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Published on: November 24, 2014
The effects of oncolytic reovirus in canine lymphoma cell lines
C C Hwang1, S Umeki1, M Igase2
1Laboratory of Molecular Diagnostics and Therapeutics, The United Graduate School of Veterinary Science, Yamaguchi University, Yamaguchi, Japan.
Abstract:
Reovirus is a potent oncolytic virus in many human neoplasms that has reached phase II and III clinical trials. Our laboratory has previously reported the oncolytic effects of reovirus in canine mast cell tumour (MCT). In order to further explore the potential of reovirus in veterinary oncology, we tested the susceptibility of reovirus in 10 canine lymphoma cell lines. Reovirus-induced cell death, virus replication and infectivity were confirmed in four cell lines with variable levels of susceptibility. The level of Ras activation varied among the cell lines with no correlation with reovirus susceptibility. Reovirus-susceptible cell lines underwent apoptosis as proven by propidium iodide (PI) staining, Annexin V-FITC/PI assay, cleavage of PARP and inhibition of cell death by caspase inhibitor. A single intratumoral injection of reovirus suppressed the growth of canine lymphoma subcutaneous tumour in NOD/SCID mice. Unlike canine MCT, canine lymphoma is less susceptible to reovirus.
Insights
Reovirus shows potential as an oncolytic virus for canine lymphoma, though less susceptible than canine mast cell tumors. Further research is needed to optimize its use in veterinary oncology.
Area of Science:
- Veterinary Oncology
- Virology
- Molecular Biology
Background:
- Reovirus demonstrates oncolytic potential in human cancers and canine mast cell tumors.
- Exploring novel viral therapies for canine cancers is crucial.
Purpose of the Study:
- To evaluate the susceptibility of canine lymphoma cell lines to reovirus.
- To investigate reovirus replication, infectivity, and cell death mechanisms in canine lymphoma.
Main Methods:
- Testing reovirus on 10 canine lymphoma cell lines.
- Assessing virus replication, infectivity, and apoptosis (propidium iodide staining, Annexin V-FITC/PI assay, PARP cleavage).
- Evaluating tumor suppression in NOD/SCID mice after intratumoral reovirus injection.
Main Results:
- Reovirus induced cell death, replication, and infectivity in four of ten canine lymphoma cell lines.
- Apoptosis was confirmed as the mechanism of cell death in susceptible cell lines.
- Reovirus injection suppressed subcutaneous canine lymphoma tumor growth in mice.
- Canine lymphoma exhibited lower susceptibility to reovirus compared to canine mast cell tumors.
Conclusions:
- Reovirus exhibits oncolytic activity against a subset of canine lymphoma cell lines.
- Canine lymphoma is less susceptible to reovirus than canine mast cell tumors.
- Reovirus warrants further investigation for veterinary oncology applications in canine lymphoma.
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