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NF-Kβ Activation in U266 Cells on Mesenchymal Stem Cells
Sara Zahedi1, Karim Shamsasenjan1, Aliakbar Movassaghpour1
1Hematology and Oncology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Advanced Pharmaceutical Bulletin
|October 22, 2016
Summary
Mesenchymal stem cells (MSCs) promote Multiple Myeloma (MM) cell growth and CD54 expression. MSCs also activate the NF-κB pathway in MM cells, suggesting it as a therapeutic target.
Area of Science:
- Hematology
- Cell Biology
- Cancer Research
Background:
- Mesenchymal Stem Cells (MSCs) are key components of the bone marrow microenvironment.
- Multiple Myeloma (MM) is a significant hematological malignancy.
- MSCs influence MM cells, notably through the NF-κB signaling pathway, which is crucial for MM cell survival and drug resistance.
Purpose of the Study:
- To investigate the interaction between U266 MM cells and Umbilical Cord Blood-derived MSCs (UCB-MSCs).
- To determine the effect of UCB-MSCs on MM cell proliferation, CD54 expression, and key signaling pathways.
Main Methods:
- U266 cells were co-cultured with UCB-MSCs or their conditioned medium.
- Proliferation was assessed using MTT assay.
- CD54 expression was measured by flow cytometry.
- Gene expression (CXCL1, CCL4, IL-6, IL-8) and NF-κB pathway activation (p65 phosphorylation) were analyzed via RT-PCR and Western blotting.
Main Results:
- UCB-MSCs significantly increased U266 cell proliferation and CD54 expression.
- UCB-MSCs altered the expression of CCL4, IL-6, IL-8, and CXCL1 in U266 cells.
- Phosphorylation of p65 in the NF-κB pathway was elevated in U266 cells upon interaction with UCB-MSCs.
Conclusions:
- UCB-MSCs support MM cell proliferation and modulate immune markers.
- MSCs activate the NF-κB signaling pathway in MM cells.
- Targeting the NF-κB pathway presents a potential therapeutic strategy for MM.
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