Article Summary
李响 李郑 程燚 贾晓兰 王劲.三七总皂甙对人急性髓系白血病细胞株U937 的抑制增殖及诱导凋亡作用[J].现代生物医学进展英文版,2016,16(4):657-660.
三七总皂甙对人急性髓系白血病细胞株U937 的抑制增殖及诱导凋亡作用
Antiproliferative and Proapoptotic Effects of Panax Notoginsenosides onAcute Myelogenous Leukemia Cells U937
  
DOI:
中文关键词: 三七总皂甙  细胞凋亡  白血病  Bax  Bcl-2
英文关键词: Panax notoginsenosides  Apoptosis  Acute myelogenous leukemia  Bax  Bcl-2
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Author NameAffiliation
李响 李郑 程燚 贾晓兰 王劲 第三军医大学第三附属医院血液科第三军医大学第三附属医院肿瘤中心总参管理保障部北极寺老干局门诊部 
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中文摘要:
      目的:观察三七总皂甙( panax notoginsenosides,PNS )对人急性髓系白血病细胞株U937 凋亡的影响,并探讨PNS 对Bax 和 Bcl-2 蛋白表达的影响。方法:将处于对数生长期的U937 细胞分为5 组:正常对照组及PNS 组(5 mg/L、10 mg/L、20 mg/L、40 mg/L),药物作用12 h、24 h、48 h后,CCK-8 比色法检测PNS 对肿瘤细胞的相对细胞活力的影响;流式细胞术检测PNS促进细胞 凋亡的能力;RT-PCR 和Western blot 法分别检测不同浓度的PNS 对Bax 和Bcl-2 蛋白表达的影响。结果:CCK-8 分析显示, PNS 在低浓度(≤ 40 mg/L)能明显抑制肿瘤细胞的活力,40 mg/L 处理组较正常对照组细胞活力在3 个时间点分别下降47%、 72%、85%;与对照组相比,处理组的凋亡率显著增加,10 mg/L、20 mg/L、40 mg/L 实验组凋亡率分别上升7%、10%、43%;PNS能明 显增加细胞内Bax mRNA及蛋白的表达,抑制Bcl-2 mRNA及蛋白的表达。结论:PNS 具有抑制人急性髓系白血病细胞株U937 的增殖抑制及凋亡诱导作用,并能影响Bax 和Bcl-2 蛋白的表达。文章探讨了PNS 抑制肿瘤发展可能存在的作用机制,为将来进 一步研发PNS 作为白血病治疗药物奠定基础。
英文摘要:
      Objective:To investigate the induced-apoptosis effect of Panax notoginsenosides (PNS) in Acute myelogenous leukemia cells U937 and the effect of PNS on Bax and Bcl-2 protein expression.Methods:Cultured-activated U937 cells were divided into 5 groups: normal control group, PNS-treated group (5, 10, 20, 40 mg/L). The cell viability was assessed by CCK-8 Assay after 12h, 24 h and 48 h treated by PNS. After being treated with different concentrations of PNS for 24 hours, the cell apoptosis was determined by flow cytometry. The expression of Bax and Bcl-2 mRNA and protein level were observed by RT-PCR and Western blotting, respectively.Results:PNS inhibited the growth of tumor cells in the low concentration(≤ 40 mg/L)with a dose-dependent manner. After treated by PNS for 12 h, 24 h and 48 h, compared to the normal control group, the cell viability of 40 mg/L treated group was decreased 47%、72%、 85%, respectively. Further study on PNS showed that it induced apoptosis in U937 cell line. 10 mg/L, 20 mg/L, 40 mg/L PNS increased the apoptosis rate by 7%, 10% and 43%, respectively, compared to that in the control group. The expression of Bax mRNA was upregulated by PNS, wheras the mRNA level of Bcl-2 was downregulated. A Western blotting analysis indicated that PNS increased the expression of the Bax, decreased the expression of Bcl-2.Conclusion:These results indicate that PNS exhibits significant activity against acute myelogenous leukemia cells U937 in vitro and can induce apoptosis besides it can influence the expression of Bax and Bcl-2. PNS is a potential therapeutic agent for acute myelogenous leukemia.
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