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1.
J Comp Pathol ; 173: 49-57, 2019 Nov.
Article in English | MEDLINE | ID: mdl-31812173

ABSTRACT

Malignant melanomas (MMs) represent 7% of all malignant neoplasms in dogs. Oral melanocytic neoplasms are often malignant and associated with poor prognosis. There are no universally accepted prognostic markers for canine oral melanoma. Galectin (Gal)-3 is a prognostic marker for human neoplasms such as thyroid, gastric, colorectal and prostate cancers. The protein is related to processes that favour cancer progression, such as angiogenesis, proliferation and apoptosis. The aim of the present study was to characterize the immunohistochemical expression of Gal-3 in canine oral melanomas and to compare it with post-surgical survival, the expression of apoptosis-related proteins and other known prognostic tools. Twenty-seven samples of canine oral melanomas were evaluated for Gal-3, B-cell lymphoma (BCL) 2, caspase (CASP) 3 and Ki67 expression, mitotic index and degree of nuclear atypia. Gal-3 cytoplasmic positivity was correlated positively, while nuclear positivity was correlated negatively, with survival. The intensity of BCL2 labelling was also correlated positively with Gal-3 cytoplasmic positivity. Higher nuclear atypia was observed in dogs with melanoma that died due to the tumour, as well as in dogs that survived for <1 year after surgery. We have confirmed the importance of nuclear atypia for MMs and suggest that Gal-3 is a valuable prognostic indicator for this neoplasm. More in-depth studies are needed to unveil Gal-3 functions in canine MMs using larger sample sizes.


Subject(s)
Biomarkers, Tumor/metabolism , Dog Diseases , Galectin 3/metabolism , Melanoma/veterinary , Mouth Neoplasms/veterinary , Animals , Biomarkers, Tumor/analysis , Dog Diseases/metabolism , Dog Diseases/pathology , Dogs , Galectin 3/analysis
2.
Vet Comp Oncol ; 15(2): 606-614, 2017 Jun.
Article in English | MEDLINE | ID: mdl-27041588

ABSTRACT

Canine mast cell tumour (MCT) is a biologically heterogeneous disease. The extracellular matrix degradation promoted by matrix metalloproteinases (MMPs) has been studied in an attempt to elucidate the mechanisms involved in the biological behaviour of tumours. The aim of this study was to characterize the expression of MMP-2 and -9 and tissue inhibitors of metalloproteinase (TIMP)-1 and -2 in canine cutaneous MCTs and to evaluate their prognostic values. Immunohistochemical staining for MMP-2, MMP-9, TIMP-2 and TIMP-1 was performed in 46 canine cases of MCTs. TIMP-1 expression showed an independent prognostic value for post-surgical survival and disease-related mortality. Dogs with MCTs showing less than 22.9% mast cell TIMP-1 positivity were more prone to die because of the disease and had a shorter post-surgical survival. This article suggests the involvement of TIMP-1 in MCT progression, by contributing to a good outcome in patients with MCTs.


Subject(s)
Dog Diseases/enzymology , Mastocytoma, Skin/veterinary , Tissue Inhibitor of Metalloproteinase-1/metabolism , Animals , Dog Diseases/diagnosis , Dog Diseases/mortality , Dogs , Female , Male , Mastocytoma, Skin/diagnosis , Mastocytoma, Skin/enzymology , Mastocytoma, Skin/mortality , Matrix Metalloproteinase 2/metabolism , Matrix Metalloproteinase 9/metabolism , Prognosis , Survival Analysis , Tissue Inhibitor of Metalloproteinase-2/metabolism
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