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Equine penile squamous cell carcinoma: expression of biomarker proteins and EcPV2

Equine penile squamous cell carcinoma (EpSCC) is a relatively common cutaneous neoplasm with a poor prognosis. In this study, we aimed to determine the protein expression and colocalisation of FRA1, c-Myc, Cyclin D1, and MMP7 in normal (NT), tumour (T), hyperplastic epidermis and/or squamous papillo...

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Autores principales: Arthurs, Callum, Suarez-Bonnet, Alejandro, Willis, Claire, Xie, Boyu, Machulla, Natalie, Mair, Tim S., Cao, Kevin, Millar, Michael, Thrasivoulou, Christopher, Priestnall, Simon L., Ahmed, Aamir
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7217868/
https://www.ncbi.nlm.nih.gov/pubmed/32398763
http://dx.doi.org/10.1038/s41598-020-64014-3
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author Arthurs, Callum
Suarez-Bonnet, Alejandro
Willis, Claire
Xie, Boyu
Machulla, Natalie
Mair, Tim S.
Cao, Kevin
Millar, Michael
Thrasivoulou, Christopher
Priestnall, Simon L.
Ahmed, Aamir
author_facet Arthurs, Callum
Suarez-Bonnet, Alejandro
Willis, Claire
Xie, Boyu
Machulla, Natalie
Mair, Tim S.
Cao, Kevin
Millar, Michael
Thrasivoulou, Christopher
Priestnall, Simon L.
Ahmed, Aamir
author_sort Arthurs, Callum
collection PubMed
description Equine penile squamous cell carcinoma (EpSCC) is a relatively common cutaneous neoplasm with a poor prognosis. In this study, we aimed to determine the protein expression and colocalisation of FRA1, c-Myc, Cyclin D1, and MMP7 in normal (NT), tumour (T), hyperplastic epidermis and/or squamous papilloma (Hyp/Pap), poorly-differentiated (PDSCC), or well-differentiated (WDSCC) EpSCC using a tissue array approach. Further objectives were to correlate protein expression to (i) levels of inflammation, using a convolutional neural network (ii) equine papillomavirus 2 (EcPV2) infection, detected using PCR amplification. We found an increase in expression of FRA1 in EpSCC compared to NT samples. c-Myc expression was higher in Hyp/Pap and WDSCC but not PDSCC whereas MMP7 was reduced in WDSCC compared with NT. There was a significant increase in the global intersection coefficient (GIC) of FRA1 with MMP7, c-Myc, and Cyclin D1 in EpSCC. Conversely, GIC for MMP7 with c-Myc was reduced in EpSCC tissue. Inflammation was positively associated with EcPV2 infection in both NT and EpSCC but not Hyp/Pap. Changes in protein expression could be correlated with EcPV2 for Cyclin D1 and c-Myc. Our results evaluate novel biomarkers of EpSCC and a putative correlation between the expression of biomarkers, EcPV2 infection and inflammation.
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spelling pubmed-72178682020-05-19 Equine penile squamous cell carcinoma: expression of biomarker proteins and EcPV2 Arthurs, Callum Suarez-Bonnet, Alejandro Willis, Claire Xie, Boyu Machulla, Natalie Mair, Tim S. Cao, Kevin Millar, Michael Thrasivoulou, Christopher Priestnall, Simon L. Ahmed, Aamir Sci Rep Article Equine penile squamous cell carcinoma (EpSCC) is a relatively common cutaneous neoplasm with a poor prognosis. In this study, we aimed to determine the protein expression and colocalisation of FRA1, c-Myc, Cyclin D1, and MMP7 in normal (NT), tumour (T), hyperplastic epidermis and/or squamous papilloma (Hyp/Pap), poorly-differentiated (PDSCC), or well-differentiated (WDSCC) EpSCC using a tissue array approach. Further objectives were to correlate protein expression to (i) levels of inflammation, using a convolutional neural network (ii) equine papillomavirus 2 (EcPV2) infection, detected using PCR amplification. We found an increase in expression of FRA1 in EpSCC compared to NT samples. c-Myc expression was higher in Hyp/Pap and WDSCC but not PDSCC whereas MMP7 was reduced in WDSCC compared with NT. There was a significant increase in the global intersection coefficient (GIC) of FRA1 with MMP7, c-Myc, and Cyclin D1 in EpSCC. Conversely, GIC for MMP7 with c-Myc was reduced in EpSCC tissue. Inflammation was positively associated with EcPV2 infection in both NT and EpSCC but not Hyp/Pap. Changes in protein expression could be correlated with EcPV2 for Cyclin D1 and c-Myc. Our results evaluate novel biomarkers of EpSCC and a putative correlation between the expression of biomarkers, EcPV2 infection and inflammation. Nature Publishing Group UK 2020-05-12 /pmc/articles/PMC7217868/ /pubmed/32398763 http://dx.doi.org/10.1038/s41598-020-64014-3 Text en © The Author(s) 2020 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Arthurs, Callum
Suarez-Bonnet, Alejandro
Willis, Claire
Xie, Boyu
Machulla, Natalie
Mair, Tim S.
Cao, Kevin
Millar, Michael
Thrasivoulou, Christopher
Priestnall, Simon L.
Ahmed, Aamir
Equine penile squamous cell carcinoma: expression of biomarker proteins and EcPV2
title Equine penile squamous cell carcinoma: expression of biomarker proteins and EcPV2
title_full Equine penile squamous cell carcinoma: expression of biomarker proteins and EcPV2
title_fullStr Equine penile squamous cell carcinoma: expression of biomarker proteins and EcPV2
title_full_unstemmed Equine penile squamous cell carcinoma: expression of biomarker proteins and EcPV2
title_short Equine penile squamous cell carcinoma: expression of biomarker proteins and EcPV2
title_sort equine penile squamous cell carcinoma: expression of biomarker proteins and ecpv2
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7217868/
https://www.ncbi.nlm.nih.gov/pubmed/32398763
http://dx.doi.org/10.1038/s41598-020-64014-3
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