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
Hauptverfasser: Sastre-Garau, Xavier, Peter, Martine, Avril, Marie-Françoise, Laude, Hélène, Couturier, Jérôme, Rozenberg, Flore, Almeida, Anna, Boitier, Françoise, Carlotti, Agnès, Couturaud, Benoıt, Dupin, Nicolas
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container_title The Journal of pathology
container_volume 218
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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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. 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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. 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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. 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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. 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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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