MicroRNA Expression in Formalin-Fixed, Paraffin-Embedded Samples of Canine Cutaneous and Oral Melanoma by RT-qPCR

Author:

Zamarian Valentina1,Catozzi Carlotta1,Ressel Lorenzo2ORCID,Finotello Riccardo3,Ceciliani Fabrizio1,Vilafranca Miguel4,Altimira Jaume4,Lecchi Cristina1ORCID

Affiliation:

1. Dipartimento di Medicina Veterinaria, Università degli Studi di Milano, Milano, Italy

2. Department of Veterinary Pathology, Public Health Institute of Veterinary Science, University of Liverpool, Neston, UK

3. Department of Small Animal Clinical Science, Institute of Veterinary Science, University of Liverpool, Neston, UK

4. HISTOVET Veterinary Diagnostic Service, Barcelona, Spain

Abstract

MicroRNAs (miRNAs) are a class of small, noncoding RNA that post-transcriptionally regulate protein expression. miRNAs are emerging as clinical biomarkers of many diseases, including tumors. The aim of this study was to investigate whether miRNA expression could vary in melanoma samples derived from formalin-fixed, paraffin-embedded (FFPE) tissues. The study included 4 groups: (1) 9 samples of oral canine malignant melanoma, (2) 10 samples of cutaneous malignant melanoma, (3) 5 samples of healthy oral mucosa, and (4) 7 samples of healthy skin. The expression levels of 6 miRNAs—miR-145, miR-146a, miR-425-5p, miR-223, miR-365, and miR-134—were detected and assessed by quantitative reverse transcription polymerase chain reaction (RT-qPCR) using TaqMan probes. Cutaneous canine malignant melanoma showed a decrease of the expression level of miR-145 and miR-365 and an increase of miR-146a and miR-425-5p compared to control samples. MiR-145 was also downregulated in oral canine malignant melanoma. The miRNAs with decreased expression may regulate genes involved in RAS, Rap1, and transforming growth factor β (TGF-β) signaling pathways, as well as upregulated genes associated with phosphatidylinositol signaling system, adherens junction, and RAS signaling pathways. In conclusion, miR-145, miR-365, miR-146a, and miR-425-5p were differentially expressed in canine malignant melanoma and healthy FFPE samples, suggesting that they may play a role in canine malignant melanoma pathogenesis.

Publisher

SAGE Publications

Subject

General Veterinary

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