郑玲1*,吕寒静1,Mouad Edderkaoui2,Stephen J Pandol2.XIAP抑制剂Embelin体外对人胰腺癌细胞株的抑制效应与机制研究[J].山西医科大学学报,2009,40(1):20~23 |
XIAP抑制剂Embelin体外对人胰腺癌细胞株的抑制效应与机制研究 |
Inhibitive effect of a XIAP inhibitor Embelin on human pancreatic carcinoma cells and its mechanism |
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DOI: |
中文关键词: Embelin 人胰腺癌细胞株 凋亡 增殖 |
英文关键词: Embelin human pancreatic carcinoma cell apoptosis proliferation |
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中文摘要: |
目的〓
探讨XIAP小分子抑制剂Embelin体外对人胰腺癌细胞株MIAPaCa 2的抑制效应与机制。
〓方法〓
将生长至第4-12代之间的MIAPaca 2细胞分为DMSO对照组与Embelin实验组,在实验组细胞中加入不同浓度的Embelin共孵育72 h,收集细胞并裂解后取上清液用细胞凋亡试剂盒检测组蛋白(凋亡指标)的OD值水平。MIAPaca 2细胞加入不同浓度的Embelin共孵育60 h后再加入3H胸腺嘧啶继续孵育12 h,取细胞裂解液用同位素γ闪烁计数仪检测3H CPM数值以判断细胞增殖程度。对DMSO对照组与Embelin实验组的组蛋白OD值与3H CPM数值分别进行比较分析。
〓结果〓
Embelin实验组的MIAPaCa 2细胞株组蛋白OD值显著高于DMSO对照组而3H CPM数值明显低于DMSO对照组(P<0.01),且实验组Embelin的作用浓度与组蛋白OD值呈正相关(r=0.996,P<0.01),而与3H CPM数值呈负相关(r=-0.993,P<0.01)。
〓结论〓
Embelin呈剂量依赖性地诱导人胰腺癌细胞株MIAPaCa 2凋亡并抑制其增殖,有肿瘤抑制效应。 |
英文摘要: |
Objective〓
To explore the inhibitive effect of Embelin,a small molecule XIAP inhibitor,on human pancreatic carcinoma cells MIAPaCa 2 and its mechanism.
〓Methods〓
MIAPaCa 2 cells of generation 4 to generation 12 were divided into Embelin group and DMSO control group.MIAPaCa 2 cells in Embelin group were cultured with different concentrations of Embelin for 72 h,harvested and lysed.And then histone levels were determined with cell death detection ELISAPLUS kit.MIAPaCa 2 cells were cultured with diffe rent concentrations of Embelin for 60 h,and then cultured with 3H thymidine for 12 h.Then 3H CPM values were measured with scintillation counter in cell lysis supernatants.
〓Results〓
OD values of histone in Embelin group were higher than those in DMSO control group(P<0.01),while 3H CPM values in Embelin group were lower than those in DMSO control group(P<0.01).Embelin concentrations in Embelin group were positively related with histone OD values(r=0.996,P<0.01),but negatively related with 3H CPM values(r=-0.993,P<0.01).
〓Conclusion〓
Embelin may have anti tumor effect on human carcinoma cells by inducing the apoptosis of human pancreatic carcinoma cell MIAPaCa 2 and inhibiting dose dependently its proliferation. |
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