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Published on: October 11, 2019
Expression profile of immunoregulatory factors in canine tumors
Kohei Murakami1, Saki Miyatake1, Jiro Miyamae1
1Laboratory of Immunology, Faculty of Veterinary Medicine, Okayama University of Science, Imabari, Ehime 794-8555, Japan.
Abstract:
Cancers utilize a variety of molecules to escape host immune responses. Better understanding the immune environment surrounding cancer may facilitate application of innovative cancer immunotherapies, such as immune checkpoint inhibitors, to dogs as well as humans. In this study, we screened the expression of 20 immune regulatory molecules in diverse canine tumors (n = 59). Quantitative RT-PCR (qPCR) analysis revealed that some immune regulatory molecules, such as LGALS9 (coding Galectin-9) and CD48, were expressed in most canine tumors, but other molecules, such as CD274 (coding PD-L1), IL4I1, PVR, TNFSF18, ICOSLG, and TNFSF4, were rarely expressed. NECTIN2 was highly expressed in epithelial tumors but was low in non-epithelial tumors. In contrast, VSIR and CD200 expressions were low in epithelial tumors but high in non-epithelial tumors. Interestingly, several tumors expressed distinctive immunoregulatory factors. Hepatocellular carcinomas expressed FGL1, mast cell tumors expressed PDCD1LG2 (coding PD-L2), transitional cell carcinomas expressed VTCN1 (coding B7x), and lymphomas and squamous cell carcinomas expressed CD70. Consistent with qPCR results, immunofluorescence staining confirmed that hepatocellular carcinomas expressed FGL-1 protein. Thus, this study reveals the expression profile of immunoregulatory molecules in canine tumors and opens the door to better understanding the relationship between canine tumors and host immunity.
Insights
This study maps immune molecules in canine tumors, finding Galectin-9 and CD48 are common. This research aids developing novel immunotherapies for canine cancers, similar to human treatments.
Area of Science:
- Veterinary Oncology
- Immunology
- Molecular Biology
Background:
- Cancers employ immune evasion strategies.
- Understanding the tumor immune microenvironment is crucial for developing effective immunotherapies.
- Canine cancer research can inform human cancer treatment strategies.
Purpose of the Study:
- To profile the expression of 20 immune regulatory molecules across diverse canine tumors.
- To identify potential therapeutic targets for canine cancer immunotherapy.
Main Methods:
- Quantitative RT-PCR (qPCR) was used to screen molecule expression in 59 canine tumors.
- Immunofluorescence staining confirmed protein expression for specific molecules.
Main Results:
- Galectin-9 (LGALS9) and CD48 were widely expressed across canine tumors.
- Programmed Death-Ligand 1 (CD274) and others were rarely expressed.
- Specific molecules like FGL1, PD-L2, B7x (VTCN1), and CD70 showed distinct expression patterns in certain tumor types (e.g., hepatocellular carcinoma, mast cell tumors, transitional cell carcinomas, lymphomas, squamous cell carcinomas).
- NECTIN2 and VSIR/CD200 expression varied between epithelial and non-epithelial tumors.
Conclusions:
- This study provides a comprehensive expression profile of immune regulatory molecules in canine tumors.
- The findings highlight specific molecules and tumor types that may benefit from targeted immunotherapies.
- This research advances the understanding of canine anti-tumor immunity and supports the development of novel veterinary cancer treatments.
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