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首页> 外文期刊>Cancer Cell International >Synergistic effects of isomorellin and forbesione with doxorubicin on apoptosis induction in human cholangiocarcinoma cell lines
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Synergistic effects of isomorellin and forbesione with doxorubicin on apoptosis induction in human cholangiocarcinoma cell lines

机译:异雷莫林和福布斯与阿霉素对人胆管癌细胞株凋亡的协同作用

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Background Chemotherapy for advanced cholangiocarcinoma (CCA) is largely ineffective, but innovative combinations of chemotherapeutic agents and natural compounds represent a promising strategy. In our previous studies, isomorellin and forbesione, caged xanthones isolated from Garcinia hanburyi, were found to induce cell cycle arrest and apoptosis in CCA cell lines. The subject of our inquiry is the synergistic effect(s) of these caged xanthones with doxorubicin on growth inhibition and apoptosis induction in human CCA cell lines. Methods KKU-100, KKU-M139 and KKU-M156 cell lines and Chang cells were treated with either isomorellin or forbesione alone or in combination with doxorubicin. Cell viability was determined using the sulforhodamine B assay. The combined effects of plant compounds with doxorubicin were analyzed using the isobologram and combination index method of Chou-Talalay. Apoptosis was determined by ethidium bromide/acridine orange staining. Protein expressions were determined by Western blot analysis. Results Isomorellin or forbesione alone inhibited the growth of these CCA cell lines in a dose-dependent manner and showed selective cytotoxicity against CCA cells but not against Chang cells. Isomorellin/doxorubicin combination showed a synergistic growth inhibitory effect on KKU-M139 and KKU-M156 cells, while the forbesione/doxorubicin combination showed a synergistic growth inhibitory effect on KKU-100 and KKU-M139 cells. The percentages of apoptotic cells were significantly higher in the combined treatments than in the respective single drug treatments. The combined treatments strongly enhanced the expression of Bax/Bcl-2, activated caspase-9 and caspase-3, while suppressing the expression of survivin, procaspase-9 and procaspase-3, compared with single drug treatments. The degree of suppression of NF-κB activation mediated by a decrease in the expression of NF-κB/p65, a reduction of the pIκB-α level and an increase in the IκB-α protein level, was significantly higher in the combined treatment groups than in the single drug treatment groups. The degree of suppression of MRP1 protein expression was also significantly higher in the combined treatment than in the single drug treatment groups. Conclusion The combinations of isomorellin/doxorubicin and forbesione/doxorubicin showed significant synergistic effects on the growth inhibition and apoptosis induction in KKU-M156 and KKU-100 cells. Caged xanthones may be useful adjunct treatments with chemotherapy for Opisthorchis viverrini (OV)-associated CCA.
机译:背景晚期胆管癌(CCA)的化学疗法在很大程度上无效,但是化学治疗剂和天然化合物的创新组合代表了一种有前途的策略。在我们之前的研究中,发现从汉黄藤中分离的笼状黄嘌呤异黄酮和forbesione诱导了CCA细胞系的细胞周期停滞和凋亡。我们所研究的主题是这些笼中的氧杂蒽与阿霉素对人CCA细胞系中生长抑制和凋亡诱导的协同作用。方法分别用异美瑞林或福贝生或与阿霉素联合处理KKU-100,KKU-M139和KKU-M156细胞系和Chang细胞。使用磺基罗丹明B测定法测定细胞活力。使用Chou-Talalay的等效线图和结合指数法分析了植物化合物与阿霉素的联合作用。通过溴化乙锭/ ac啶橙染色确定细胞凋亡。通过蛋白质印迹分析确定蛋白质表达。结果单独的异瑞林或forbessione可以剂量依赖性地抑制这些CCA细胞系的生长,并显示出对CCA细胞的选择性细胞毒性,但对Chang细胞没有选择性。异瑞林/阿霉素组合对KKU-M139和KKU-M156细胞具有协同生长抑制作用,而福斯本/阿霉素组合对KKU-100和KKU-M139细胞具有协同生长抑制作用。联合治疗中凋亡细胞的百分比显着高于相应的单一药物治疗。与单一药物治疗相比,联合治疗强烈增强了Bax / Bcl-2,活化的caspase-9和caspase-3的表达,同时抑制了survivin,procaspase-9和procaspase-3的表达。联合治疗组中由NF-κB/ p65表达降低,pIκB-α水平降低和IκB-α蛋白水平升高介导的NF-κB活化抑制程度明显更高比单药治疗组要多。在联合治疗中,MRP1蛋白表达的抑制程度也明显高于单一药物治疗组。结论异瑞林/阿霉素和苯甲酸/阿霉素的组合对KKU-M156和KKU-100细胞的生长抑制和凋亡诱导具有明显的协同作用。笼养的氧杂蒽酮可能是对与阿维斯匹氏菌(OV)相关的CCA进行化疗的有用辅助疗法。

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