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黄芪苷通过上调miR-125b降低己糖激酶2,从而在体内外抑制肝癌细胞增殖。

Astragalin Reduces Hexokinase 2 through Increasing miR-125b to Inhibit the Proliferation of Hepatocellular Carcinoma Cells in Vitro and in Vivo.

作者信息

Li Wei, Hao Ji, Zhang Lang, Cheng Zhuo, Deng Xukun, Shu Guangwen

机构信息

School of Pharmaceutical Sciences, South-Central University for Nationalities , Wuhan, China 430074.

National Demonstration Center for Experimental Ethnopharmacology Education, South-Central University for Nationalities , Wuhan, China 430074.

出版信息

J Agric Food Chem. 2017 Jul 26;65(29):5961-5972. doi: 10.1021/acs.jafc.7b02120. Epub 2017 Jul 11.

DOI:10.1021/acs.jafc.7b02120
PMID:28654261
Abstract

Astragalin (ASG) can be found in a variety of food components. ASG exhibits cytotoxic effects on several different types of malignant cells. However, its effects on hepatocellular carcinoma (HCC) cells and the underlying molecular mechanisms have remained to be fully elucidated. Here, we revealed that ASG remarkably suppressed the proliferation of HCC cells. In HCC cells, ASG inhibited glucose glycolysis and promoted oxidative phosphorylation, resulting in a surge of reactive oxygen species (ROS). Mechanistically, ASG suppressed the expression of hexokinase 2 (HK2). This event was indispensible for ASG-mediated metabolic reprogramming, ROS accumulation, and subsequent growth arrest. Our further investigations unveiled that ASG repressed HK2 expression via increasing miR-125b. In vivo experiments showed that gavage of ASG decreased the proliferation of Huh-7 HCC xenografts in nude mice and inhibited the growth of transplanted H22 HCC cells in Kunming mice. Declined HCC tumor growth in vivo was associated with boosted miR-125b and reduced expression of HK2 in tumor tissues. Collectively, our results demonstrated that ASG is able to suppress the proliferation of HCC cells both in vitro and in vivo. Inhibition of HK2 through upregulating miR-125b and subsequent metabolic reprogramming is implicated in the antiproliferative effects of ASG on HCC cells.

摘要

黄芪苷(ASG)存在于多种食物成分中。ASG对几种不同类型的恶性细胞具有细胞毒性作用。然而,其对肝癌(HCC)细胞的作用及潜在分子机制仍有待充分阐明。在此,我们发现ASG显著抑制HCC细胞的增殖。在HCC细胞中,ASG抑制糖酵解并促进氧化磷酸化,导致活性氧(ROS)激增。机制上,ASG抑制己糖激酶2(HK2)的表达。这一事件对于ASG介导的代谢重编程、ROS积累及随后的生长停滞不可或缺。我们的进一步研究表明,ASG通过增加miR-125b来抑制HK2表达。体内实验表明,灌胃ASG可降低裸鼠中Huh-7 HCC异种移植瘤的增殖,并抑制昆明小鼠中移植的H22 HCC细胞的生长。体内HCC肿瘤生长的下降与肿瘤组织中miR-125b的升高和HK2表达的降低有关。总体而言,我们的结果表明ASG能够在体外和体内抑制HCC细胞的增殖。通过上调miR-125b抑制HK2及随后的代谢重编程与ASG对HCC细胞的抗增殖作用有关。

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