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作 者:杨伟霞[1] 陆少锋[1] 贾宁[1] 赵冠耀[1]
机构地区:[1]佛山市高明区人民医院药剂科,广东佛山528500
出 处:《中华中医药学刊》2015年第8期2008-2010,I0033,I0034,共5页Chinese Archives of Traditional Chinese Medicine
摘 要:目的:探讨川芎嗪诱导人胃癌细胞株SGC-7901/ADR凋亡及对MDR1、GST-π表达的调控作用。方法:不同剂量(0~120μM)川芎嗪内酯与人胃癌细胞株SGC-7901/ADR同培养不同时间(24、48及72 h),50μM 5-氟尿嘧啶(5-FU)作为阳性对照组,采用CCK8法测定细胞的增殖,流式细胞术测定细胞凋亡率。用不同剂量的川芎嗪与细胞培养48 h后,采用Western blot测定MDR1、GST-π蛋白的表达情况,用半定量RT-PCR测定MDR1、GST-πmRNA表达。结果:不同浓度川芎嗪处理人胃癌细胞株SGC-7901,川芎嗪抑制SGC-7901细胞增殖呈浓度及作用时间依赖性且120μM川芎嗪的抑制率与阳性对照组相当;而且应用流式细胞仪检测发现川芎嗪作用于人胃癌细胞株SGC-7901 48 h后,细胞出现凋亡。Western blot及半定量RT-PCR检测细胞中MDR1、GST-π及其mRNA的表达,结果显示,川芎嗪可下调MDR1、GST-π表达,下调作用与TMZ相当甚至更具优势。结论:川芎嗪能够抑制人胃癌细胞株SGC-7901的增殖,诱导其凋亡,且能抑制细胞中MDR1、GST-π的表达,其表达量与川芎嗪剂量呈现明显的时间-浓度效应关系。Objective : To investigate the effect of tetramethylpyrazine on proliferation and apoptosis and MDR1 and GST -π expressions in human gastric carcinoma cell line SGC - 7901. Methods : SGC - 7901 cells were treated with tet- ramethylpyrazine at different concentrations (0 ~ 100 μM) for 24,48 and 72 h,respectively. Cell proliferation was detec- ted by CCKS. The apoptosis rate of SGC - 7901 cells after treated with tetramethylpyr .azine for 48 h was evaluated by flow cytometry. The expressions of MDR1 ,GST-π and MDR1 ,GST-π mRNA were determined by Western blot and QRT- PCR, respectively. Results: Tetramethylpyrazine inhibited the proliferation of SGC -7901 cells and the inhibitory rates increased at a dose - time - dependent manner. Compared to the control group, the expressions of MDR1, GST -π and MDR1, GST -π mRNA in the treatment groups were significantly down - regulated. Conclusion : Tetramethylpyrazine in- hibits proliferation and apeptosis in human gastric carcinoma cell line SGC -7901, which may be through the down- regulation of MDR1 and GST-π expressions in cells.
关 键 词:川芎嗪 人胃癌细胞株SGC-7901 MDR1 GST-Π
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