# Differential HER2 Expression Across Feline Nasal Carcinoma and Its Relationship with Proliferation and p53 Status

**Authors:** Maral Anjomanibenisi, Ginevra Martinoli, Michele Olei, Barbara Bacci, Barbara Brunetti

PMC · DOI: 10.3390/vetsci13030212 · Veterinary Sciences · 2026-02-25

## TL;DR

This study examines feline nasal carcinomas, finding that HER2 overexpression is common in adenocarcinomas, suggesting a potential target for future treatments.

## Contribution

The study identifies HER2 as a potential biomarker for feline nasal adenocarcinomas, offering new insights for targeted therapies.

## Key findings

- HER2 overexpression was detected in approximately one-third of feline nasal carcinomas, particularly in adenocarcinomas.
- p53 expression was uncommon and observed exclusively in non-adenocarcinoma tumors.
- Ki-67 proliferation indices were low, while PCNA showed high positivity across all cases.

## Abstract

Feline nasal carcinomas are rare, locally aggressive malignant tumors that typically occur in older cats. Information on their biological and immunohistochemical features is still limited. In this study, 23 feline nasal carcinomas were evaluated to describe their histological characteristics and the expression of selected immunohistochemical markers, including Ki-67, PCNA, p53, and HER2. Most tumors were adenocarcinomas, particularly of the acinar subtype. Ki-67 expression was generally low, while PCNA showed high positivity in all cases. p53 expression was uncommon. Notably, HER2 overexpression was detected in approximately one-third of the tumors, particularly in adenocarcinomas. These results provide baseline immunohistochemical data for feline nasal carcinomas and identify HER2 as a potential biomarker for future diagnostic and therapeutic investigations.

Feline nasal carcinomas are rare but clinically aggressive neoplasms. This study characterizes their histopathological features and evaluates HER2, p53, Ki-67, and PCNA expression using immunohistochemistry and digital image analysis, aiming to provide a comprehensive biological characterization with potential prognostic and therapeutic implications. Tumors were classified into adenocarcinomas (AC) and non-adenocarcinomas (non-AC). Among the 23 cases examined, adenocarcinoma was the most common subtype (17 cases). HER2 was scored as 3+ in 7 cases, 2+ in 8 cases, 1+ in 5 cases, and 3 cases were scored 0. A statistically significant association was found between histological type and HER2 expression (Fisher’s exact test, p = 0.02), with a higher prevalence of HER2 positivity in adenocarcinomas. Evaluation of p53 expression according to histological grouping showed a trend toward significance (p = 0.0593), with p53 positivity observed exclusively in non-AC. The Ki-67 index had a median of 4.4 (min 0.5, max 21.06), and the PCNA index had a median of 82.26 (min 19.55, max 100). No significant associations were identified between the Ki-67 labeling index and HER2 expression, histotype, and the inflammatory infiltrate. Finally, Pearson correlation analysis revealed no significant correlation between Ki-67 and PCNA indices (p = 0.32). The overexpression of HER2 lays the groundwork for the possible use of anti-HER2 targeted drugs in this tumor type, particularly in adenocarcinomas. These findings provide baseline immunohistochemical data for feline nasal carcinomas and highlight HER2 as a relevant biomarker for future diagnostic and therapeutic research.

## Linked entities

- **Genes:** ERBB2 (erb-b2 receptor tyrosine kinase 2) [NCBI Gene 2064], TP53 (tumor protein p53) [NCBI Gene 7157], Mki67 (antigen identified by monoclonal antibody Ki 67) [NCBI Gene 17345], PCNA (proliferating cell nuclear antigen) [NCBI Gene 5111]

## Full-text entities

- **Genes:** HER2 [NCBI Gene 751824], PCNA [NCBI Gene 101080704], S100A1 (S100 calcium binding protein A1) [NCBI Gene 6271] {aka S100, S100-alpha, S100A}, PCNA (proliferating cell nuclear antigen) [NCBI Gene 5111] {aka ATLD2}, ERBB2 (erb-b2 receptor tyrosine kinase 2) [NCBI Gene 2064] {aka CD340, HER-2, HER-2/neu, HER2, MLN 19, MLN-19}, COX2 (cytochrome c oxidase subunit II) [NCBI Gene 4513] {aka COII, MTCO2}, TP53 (tumor protein p53) [NCBI Gene 7157] {aka BCC7, BMFS5, LFS1, P53, TRP53}, TP53 [NCBI Gene 493847]
- **Diseases:** Acinar adenocarcinoma (MESH:D018267), paranasal sinus tumors (MESH:D010255), rhinitis (MESH:D012220), Papillary adenocarcinoma (MESH:D000231), sinonasal carcinoma (MESH:C537344), Tumor (MESH:D009369), breast cancer (MESH:D001943), epistaxis (MESH:D004844), cell (MESH:D002292), necrosis (MESH:D009336), lymphoma (MESH:D008223), oral squamous cell carcinoma (MESH:D000077195), Squamous cell carcinoma (MESH:D002294), inflammatory (MESH:D007249), AC (MESH:D000230), Transitional carcinoma (MESH:D002295), injury to (MESH:D014947), facial deformity (MESH:D005153), H&amp;E (MESH:D016751), sarcomas (MESH:D012509), hemorrhage (MESH:D006470), neoplastic disease (MESH:D004194), metastases (MESH:D009362), nasal carcinogenesis (MESH:D063646), pulmonary carcinomas (MESH:D008175), Non-Small Cell lung cancer (MESH:D002289), Feline nasal carcinomas (MESH:D009669), nasal mass (MESH:D009668), Undifferentiated carcinoma (MESH:D002277), dyspnea (MESH:D004417), pulmonary (MESH:D008171)
- **Chemicals:** formalin (MESH:D005557), paraffin (MESH:D010232), methanol (MESH:D000432), H&amp;E (MESH:D006371), H2O2 (MESH:D006861), Hematoxylin (MESH:D006416), 3-amino-9-ethylcarbazole (MESH:C020702), citrate (MESH:D019343), ABC (-), ethanol (MESH:D000431), 3,3'-diaminobenzidine (MESH:D015100), Eosin (MESH:D004801), DAB (MESH:C000469)
- **Species:** Canis lupus familiaris (dog, subspecies) [taxon 9615], Felis catus (cat, species) [taxon 9685], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13030173/full.md

## References

48 references — full list in the complete paper: https://tomesphere.com/paper/PMC13030173/full.md

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Source: https://tomesphere.com/paper/PMC13030173