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  3. Immunohistochemical Investigation into Protein Expression Patterns of FOXO4, IRF8 and LEF1 in Canine Osteosarcoma.
 

Immunohistochemical Investigation into Protein Expression Patterns of FOXO4, IRF8 and LEF1 in Canine Osteosarcoma.

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BORIS DOI
10.48350/197091
Date of Publication
May 20, 2024
Publication Type
Article
Division/Institute

Institut für Tierpath...

Contributor
De Brot, Simone Danielle
Institut für Tierpathologie (ITPA) - Labor Krebstherapieresistenz
Institut für Tierpathologie (ITPA) - Lehre & Diagnostik
Cobb, Jack
Alibhai, Aziza A
Jackson-Oxley, Jorja
Haque, Maria
Patke, Rodhan
Harris, Anna E
Woodcock, Corinne L
Lothion-Roy, Jennifer
Varun, Dhruvika
Thompson, Rachel
Gomes, Claudia
Kubale, Valentina
Dunning, Mark D
Jeyapalan, Jennie N
Mongan, Nigel P
Rutland, Catrin S
Subject(s)

600 - Technology::630...

Series
Cancers
ISSN or ISBN (if monograph)
2072-6694
Publisher
MDPI AG
Language
English
Publisher DOI
10.3390/cancers16101945
PubMed ID
38792023
Uncontrolled Keywords

cancer identification...

Description
Osteosarcoma (OSA) is the most common type of primary bone malignancy in people and dogs. Our previous molecular comparisons of canine OSA against healthy bone resulted in the identification of differentially expressed protein-expressing genes (forkhead box protein O4 (FOXO4), interferon regulatory factor 8 (IRF8), and lymphoid enhancer binding factor 1 (LEF1)). Immunohistochemistry (IHC) and H-scoring provided semi-quantitative assessment of nuclear and cytoplasmic staining alongside qualitative data to contextualise staining (n = 26 patients). FOXO4 was expressed predominantly in the cytoplasm with significantly lower nuclear H-scores. IRF8 H-scores ranged from 0 to 3 throughout the cohort in the nucleus and cytoplasm. LEF1 was expressed in all patients with significantly lower cytoplasmic staining compared to nuclear. No sex or anatomical location differences were observed. While reduced levels of FOXO4 might indicate malignancy, the weak or absent protein expression limits its primary use as diagnostic tumour marker. IRF8 and LEF1 have more potential for prognostic and diagnostic uses and facilitate further understanding of their roles within their respective molecular pathways, including Wnt/beta-catenin/LEF1 signalling and differential regulation of tumour suppressor genes. Deeper understanding of the mechanisms involved in OSA are essential contributions towards the development of novel diagnostic, prognostic, and treatment options in human and veterinary medicine contexts.
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/177653
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cancers-16-01945-v2.pdftextAdobe PDF5.15 MBAttribution (CC BY 4.0)publishedOpen
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