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http://dx.doi.org/10.17555/jvc.2019.12.36.6.319

Immunohistochemical Expression of Receptor Tyrosine Kinase (RTK) in Canine Brain Tumors  

Jung, Hae-Won (Institute of Animal Medicine, College of Veterinary Medicine, Gyeongsang National University)
Song, Joong-Hyun (Institute of Animal Medicine, College of Veterinary Medicine, Gyeongsang National University)
Yu, Do-Hyeon (Institute of Animal Medicine, College of Veterinary Medicine, Gyeongsang National University)
An, Su-Jin (Institute of Animal Medicine, College of Veterinary Medicine, Gyeongsang National University)
Sur, Jung-Hyang (Department of Pathobiology, Small Animal Tumor Diagnostic Center, College of Veterinary Medicine, Konkuk University)
Kim, Young Joo (College of Veterinary Medicine, Western University of Health Sciences)
Han, Donghyun (Section of Veterinary Research and Academic Consulting, Veteran, Inc.)
Jung, Dong-In (Institute of Animal Medicine, College of Veterinary Medicine, Gyeongsang National University)
Publication Information
Journal of Veterinary Clinics / v.36, no.6, 2019 , pp. 319-324 More about this Journal
Abstract
Receptor tyrosine kinases (RTK) are major promising targets in anticancer therapy in human and veterinary medicine. Using immunohistochemistry method, we evaluated the expressionof five types RTK (PDGFR-α, PDGFR-β, VEGFR 2, c-Kit and Abl) in the six canine brain tumor samples (2 meningioma, 2 astrocytoma, 1 ependymoma and 1 choroid plexus papilloma). A total of five samples expressed PDGFR-β (5/6), one sample, the choroid plexus papilloma, expressed c-Kit (1/6), and a total of two samples expressed Abl (2/6). None of the samples showed expression of PDGFR-α and VEGFR 2. We demonstrate that a significant portion of canine brain tumors express tyrosine receptors for growth factors and show that these receptors generally localize to tumor cell membranes and the cytoplasm. Evaluation of immunohistochemical expression for the RTKs PDGFR-β, c-Kit, and Alb in canine brain samples reveals an interesting potential for molecular targeting by TKIs in therapeutic studies of canine brain tumors, and more studies will be needed to assess the interactions and efficacy of these RTKs and TKIs. Based on these results, we have some evidence for novel chemotherapeutic trials using TKIs for canine nervous tumors.
Keywords
dog; tyrosine kinase inhibitor; brain tumor; receptor tysine kinase;
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