Vimentin and Ki-67 immunolabeling in canine gastric carcinomas and their prognostic value

Author:

Flores Ana R.1234,Rêma Alexandra1,Mesquita João R.5,Taulescu Marian67ORCID,Seixas Fernanda34,Gärtner Fátima128,Amorim Irina128

Affiliation:

1. Institute of Biomedical Sciences Abel Salazar (ICBAS), University of Porto, Porto, Portugal

2. Institute of Molecular Pathology and Immunology of the University of Porto, Porto, Portugal

3. University of Trás-os-Montes and Alto Douro, Vila Real, Portugal

4. Associate Laboratory for Animal and Veterinary Sciences, Vila Real, Portugal

5. Instituto de Saúde Pública da Universidade do Porto, Porto, Portugal

6. University of Agricultural Sciences and Veterinary Medicine of Cluj-Napoca, Cluj-Napoca, Romania

7. Synevovet Laboratory, Chiajna, Romania

8. i3S-Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal

Abstract

This study evaluated the expression of vimentin and Ki-67 proliferative index (PI) by immunohistochemistry in 30 canine gastric carcinomas (GCs) and a possible association with clinical and pathological features and patient’s survival time. Vimentin immunoreactivity was assessed in neoplastic cells (in primary lesions, emboli, and metastases) and tumor-associated stroma (TAS) of canine GCs. Ki-67 PI was quantified in the neoplastic epithelial component. Vimentin immunolabeling in neoplastic cells was found in 30% of the primary lesions, in 82% of the neoplastic emboli, and in 50% of the metastases; in TAS, it was observed in all cases. A mean of 16% of the TAS was immunolabeled for vimentin. High vimentin immunolabeling in the TAS (>16%) was detected in 40% of cases. The average value of Ki-67 PI was 50%, and 80% of the lesions had Ki-67 PI above 20%. Vimentin immunolabeling in neoplastic cells was more frequent in less-differentiated carcinomas (diffuse [29%] and indeterminate types [75%]) than well-differentiated carcinomas (intestinal type [0%], P = .049). No significant differences were observed in vimentin immunolabeling in the TAS or Ki-67 PI according to histological diagnosis, depth of invasion, presence of neoplastic emboli or metastases. However, vimentin immunolabeling in the TAS was positively correlated with Ki-67 PI ( r = .394, P = .031). Furthermore, a moderate negative correlation was observed between Ki-67 PI and survival time ( r = −0.540). Our results suggest that vimentin and Ki-67 PI have potential for providing prognostic information in cases of canine GCs.

Publisher

SAGE Publications

Subject

General Veterinary

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