Abstract
Human epidermal growth factor receptor (HER2) is a tumor biomarker that when overexpressed and/or amplified is associated with a poor prognosis for women with breast cancer. This specific tumor subtype is eligible for a specific immunotherapy that increases survival period. However, in feline oncology, only a few studies have been performed on molecular characterization of feline (fHER2) in feline mammary carcinoma (FMC), and the available data are inconsistent. In this study, fHER2 protein levels and gene status in FMC were evaluated by immunohistochemistry and in situ hybridization. After being optimized, these techniques revealed that fHER2 is overexpressed in 33% of FMC cases, although fHER2 and fTOP2A gene amplification could not be observed. Our results support the possibility of using FMC as a natural model for comparative oncology. Additional data obtained may also improve the diagnostics, and consequently the treatment, of this type of tumor in veterinary medicine.
| Original language | English |
|---|---|
| Pages (from-to) | 876-882 |
| Number of pages | 7 |
| Journal | Microscopy and Microanalysis |
| Volume | 19 |
| Issue number | 4 |
| DOIs | |
| Publication status | Published - 1 Aug 2013 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- Feline human epidermal growth factor receptor-2 gene homolog (fHER2)
- Feline mammary carcinomas (FMC)
- Feline topoisomerase 2 alpha gene homolog (fTOP2A)
- Gene amplification
- Immunohistochemistry (IHC)
- In situ hybridization (ISH)
- Protein overexpression
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