54f93a8234f80b1ee863</citedby><cites>FETCH-LOGICAL-c5122-d42af370d3c394a50cc1751768d6d02b7402ffd009e4b54f93a8234f80b1ee863</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.2532$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fpath.2532$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=21304596$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19291712$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sastre-Garau, Xavier</creatorcontrib><creatorcontrib>Peter, Martine</creatorcontrib><creatorcontrib>Avril, Marie-Françoise</creatorcontrib><creatorcontrib>Laude, Hélène</creatorcontrib><creatorcontrib>Couturier, Jérôme</creatorcontrib><creatorcontrib>Rozenberg, Flore</creatorcontrib><creatorcontrib>Almeida, Anna</creatorcontrib><creatorcontrib>Boitier, Françoise</creatorcontrib><creatorcontrib>Carlotti, Agnès</creatorcontrib><creatorcontrib>Couturaud, Benoıt</creatorcontrib><creatorcontrib>Dupin, Nicolas</creatorcontrib><title>Merkel cell carcinoma of the skin: pathological and molecular evidence for a causative role of MCV in oncogenesis</title><title>The Journal of pathology</title><addtitle>J. Pathol</addtitle><description>Merkel cell carcinoma (MCC), a skin tumour with neuroendocrine features, was recently found to be associated with a new type of human polyomavirus, called Merkel cell virus (MCV). We investigated the specificity of this association as well as a causal role of MCV in oncogenesis. DNA and RNA from ten cases of MCC were analysed using PCR and RT-PCR. DNA from 1241 specimens of a wide range of human tumours was also analysed. The DIPS technique was used to identify the integration locus of viral DNA sequences. Array CGH was performed to analyse structural alterations of the cell genome. MCV DNA sequences were found in all ten cases of MCC and in none of the 1241 specimens of other tumour types. Clonal integration of MCV into the host genome was seen in all MCC cases and was checked by FISH in one case. A recurrent pattern of conserved viral sequences which encompassed the replication origin, the small tumour (ST), and the 5' part of the large tumour (LT) antigen DNA sequences was observed. Both ST and LT viral sequences were found to be significantly expressed in all MCCs. Neither recurrent site of integration nor alteration of cellular genes located near the viral sequences was observed. The tight association of MCV with MCC, the clonal pattern of MCV integration, and the expression of the viral oncoproteins strongly support a causative role for MCV in the tumour process. This information will help the development of novel approaches for the assessment and therapy of MCC and biologically related tumours. Copyright © 2009 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.</description><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Biological and medical sciences</subject><subject>Carcinoma, Merkel Cell - pathology</subject><subject>Carcinoma, Merkel Cell - virology</subject><subject>Comparative Genomic Hybridization</subject><subject>Dermatology</subject><subject>DNA, Viral - analysis</subject><subject>Female</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>human polyomavirus</subject><subject>Humans</subject><subject>In Situ Hybridization, Fluorescence</subject><subject>Investigative techniques, diagnostic techniques (general aspects)</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Merkel cell carcinoma</subject><subject>Merkel cell virus</subject><subject>Merkel Cells - pathology</subject><subject>Merkel Cells - virology</subject><subject>Middle Aged</subject><subject>Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques</subject><subject>Polyomavirus</subject><subject>Polyomavirus - pathogenicity</subject><subject>Polyomavirus Infections - complications</subject><subject>RNA, Viral - analysis</subject><subject>Skin Neoplasms - pathology</subject><subject>Skin Neoplasms - virology</subject><subject>small T oncogene</subject><subject>Tumors of the skin and soft tissue. Premalignant lesions</subject><subject>viral integration</subject><subject>viral oncogenesis</subject><subject>Virus Integration</subject><subject>Virus Replication</subject><issn>0022-3417</issn><issn>1096-9896</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU9P3DAQxa2qVVmgh36B1pci9RDwnziJe0NLgUpQKgGlN8vrjBd3k3ixE1q-fR0loqeqF8_Bv3nz3gxCbyk5pISwo63u7w-Z4OwFWlAii0xWsniJFumPZTyn5Q7ajfEnIURKIV6jHSqZpCVlC_RwCWEDDTbQpEcH4zrfauwt7u8Bx43rPuFR3jd-7YxusO5q3PoGzNDogOHR1dAZwNYHrJPAEHXvHgGHhIwql8vv2HXYd8avoYPo4j56ZXUT4c1c99Dt6eeb5Xl2cXX2ZXl8kRlBk-06Z9ryktTccJlrQYyhpaBlUdVFTdiqzAmztk6RIF-J3EquK8ZzW5EVBagKvocOJt1t8A8DxF61Lo4xdQd-iKpI-Ykk_wcZEUUpeJ7AjxNogo8xgFXb4FodnhQlajyEGjelxkMk9t0sOqxaqP-S8-YT8GEGdEx7tUF3xsVnjlFOciFHd0cT98s18PTvierb8c35PDqbOlzs4fdzhw6blJmXQt19PVPi5OT0enlXqR-Jfz_xVnul1yG5uL1mJBmgRSqC8T__p7dh</recordid><startdate>200905</startdate><enddate>200905</enddate><creator>Sastre-Garau, Xavier</creator><creator>Peter, Martine</creator><creator>Avril, Marie-Françoise</creator><creator>Laude, Hélène</creator><creator>Couturier, Jérôme</creator><creator>Rozenberg, Flore</creator><creator>Almeida, Anna</creator><creator>Boitier, Françoise</creator><creator>Carlotti, Agnès</creator><creator>Couturaud, Benoıt</creator><creator>Dupin, Nicolas</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>7TO</scope><scope>7U9</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>200905</creationdate><title>Merkel cell carcinoma of the skin: pathological and molecular evidence for a causative role of MCV in oncogenesis</title><author>Sastre-Garau, Xavier ; Peter, Martine ; Avril, Marie-Françoise ; Laude, Hélène ; Couturier, Jérôme ; Rozenberg, Flore ; Almeida, Anna ; Boitier, Françoise ; Carlotti, Agnès ; Couturaud, Benoıt ; Dupin, Nicolas</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5122-d42af370d3c394a50cc1751768d6d02b7402ffd009e4b54f93a8234f80b1ee863</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Biological and medical sciences</topic><topic>Carcinoma, Merkel Cell - pathology</topic><topic>Carcinoma, Merkel Cell - virology</topic><topic>Comparative Genomic Hybridization</topic><topic>Dermatology</topic><topic>DNA, Viral - analysis</topic><topic>Female</topic><topic>Gene Expression Regulation, Neoplastic</topic><topic>human polyomavirus</topic><topic>Humans</topic><topic>In Situ Hybridization, Fluorescence</topic><topic>Investigative techniques, diagnostic techniques (general aspects)</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Merkel cell carcinoma</topic><topic>Merkel cell virus</topic><topic>Merkel Cells - pathology</topic><topic>Merkel Cells - virology</topic><topic>Middle Aged</topic><topic>Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques</topic><topic>Polyomavirus</topic><topic>Polyomavirus - pathogenicity</topic><topic>Polyomavirus Infections - complications</topic><topic>RNA, Viral - analysis</topic><topic>Skin Neoplasms - pathology</topic><topic>Skin Neoplasms - virology</topic><topic>small T oncogene</topic><topic>Tumors of the skin and soft tissue. Premalignant lesions</topic><topic>viral integration</topic><topic>viral oncogenesis</topic><topic>Virus Integration</topic><topic>Virus Replication</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sastre-Garau, Xavier</creatorcontrib><creatorcontrib>Peter, Martine</creatorcontrib><creatorcontrib>Avril, Marie-Françoise</creatorcontrib><creatorcontrib>Laude, Hélène</creatorcontrib><creatorcontrib>Couturier, Jérôme</creatorcontrib><creatorcontrib>Rozenberg, Flore</creatorcontrib><creatorcontrib>Almeida, Anna</creatorcontrib><creatorcontrib>Boitier, Françoise</creatorcontrib><creatorcontrib>Carlotti, Agnès</creatorcontrib><creatorcontrib>Couturaud, Benoıt</creatorcontrib><creatorcontrib>Dupin, Nicolas</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>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>The Journal of pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sastre-Garau, Xavier</au><au>Peter, Martine</au><au>Avril, Marie-Françoise</au><au>Laude, Hélène</au><au>Couturier, Jérôme</au><au>Rozenberg, Flore</au><au>Almeida, Anna</au><au>Boitier, Françoise</au><au>Carlotti, Agnès</au><au>Couturaud, Benoıt</au><au>Dupin, Nicolas</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Merkel cell carcinoma of the skin: pathological and molecular evidence for a causative role of MCV in oncogenesis</atitle><jtitle>The Journal of pathology</jtitle><addtitle>J. Pathol</addtitle><date>2009-05</date><risdate>2009</risdate><volume>218</volume><issue>1</issue><spage>48</spage><epage>56</epage><pages>48-56</pages><issn>0022-3417</issn><eissn>1096-9896</eissn><coden>JPTLAS</coden><abstract>Merkel cell carcinoma (MCC), a skin tumour with neuroendocrine features, was recently found to be associated with a new type of human polyomavirus, called Merkel cell virus (MCV). We investigated the specificity of this association as well as a causal role of MCV in oncogenesis. DNA and RNA from ten cases of MCC were analysed using PCR and RT-PCR. DNA from 1241 specimens of a wide range of human tumours was also analysed. The DIPS technique was used to identify the integration locus of viral DNA sequences. Array CGH was performed to analyse structural alterations of the cell genome. MCV DNA sequences were found in all ten cases of MCC and in none of the 1241 specimens of other tumour types. Clonal integration of MCV into the host genome was seen in all MCC cases and was checked by FISH in one case. A recurrent pattern of conserved viral sequences which encompassed the replication origin, the small tumour (ST), and the 5' part of the large tumour (LT) antigen DNA sequences was observed. Both ST and LT viral sequences were found to be significantly expressed in all MCCs. Neither recurrent site of integration nor alteration of cellular genes located near the viral sequences was observed. The tight association of MCV with MCC, the clonal pattern of MCV integration, and the expression of the viral oncoproteins strongly support a causative role for MCV in the tumour process. This information will help the development of novel approaches for the assessment and therapy of MCC and biologically related tumours. Copyright © 2009 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>19291712</pmid><doi>10.1002/path.2532</doi><tpages>9</tpages></addata></record> |
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subjects | Aged Aged, 80 and over Biological and medical sciences Carcinoma, Merkel Cell - pathology Carcinoma, Merkel Cell - virology Comparative Genomic Hybridization Dermatology DNA, Viral - analysis Female Gene Expression Regulation, Neoplastic human polyomavirus Humans In Situ Hybridization, Fluorescence Investigative techniques, diagnostic techniques (general aspects) Male Medical sciences Merkel cell carcinoma Merkel cell virus Merkel Cells - pathology Merkel Cells - virology Middle Aged Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques Polyomavirus Polyomavirus - pathogenicity Polyomavirus Infections - complications RNA, Viral - analysis Skin Neoplasms - pathology Skin Neoplasms - virology small T oncogene Tumors of the skin and soft tissue. Premalignant lesions viral integration viral oncogenesis Virus Integration Virus Replication |
title | Merkel cell carcinoma of the skin: pathological and molecular evidence for a causative role of MCV in oncogenesis |
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