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机构地区:[1]重庆医科大学附属第一医院耳鼻咽喉科,重庆400016
出 处:《重庆医科大学学报》2008年第8期967-969,共3页Journal of Chongqing Medical University
摘 要:目的:研究天然有效成分粉防己碱(Tetrandrine,TET)对喉癌耐药细胞株KBV200的耐药逆转作用。方法:本研究以喉癌耐药细胞株KBV200为研究对象,采用粉防己碱逆转KBV200对常用抗肿瘤药物阿霉素的多药耐药作用,以经典逆转剂维拉帕米(Verapamil,VRP)为对照组,用四甲基偶氮唑蓝(MTT)法测定其对实验细胞的增殖抑制率。结果:低毒剂量的粉防己碱能逆转实验细胞株对阿霉素的多药耐药(Multidrug resistance,MDR)作用,逆转指数为22.96;维拉帕米逆转指数为9.31。结论:低毒浓度的天然药物粉防己碱能逆转喉癌耐药细胞株KBV200对阿霉素的耐药作用,其逆转效果优于经典逆转剂维拉帕米。Objective:To study the reversal effect of tetrandrine on muhidrug resistance of KBV200 cell line in order to provide experimental data for clinical individual chemotherapy. Methods:MTT reduction assay was used to investgate the inhibition of Adriamycin on KBV200cell line,and the reversal effects of Tetrandrine and Verapamil on the cell line. Results:Verapamil and Tetrandrine had the reveral effects on the cell line,and the reversal indexes of Tetrandrine and Veramil were 22.96 and 9.31, respectively. Conclusion:KBV200 cell line was muhidrug resistance to Adriamycin but Tetrandrine had reversal effects on its muhidrug resistance.
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