miR-106B-25 Cluster expression: a comparative human and canine osteosarcoma study

BackgroundOsteosarcoma (OS) is the most common primary malignant bone tumour in dogs and human beings, characterised by similar genetic and clinical features. With the aim to define similarities and differences in the biological aspects involved in OS progression, a comparative study was performed t...

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Published inVeterinary record open Vol. 7; no. 1; pp. e000379 - n/a
Main Authors Leonardi, Leonardo, Benassi, Maria Serena, Pollino, Serena, Locaputo, Carmen, Pazzaglia, Laura
Format Journal Article
LanguageEnglish
Published United States British Veterinary Association 01.01.2020
Blackwell Publishing Ltd
BMJ Publishing Group
Wiley
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Summary:BackgroundOsteosarcoma (OS) is the most common primary malignant bone tumour in dogs and human beings, characterised by similar genetic and clinical features. With the aim to define similarities and differences in the biological aspects involved in OS progression, a comparative study was performed to create a model to improve patient outcome.MethodsFirst, the expression of microRNAs (miRNAs) belonging to the cluster miR-106b-25 (miR-106b, miR-25 and miR-93-5p) in human and canine OS tissue was compared.ResultsmiR-25 and miR-106b presented a variable expression not significantly different from the corresponding normal bone, while miR-93-5p expression was increased in all OS specimens, with higher levels in the canine subset compared with human. Accordingly, its target p21 presented a weaker and less homogeneous immunostaining distribution in the canine group. Given the high expression of miR-93-5p in all OS specimens, the functional response of human 143B and canine DAN OS cells to miRNA inhibition was evaluated. Although p21 expression increased after miR-93-5p inhibition both at mRNA and protein level, a more significant cell response in terms of proliferation and apoptosis was seen in canine OS cells.ConclusionsIn conclusion, canine OS tissue and cell line presented higher expression levels of miR-93-5p than human OS. In addition, the introduction of miR-93-5p inhibitor caused a cell response in 143B and DAN that differed for the more intense functional impact in the canine OS cell line.
Bibliography:ObjectType-Article-1
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content type line 23
ISSN:2052-6113
2399-2050
2052-6113
DOI:10.1136/vetreco-2019-000379