Localization of integrin αvß3 and vascular endothelial growth factor receptor-2 (KDR/Flk-1) in cutaneous and oral melanomas of dog

• N.G. Rawlings ^[1] ; E. Simko ^[1] ; T. Bebchuk ^[1] ; S.J. Caldwell ^[1] ; B. Singh ^[1]
  1. [1] University of Saskatchewan

     University of Saskatchewan

     Canadá

     
• Localización: Histology and histopathology: cellular and molecular biology, ISSN-e 1699-5848, ISSN 0213-3911, Vol. 18, Nº. 3, 2003, págs. 819-826
• Idioma: inglés
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• Resumen

  • Melanomas are common neoplasms of dogs and arise from pigment-producing cells called melanocytes or melanoblasts. Melanomas of skin are often easily cured by surgical excision, but those of oral mucosa are aggressive, metastasize to the regional lymph nodes and lungs, and respond poorly to conventional therapy. Tumor growth is sustained by proliferation of microvessels via a process called angiogenesis. Integrin α vß3 is expressed in proliferating but not in quiescent microvessels suggesting a role in angiogenesis. Vascular endothelial growth factor (VEGF) manifests its mitogenic and angiogenic effects mainly via VEGF receptor-2 (VEGFR-2/Flk-1). We conducted this immunocytochemical study to investigate the expression of integrin α vß3 and VEGFR-2 in archival and fresh samples from cases of canine melanomas. Results show that integrin α vß3 was expressed in 72% and 88% of cutaneous and oral melanomas, respectively, and the expression was restricted to and immediately around the melanocytes and endothelial cells. VEGFR-2 staining of selected cases of melanoma revealed that its expression overlapped with the α v β 3 integrin. Dual immuno-gold electron microscopy confirmed co-localization of integrin α vß3 and VEGFR-2 in melanocytes and endothelial cells. These data demonstrate expression and co-localization of integrin α vß3 and VEGFR-2 in cutaneous and oral melanomas of dogs.