Pan-tumour analysis of COX-2 expression in dogs
Copyright © 2024 Elsevier Ltd. All rights reserved..
Cyclooxgenase-2 (COX-2) is associated with inflammatory microenvironment and tumour progression. COX-2 expression was reported in canine tumours, and anti-COX treatment showed therapeutic effects in selected tumour types. Currently, direct comparisons between different tumour types or reports were impossible due to varying evaluation protocols. Additionally, COX-2 expression in relatively uncommon tumours were yet to be evaluated. Here, we analysed COX-2 expression across various tumour types in dogs in a consistent protocol, aiming to revisit accumulated evidence in the field and report novel candidate tumours for anti-COX therapy. COX-2 expression in 32 histological types of tumours, which consisted of 347 samples in total, was investigated using immunohistochemistry followed by the Belshaw's method scoring (range: 0-12). More than the half of the samples expressed COX-2 in mast cell tumours, transitional cell carcinoma in the urinary tract, squamous cell carcinoma, liposarcoma, and melanoma, with COX-2 median scores ranging from 1-8. On the other hand, <20% tissues expressed COX-2 in the half of tumour types investigated. Overall COX-2 positive rate was 27%. In conclusion, the results confirmed COX-2 expression in the well-known COX-2-expresing tumour types and suggested novel candidate tumours for anti-COX-2 therapy. At the same time, overall COX-2 expression was low, and inter- and intra-histology heterogeneity was apparent. This study will provide a foundation reference for future research in canine tumours.
Medienart: |
E-Artikel |
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Erscheinungsjahr: |
2024 |
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Erschienen: |
2024 |
Enthalten in: |
Zur Gesamtaufnahme - volume:304 |
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Enthalten in: |
Veterinary journal (London, England : 1997) - 304(2024) vom: 18. Apr., Seite 106064 |
Sprache: |
Englisch |
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Beteiligte Personen: |
Eto, Shotaro [VerfasserIn] |
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Links: |
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Themen: |
COX-2 |
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Anmerkungen: |
Date Completed 16.04.2024 Date Revised 16.04.2024 published: Print-Electronic Citation Status MEDLINE |
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doi: |
10.1016/j.tvjl.2024.106064 |
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funding: |
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Förderinstitution / Projekttitel: |
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PPN (Katalog-ID): |
NLM367327783 |
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520 | |a Cyclooxgenase-2 (COX-2) is associated with inflammatory microenvironment and tumour progression. COX-2 expression was reported in canine tumours, and anti-COX treatment showed therapeutic effects in selected tumour types. Currently, direct comparisons between different tumour types or reports were impossible due to varying evaluation protocols. Additionally, COX-2 expression in relatively uncommon tumours were yet to be evaluated. Here, we analysed COX-2 expression across various tumour types in dogs in a consistent protocol, aiming to revisit accumulated evidence in the field and report novel candidate tumours for anti-COX therapy. COX-2 expression in 32 histological types of tumours, which consisted of 347 samples in total, was investigated using immunohistochemistry followed by the Belshaw's method scoring (range: 0-12). More than the half of the samples expressed COX-2 in mast cell tumours, transitional cell carcinoma in the urinary tract, squamous cell carcinoma, liposarcoma, and melanoma, with COX-2 median scores ranging from 1-8. On the other hand, <20% tissues expressed COX-2 in the half of tumour types investigated. Overall COX-2 positive rate was 27%. In conclusion, the results confirmed COX-2 expression in the well-known COX-2-expresing tumour types and suggested novel candidate tumours for anti-COX-2 therapy. At the same time, overall COX-2 expression was low, and inter- and intra-histology heterogeneity was apparent. This study will provide a foundation reference for future research in canine tumours | ||
650 | 4 | |a Journal Article | |
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700 | 1 | |a Shinada, Masahiro |e verfasserin |4 aut | |
700 | 1 | |a Saeki, Kohei |e verfasserin |4 aut | |
700 | 1 | |a Tsuboi, Masaya |e verfasserin |4 aut | |
700 | 1 | |a Kamoto, Satoshi |e verfasserin |4 aut | |
700 | 1 | |a Yoshitake, Ryohei |e verfasserin |4 aut | |
700 | 1 | |a Chambers, James |e verfasserin |4 aut | |
700 | 1 | |a Uchida, Kazuyuki |e verfasserin |4 aut | |
700 | 1 | |a Kato, Daiki |e verfasserin |4 aut | |
700 | 1 | |a Nishimura, Ryohei |e verfasserin |4 aut | |
700 | 1 | |a Nakagawa, Takayuki |e verfasserin |4 aut | |
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