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

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作者
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
机构
[1] Prostate Cancer Research Centre at the Centre for Stem Cells and Regenerative Medicine,
[2] King’s College London,undefined
[3] Department of Pathobiology and Population Sciences,undefined
[4] Royal Veterinary College,undefined
[5] Bell Equine Veterinary Clinic,undefined
[6] Queen’s Medical Research Institute,undefined
[7] University of Edinburgh,undefined
[8] Research Department of Cell and Developmental Biology,undefined
[9] The Centre for Cell and Molecular Dynamics,undefined
[10] Rockefeller Building,undefined
[11] University College London,undefined
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摘要
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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