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Open AccessJournal ArticleDOI

Clonal integration of a polyomavirus in human Merkel cell carcinoma.

Huichen Feng, +3 more
- 22 Feb 2008 - 
- Vol. 319, Iss: 5866, pp 1096-1100
TLDR
In six of eight MCV-positive MCCs, viral DNA was integrated within the tumor genome in a clonal pattern, suggesting that MCV infection and integration preceded clonal expansion of the tumor cells, and MCV may be a contributing factor in the pathogenesis of MCC.
Abstract
Merkel cell carcinoma (MCC) is a rare but aggressive human skin cancer that typically affects elderly and immunosuppressed individuals, a feature suggestive of an infectious origin. We studied MCC samples by digital transcriptome subtraction and detected a fusion transcript between a previously undescribed virus T antigen and a human receptor tyrosine phosphatase. Further investigation led to identification and sequence analysis of the 5387-base-pair genome of a previously unknown polyomavirus that we call Merkel cell polyomavirus (MCV or MCPyV). MCV sequences were detected in 8 of 10 (80%) MCC tumors but only 5 of 59 (8%) control tissues from various body sites and 4 of 25 (16%) control skin tissues. In six of eight MCV-positive MCCs, viral DNA was integrated within the tumor genome in a clonal pattern, suggesting that MCV infection and integration preceded clonal expansion of the tumor cells. Thus, MCV may be a contributing factor in the pathogenesis of MCC.

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Journal ArticleDOI

An Update on Tumors of the Lacrimal Gland.

TL;DR: An update on the clinical, radiological, histological, and molecular features, along with treatment strategies for tumors of the lacrimal gland are presented.
Journal ArticleDOI

Detection of Merkel cell polyomavirus with a tumour-specific signature in non-small cell lung cancer

TL;DR: The expression of a viral oncoprotein, the presence of integrated MCPyV, and a truncated LT gene with a preserved retinoblastoma tumour-suppressor protein-binding domain in NSCLCs support the possibility that M CPyV is partly associated with the pathogenesis of NSCLC in a subset of patients.
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Human oncogenic viruses: nature and discovery.

TL;DR: Although individual human tumour viruses exert their malignant effects in different ways, there are common features that illuminate mechanisms of oncogenesis more generally, whether or not there is a viral aetiology.
Journal ArticleDOI

Human polyomaviruses and cancer: an overview.

TL;DR: Present evidence only supports the role of MCPyV as a carcinogen to humans, and a summarized discussion on the current knowledge concerning the roleof MCPYV, TSPyV, JCPy V and BKPyV in human cancers is presented.
Journal ArticleDOI

Merkel cell carcinoma: histopathologic and prognostic features according to the immunohistochemical expression of Merkel cell polyomavirus large T antigen correlated with viral load

TL;DR: Depending on MCPyV involvement, 2 MCC subgroups can be distinguished on histopathologic criteria, and the CM2B4 antibody is able to differentiate them reliably.
References
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SV40 large tumor antigen forms a specific complex with the product of the retinoblastoma susceptibility gene

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Journal ArticleDOI

Identification of a novel polyomavirus from patients with acute respiratory tract infections.

TL;DR: The presence of multiple instances of the virus in two continents suggests that this virus is geographically widespread in the human population and raises the possibility that the WU virus may be a human pathogen.
Journal ArticleDOI

Identification of a Third Human Polyomavirus

TL;DR: The identification of a previously unknown polyomvirus provisionally named KI polyomavirus, which is phylogenetically related to other primatepolyomaviruses in the early region of the genome but has very little homology to known polyomVirus in the late region, illustrates how unbiased screening of respiratory tract samples can be used for the discovery of diverse virus types.
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