Cargando…
Detection of Merkel Cell Polyomavirus in Seborrheic Keratosis
Seborrheic keratosis (SK) is the most common benign cutaneous neoplasm. A subset shows increased p16 expression. Since SK shares several features with verruca vulgaris, e.g., increased p16 expression, human papillomaviruses (HPV) have been suggested as possible causal agents. However, a relevant ass...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5767171/ https://www.ncbi.nlm.nih.gov/pubmed/29375515 http://dx.doi.org/10.3389/fmicb.2017.02648 |
_version_ | 1783292481756987392 |
---|---|
author | Hillen, Lisa M. Rennspiess, Dorit Speel, Ernst-Jan Haugg, Anke M. Winnepenninckx, Véronique zur Hausen, Axel |
author_facet | Hillen, Lisa M. Rennspiess, Dorit Speel, Ernst-Jan Haugg, Anke M. Winnepenninckx, Véronique zur Hausen, Axel |
author_sort | Hillen, Lisa M. |
collection | PubMed |
description | Seborrheic keratosis (SK) is the most common benign cutaneous neoplasm. A subset shows increased p16 expression. Since SK shares several features with verruca vulgaris, e.g., increased p16 expression, human papillomaviruses (HPV) have been suggested as possible causal agents. However, a relevant association could not be established between HPV and SK. In the present study we aimed to investigate the presence of Merkel cell polyomavirus (MCPyV) in relation to p16 expression in SK. P16 expression was investigated using immunohistochemistry (IHC). Presence of MCPyV was assessed in 23 formalin-fixed paraffin-embedded tissue samples of SK by molecular techniques (i.e., PCR and FISH) and IHC. 16/23 SK showed strong to moderate p16 expression. 6/23 of SK were MCPyV positive by PCR which was confirmed by FISH. Of interest, two samples with strong FISH signals also showed MCPyV expression as tested by IHC. Samples with weaker signal intensity were negative in IHC. P16 expression was not associated with the presence of MCPyV. Concluding, the detection of MCPyV DNA by PCR and FISH in SK reflects the widespread prevalence of MCPyV in the skin. However, low detection rates exclude MCPyV as a major pathogenic factor in SK, most likely representing a coincidental infection. P16 IHC does not appear as useful adjunctive surrogate marker for the presence of MCPyV in SK. |
format | Online Article Text |
id | pubmed-5767171 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-57671712018-01-26 Detection of Merkel Cell Polyomavirus in Seborrheic Keratosis Hillen, Lisa M. Rennspiess, Dorit Speel, Ernst-Jan Haugg, Anke M. Winnepenninckx, Véronique zur Hausen, Axel Front Microbiol Microbiology Seborrheic keratosis (SK) is the most common benign cutaneous neoplasm. A subset shows increased p16 expression. Since SK shares several features with verruca vulgaris, e.g., increased p16 expression, human papillomaviruses (HPV) have been suggested as possible causal agents. However, a relevant association could not be established between HPV and SK. In the present study we aimed to investigate the presence of Merkel cell polyomavirus (MCPyV) in relation to p16 expression in SK. P16 expression was investigated using immunohistochemistry (IHC). Presence of MCPyV was assessed in 23 formalin-fixed paraffin-embedded tissue samples of SK by molecular techniques (i.e., PCR and FISH) and IHC. 16/23 SK showed strong to moderate p16 expression. 6/23 of SK were MCPyV positive by PCR which was confirmed by FISH. Of interest, two samples with strong FISH signals also showed MCPyV expression as tested by IHC. Samples with weaker signal intensity were negative in IHC. P16 expression was not associated with the presence of MCPyV. Concluding, the detection of MCPyV DNA by PCR and FISH in SK reflects the widespread prevalence of MCPyV in the skin. However, low detection rates exclude MCPyV as a major pathogenic factor in SK, most likely representing a coincidental infection. P16 IHC does not appear as useful adjunctive surrogate marker for the presence of MCPyV in SK. Frontiers Media S.A. 2018-01-09 /pmc/articles/PMC5767171/ /pubmed/29375515 http://dx.doi.org/10.3389/fmicb.2017.02648 Text en Copyright © 2018 Hillen, Rennspiess, Speel, Haugg, Winnepenninckx and zur Hausen. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Hillen, Lisa M. Rennspiess, Dorit Speel, Ernst-Jan Haugg, Anke M. Winnepenninckx, Véronique zur Hausen, Axel Detection of Merkel Cell Polyomavirus in Seborrheic Keratosis |
title | Detection of Merkel Cell Polyomavirus in Seborrheic Keratosis |
title_full | Detection of Merkel Cell Polyomavirus in Seborrheic Keratosis |
title_fullStr | Detection of Merkel Cell Polyomavirus in Seborrheic Keratosis |
title_full_unstemmed | Detection of Merkel Cell Polyomavirus in Seborrheic Keratosis |
title_short | Detection of Merkel Cell Polyomavirus in Seborrheic Keratosis |
title_sort | detection of merkel cell polyomavirus in seborrheic keratosis |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5767171/ https://www.ncbi.nlm.nih.gov/pubmed/29375515 http://dx.doi.org/10.3389/fmicb.2017.02648 |
work_keys_str_mv | AT hillenlisam detectionofmerkelcellpolyomavirusinseborrheickeratosis AT rennspiessdorit detectionofmerkelcellpolyomavirusinseborrheickeratosis AT speelernstjan detectionofmerkelcellpolyomavirusinseborrheickeratosis AT hauggankem detectionofmerkelcellpolyomavirusinseborrheickeratosis AT winnepenninckxveronique detectionofmerkelcellpolyomavirusinseborrheickeratosis AT zurhausenaxel detectionofmerkelcellpolyomavirusinseborrheickeratosis |