Merkel cell polyomavirus detection in Merkel cell cancer tumors in Northern Germany using PCR and protein expression

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Merkel cell polyomavirus detection in Merkel cell cancer tumors in Northern Germany using PCR and protein expression. / Leitz, Miriam; Stieler, Kristin; Grundhoff, Adam; Moll, Ingrid; Brandner, Johanna M; Fischer, Nicole.

In: J MED VIROL, Vol. 86 , No. 10, 2014, p. 1813-1819.

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@article{0c3400604c2d4041b3a88c5304210e9a,
title = "Merkel cell polyomavirus detection in Merkel cell cancer tumors in Northern Germany using PCR and protein expression",
abstract = "Merkel cell carcinoma is a highly malignant skin cancer which predominantly occurs in elderly and immunocompromised persons. The identification of the Merkel cell polyomavirus (MCPyV) has inaugurated a new understanding of Merkel cell carcinoma pathogenesis. The frequent detection of the virus in Merkel cell carcinoma tissue (70-90%), its monoclonal integration in the tumor cells and the expression of viral oncogenes highly suggest that MCPyV is causally linked to the pathogenesis of the majority of Merkel cell cancer (MCC) cases. Using qualitative and quantitative PCR together with immunohistochemical staining this study aimed at characterizing the presence of MCPyV sequences and viral early gene expression in a cohort of MCC cases (n = 32) selected in Northern Germany. 40-57% of the cases were identified as MCPyV positive with 40.6% of the cases positive by immunohistochemical staining and 51.6-57.6% positive by PCR. Interestingly, in the majority (64%) of LT-Antigen positive tumors only 25-50% of tumor cells express LT-Antigen. These data are in accord with published studies describing heterogeneity in MCPyV viral loads and suggest that detection of MCPyV in Merkel cell carcinoma by PCR should be undertaken using multiple primer pairs. J. Med. Virol. {\textcopyright} 2013 Wiley Periodicals, Inc.",
author = "Miriam Leitz and Kristin Stieler and Adam Grundhoff and Ingrid Moll and Brandner, {Johanna M} and Nicole Fischer",
note = "{\textcopyright} 2013 Wiley Periodicals, Inc.",
year = "2014",
doi = "10.1002/jmv.23808",
language = "English",
volume = "86 ",
pages = "1813--1819",
journal = "J MED VIROL",
issn = "0146-6615",
publisher = "Wiley-Liss Inc.",
number = "10",

}

RIS

TY - JOUR

T1 - Merkel cell polyomavirus detection in Merkel cell cancer tumors in Northern Germany using PCR and protein expression

AU - Leitz, Miriam

AU - Stieler, Kristin

AU - Grundhoff, Adam

AU - Moll, Ingrid

AU - Brandner, Johanna M

AU - Fischer, Nicole

N1 - © 2013 Wiley Periodicals, Inc.

PY - 2014

Y1 - 2014

N2 - Merkel cell carcinoma is a highly malignant skin cancer which predominantly occurs in elderly and immunocompromised persons. The identification of the Merkel cell polyomavirus (MCPyV) has inaugurated a new understanding of Merkel cell carcinoma pathogenesis. The frequent detection of the virus in Merkel cell carcinoma tissue (70-90%), its monoclonal integration in the tumor cells and the expression of viral oncogenes highly suggest that MCPyV is causally linked to the pathogenesis of the majority of Merkel cell cancer (MCC) cases. Using qualitative and quantitative PCR together with immunohistochemical staining this study aimed at characterizing the presence of MCPyV sequences and viral early gene expression in a cohort of MCC cases (n = 32) selected in Northern Germany. 40-57% of the cases were identified as MCPyV positive with 40.6% of the cases positive by immunohistochemical staining and 51.6-57.6% positive by PCR. Interestingly, in the majority (64%) of LT-Antigen positive tumors only 25-50% of tumor cells express LT-Antigen. These data are in accord with published studies describing heterogeneity in MCPyV viral loads and suggest that detection of MCPyV in Merkel cell carcinoma by PCR should be undertaken using multiple primer pairs. J. Med. Virol. © 2013 Wiley Periodicals, Inc.

AB - Merkel cell carcinoma is a highly malignant skin cancer which predominantly occurs in elderly and immunocompromised persons. The identification of the Merkel cell polyomavirus (MCPyV) has inaugurated a new understanding of Merkel cell carcinoma pathogenesis. The frequent detection of the virus in Merkel cell carcinoma tissue (70-90%), its monoclonal integration in the tumor cells and the expression of viral oncogenes highly suggest that MCPyV is causally linked to the pathogenesis of the majority of Merkel cell cancer (MCC) cases. Using qualitative and quantitative PCR together with immunohistochemical staining this study aimed at characterizing the presence of MCPyV sequences and viral early gene expression in a cohort of MCC cases (n = 32) selected in Northern Germany. 40-57% of the cases were identified as MCPyV positive with 40.6% of the cases positive by immunohistochemical staining and 51.6-57.6% positive by PCR. Interestingly, in the majority (64%) of LT-Antigen positive tumors only 25-50% of tumor cells express LT-Antigen. These data are in accord with published studies describing heterogeneity in MCPyV viral loads and suggest that detection of MCPyV in Merkel cell carcinoma by PCR should be undertaken using multiple primer pairs. J. Med. Virol. © 2013 Wiley Periodicals, Inc.

U2 - 10.1002/jmv.23808

DO - 10.1002/jmv.23808

M3 - SCORING: Journal article

C2 - 24307009

VL - 86

SP - 1813

EP - 1819

JO - J MED VIROL

JF - J MED VIROL

SN - 0146-6615

IS - 10

ER -