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18β-甘草次酸哌嗪衍生物抗肝癌SMMC-7721细胞活性研究 被引量:4

Effects of 18β-glycyrrhetinic acid derivatives containing piperazine on SMMC-7721 cell activity
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摘要 目的研究18β-甘草次酸哌嗪衍生物D34、D35对SMMC-7721细胞增殖的的抑制作用及对凋亡的影响。方法用18β-甘草次酸哌嗪衍生物D34、D35以不同浓度、不同时间段处理SMMC-7721细胞,显微镜下观察其对肝癌SMMC-7721细胞形态结构的影响;MTT法检测18β-甘草次酸哌嗪衍生物D34、D35对SMMC-7721细胞的增殖抑制率;Hoechst-33258细胞凋亡染色试剂盒检测细胞凋亡情况;Annexin V-FITC/PI双染法检测细胞凋亡率。结果MTT检测结果表明,18β-甘草次酸哌嗪衍生物D34、D35能够抑制肝癌SMMC-7721细胞增殖,且呈浓度依赖性(P<0.05);流式细胞仪检测细胞凋亡率,D35为26.71%、D34为36.95%。结论 18β-甘草次酸哌嗪衍生物D34、D35对SMMC-7721细胞有增殖抑制作用和促凋亡作用,且优于18β-甘草次酸(GA)。 Objective To study the effects of 18β-glycyrrhetinic acid derivatives containing piperazine D34 and D35 on the proliferation and apoptosis of SMMC-7721cells. Methods The morphology of the cells treated with 18β-glycyrrhetinic acid derivatives containing piperazine D34 and D35 was observed under the microscope. The cellular inhibition rate was detected by MTT; apoptosis was detected by Hoechst-33258 Staining Kit; and apoptosis rate was analyzed by flow cytometry method. Results The proliferation of SMMC-7721 cells was significantly inhibited by 18β-glycyrrhetinic acid derivatives containing piperazine D34 and D35 in a dose-dependent manner (P〈0.05). Conclusion 18β-glycyrrhetinic acid derivatives containing piperazine D34 and D35 can inhibit the proliferation and induce the apoptosis of SMMC-7721 cells, and they are superior to GA.
出处 《西安交通大学学报(医学版)》 CAS CSCD 北大核心 2016年第6期795-798,809,共5页 Journal of Xi’an Jiaotong University(Medical Sciences)
基金 国家自然科学基金资助项目(No.21062014)~~
关键词 18Β-甘草次酸 哌嗪衍生物 SMMC-7721 细胞凋亡 18β-glycyrrhetinic acid piperazine derivative SMMC-7721 apoptosis
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