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AnimalsAnimals
  • Article
  • Open Access

20 January 2025

13 Pages

Immunohistochemical Expression of Vascular Endothelial Growth Factor (VEGF) in Primary Canine Mast Cell Tumors and Related Regional Lymph Node Metastasis

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1
Department of Veterinary Medicine and Surgery, Agricultural and Veterinary Sciences, Universidade Estadual Paulista, Jaboticabal 14884-900, Brazil
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Department of Veterinary Medicine and Surgery, Veterinary School, Universidade Federal de Minas Gerais, Belo Horizonte 31310-250, Brazil
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Maylla Gava Patologia Veterinaria, Praia das Gaivotas, Vila Velha 29102-571, Brazil
4
Department of Veterinary Clinical Science, Jockey Club College of Veterinary Medicine, City University of Hong Kong, Kowloon, Hong Kong
This article belongs to the Section Veterinary Clinical Studies

Simple Summary

VEGF (vascular endothelial growth factor) is a cellular growth factor involved in angiogenesis. It has been detected in many canine neoplasms and it is recognized as a potential target for drug therapy. This study evaluated the immunohistochemical expression of VEGF in canine mast cell tumors and their respective lymph node metastases in order to determine the concordance of this expression and the correlation with other prognostic factors and patient survival. Only 14.3% expressed VEGF both on the primary tumor and its respective metastasis, with fair agreement (Κ = 0.250). VEGF immunolabeling had no influence on survival time.

Abstract

Vascular endothelial growth factor (VEGF) is an important regulator of angiogenesis and has been identified as an autocrine growth factor for neoplastic cells of several tumors. The aim of this study was to evaluate VEGF expression in canine mast cell tumors and their respective lymph node metastases. For this purpose, 28 patients with mast cell tumors and confirmed regional lymph node metastasis were selected. The samples were submitted for analysis with immunohistochemistry. VEGF was expressed in 14/28 patients (50%) and 35.7% of primary MCTs (10/28), and only 14.3% expressed VEGF in both the primary tumor and its respective metastasis (4/28), with fair agreement (Κ = 0.250). There was a weak correlation between VEGF and tumor size (p = 0.016, rs = 0.045). In this cohort, survival time was correlated with Kiupel grade, mitotic index, tumor necrosis, tumor location, and systemic treatment. VEGF immunolabeling had no influence on survival; however, patients with positive expression may benefit from specific therapy.

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