| 注册
首页|期刊导航|重庆医学|姜黄素抑制多药耐药肝癌细胞HepG2/ADM的增殖及其机制研究

姜黄素抑制多药耐药肝癌细胞HepG2/ADM的增殖及其机制研究

耿燕娜 武毅君 张文鑫

重庆医学2017,Vol.46Issue(31):4329-4331,3.
重庆医学2017,Vol.46Issue(31):4329-4331,3.DOI:10.3969/j.issn.1671-8348.2017.31.003

姜黄素抑制多药耐药肝癌细胞HepG2/ADM的增殖及其机制研究

Study on effect of curcumin in inhibiting proliferation of multidrug resistant liver cancer HepG2/ADM cells and its mechanism

耿燕娜 1武毅君 2张文鑫3

作者信息

  • 1. 河南大学淮河医院药学部,河南开封475000
  • 2. 河南大学药学院,河南开封475000
  • 3. 河南中医药大学第一附属医院,郑州450000
  • 折叠

摘要

Abstract

Objective To observe the inhibitory effect of curcumin on the proliferation of multidrug resistance liver cancer line HepG2/ADM cells and to explore its mechanisms.Methods HepG2/ADM cells were prepared and cultured in vitro,and treated by different concentrations (5,10,20,40 μmol/L) of curcumin for 24,48,72 h respectively.The effect of curcumin on proliferation of HepG2/ADM cells was measured by CCK-8 reagent;the concentration of intracellular rhodamine-123 (Rh-123) and adriamycin (ADM) were determined by flow cytometry;the level change of intracellular mdr-1 mRNA in each group was determined by RT-PCR,the P-gp protein level was detected by Western blot.Results Compared with the blank control and DMSO group,curucmin had more obvious inhibitory effect on HepG2/ADM cells proliferation (P<0.05),and could more remarkably inhibit the intracellular Rh-123 excretion(P<0.05).The RT-PCR and Western blot results showed that curcumm more significantly decrease the mdr-1 mRNA and P-gp protein levels in dose-time dependent manner (P<0.05).Conclusion Curcumin could significantly inhibit the proliferation of multidrug-resistant HepG2/ADM cells,and its mechanism may be related with inhibiting mdr-1 gene expression and its encoded P-gp protein level,which are closely related with MDR.

关键词

姜黄素/多药耐药/P-糖蛋白/HepG2/ADM细胞

Key words

curcumin/multidrug-resistance/P-gp/HepG2/ADM cells

分类

医药卫生

引用本文复制引用

耿燕娜,武毅君,张文鑫..姜黄素抑制多药耐药肝癌细胞HepG2/ADM的增殖及其机制研究[J].重庆医学,2017,46(31):4329-4331,3.

基金项目

河南省医学科技公关计划项目(201404035). (201404035)

重庆医学

1671-8348

访问量3
|
下载量0
段落导航相关论文