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Updated: Feb 16, 2026

Repression of Multiple Myeloma Cell Growth In Vivo by Single-wall Carbon Nanotube SWCNT-delivered MALAT1 Antisense Oligos
Published on: December 13, 2018
[Targeting Notch1 Gene Inhibits the Proliferation of Multiple Myeloma Cells]
Mei-Ling Li1, Mei-Qiong Chen2, Peng Zhang2
1Department of Hematology, Xiamen University Zhongshan Hospital, Xiamen 361004, Fujian Province, China; Department of Hematology, Guizhou Medical University Third Hospital, Duyun 558000, Guizhou Province, China.
Objective:
To investigate the effects of Notch1 gene silencing on the proliferation and apoptosis of multiple myeloma cells, and to find the new targets for the treatment of multiple myeloma.
Methods:
Notch1-shRNA targeted silencing Notch1 gene was transfected into multiple myeloma RPMI8226 cells, the CCK-8 and flow cytometry were used to detect the proliferation and apoptosis of myeloma cells after Notch1-shRNA transfection, the real-time fluorescence quantitative PCR was used to analyze expression level of Notch1 mRNA, and the Western blot were used to detect the expression level of Notch1 signaling pathway-related protein, such as Hes-1, Jagged-1, Jagged-2, BCL-2, PTEN, AKT and P-AKT.
Results:
The mRNA and protein expression levels of Notch1-shRNA transfected cells were significantly inhibited in the experimental group assayed by real time fluorescence quantitative PCR and Western blot, the mRNA and protein expression level were down-regulated to 66% + 0.1%, 88% + 3.4% respectively, as compared with the control group(P<0.05). CCK-8 results confirmed that the cell proliferation rate was significantly decreased in the experimental group 48 hours after transfection. Flow cytometry results showed that the cell apoptosis rate was significantly higher in the experimental group than that in the control group. The expression levels of downstream protein Hes1, p-AKT and BCL-2 were decreased, the level of PTEN increased significantly after Notch1 gene silencing.
Conclusion:
Notch1 gene silencing by transfection of Notch1-shRNA can inhibit the proliferation of myeloma cells and induce their apoptosis, and its mechanism is related to the activation of PTEN gene and p-AKT signaling. Notch1 signal can be used as a potential target for multiple myeloma therapy.
Insights
Notch1 gene silencing inhibits multiple myeloma cell proliferation and induces apoptosis. This suggests Notch1 signaling is a potential therapeutic target for multiple myeloma treatment.
Area of Science:
- Molecular Biology
- Cancer Research
- Cell Biology
Background:
- Multiple myeloma is a hematologic malignancy characterized by uncontrolled proliferation of plasma cells.
- The Notch1 signaling pathway plays a role in cell growth and survival, making it a potential target for cancer therapy.
Purpose of the Study:
- To investigate the impact of Notch1 gene silencing on multiple myeloma cell proliferation and apoptosis.
- To explore Notch1 as a potential therapeutic target for multiple myeloma.
Main Methods:
- Utilized Notch1-shRNA to silence the Notch1 gene in RPMI8226 multiple myeloma cells.
- Assessed cell proliferation using CCK-8 assays and apoptosis via flow cytometry.
- Analyzed Notch1 mRNA and protein expression, along with downstream signaling proteins (Hes-1, Jagged-1, Jagged-2, BCL-2, PTEN, AKT, P-AKT) using real-time PCR and Western blot.
Main Results:
- Notch1 gene silencing significantly reduced Notch1 mRNA and protein expression in myeloma cells.
- Observed a significant decrease in cell proliferation and a significant increase in apoptosis following Notch1 silencing.
- Noted downregulation of Hes1, p-AKT, and BCL-2, and upregulation of PTEN expression.
Conclusions:
- Notch1 gene silencing effectively inhibits multiple myeloma cell proliferation and induces apoptosis.
- The mechanism involves the activation of PTEN and modulation of the p-AKT signaling pathway.
- Notch1 signaling represents a promising therapeutic target for multiple myeloma.
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