Protease-Activated Receptor-2 Is Associated With Adverse Outcomes in Canine Mammary Carcinoma.


Journal

Veterinary pathology
ISSN: 1544-2217
Titre abrégé: Vet Pathol
Pays: United States
ID NLM: 0312020

Informations de publication

Date de publication:
01 2021
Historique:
pubmed: 16 10 2020
medline: 18 9 2021
entrez: 15 10 2020
Statut: ppublish

Résumé

Protease-activated receptor-2 (PAR2) is a G protein-coupled receptor that is activated by serine proteases. In humans, PAR2 is highly expressed in various cancers, including breast cancer, and is associated with cancer progression and metastasis. However, the expression and roles of PAR2 in canine mammary carcinoma remain unclear. The purpose of this study was to examine the expression of PAR2 in canine mammary carcinoma, the association between PAR2 expression and clinical characteristics, and the role of PAR2 in the metastatic phenotypes of tumor cells. Mammary carcinoma from 31 dogs and 10 normal mammary glands were included in this study, and used for immunohistochemical analysis of PAR2 expression. Normal mammary glands did not express PAR2. In contrast, mammary carcinomas showed PAR2 immunoreactivity in the cytoplasm, and its expression level varied between specimens from negative to strongly positive. The overall survival of dogs with high PAR2 expression was shorter than that of dogs with low PAR2 expression. Moreover, PAR2 expression level was associated with the presence of lymph node involvement, advanced clinical stage, and high histopathological grade. In vitro analyses revealed that a PAR2 agonist accelerated cell migration and invasion in a canine mammary carcinoma cell line. In addition, the PAR2 agonist induced epithelial-mesenchymal transition and actin polymerization. These results suggest that PAR2 expression plays a role in tumor progression and clinical outcomes in canine mammary carcinoma.

Identifiants

pubmed: 33054598
doi: 10.1177/0300985820963087
doi:

Substances chimiques

Receptor, PAR-2 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

53-62

Auteurs

Kenjiro Kaji (K)

Department of Veterinary Clinical Pathobiology, Graduate School of Agricultural and Life Sciences, 13143The University of Tokyo, Japan.

Noriyuki Kaji (N)

Department of Veterinary Clinical Pathobiology, Graduate School of Agricultural and Life Sciences, 13143The University of Tokyo, Japan.

Masatoshi Hori (M)

Department of Veterinary Clinical Pathobiology, Graduate School of Agricultural and Life Sciences, 13143The University of Tokyo, Japan.

Kosei Sakai (K)

Department of Veterinary Clinical Pathobiology, Graduate School of Agricultural and Life Sciences, 13143The University of Tokyo, Japan.

Tomohiro Yonezawa (T)

Department of Veterinary Clinical Pathobiology, Graduate School of Agricultural and Life Sciences, 13143The University of Tokyo, Japan.

Shingo Maeda (S)

Department of Veterinary Clinical Pathobiology, Graduate School of Agricultural and Life Sciences, 13143The University of Tokyo, Japan.

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Classifications MeSH