ReviewFrontiers in immunology2025
Comparative pathophysiology and molecular insights into cutaneous and non-cutaneous canine skin cancers: focus on melanoma, mast cell tumors, and squamous cell carcinoma.
Review in Frontiers in immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
3 citing papers in PubMed.
- Tumor-Specific Classification of Canine Cutaneous and Subcutaneous Tumors Using Heat-Diffusion Imaging and Artificial Intelligence.Veterinary sciences · 2026Article
- Serum Proteomic Analysis Using Gel-Based Liquid Chromatography Tandem Mass Spectrometry Reveals Differences Between Canine Oral Malignancies and Non-Malignant Conditions.Veterinary medicine and science · 2026Article
- Stemness and Survival: CD117Cells · 2026Article
Corrections and comments
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Authors and funding
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Skin cancer is one of the most frequently diagnosed neoplasms in dogs, encompassing a range of malignancies with significant clinical implications. Among them, mast cell tumors (MCTs), melanomas, and squamous cell carcinomas (SCCs) signify the most common and clinically relevant types, each posing distinct therapeutic challenges and exhibiting pathophysiological mechanisms. MCTs, accounting for approximately 21% of canine skin tumors, are often driven by mutations in the KIT proto-oncogene, leading to an uncontrolled proliferation of mast cells. Melanomas, while typically benign in cutaneous forms, exhibit aggressive behavior in oral and digital locations, with BRAF and NRAS mutations playing an integral role in tumor growth. Furthermore, SCCs, primarily associated with chronic ultraviolet (UV) radiation exposure, demonstrate significant genomic modifications, including mutations in TP53 and increased expression of COX-2, resulting in carcinogenesis. Accurate diagnosis of these tumors significantly relies on cytology, histopathology, and immunohistochemical markers. Moreover, advanced imaging techniques such as computed tomography (CT) and positron emission tomography (PET) can potentially enhance staging and prognostication. Treatment modalities vary based on tumor type and stage, including surgical excision, radiation therapy, chemotherapy, and emerging targeted therapies. Tyrosine kinase inhibitors (TKIs), such as toceranib phosphate (Palladia) and masitinib, have demonstrated efficacy in MCTs. Likewise, immunotherapies, including the
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