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

  • Callum Arthurs
  • , Alejandro Suarez-Bonnet
  • , Claire Willis
  • , Boyu Xie
  • , Natalie Machulla
  • , Tim S Mair
  • , Kevin Cao
  • , Michael Millar
  • , Christopher Thrasivoulou
  • , Simon L Priestnall
  • , Aamir Ahmed
  • Prostate Cancer Research Centre at the Centre for Stem Cells and Regenerative Medicine
  • Royal Veterinary College
  • Bell Equine Veterinary Clinic, Maidstone, UK.
  • Authors' Affiliations: MRC Centre for Inflammation Research, The Queen's Medical Research Institute; MRC Centre for Regenerative Medicine; School of Chemistry, Joseph Black Building, University of Edinburgh, Edinburgh; Department of Thoracic Oncology, Papworth Hospital NHS Foundation Trust, Cambridge; and Department of Respiratory Medicine and Allergy, Kings College Denmark Hill Campus, London, United Kingdom.
  • Research Department of Cell and Developmental Biology, The Centre for Cell and Molecular Dynamics, Rockefeller Building, University College London, London, United Kingdom.

Research output: Contribution to journal › Article › peer-review

17 Citations (Scopus)

Abstract

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.

Original languageEnglish
Article number7863
JournalScientific Reports
Volume10
Issue number1
Early online date12 May 2020
DOIs
Publication statusPublished - 1 Dec 2020

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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