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作 者:屈艺[1] 刘菽秋[1] 李大成[1] 张旋波[1] 白绍怀[1] 唐心曜[1] 张泰怀[1] 刘柏林[1]
出 处:《天然产物研究与开发》2006年第6期932-936,共5页Natural Product Research and Development
基 金:This work was supported by National Nature Science Fund (39470876)
摘 要:为寻找能有效逆转肿瘤细胞多药耐药性的药物,通过体外细胞实验对Ams-11、Fw-13、Tul-17三种中药制剂逆转肿瘤细胞多药耐药性的作用进行了分析。并用流式细胞仪测定了Tul-17处理细胞后药物累积程度的变化及细胞P糖蛋白表达情况。为进一步研究体外细胞实验筛选出的多药耐药逆转剂在体内的药效学,将其中Fw13用于人白血病K562/ADR裸鼠移植瘤逆转试验。结果:在无细胞毒性的剂量范围内,该三种中药制剂均能明显增强多药耐药细胞对抗癌药物的敏感性,而且其逆转作用呈剂量依赖关系。Tu-17处理后,K562耐药细胞表达的P糖蛋白较对照降低1.5倍,对罗丹明123的累积量是对照的2.5倍。用Fw13治疗人白血病K562/ADR裸鼠移植瘤,可将硫酸长春新碱(VCR)对K562/ADR的抑瘤率从19.79%提高到86.59%,与单独VCR治疗疗效有显著性差异(P<0.05)。结果表明,这三种中药制剂可望成为肿瘤多药耐药逆转剂,在肿瘤化疗中发挥作用。The aim of this project was to find some kinds of Chinese medicines as effective agents for reversal of cancer multidrug resistance. Based on the present authors'previous researches, thirty-two kinds of Chinese medicines as research materials were selected and examined. Using cell growth inhibition assay,the authors found that three of them,Ams-11,Fw-13 and Tul- 17 ,in the doses free from cytotoxieity could enhance the senstivity of multidrug resistant cells to anfieancer drugs in a dose-dependent way. Through mechanistic studies, the authors demonstrated that Tul-17 could increase the accumulation of MDR drugs, and attenuate the expression level of P-glyeoprotein (Pgp),Animal test with Fw-13 also proved the MDR reversal effect of this medicine. Taken together, the results indicate that these three Chinese medicines might be potential effective MDR reversal agents,
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