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Emerging role of human polyomaviruses 6 and 7 in human cancers

BACKGROUND: Currently 12 human polyomaviruses (HPyVs) have been identified, 6 of which have been associated with human diseases, including cancer. The discovery of the Merkel cell polyomavirus and its role in the etiopathogenesis in the majority of Merkel cell carcinomas has drawn significant attent...

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Autores principales: Klufah, Faisal, Mobaraki, Ghalib, Liu, Dan, Alharbi, Raed A., Kurz, Anna Kordelia, Speel, Ernst Jan M., Winnepenninckx, Véronique, zur Hausen, Axel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8130262/
https://www.ncbi.nlm.nih.gov/pubmed/34001216
http://dx.doi.org/10.1186/s13027-021-00374-3
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author Klufah, Faisal
Mobaraki, Ghalib
Liu, Dan
Alharbi, Raed A.
Kurz, Anna Kordelia
Speel, Ernst Jan M.
Winnepenninckx, Véronique
zur Hausen, Axel
author_facet Klufah, Faisal
Mobaraki, Ghalib
Liu, Dan
Alharbi, Raed A.
Kurz, Anna Kordelia
Speel, Ernst Jan M.
Winnepenninckx, Véronique
zur Hausen, Axel
author_sort Klufah, Faisal
collection PubMed
description BACKGROUND: Currently 12 human polyomaviruses (HPyVs) have been identified, 6 of which have been associated with human diseases, including cancer. The discovery of the Merkel cell polyomavirus and its role in the etiopathogenesis in the majority of Merkel cell carcinomas has drawn significant attention, also to other novel HPyVs. In 2010, HPyV6 and HPyV7 were identified in healthy skin swabs. Ever since it has been speculated that they might contribute to the etiopathogenesis of skin and non-cutaneous human cancers. MAIN BODY: Here we comprehensively reviewed and summarized the current evidence potentially indicating an involvement of HPyV6 and HPyV7 in the etiopathogenesis of neoplastic human diseases. The seroprevalence of both HPyV6 and 7 is high in a normal population and increases with age. In skin cancer tissues, HPyV6- DNA was far more often prevalent than HPyV7 in contrast to cancers of other anatomic sites, in which HPyV7 DNA was more frequently detected. CONCLUSION: It is remarkable to find that the detection rate of HPyV6-DNA in tissues of skin malignancies is higher than HPyV7-DNA and may indicate a role of HPyV6 in the etiopathogenesis of the respected skin cancers. However, the sheer presence of viral DNA is not enough to prove a role in the etiopathogenesis of these cancers.
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spelling pubmed-81302622021-05-18 Emerging role of human polyomaviruses 6 and 7 in human cancers Klufah, Faisal Mobaraki, Ghalib Liu, Dan Alharbi, Raed A. Kurz, Anna Kordelia Speel, Ernst Jan M. Winnepenninckx, Véronique zur Hausen, Axel Infect Agent Cancer Review BACKGROUND: Currently 12 human polyomaviruses (HPyVs) have been identified, 6 of which have been associated with human diseases, including cancer. The discovery of the Merkel cell polyomavirus and its role in the etiopathogenesis in the majority of Merkel cell carcinomas has drawn significant attention, also to other novel HPyVs. In 2010, HPyV6 and HPyV7 were identified in healthy skin swabs. Ever since it has been speculated that they might contribute to the etiopathogenesis of skin and non-cutaneous human cancers. MAIN BODY: Here we comprehensively reviewed and summarized the current evidence potentially indicating an involvement of HPyV6 and HPyV7 in the etiopathogenesis of neoplastic human diseases. The seroprevalence of both HPyV6 and 7 is high in a normal population and increases with age. In skin cancer tissues, HPyV6- DNA was far more often prevalent than HPyV7 in contrast to cancers of other anatomic sites, in which HPyV7 DNA was more frequently detected. CONCLUSION: It is remarkable to find that the detection rate of HPyV6-DNA in tissues of skin malignancies is higher than HPyV7-DNA and may indicate a role of HPyV6 in the etiopathogenesis of the respected skin cancers. However, the sheer presence of viral DNA is not enough to prove a role in the etiopathogenesis of these cancers. BioMed Central 2021-05-17 /pmc/articles/PMC8130262/ /pubmed/34001216 http://dx.doi.org/10.1186/s13027-021-00374-3 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Review
Klufah, Faisal
Mobaraki, Ghalib
Liu, Dan
Alharbi, Raed A.
Kurz, Anna Kordelia
Speel, Ernst Jan M.
Winnepenninckx, Véronique
zur Hausen, Axel
Emerging role of human polyomaviruses 6 and 7 in human cancers
title Emerging role of human polyomaviruses 6 and 7 in human cancers
title_full Emerging role of human polyomaviruses 6 and 7 in human cancers
title_fullStr Emerging role of human polyomaviruses 6 and 7 in human cancers
title_full_unstemmed Emerging role of human polyomaviruses 6 and 7 in human cancers
title_short Emerging role of human polyomaviruses 6 and 7 in human cancers
title_sort emerging role of human polyomaviruses 6 and 7 in human cancers
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8130262/
https://www.ncbi.nlm.nih.gov/pubmed/34001216
http://dx.doi.org/10.1186/s13027-021-00374-3
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