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川芎嗪逆转人胃癌耐药细胞SGC7901/ADM多药耐药的实验研究
引用本文:曲正,侯培珍,曲伟,王颖慧. 川芎嗪逆转人胃癌耐药细胞SGC7901/ADM多药耐药的实验研究[J]. 包头医学院学报, 2005, 21(3): 220-221
作者姓名:曲正  侯培珍  曲伟  王颖慧
作者单位:包头医学院第一附属医院,内蒙古,包头,014010
摘    要:目的:观察中药钙通道阻滞剂川芎嗪(TMP)对胃癌耐药细胞系SGC7901/ADM多药耐药(MDR)的逆转.方法:采用四唑氮蓝(MTT)法以川芎嗪为逆转剂,观察化疗药物对SGC7901/ADM的杀伤作用.结果:采用非细胞毒剂量的300mg/L TMP,能提高5-Fu的细胞杀伤作用.结论:TMP是一种有效的逆转胃癌MDR的中药逆转剂.

关 键 词:胃肿瘤  川芎嗪  多药耐药
文章编号:1006-740X(2005)03-0220-02
收稿时间:2005-03-16
修稿时间:2005-03-16

Reversal of Multidrug Resistance of SGC7901/ADM Gastric Carcinoma Cell Line by Tetramethylpyrazine
Qu Zheng,HOU Peizhen,QU Wei,Wang Yinghui. Reversal of Multidrug Resistance of SGC7901/ADM Gastric Carcinoma Cell Line by Tetramethylpyrazine[J]. Journal of Baotou Medical College, 2005, 21(3): 220-221
Authors:Qu Zheng  HOU Peizhen  QU Wei  Wang Yinghui
Abstract:Objective:To investigate the reversal of multidrug resistance (MDR) of gastric carcinoma cell line SGC7901/ADM by traditional Chinese medicine tetramethylpyrazine(TMP).Methods:MTT assay was used to investigate the cytotoxicity of the drugs against human gastric carcinoma cell line SGC7901/ADM in vitro.Results:The cytotoxicity of 5-Fu to SGC7901/ADM was enhanced by TMP at nontoxic doses.Conclusion:TMP may be a safe and effective revertant to MDR.
Keywords:Gastric carcinoma   Tetramethylpyrazine    Muhidrug - resistant
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