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从朝鲜忍冬中分离得到的多酚提取物诱导 HepG2 细胞 G2/M 期细胞周期阻滞和凋亡:涉及 PI3K/Akt 和 MAPKs。

Polyphenolic extract isolated from Korean Lonicera japonica Thunb. induce G2/M cell cycle arrest and apoptosis in HepG2 cells: involvements of PI3K/Akt and MAPKs.

机构信息

Research Institute of Life Science, College of Veterinary Medicine, Gyeongsang National University, Gazwa, Jinju 660-701, Republic of Korea.

出版信息

Food Chem Toxicol. 2012 Jul;50(7):2407-16. doi: 10.1016/j.fct.2012.04.034. Epub 2012 Apr 27.

Abstract

Lonicera japonica Thunb. (L. japonica T.) has been used in Korean traditional medicine for long time because of its anti-cancer and hepatic protective effect. In this study, we investigated polyphenolic extract in L. japonica T. using high-performance liquid chromatography coupled with tandem mass spectrometry (HPLC-MS/MS) and its anti-cancer effect on hepatocarcinoma cells. Human HepG2 cell line was treated with various concentrations of polyphenolic extract. Apoptosis was detective by cell morphology, cell cycle analysis and immunoblot analysis. Polyphenolic extract inhibited cell proliferation at 48h in a dose-dependent manner. Polyphenolic extract affected HepG2 cell viability by inhibiting cell cycle progression at the G2/M transition and inducing apoptosis. Polyphenolic extract also decreased the expression of CDK1, CDC25C, cyclin B1, pro-caspases-3 and -9 and poly ADP ribose polymerase, and affected the levels of mitochondrial apoptotic-related proteins. The phosphorylation of extracellular signal-related kinase ½ (ERK 1/2), c-Jun N-terminal kinase (JNK), and p-38 mitogen-activated protein kinases (MAPKs) were increased in HepG2 cells treated with polyphenolic extract, whereas Akt was dephosphorylated. These results indicate that inhibition of PI3K/Akt and activation of MAPKs are pivotal in G2/M cell cycle arrest and apoptosis of human hepatocarcinoma cells mediated by polyphenolic extract.

摘要

忍冬(Lonicera japonica Thunb.)在韩国传统医学中被长期应用,因为它具有抗癌和保肝作用。在这项研究中,我们使用高效液相色谱-串联质谱法(HPLC-MS/MS)研究了忍冬中的多酚提取物及其对肝癌细胞的抗癌作用。用人 HepG2 细胞系用不同浓度的多酚提取物处理。通过细胞形态学、细胞周期分析和免疫印迹分析检测细胞凋亡。多酚提取物以剂量依赖的方式在 48 小时内抑制细胞增殖。多酚提取物通过抑制细胞周期在 G2/M 期转变和诱导细胞凋亡来影响 HepG2 细胞活力。多酚提取物还降低了 CDK1、CDC25C、cyclin B1、pro-caspase-3 和 -9 以及聚 ADP 核糖聚合酶的表达,并影响线粒体凋亡相关蛋白的水平。用多酚提取物处理 HepG2 细胞后,细胞外信号相关激酶 1/2(ERK 1/2)、c-Jun N-末端激酶(JNK)和 p-38 丝裂原活化蛋白激酶(p38 MAPKs)的磷酸化增加,而 Akt 去磷酸化。这些结果表明,PI3K/Akt 的抑制和 MAPKs 的激活在多酚提取物介导的人肝癌细胞 G2/M 细胞周期阻滞和凋亡中起关键作用。

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