MicroRNA Expression in Formalin-Fixed, Paraffin-Embedded Samples of Canine Cutaneous and Oral Melanoma by RT-qPCR.
Animals
Biomarkers, Tumor
/ genetics
Cohort Studies
Dog Diseases
/ diagnosis
Dogs
Down-Regulation
Gene Expression Regulation, Neoplastic
/ genetics
Immunohistochemistry
/ veterinary
Melanoma
/ diagnosis
MicroRNAs
/ genetics
Mouth Neoplasms
/ diagnosis
Paraffin Embedding
/ veterinary
Real-Time Polymerase Chain Reaction
/ veterinary
Skin Neoplasms
/ diagnosis
Up-Regulation
Melanoma, Cutaneous Malignant
RT-qPCR
canine
cutaneous melanoma
dog
microRNAs
oral melanoma
Journal
Veterinary pathology
ISSN: 1544-2217
Titre abrégé: Vet Pathol
Pays: United States
ID NLM: 0312020
Informations de publication
Date de publication:
11 2019
11 2019
Historique:
pubmed:
19
9
2019
medline:
24
3
2020
entrez:
19
9
2019
Statut:
ppublish
Résumé
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.
Identifiants
pubmed: 31526125
doi: 10.1177/0300985819868646
doi:
Substances chimiques
Biomarkers, Tumor
0
MicroRNAs
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM