Effect of proteasome inhibitors on canine lymphoma cell response to CHOP chemotherapy in vitro.
Nicholas E PrevedelMiles W MeeGeoffrey A WoodBrenda Lynn CoomberPublished in: Veterinary and comparative oncology (2024)
The standard treatment for canine lymphoma is the CHOP chemotherapy regimen. Proteasome inhibitors have been employed with CHOP for the treatment of human haematological malignancies but remain to be fully explored in canine lymphoma. We identified an association between poor response to CHOP chemotherapy and high mRNA expression levels of proteasomal subunits in a cohort of 15 canine lymphoma patients, and sought to determine the effect of proteasome inhibitors on the viability of a canine B-cell lymphoma cell line (CLBL-1). The aim of this study was to investigate whether proteasome inhibitors sensitize these cells to the CHOP agents doxorubicin, vincristine and cyclophosphamide (as 4-hydroxycyclophosphamide/4-HC). CLBL-1 cells were sensitive to proteasome inhibition by bortezomib and ixazomib. The IC 50 of bortezomib was 15.1 nM and of ixazomib was 59.14 nM. Proteasome inhibitors plus doxorubicin had a synergistic effect on CLBL-1 viability; proteosome inhibitors plus vincristine showed different effects depending on the combination ratio, and there was an antagonistic effect with 4-HC. These results may have clinical utility, as proteasome inhibition could potentially be used with a synergizing CHOP compound to improve responsiveness to chemotherapy for canine lymphoma patients.
Keyphrases
- diffuse large b cell lymphoma
- end stage renal disease
- newly diagnosed
- induced apoptosis
- ejection fraction
- chronic kidney disease
- locally advanced
- peritoneal dialysis
- stem cells
- endothelial cells
- photodynamic therapy
- cell cycle arrest
- low dose
- prognostic factors
- single cell
- squamous cell carcinoma
- multiple myeloma
- patient reported outcomes
- cell therapy
- signaling pathway
- mesenchymal stem cells
- high dose
- cancer therapy
- cell proliferation
- combination therapy