Peer-reviewed veterinary case report
Galectin-3 and BCL2 protein link in dog skin mast cell tumors
By Vargas, Thiago Henrique M et al.·Published in Acta veterinaria Hungarica·2021·1Laborató, Brazil·View original on PubMed →
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Original publication title: Galectin-3 immunolabelling correlates with BCL2 expression in canine cutaneous mast cell tumours.
- Species:
- dog
Plain-English summary
A study looked at skin tumors called mast cell tumors (MCTs) in dogs, which are the most common type of skin cancer in these pets. Researchers examined 34 cases of MCTs that had been surgically removed to see if a protein called Galectin-3 (Gal-3) could help predict how aggressive the cancer might be. They found that while Gal-3 was present in many of the tumors, it didn't provide clear information about the tumor's behavior or the dog's survival after surgery. This means that while Gal-3 is linked to another protein called BCL2, it may not be a reliable way to judge the seriousness of MCTs in dogs.
People also search for: dog skin tumor treatment · mast cell tumor prognosis in dogs · Galectin-3 in canine cancer
Abstract
Mast cell tumour (MCT) is the most frequent skin neoplasm in dogs. These tumours are characterised by variable behaviour and clinical presentation that make prognosis an important and challenging task in the veterinary practice. Galectin-3 (Gal-3) is known to influence several biological processes that are important in the cancer context and has been described as a prognostic marker for several human cancers. The aim of the present work was to characterise Gal-3 immunolabelling in canine cutaneous MCTs and to investigate its value as a prognostic marker for the disease. Thirty-four random cases of canine cutaneous MCT that were surgically treated with wide margins were included in this study. Gal-3 expression was evaluated using immunohistochemistry and the results were compared with the expression of apoptosis-related proteins, Ki67 index, histopathological grades, mortality due to the disease and post-surgical survival. The majority of the MCTs (65.8%) were positive for Gal-3. Gal-3 immunolabelling was variable among the samples (2.7%-86.8% of the neoplastic cells). The protein was located in the cytoplasm or in the cytoplasm and the nucleus. Gal-3 positivity was correlated with BCL2 expression (P < 0.001; r = 0.604), but not with Ki67 and BAX. No significant differences were detected between histological grades or in the survival analysis. Gal-3 expression correlates with BCL2 expression in MCTs. Although an efficient marker for several human neoplasms, the results presented herein suggest that Gal-3 immunolabelling is not an independent prognostic indicator for this disease.
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Search related cases →Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/34111022/