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Updated: Jan 29, 2026

Induction of Mesenchymal-Epithelial Transitions in Sarcoma Cells
Published on: April 7, 2017
Anti-tumour activity of oncolytic reovirus against canine histiocytic sarcoma cells
Masaya Igase1, Kazuha Shousu2, Noriyuki Fujiki2
1Laboratory of Molecular Diagnostics and Therapeutics, The United Graduate School of Veterinary Science, Yamaguchi University, Yamaguchi, Japan.
Abstract:
Canine histiocytic sarcoma is an aggressive, fatal neoplastic disease with a poor prognosis. Lomustine is generally accepted as the first-line systemic therapy, although this compound does not provide complete regression. Therefore, research into a novel approach against canine histiocytic sarcoma is needed. However, anti-tumour effects of oncolytic therapy using reovirus against histiocytic sarcoma are unknown. Here, we showed that reovirus has oncolytic activity in canine histiocytic sarcoma cell lines in vitro and in vivo. We found that reovirus can replicate and induce caspase-dependent apoptosis in canine histiocytic sarcoma cell lines. A single intra-tumoural injection of reovirus completely suppressed the growth of subcutaneously grafted tumours in NOD/SCID mice. Additionally, we demonstrated that susceptibility to reovirus-induced cell death was attributable to the extent of expression of type I interferons induced by reovirus infection in vitro. In conclusion, oncolytic reovirus appears to be an effective treatment option for histiocytic sarcoma, and therefore warrants further investigation in early clinical trials.
Insights
Oncolytic reovirus shows promise for treating canine histiocytic sarcoma. This novel therapy demonstrated significant anti-tumour effects in cell lines and animal models, warranting further clinical trials.
Area of Science:
- Veterinary Oncology
- Viral Oncology
- Cancer Therapeutics
Background:
- Canine histiocytic sarcoma is a fatal cancer with limited treatment options.
- Current first-line therapy, lomustine, offers incomplete tumor regression.
- Novel therapeutic strategies are urgently needed for canine histiocytic sarcoma.
Purpose of the Study:
- To investigate the anti-tumour effects of oncolytic reovirus against canine histiocytic sarcoma.
- To evaluate reovirus efficacy in vitro and in vivo models.
Main Methods:
- Assessed reovirus oncolytic activity in canine histiocytic sarcoma cell lines.
- Evaluated reovirus replication and apoptosis induction.
- Tested reovirus efficacy via intra-tumoural injection in mouse models.
- Determined factors influencing susceptibility to reovirus-induced cell death.
Main Results:
- Reovirus exhibited oncolytic activity in canine histiocytic sarcoma cell lines.
- Reovirus replicated and induced caspase-dependent apoptosis in cancer cells.
- Intra-tumoural reovirus injection completely suppressed tumor growth in vivo.
- Susceptibility correlated with type I interferon expression.
Conclusions:
- Oncolytic reovirus demonstrates significant efficacy against canine histiocytic sarcoma.
- Reovirus warrants further investigation in early-stage clinical trials for this disease.
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