Determining the Expression Levels of Circulating Tumour Cell Markers in Canine Mammary Tumours
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Erişim
info:eu-repo/semantics/openAccessTarih
2021Yazar
Değirmencioğlu, SevginUçmak, Zeynep Günay
Kahraman, Özlem Timirci
Gültekin, Güldal İnal
Yaylım, İlhan
Güvenç, Kazım
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Uçmak, Z. G., Kahraman, Ö. T., Gültekin, G. İ., Değirmencioğlu, S., Yaylım, İ., & Güvenç, K. (2021). Determining the expression levels of circulating tumour cell markers in canine mammary tumours. Acta Veterinaria Brno, 90(2), 191-200.Özet
Detection of the circulating tumour cells (CTC) in dogs with a mammary tumour is a useful tool to reveal the micrometastases long before metastases are recognised clinically. The aim of this study was to evaluate the association of the epidermal growth factor receptor (EGFR), claudin 7 (CLND7) and epithelial cell adhesion molecule (EPCAM) with the clinical indices and to reveal the diagnostic importance of these biomarkers in canine mammary tumours (CMTs). Peripheral blood (PB) samples were collected from 45 bitches (group MT) which had single mass with malignant epithelial tumours and 9 healthy bitches (group H). Real time PCR (rt-PCR) was performed to determine the expression levels of EGFR, CLDN7, and EPCAM. Mean values of EGFR and CLDN7 expressions were significantly higher in group MT compared to group H (P < 0.01 and P < 0.001, respectively). The expression level of CLDN7 was positively correlated with EGFR and EPCAM (P < 0.001 and P < 0.05, respectively). The EPCAM expression was associated with increased tumour size (P < 0.05) and EPCAM tended to decrease in the presence of skin ulceration on tumour (P = 0.05). Furthermore, expression levels of EGFR in intact dogs were significantly higher compared to spayed dogs in group MT (P < 0.01). The EGFR expression was significantly higher in the presence of metastases (P < 0.05). Also, increased EGFR was determined in grade 2 compared to grade 1 (P < 0.05). In conclusion, these results show that EGFR, CLDN7, EPCAM markers are measureable in PB and they may provide valuable information about the clinical pathophysiology of CMT.