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Ultrastructural Proof of Polyomavirus in Merkel Cell Carcinoma Tumour Cells and Its Absence in Small Cell Carcinoma of the Lung

BACKGROUND: A new virus called the Merkel Cell Polyomavirus (MCPyV) has recently been found in Merkel Cell Carcinoma (MCC). MCC is a rare aggressive small cell neuroendocrine carcinoma primarily derived from the skin, morphologically indistinguishable from small cell lung carcinoma (SCLC). So far th...

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Autores principales: Wetzels, Charlotte T. A. H., Hoefnagel, Jolanda G. M., Bakkers, Judith M. J. E., Dijkman, Henry B. P. M., Blokx, Willeke A. M., Melchers, Willem J. G.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2654729/
https://www.ncbi.nlm.nih.gov/pubmed/19305499
http://dx.doi.org/10.1371/journal.pone.0004958
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author Wetzels, Charlotte T. A. H.
Hoefnagel, Jolanda G. M.
Bakkers, Judith M. J. E.
Dijkman, Henry B. P. M.
Blokx, Willeke A. M.
Melchers, Willem J. G.
author_facet Wetzels, Charlotte T. A. H.
Hoefnagel, Jolanda G. M.
Bakkers, Judith M. J. E.
Dijkman, Henry B. P. M.
Blokx, Willeke A. M.
Melchers, Willem J. G.
author_sort Wetzels, Charlotte T. A. H.
collection PubMed
description BACKGROUND: A new virus called the Merkel Cell Polyomavirus (MCPyV) has recently been found in Merkel Cell Carcinoma (MCC). MCC is a rare aggressive small cell neuroendocrine carcinoma primarily derived from the skin, morphologically indistinguishable from small cell lung carcinoma (SCLC). So far the actual presence of the virus in MCC tumour cells on a morphological level has not been demonstrated, and the presence of MCPyV in other small cell neuroendocrine carcinomas has not been studied yet. METHODOLOGY/PRINCIPAL FINDINGS: We investigated MCC tissue samples from five patients and SCLCs from ten patients for the presence of MCPyV-DNA by PCR and sequencing. Electron microscopy was used to search ultrastructurally for morphological presence of the virus in MCPyV-DNA positive samples. MCPyV was detected in two out of five primary MCCs. In one MCC patient MCPyV-DNA was detected in the primary tumour as well as in the metastasis, strongly suggesting integration of MCPyV in the cellular DNA of the tumour in this patient. In the primary MCC of another patient viral particles in tumour cell nuclei and cytoplasm were identified by electron microscopy, indicating active viral replication in the tumour cells. In none of the SCLCs MCPyV-DNA was detected. CONCLUSIONS/SIGNIFICANCE: Our results strongly suggest that MCPyV is an oncogenic polyomavirus in humans, and is potentially causally related to the development of MCC but not to the morphological similar SCLC.
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spelling pubmed-26547292009-03-23 Ultrastructural Proof of Polyomavirus in Merkel Cell Carcinoma Tumour Cells and Its Absence in Small Cell Carcinoma of the Lung Wetzels, Charlotte T. A. H. Hoefnagel, Jolanda G. M. Bakkers, Judith M. J. E. Dijkman, Henry B. P. M. Blokx, Willeke A. M. Melchers, Willem J. G. PLoS One Research Article BACKGROUND: A new virus called the Merkel Cell Polyomavirus (MCPyV) has recently been found in Merkel Cell Carcinoma (MCC). MCC is a rare aggressive small cell neuroendocrine carcinoma primarily derived from the skin, morphologically indistinguishable from small cell lung carcinoma (SCLC). So far the actual presence of the virus in MCC tumour cells on a morphological level has not been demonstrated, and the presence of MCPyV in other small cell neuroendocrine carcinomas has not been studied yet. METHODOLOGY/PRINCIPAL FINDINGS: We investigated MCC tissue samples from five patients and SCLCs from ten patients for the presence of MCPyV-DNA by PCR and sequencing. Electron microscopy was used to search ultrastructurally for morphological presence of the virus in MCPyV-DNA positive samples. MCPyV was detected in two out of five primary MCCs. In one MCC patient MCPyV-DNA was detected in the primary tumour as well as in the metastasis, strongly suggesting integration of MCPyV in the cellular DNA of the tumour in this patient. In the primary MCC of another patient viral particles in tumour cell nuclei and cytoplasm were identified by electron microscopy, indicating active viral replication in the tumour cells. In none of the SCLCs MCPyV-DNA was detected. CONCLUSIONS/SIGNIFICANCE: Our results strongly suggest that MCPyV is an oncogenic polyomavirus in humans, and is potentially causally related to the development of MCC but not to the morphological similar SCLC. Public Library of Science 2009-03-23 /pmc/articles/PMC2654729/ /pubmed/19305499 http://dx.doi.org/10.1371/journal.pone.0004958 Text en Wetzels et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Wetzels, Charlotte T. A. H.
Hoefnagel, Jolanda G. M.
Bakkers, Judith M. J. E.
Dijkman, Henry B. P. M.
Blokx, Willeke A. M.
Melchers, Willem J. G.
Ultrastructural Proof of Polyomavirus in Merkel Cell Carcinoma Tumour Cells and Its Absence in Small Cell Carcinoma of the Lung
title Ultrastructural Proof of Polyomavirus in Merkel Cell Carcinoma Tumour Cells and Its Absence in Small Cell Carcinoma of the Lung
title_full Ultrastructural Proof of Polyomavirus in Merkel Cell Carcinoma Tumour Cells and Its Absence in Small Cell Carcinoma of the Lung
title_fullStr Ultrastructural Proof of Polyomavirus in Merkel Cell Carcinoma Tumour Cells and Its Absence in Small Cell Carcinoma of the Lung
title_full_unstemmed Ultrastructural Proof of Polyomavirus in Merkel Cell Carcinoma Tumour Cells and Its Absence in Small Cell Carcinoma of the Lung
title_short Ultrastructural Proof of Polyomavirus in Merkel Cell Carcinoma Tumour Cells and Its Absence in Small Cell Carcinoma of the Lung
title_sort ultrastructural proof of polyomavirus in merkel cell carcinoma tumour cells and its absence in small cell carcinoma of the lung
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2654729/
https://www.ncbi.nlm.nih.gov/pubmed/19305499
http://dx.doi.org/10.1371/journal.pone.0004958
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