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Published on: June 6, 2025
[TLR4 signals are involved in multiple myeloma cell proliferation and apoptosis]
Han-Ying Bao1, Li-Juan Wang, Yang Yang
1The First Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou 310003, China.
Objective:
To investigate the TLR4 signaling in multiple myeloma cell proliferation and apoptosis.
Methods:
TLR4 gene transcription and protein expression were detected by RT-PCR and PE flow cytometry staining; the cells proliferation were detected by MTT assay; doxorubicin-induced apoptosis of cells was detected by AnnexinV-PI double staining flow cytometry.
Result:
TLR4 gene transcription and protein expression was detected in the myeloma cell lines. Under the lipopolysaccharides (LPS) stimulation, MM1-s cells TLR4 positive proliferation significantly increased (P<0.05), but not found in U266 cells TLR4 negative; MM1-s cells showed the resistance to doxorubisin-induced apoptosis, but LPS did not protect doxorubicin-induced U266 cell apoptosis.
Conclusion:
TLR4 signaling may play an important role both in multiple myeloma proliferation and survival.
Insights
Toll-like receptor 4 (TLR4) signaling promotes multiple myeloma cell proliferation and enhances resistance to doxorubicin-induced apoptosis, suggesting a key role in cancer survival.
Area of Science:
- Immunology
- Oncology
- Molecular Biology
Context:
- Multiple myeloma (MM) is a hematological malignancy characterized by uncontrolled proliferation of plasma cells.
- The role of Toll-like receptor 4 (TLR4) signaling in MM pathogenesis remains incompletely understood.
- Investigating TLR4's impact on MM cell behavior is crucial for developing targeted therapies.
Purpose:
- To elucidate the function of TLR4 signaling in multiple myeloma cell proliferation.
- To determine the effect of TLR4 activation on doxorubicin-induced apoptosis in myeloma cells.
- To analyze TLR4 gene and protein expression in MM cell lines.
Summary:
- TLR4 gene and protein expression were assessed in MM cell lines using RT-PCR and flow cytometry.
- Lipopolysaccharide (LPS) stimulation significantly increased proliferation in TLR4-positive MM1-s cells, but not in TLR4-negative U266 cells.
- MM1-s cells exhibited resistance to doxorubicin-induced apoptosis, while LPS did not confer protection in U266 cells.
Impact:
- TLR4 signaling is implicated in promoting multiple myeloma cell proliferation.
- TLR4 activation may contribute to chemoresistance by inhibiting apoptosis.
- Findings suggest TLR4 as a potential therapeutic target for overcoming MM progression and drug resistance.
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