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靶向Notch1基因抑制多发性骨髓瘤细胞的增殖

[Targeting Notch1 Gene Inhibits the Proliferation of Multiple Myeloma Cells].

作者信息

Li Mei-Ling, Chen Mei-Qiong, Zhang Peng, Lu Quan-Yi

机构信息

Department of Hematology, Xiamen University Zhongshan Hospital, Xiamen 361004, Fujian Province, China; Department of Hematology, Guizhou Medical University Third Hospital, Duyun 558000, Guizhou Province, China.

Department of Hematology, Xiamen University Zhongshan Hospital, Xiamen 361004, Fujian Province, China.

出版信息

Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2017 Dec;25(6):1707-1712. doi: 10.7534/j.issn.1009-2137.2017.06.023.

Abstract

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.

摘要

目的

探讨Notch1基因沉默对多发性骨髓瘤细胞增殖和凋亡的影响,寻找治疗多发性骨髓瘤的新靶点。

方法

将靶向沉默Notch1基因的Notch1-shRNA转染至多发性骨髓瘤RPMI8226细胞,采用CCK-8法和流式细胞术检测Notch1-shRNA转染后骨髓瘤细胞的增殖和凋亡情况,采用实时荧光定量PCR分析Notch1 mRNA表达水平,采用蛋白质印迹法检测Notch1信号通路相关蛋白如Hes-1、Jagged-1、Jagged-2、BCL-2、PTEN、AKT及P-AKT的表达水平。

结果

实时荧光定量PCR和蛋白质印迹法检测结果显示,实验组Notch1-shRNA转染细胞的mRNA和蛋白表达水平均受到显著抑制,与对照组相比,mRNA和蛋白表达水平分别下调至66%±0.1%、88%±3.4%(P<0.05)。CCK-8结果证实,转染后48小时实验组细胞增殖率显著降低。流式细胞术结果显示,实验组细胞凋亡率显著高于对照组。Notch1基因沉默后,下游蛋白Hes1、p-AKT和BCL-2表达水平降低,PTEN水平显著升高。

结论

转染Notch1-shRNA沉默Notch1基因可抑制骨髓瘤细胞增殖并诱导其凋亡,其机制与PTEN基因激活及p-AKT信号有关。Notch1信号可作为多发性骨髓瘤治疗的潜在靶点。

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