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Immunohistochemical Expression of Platelet-Derived Growth Factor Receptor β (PDGFR-β) in Canine Cutaneous Peripheral
Catarina Aluai-Cunha1, Augusto Matos1,2, Irina Amorim3,4,5
1Department of Veterinary Clinics, Institute of Biomedical Sciences Abel Salazar (ICBAS), University of Porto, R. Jorge Viterbo Ferreira 228, 4050-313 Porto, Portugal.
Abstract:
As in humans, the prevalence of tumors in companion animals is increasing dramatically and there is a strong need for research on new pharmacological agents particularly for the treatment of those tumors that are resistant to conventional chemotherapy agents such as soft tissue sarcomas (STS). Because malignant (MPNST) and benign peripheral nerve sheath tumors (BPNST) are relatively common STS in dogs, the aim of this retrospective study was to evaluate the immunohistochemical (IHC) expression of PDGFR-β, contributing to its characterization as a potential target for their treatment. A total of 19 samples were included, 9 histologically classified as benign and the other 10 as malignant. The results showed diffuse immunoexpression in the cytoplasm of neoplastic cells. Six (66.7%) BPNST expressed the receptor in less than 25% of neoplastic cells and only three (33.3%) exhibited labelling in more than 25% of neoplastic cells. In contrast, all MPNST expressed PDGFR-β, and in 8 (80%) of these samples, the receptor was expressed in more than 25% of neoplastic cells, and only 2 (20%) cases expressed the receptor in less than 25% of neoplastic cells. PDGFR-β expression was significantly higher in MPNST and larger tumors, suggesting that drugs able to inhibit the activity of this tyrosine kinase receptor, such as toceranib, may be considered in the approach of unresectable tumors and/or in the context of adjuvant or neoadjuvant therapies.
Insights
Malignant peripheral nerve sheath tumors (MPNST) in dogs show higher PDGFR-β expression than benign tumors. This suggests PDGFR-β inhibitors like toceranib may treat canine soft tissue sarcomas.
Area of Science:
- Veterinary Oncology
- Cancer Biology
- Immunohistochemistry
Background:
- Companion animal tumors are increasing, necessitating novel treatments for chemotherapy-resistant cancers like soft tissue sarcomas (STS).
- Malignant (MPNST) and benign peripheral nerve sheath tumors (BPNST) are common STS in dogs, requiring targeted therapeutic strategies.
Purpose of the Study:
- To investigate the immunohistochemical (IHC) expression of PDGFR-β in canine MPNST and BPNST.
- To evaluate PDGFR-β as a potential therapeutic target for these canine soft tissue sarcomas.
Main Methods:
- Retrospective analysis of 19 canine STS samples (9 BPNST, 10 MPNST).
- Immunohistochemical staining for PDGFR-β expression in neoplastic cells.
- Quantitative assessment of PDGFR-β immunoexpression levels.
Main Results:
- PDGFR-β was diffusely expressed in the cytoplasm of neoplastic cells in all samples.
- Significantly higher PDGFR-β expression was observed in MPNST compared to BPNST.
- PDGFR-β expression correlated positively with tumor size and malignancy.
Conclusions:
- Elevated PDGFR-β expression in canine MPNST indicates its potential as a therapeutic target.
- Tyrosine kinase inhibitors targeting PDGFR-β, such as toceranib, may be beneficial for unresectable, adjuvant, or neoadjuvant therapy in canine STS.
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