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Oncolytic Myxoma virus Increases Autophagy in Multiple Myeloma
Alpay Yeşilaltay1, Dilek Muz2, Berna Erdal3
1Başkent University İstanbul Hospital, Department of Hematology, İstanbul, Türkiye
Objective:
Multiple myeloma, which affects plasma cells, is the second most common hematological malignancy. Despite the development of new drugs and treatment protocols, patient survival has not reached the desired level. In this study, we investigated the effects of Myxoma virus (MYXV), an oncolytic virus, on autophagy in myeloma cells.
Materials And Methods:
We analyzed protein expressions of ATG-5, p62, Beclin-1, LC3B, and the apoptosis marker Bcl-2 as autophagy markers in human U-266 and mouse MOPC-315 myeloma cell lines subjected to different doses of MYXV. In addition, autophagic images of myeloma cells were investigated using transmission electron microscopy (TEM).
Results:
In the first 24 h, which is the early stage of autophagy, ATG-5 and Beclin-1 expression levels were increased in the U-266 and MOPC-315 cell lines in the groups that had received MYXV at a multiplicity of infection of 15. At 48 h, a significant increase was detected in the expression of LC3B, which is a late indicator. Autophagosomes were observed in myeloma cells by TEM.
Conclusion:
MYXV shows an antimyeloma effect by increasing autophagy in myeloma cells.
Insights
Myxoma virus (MYXV) increases autophagy in multiple myeloma cells, demonstrating an anti-myeloma effect. This study explored MYXV
Area of Science:
- Oncology
- Virology
- Cell Biology
Background:
- Multiple myeloma is a prevalent hematological malignancy affecting plasma cells.
- Current treatments for multiple myeloma have limitations in improving patient survival rates.
- Oncolytic viruses are being explored as a therapeutic strategy for cancer treatment.
Purpose of the Study:
- To investigate the impact of Myxoma virus (MYXV) on autophagy in multiple myeloma cells.
- To evaluate MYXV as a potential therapeutic agent against multiple myeloma.
Main Methods:
- Analyzed autophagy markers (ATG-5, p62, Beclin-1, LC3B) and apoptosis marker (Bcl-2) protein expression.
- Utilized human U-266 and mouse MOPC-315 myeloma cell lines.
- Employed transmission electron microscopy (TEM) to visualize autophagosomes.
Main Results:
- MYXV treatment increased ATG-5 and Beclin-1 expression within 24 hours in myeloma cell lines.
- A significant increase in the late autophagy indicator LC3B was observed at 48 hours post-MYXV treatment.
- TEM confirmed the presence of autophagosomes in MYXV-treated myeloma cells.
Conclusions:
- Myxoma virus (MYXV) induces autophagy in multiple myeloma cells.
- MYXV exhibits an anti-myeloma effect through the induction of autophagy.
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