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Epidermal growth factor receptor expression in canine transitional cell carcinoma
Kiwamu Hanazono1, Shinya Fukumoto, Yoshio Kawamura
1Department of Small Animal Clinical Sciences, School of Veterinary Medicine, Rakuno Gakuen University, 582 Bunkyodai Midorimachi, Ebetsu-shi, Hokkaido 069-8501, Japan.
The Journal of Veterinary Medical Science
|September 17, 2014
Summary
High epidermal growth factor receptor (EGFR) protein expression is a potential diagnostic marker for canine transitional cell carcinoma (TCC). This study found significantly increased EGFR in TCC compared to normal bladders, aiding diagnosis.
Area of Science:
- Veterinary Oncology
- Molecular Pathology
- Canine Cancer Research
Background:
- Transitional cell carcinoma (TCC) is a common and often fatal urinary bladder tumor in dogs.
- Epidermal growth factor receptor (EGFR) overexpression is linked to human bladder cancer, but its role in canine TCC is unestablished.
Purpose of the Study:
- To investigate EGFR protein and mRNA expression in canine normal bladder, polypoid cystitis, and TCC.
- To determine if EGFR expression can serve as a diagnostic marker for canine TCC.
Main Methods:
- Immunohistochemistry was used to assess EGFR protein expression.
- Real-time polymerase chain reaction (PCR) was employed to quantify EGFR mRNA levels.
- Samples included normal bladder (n=5), polypoid cystitis (n=5), and TCC (n=25).
Main Results:
- EGFR protein expression was significantly higher in TCC compared to normal bladder (P<0.001) and polypoid cystitis (P<0.005).
- High EGFR protein expression showed a significant association with TCC (P<0.01), with 72% sensitivity and 100% specificity.
- A strong positive correlation (r=0.88, P<0.05) was observed between EGFR mRNA and protein levels in TCC.
Conclusions:
- Intense EGFR protein expression is significantly elevated in canine TCC.
- EGFR protein expression shows potential as a valuable diagnostic marker for canine TCC.
- The correlation between mRNA and protein expression supports EGFR's role in canine TCC pathogenesis.

