Feng Duo, Zhou Shi-Qi, Zhou Ya-Xi, Jiang Yong-Jun, Sun Qiao-di, Song Wei, Cui Qian-Qian, Yan Wen-Jie, Wang Jing
College of Biochemical Engineering, Beijing Union University, Beijing, China.
Beijing Key Laboratory of Bioactive Substances and Functional Food, College of Biochemical Engineering, Beijing Union University, Beijing, China.
Front Nutr. 2023 Feb 6;10:1117364. doi: 10.3389/fnut.2023.1117364. eCollection 2023.
To study the anti-tumor effect of , HepG2 cells were treated with 0, 3.5, 10.5, 21, 31.5, and 42 μg/ml of total glycosides (TG) from . The HepG2 cell survival rate and 50% inhibition concentration (IC) were detected using the CCK-8 method, and the level of reactive oxygen species (ROS) was detected by using a DCFH-DA fluorescence probe. Finally, a Seahorse XFe24 energy analyzer (Agilent, United States) was used to detect cell mitochondrial pressure and glycolytic pressure. The results showed that TG could reduce the survival rate of HepG2 cells and that the IC level was 35.28 μg/ml. With increasing TG concentration, the level of ROS showed a concentration-dependent upward trend. Energy metabolism showed that each dose group of TG could significantly decline the mitochondrial respiratory and glycolytic functions of HepG2 cells. In conclusion, TG could significantly inhibit the mitochondrial respiration and glycolysis functions of HepG2 cells, increase the level of ROS, and inhibit cell proliferation. Thus, this experiment pointed out that can be used as a source of anti-cancer foods or drugs in the future. However, further studies on its mechanisms and clinical applications are needed.
为研究[具体物质]总苷(TG)的抗肿瘤作用,用0、3.5、10.5、21、31.5和42μg/ml的[具体物质]总苷处理HepG2细胞。采用CCK - 8法检测HepG2细胞存活率和50%抑制浓度(IC),并使用DCFH - DA荧光探针检测活性氧(ROS)水平。最后,使用海马XFe24能量分析仪(美国安捷伦公司)检测细胞线粒体压力和糖酵解压力。结果表明,TG可降低HepG2细胞的存活率,IC水平为35.28μg/ml。随着TG浓度增加,ROS水平呈浓度依赖性上升趋势。能量代谢显示,TG各剂量组均可显著降低HepG2细胞的线粒体呼吸和糖酵解功能。总之,TG可显著抑制HepG2细胞的线粒体呼吸和糖酵解功能,提高ROS水平,并抑制细胞增殖。因此,本实验指出[具体物质]未来可作为抗癌食品或药物的来源。然而,需要对其作用机制和临床应用进行进一步研究。