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Chinese Journal of Clinical Pharmacology and Therapeutics ›› 2014, Vol. 19 ›› Issue (2): 139-144.

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Reversal of human hepatic cancer multidrug resistance is induced by AstragalosideⅡ in BEL-7402/FU cells

WANG Pei-pei1, XU Du-juan2, HUANG Can3, XU Wen-ke1, LUAN Jia-jie1   

  1. 1Department of Pharmacy, Yijishan Affiliated Hospital of Wannan Medical College, Wuhu 241001, Anhui, China;
    2The First Affiliated Hospital of Anhui Medical University, Third-Grade Pharmaceutical Chemistry Laboratory of State Administration of Traditional Chinese Medicine, Hefei 230022, Anhui, China;
    3Department of Pharmacy, Anqing Shili Hospital, Anqing 246003, Anhui, China
  • Received:2013-06-25 Revised:2014-02-17 Online:2014-02-26 Published:2014-03-31

Abstract: AIM: To investigate the effect of AstragalosideⅡ on the reversal of multidrug resistance in human hepatic cancer cells.METHODS: Susceptibility of chemotherapy drugs and relative reversal fold was evaluated by MTT. The mRNA level of MDR1 gene was detected by RT-PCR and the P-glycoprotein expression was detected by immunocytochemistry method. Intracellular Rhodamine123 accumulation was determined by flowcytometry.RESULTS: BEL-7402/FU cells showed resistance to three chemotherapy drugs 5-fluorouracil, Adriamycin and Mitomycin, their resistance index were 19.64, 1.98, 1.92. Astragaloside Ⅱ(0.04, 0.08 mg/mL) relative reversal fold were 1.49, 1.81 to 5-fluorouracil. Astragaloside Ⅱ(0.08 mg/mL, 0.16 mg/mL) could downregulate the expression of MDR1 mRNA and P-glycoprotein, increase the intracellular Rhodamine123 fluorescence.CONCLUSION: Astragaloside Ⅱ could reverse the drug resistance of Bel-7402/FU cells via regulating down the expression of MDR1 mRNA, inhibit the expression and function of P-glycoprotein.

Key words: Astragaloside Ⅱ, P-glycoprotein, multidrug resistance, hepatocellular carcinoma

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