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黄连素通过靶向Sp1上调miR-22-3p以抑制肝癌细胞增殖。

Berberine upregulates miR-22-3p to suppress hepatocellular carcinoma cell proliferation by targeting Sp1.

作者信息

Chen Jie, Wu Fei-Xiang, Luo Hong-Lin, Liu Jun-Jie, Luo Tao, Bai Tao, Li Le-Qun, Fan Xiao-Hui

机构信息

Department of Hepatobiliary Surgery, Affiliated Tumor Hospital of Guangxi Medical University Nanning 530021, China.

School of Preclinical Medicine, Guangxi Medical University Nanning 530021, China.

出版信息

Am J Transl Res. 2016 Nov 15;8(11):4932-4941. eCollection 2016.

Abstract

MicroRNA-22-3p (miR-22-3p) is downregulated in hepatocellular carcinoma (HCC), which contributes to the development and progression of HCC. In this study, berberine treatment upregulated miR-22-3p expression in HepG2 cells. Therefore, we investigated whether berberine suppresses the proliferation of HCC cells and explored the underlying mechanism. The HCC HepG2 cell line was treated with a gradient of berberine concentrations (0-300 μM) for 48 h, and 100 μM berberine inhibited cell growth at 24 h. The HepG2 cells were then incubated with 100 μM berberine for 0-48 h, and after treatment for 24 h, berberine markedly suppressed HepG2 cell growth and significantly upregulated miR-22-3p expression. Berberine also downregulated the expression of SP1, CCND1, and BCL2, determined with western blotting. Dual luciferase reporter assays and western blot analyses showed that miR-22-3p directly targeted SP1, thereby suppressing the expression of its downstream targets, CCND1 and BCL2. SP1 knockdown with small interfering RNA also reduced CCND1 and BCL2 expression in HepG2 cells. Therefore, we conclude that berberine treatment suppresses cancer cell growth by regulating miR-22-3p and SP1 and its downstream targets, CCND1 and BCL2, in HCC.

摘要

微小RNA-22-3p(miR-22-3p)在肝细胞癌(HCC)中表达下调,这促进了HCC的发生和发展。在本研究中,黄连素处理上调了HepG2细胞中miR-22-3p的表达。因此,我们研究了黄连素是否能抑制HCC细胞的增殖,并探讨其潜在机制。将HCC HepG2细胞系用不同浓度梯度(0-300μM)的黄连素处理48小时,100μM黄连素在24小时时抑制细胞生长。然后将HepG2细胞与100μM黄连素孵育0-48小时,处理24小时后,黄连素显著抑制HepG2细胞生长并显著上调miR-22-3p表达。通过蛋白质印迹法测定,黄连素还下调了SP1、CCND1和BCL2的表达。双荧光素酶报告基因检测和蛋白质印迹分析表明,miR-22-3p直接靶向SP1,从而抑制其下游靶点CCND1和BCL2的表达。用小干扰RNA敲低SP1也降低了HepG2细胞中CCND1和BCL2的表达。因此,我们得出结论,黄连素处理通过调节miR-22-3p和SP1及其下游靶点CCND1和BCL2来抑制HCC癌细胞的生长。

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