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Mus musculus papillomavirus 1 is a key driver of skin cancer development upon immunosuppression

Epidemiological and experimental data implicate cutaneous human papillomavirus infection as co‐factor in the development of cutaneous squamous cell carcinomas (cSCCs), particularly in immunocompromised organ transplant recipients (OTRs). Herein, we established and characterized a skin cancer model,...

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Autores principales: Dorfer, Sonja, Strasser, Katharina, Schröckenfuchs, Georg, Bonelli, Michael, Bauer, Wolfgang, Kittler, Harald, Cataisson, Christophe, Fischer, Michael B., Lichtenberger, Beate M., Handisurya, Alessandra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7894140/
https://www.ncbi.nlm.nih.gov/pubmed/33063442
http://dx.doi.org/10.1111/ajt.16358
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author Dorfer, Sonja
Strasser, Katharina
Schröckenfuchs, Georg
Bonelli, Michael
Bauer, Wolfgang
Kittler, Harald
Cataisson, Christophe
Fischer, Michael B.
Lichtenberger, Beate M.
Handisurya, Alessandra
author_facet Dorfer, Sonja
Strasser, Katharina
Schröckenfuchs, Georg
Bonelli, Michael
Bauer, Wolfgang
Kittler, Harald
Cataisson, Christophe
Fischer, Michael B.
Lichtenberger, Beate M.
Handisurya, Alessandra
author_sort Dorfer, Sonja
collection PubMed
description Epidemiological and experimental data implicate cutaneous human papillomavirus infection as co‐factor in the development of cutaneous squamous cell carcinomas (cSCCs), particularly in immunocompromised organ transplant recipients (OTRs). Herein, we established and characterized a skin cancer model, in which Mus musculus papillomavirus 1 (MmuPV1) infection caused cSCCs in cyclosporine A (CsA)‐treated mice, even in the absence of UV light. Development of cSCCs and their precursors were observed in 70% of MmuPV1‐infected, CsA‐treated mice on back as well as on tail skin. Immunosuppression by systemic CsA, but not UV‐B irradiation, was a prerequisite, as immunocompetent or UV‐B–irradiated mice did not develop skin malignancies after infection. In the virus‐driven cSCCs the MmuPV1‐E6/E7 oncogenes were abundantly expressed, and transcriptional activity and productive infection demonstrated. MmuPV1 infection induced the expression of phosphorylated H2AX, but not degradation of proapoptotic BAK in the cSCCs. Transfer of primary cells, established from a MmuPV1‐induced cSCC from back skin, into athymic nude mice gave rise to secondary cSCCs, which lacked viral DNA, demonstrating that maintenance of the malignant phenotype was virus independent. This papillomavirus‐induced skin cancer model opens future investigations into viral involvement, pathogenesis, and cancer surveillance, aiming at understanding and controlling the high incidence of skin cancer in OTRs.
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spelling pubmed-78941402021-03-02 Mus musculus papillomavirus 1 is a key driver of skin cancer development upon immunosuppression Dorfer, Sonja Strasser, Katharina Schröckenfuchs, Georg Bonelli, Michael Bauer, Wolfgang Kittler, Harald Cataisson, Christophe Fischer, Michael B. Lichtenberger, Beate M. Handisurya, Alessandra Am J Transplant ORIGINAL ARTICLES Epidemiological and experimental data implicate cutaneous human papillomavirus infection as co‐factor in the development of cutaneous squamous cell carcinomas (cSCCs), particularly in immunocompromised organ transplant recipients (OTRs). Herein, we established and characterized a skin cancer model, in which Mus musculus papillomavirus 1 (MmuPV1) infection caused cSCCs in cyclosporine A (CsA)‐treated mice, even in the absence of UV light. Development of cSCCs and their precursors were observed in 70% of MmuPV1‐infected, CsA‐treated mice on back as well as on tail skin. Immunosuppression by systemic CsA, but not UV‐B irradiation, was a prerequisite, as immunocompetent or UV‐B–irradiated mice did not develop skin malignancies after infection. In the virus‐driven cSCCs the MmuPV1‐E6/E7 oncogenes were abundantly expressed, and transcriptional activity and productive infection demonstrated. MmuPV1 infection induced the expression of phosphorylated H2AX, but not degradation of proapoptotic BAK in the cSCCs. Transfer of primary cells, established from a MmuPV1‐induced cSCC from back skin, into athymic nude mice gave rise to secondary cSCCs, which lacked viral DNA, demonstrating that maintenance of the malignant phenotype was virus independent. This papillomavirus‐induced skin cancer model opens future investigations into viral involvement, pathogenesis, and cancer surveillance, aiming at understanding and controlling the high incidence of skin cancer in OTRs. John Wiley and Sons Inc. 2020-11-03 2021-02 /pmc/articles/PMC7894140/ /pubmed/33063442 http://dx.doi.org/10.1111/ajt.16358 Text en © 2020 The Authors. American Journal of Transplantation published by Wiley Periodicals LLC on behalf of The American Society of Transplantation and the American Society of Transplant Surgeons This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle ORIGINAL ARTICLES
Dorfer, Sonja
Strasser, Katharina
Schröckenfuchs, Georg
Bonelli, Michael
Bauer, Wolfgang
Kittler, Harald
Cataisson, Christophe
Fischer, Michael B.
Lichtenberger, Beate M.
Handisurya, Alessandra
Mus musculus papillomavirus 1 is a key driver of skin cancer development upon immunosuppression
title Mus musculus papillomavirus 1 is a key driver of skin cancer development upon immunosuppression
title_full Mus musculus papillomavirus 1 is a key driver of skin cancer development upon immunosuppression
title_fullStr Mus musculus papillomavirus 1 is a key driver of skin cancer development upon immunosuppression
title_full_unstemmed Mus musculus papillomavirus 1 is a key driver of skin cancer development upon immunosuppression
title_short Mus musculus papillomavirus 1 is a key driver of skin cancer development upon immunosuppression
title_sort mus musculus papillomavirus 1 is a key driver of skin cancer development upon immunosuppression
topic ORIGINAL ARTICLES
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7894140/
https://www.ncbi.nlm.nih.gov/pubmed/33063442
http://dx.doi.org/10.1111/ajt.16358
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