八角莽草酸诱导人肝癌细胞HepG-2凋亡及其机制研究

朱开梅; 顾生玖; 李美波; 骆彩珍; 许有瑞; 顾小文

doi:10.13422/j.cnki.syfix.2014080154

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八角莽草酸诱导人肝癌细胞HepG-2凋亡及其机制研究

更新时间：2024-01-04

- 八角莽草酸诱导人肝癌细胞HepG-2凋亡及其机制研究
- Shikimic Acid Inducing Apoptosis on Hepatocellular Carcinoma HepG-2 Cells Through Decreasing the Ratio of Bcl-2/Bax
- 中国实验方剂学杂志 2014年20卷第8期页码：154-158
- 作者机构：
- 作者简介：
- 基金信息：
  
  广西科技攻关项目（129825-21）;广西教育厅项目（201202ZD065）;桂林市科技攻关项目（20130113-1，20130103-8，20130103-8;20120105-8）
- DOI：10.13422/j.cnki.syfix.2014080154
  中图分类号：
- 纸质出版日期：2014
- 稿件说明：
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朱开梅, 顾生玖, 李美波, 等. 八角莽草酸诱导人肝癌细胞HepG-2凋亡及其机制研究[J]. 中国实验方剂学杂志, 2014,20(8):154-158.

ZHU Kai-mei, GU Sheng-jiu, LI Mei-bo, et al. Shikimic Acid Inducing Apoptosis on Hepatocellular Carcinoma HepG-2 Cells Through Decreasing the Ratio of Bcl-2/Bax[J]. Chinese journal of experimental traditional medical formulae, 2014, 20(8): 154-158.
朱开梅, 顾生玖, 李美波, 等. 八角莽草酸诱导人肝癌细胞HepG-2凋亡及其机制研究[J]. 中国实验方剂学杂志, 2014,20(8):154-158. DOI： 10.13422/j.cnki.syfix.2014080154.

ZHU Kai-mei, GU Sheng-jiu, LI Mei-bo, et al. Shikimic Acid Inducing Apoptosis on Hepatocellular Carcinoma HepG-2 Cells Through Decreasing the Ratio of Bcl-2/Bax[J]. Chinese journal of experimental traditional medical formulae, 2014, 20(8): 154-158. DOI： 10.13422/j.cnki.syfix.2014080154.

摘要

目的：研究八角莽草酸诱导人肝癌细胞HepG-2凋亡的作用和机制。方法：取对数生长期人肝癌HepG-2细胞，随机分为药物组和对照组，用0.125，0.5，1 g·L-1不同浓度八角莽草酸作用人肝癌HepG-2细胞，采用MTT法测定莽草酸对HepG-2细胞增殖的影响；通过流式细胞仪检测在以上浓度的莽草酸对肝癌HepG-2细胞周期的影响；通过免疫细胞化学检测凋亡相关基因B细胞淋巴瘤白血病2（Bcl-2）、Bcl-2相关X蛋白（Bax蛋白）表达的改变。结果：MTT实验结果表明，各质量浓度0.125，0.5，1 g·L-1的莽草酸对人肝癌HepG-2的生长具有显著的抑制作用（P<0.05），呈现时间依赖性和剂量依赖性；流式结果表明莽草酸将人肝癌HepG-2细胞阻滞在G1期，使细胞不能顺利地进入细胞DNA合成期S期，从而抑制了该细胞的增殖。免疫细胞化学检测凋亡相关基因Bcl-2蛋白表达明显减少、Bax表达明显增加；Bcl-2/Bax比例明显降低。结论：八角莽草酸在体外诱导人肝癌HepG-2细胞大量阻滞在G1期，进入S期细胞减少，抑制细胞增殖，其作用可能通过降低Bcl-2/Bax比例来诱导细胞凋亡而实现的。

Abstract

Objective: To investigate the effects of shikimic acid on inducing hepatocellular carcinoma HepG-2 cells apoptosis in vitro. Method: The MTT assay was used

and the hepatocellular carcinoma HepG-2 cells in logarithmic phase of growth were randomly divided into control group and treatment group treated with the concentration of 0.125

0.5

1 g·L-1 shikimic acid in hepatocellular carcinoma HepG-2 cells. The cell cycle distribution was analyzed by flow cytometry. The protein expression of B cell lymphoma/leukemia-2(Bcl-2) and Bcl-2 associated x protein(Bax) was analyzed by immunocytochemical method. Result: Shikimic acid inhibited the growth of cells significantly(P<0.05). The suppression was both in a time-and dose-dependent manner. The flow cytometry showed that shikimic acid can inhibit the proliferation by preventing cells turning into S phase from G1 phase in cell cycle

at the same time

shikimic acid down-regulated the Bcl-2 expression and up-regulated the Bax expression

the ratio of Bcl-2/Bax was evident decrease. Conclusion: Shikimic acid can inhibit proliferation hepatocellular carcinoma HepG-2 cells and induce a G1 cell cycle arrest and reduce the cell population in S phase

it may induce apoptosis through decreasing the ratio of Bcl-2/Bax.

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