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丹皮酚联合阿霉素对HepG2细胞株的增殖抑制作用[J]. 肿瘤防治研究, 2008, 35(06): 386-389. DOI: 10.3971/j.issn.1000-8578.2338
引用本文: 丹皮酚联合阿霉素对HepG2细胞株的增殖抑制作用[J]. 肿瘤防治研究, 2008, 35(06): 386-389. DOI: 10.3971/j.issn.1000-8578.2338
Anti-proliferative Effect of Combining Paeonol and Doxorubicin on HepG2 Cell[J]. Cancer Research on Prevention and Treatment, 2008, 35(06): 386-389. DOI: 10.3971/j.issn.1000-8578.2338
Citation: Anti-proliferative Effect of Combining Paeonol and Doxorubicin on HepG2 Cell[J]. Cancer Research on Prevention and Treatment, 2008, 35(06): 386-389. DOI: 10.3971/j.issn.1000-8578.2338

丹皮酚联合阿霉素对HepG2细胞株的增殖抑制作用

Anti-proliferative Effect of Combining Paeonol and Doxorubicin on HepG2 Cell

  • 摘要: 目的 探讨丹皮酚联合阿霉素对HepG2细胞株的增殖抑制作用。方法 采用MTT法测定丹皮酚、阿霉素及丹皮酚联合阿霉素体外对HepG2细胞的增殖抑制率;采用两药相互作用指数评价两药相互作用性质;流式细胞仪检测细胞凋亡;原位细胞凋亡检测法观察细胞凋亡形态学变化;Western blot分析Bcl-2、Bax变化。结果 不同浓度的丹皮酚、阿霉素及联合用药对HepG2细胞株均有增殖抑制作用,呈剂量依赖性。丹皮酚在31.25mg/L分别与阿霉素在0.16、0.31mg/L联合应用时协同作用最为显著(CDI<0.7)。流式细胞仪检测联合用药组凋亡率(37%)明显高于对照组和单独用药组。TUNEL染色可见典型的凋亡形态学特征。Western blot分析表明单独用药和联合用药组Bcl-2表达降低,Bax表达上调,Bcl-2/Bax比值降低。结论 一定浓度的丹皮酚能增强阿霉素在体外对HepG2细胞株的增殖抑制作用,其作用机制为通过降低Bcl-2表达,上调Bax表达,使得Bcl-2/Bax比值降低诱导凋亡实现的。

     

    Abstract: Objective  To explore the anti2proliferative effect of combining Paeonol and Doxorubicin on Hep G2 cell and possible mechanism. Methods  The inhibitor effect of Paeonol or Doxorubicin alone or in both on Hep G2 cell was measured by MTT assay. The coefficient of drug interaction was used to analyze the nature of drug interactions. The apoptosis rate was detected by flow cytomet ry and the morphological change of apopotosis was observed by TUNEL. Bcl22 and Bax expression were assayed by Western blot . Results  Pae or Dox had anti2proliferative effect on Hep G2 cell in a dose2dependent manner. The coeffi2 cient of drug interaction ( CDI < 0. 7) was significant af ter t reatment with a combination of Pae (31. 25 mg/ L) with Dox (0. 16 、0. 31 mg/ L) . The cells showed distinctive apoptotic characteristics by TUNEL and the apoptosis rate of the combined group (37. 0 %) was higher than those of the group t reated with Pae (6. 49 %) or Dox (5. 41 %) alone at the desired concent rations by flow cytomet ry assay. The expres2 sion of Bcl22 decreased and that of Bax increased in the t reated groups, especially in the combination group . The ratio of Bcl22/ Bax decreased conspicuously. Conclusion  Pae could enhance the anti2prolifera2 tive effect of Dox on Hep G2 cell at designated concent rations and the possibility mechanism may be in2 duce apoptosis via activation of Bax and down2regulation Bcl22, which may be useful in hepatocarcinoma t reatment .

     

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