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Immunohistochemistry Screening of Different Tyrosine Kinase Receptors in Canine Solid Tumors—Part I: Proposal of a Receptor Panel to Predict Therapies

dc.contributor.authorDos Anjos, Denner Santos [UNESP]
dc.contributor.authorCiva, Patrick Antônio Sonaglio
dc.contributor.authorWerner, Juliana
dc.contributor.authorVicente, Igor Simões Tiagua
dc.contributor.authorFonseca-Alves, Carlos Eduardo [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.contributor.institutionMedicalvet Veterinary Clinic
dc.contributor.institutionWerner and Werner Laboratory
dc.contributor.institutionVetPrecision Laboratory
dc.contributor.institutionIOVET
dc.date.accessioned2025-04-29T20:01:53Z
dc.date.issued2024-08-01
dc.description.abstractThe use of tyrosine kinase inhibitors (TKI) has been growing in veterinary oncology and in the past few years several TKI have been tested in dogs. However, different from human medicine, we lack strategies to select patients to be treated with each TKI. Therefore, this study aimed to screen different tumor subtypes regarding TKI target immunoexpression as a predictor strategy to personalize the canine cancer treatment. It included 18 prostatic carcinomas, 36 soft tissue sarcomas, 20 mammary gland tumors, 6 urothelial bladder carcinomas, and 7 tumors from the endocrine system. A total of 87 patients with paraffin blocks were used to perform immunohistochemistry (IHC) of human epidermal growth factor receptor 2 (HER-2), epidermal growth factor receptors 1 (EGFR1), vascular endothelial growth factor receptor 2 (VEGFR-2), platelet derived growth factor receptor beta (PDGFR-β), c-KIT, and extracellular signal-regulated kinase 1/2 (ERK1/ERK2). The immunohistochemical screening revealed a heterogeneous protein expression among histological types with mesenchymal tumors showing the lowest expression level and carcinomas the highest expression. We have demonstrated by IHC screening that HER2, EGFR1, VEGFR-2, PDGFR-β and ERK1/ERK2 are commonly overexpressed in dogs with different carcinomas, and KIT expression is considered relatively low in the analyzed samples.en
dc.description.affiliationDepartment of Veterinary Surgery and Animal Reproduction Universidade Estadual Paulista (UNESP)
dc.description.affiliationMedicalvet Veterinary Clinic
dc.description.affiliationWerner and Werner Laboratory
dc.description.affiliationVetPrecision Laboratory
dc.description.affiliationInstitute of Veterinary Oncology IOVET
dc.description.affiliationUnespDepartment of Veterinary Surgery and Animal Reproduction Universidade Estadual Paulista (UNESP)
dc.identifierhttp://dx.doi.org/10.3390/ijms25158438
dc.identifier.citationInternational Journal of Molecular Sciences, v. 25, n. 15, 2024.
dc.identifier.doi10.3390/ijms25158438
dc.identifier.issn1422-0067
dc.identifier.issn1661-6596
dc.identifier.scopus2-s2.0-85201049581
dc.identifier.urihttps://hdl.handle.net/11449/305029
dc.language.isoeng
dc.relation.ispartofInternational Journal of Molecular Sciences
dc.sourceScopus
dc.subjectdogs
dc.subjectepidermal growth factor
dc.subjectimmunohistochemistry
dc.subjectplatelet-derived growth factor receptor
dc.subjectreceptor tyrosine kinase
dc.subjecttarget therapy
dc.subjectvascular endothelial growth factor
dc.titleImmunohistochemistry Screening of Different Tyrosine Kinase Receptors in Canine Solid Tumors—Part I: Proposal of a Receptor Panel to Predict Therapiesen
dc.typeArtigopt
dspace.entity.typePublication
unesp.author.orcid0000-0003-1804-475X[1]
unesp.author.orcid0000-0002-6702-6139[5]

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