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抗癌Ⅰ号方含药血清对HepG 2肝癌细胞增殖抑制的影响

The Effect of Anticancer Formula I on the Proliferation Inhibition of HepG2 Hepatoma Cells
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摘要 目的研究抗癌Ⅰ号方含药血清对HepG2肝癌细胞的抑制作用及其可能机制。方法用MTT法检测不同浓度的抗癌Ⅰ号方含药血清对HepG2肝癌细胞的增殖抑制作用。免疫印迹法检测各浓度组48h PI3K/Akt信号通路重要蛋白Akt及其磷酸化形式p-Akt的蛋白水平。结果不同浓度的抗癌Ⅰ号方含药血清对HepG2肝癌细胞均有抑制作用,且有一定的浓度依赖性。随着浓度升高,p-Akt/Akt值呈降低趋势,差异有统计学意义(P <0.05)。结论抗癌Ⅰ号方含药血清对HepG2肝癌细胞增殖起抑制作用,同时与药物浓度有一定的依赖性,其可能通过抑制PI3K/Akt通路激活实现。 Objective To study the inhibitory effect of anticancer Ⅰ on HepG2 hepatoma cells and its mechanism. Methods MTT method was used to detect the inhibitory effect of anticancer Ⅰ on HepG2 hepatoma cells. Western blotting was used to detect the protein levels of the important protein Akt and phosphorylated p-Akt of PI3K/Akt signaling pathway in each concentration group at 48 h. Results Different concentrations of anti-cancer Ⅰ have inhibitory effect on HepG2 hepatoma cells, and there is certain concentration dependence. With the increase of the concentration, the p-Akt/Akt value decreased, and the difference was statistically significant(P<0.05). Conclusion Anti cancer formula Ⅰ can inhibit the proliferation of HepG2 hepatoma cells, and it is dependent on the drug concentration, which may be achieved by inhibiting the activation of PI3K/Akt pathway.
作者 高卓维 符路娣 GAO Zhuowei;FU Ludi(Shunde Hospital,Guangzhou University of Chinese Medicine(Shunde District Hospital of Traditional Chinese Medicine,Guangdong Province,Foshan 528300,China;Laboratory of Molecular Biology,College of Traditional Chinese Medicine,Southern Medical University,Level III Scientific Research,Laboratory State Administration of Traditional Chinese Medicine,Guangdong Province,Guangzhou 510515,China;Experimental Animal Center,Guangzhou University of Chinese Medicine,Guangdong Province,Guangzhou 510006,China)
出处 《中国中医药现代远程教育》 2020年第13期125-127,共3页 Chinese Medicine Modern Distance Education of China
基金 国家自然科学基金【No.81703914】 中国博士后科学基金【No.2018M633089】 广东省中医药局科研课题【No.20171304】 广东省佛山市医学类科技攻关项目【No.2017AB003723】。
关键词 抗癌Ⅰ号方 HEPG2肝癌细胞 增殖抑制 anticancer Ⅰ formula HepG2 hepatoma cells cell proliferation
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