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Published on: August 23, 2019
[Mechanism Underlying the Inhibitory Effect of MiR-532-3p on the Cells Proliferation of Diffuse Large B-Cell
Yan Zhang1, Qian Yao1, Jian-Jun Jin1
1The First School of Clinic Medicine, Lanzhou University; Lanzhou 730000, Gansu Province, China.
Objective:
To investigate the effects and underlying mechanism of miR-532-3p and resibufogenin (RES) by regulating Wnt/β-catenin signaling on diffuse Large B-cell lymphoma (DLBCL) cells proliferation.
Methods:
DLBCL tissues and adjacent normal tissues were collected from patients had been diagnosed with DLBCL at the First Hospital of Lanzhou University from October 2019 to October 2021. Four groups including mimics-NC, miR-532-3p mimics, RES control and RES treatment in SU-DHL-4 cells were designed. The expression level of miR-532-3p was detected by RT-qPCR. The protein content of β-catenin was detected by Western blot. MTT assay was used to detect the proliferation activity of SU-DHL-4 cells.
Results:
miR-532-3p expression was significantly decreased in DLBCL tissues compared with adjacent normal tissues (P<0.001). The miR-532-3p content in lymphoma cells was significantly lower than that in normal lymphocytes (P<0.001). After overexpression of miR-532-3p, the viability of SU-DHL 4 cells was significantly decreased (P<0.001), with a reduced expression of β-catenin (P<0.05). RES treatment inhibited the proliferation of SU-DHL-4 cells and decreased β-catenin expression in SU-DHL-4 cells compared with the control group.
Conclusion:
Overexpression of miR-532-3p reduced Wnt/β-catenin signaling and inhibited the proliferation of lymphoma cells. Moreover, RES treatment inhibited lymphoma cells growth partially through Wnt/β-catenin signaling suppression.
Insights
This study shows that increasing miR-532-3p levels and using resibufogenin (RES) can inhibit the growth of diffuse Large B-cell lymphoma (DLBCL) cells by affecting Wnt/β-catenin signaling. Both strategies show promise in targeting lymphoma cell proliferation.
Area of Science:
- Oncology
- Molecular Biology
- Biochemistry
Background:
- Diffuse Large B-cell lymphoma (DLBCL) is an aggressive non-Hodgkin lymphoma.
- The Wnt/β-catenin signaling pathway plays a critical role in the pathogenesis and progression of various cancers, including DLBCL.
- Identifying novel therapeutic targets and agents for DLBCL is crucial.
Purpose of the Study:
- To investigate the therapeutic potential of miR-532-3p and resibufogenin (RES) in DLBCL.
- To elucidate the underlying mechanism involving the regulation of Wnt/β-catenin signaling by miR-532-3p and RES in DLBCL cells.
- To assess the impact of these interventions on DLBCL cell proliferation.
Main Methods:
- Analysis of miR-532-3p expression in DLBCL tissues and adjacent normal tissues.
- In vitro experiments using SU-DHL-4 cells treated with miR-532-3p mimics and resibufogenin (RES).
- Detection of miR-532-3p expression via RT-qPCR, β-catenin protein levels via Western blot, and cell proliferation via MTT assay.
Main Results:
- miR-532-3p expression was significantly downregulated in DLBCL tissues and cells compared to normal controls.
- Overexpression of miR-532-3p significantly reduced SU-DHL-4 cell viability and decreased β-catenin expression.
- RES treatment inhibited DLBCL cell proliferation and suppressed β-catenin expression.
Conclusions:
- Overexpression of miR-532-3p effectively inhibits DLBCL cell proliferation by suppressing the Wnt/β-catenin signaling pathway.
- Resibufogenin (RES) demonstrates anti-proliferative effects on lymphoma cells, partly through the inhibition of Wnt/β-catenin signaling.
- Both miR-532-3p and RES represent potential therapeutic strategies for DLBCL.
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