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Smac类似物Birinapant的抗肝癌作用及其相关分子机制

[Anti-hepatoma effects of Smac analogue Birinapant and its related molecular mechanism].

作者信息

Jiang Pan-Ruo, Ke Rui-Jun, Zhu Ming-Liao, Lou En-Zhe, Xie Jia-Geng, Chen Jia-Yu

机构信息

Medical School, Shaoxing University, Shaoxing 312000, China.

出版信息

Zhongguo Ying Yong Sheng Li Xue Za Zhi. 2018 Jun 8;34(6):524-529. doi: 10.12047/j.cjap.5685.2018.117.

Abstract

OBJECTIVE

To investigate the effects of Birinapant on hepatocellular carcinoma cells and its related molecular mechanisms.

METHODS

Human hepatocellular carcinoma cells QGY-7701 were treated with 0, 1, 5, 25 and 125 nmol/L Birinapant for 24, 48 and 72 hours respectively, each experiment 3 wells.The proliferation activity of cells, the apoptosis levels, the cells nuclear type, the mitochondrial membrane potential, the transcription and expression levels of genes and the cytotoxicity of Birinapant were analyzed.At the same time, 4-week-old male BALB/C mice were randomly divided into 5 groups, with 20 mice in each group.The mice were inguinal injected with QGY-7701 cells, and then subcutaneous injected with Birinapant (concentrations ranging from 0, 1, 5, 25, 125 μg/kg) in each group after two days, once every other day.On 18 day since first Birinapant injection, 10 mice were killed in each group to weigh tumor tissue and survival time was recorded from the remaining 10 mice.The effects of Birinapant on the growth of the tumor and the survival time of tumor-bearing mice were observed.

RESULTS

Compared with the negative control (NC) group, the proliferation activity of QGY-7701 was inhibited significantly after Birinapant treatment and the apoptosis levels were increased significantly (<0.01).The cell mitochondrial membrane potential was decreased and the karyotype was changed (<0.01).At the same time, the transcription and expression levels of genes cellular inhibitor of apoptosis protein 1(cIAP-1), cellular inhibitor of apoptosis protein 2(cIAP-2), ras, raf, mek and erk were significantly decreased (<0.01), while the expression levels of caspase-3 and caspase-9 genes were up-regulated (<0.01).Compared with the model group (MG), the growth of the tumor was inhibited significantly and the survival time of the tumor-bearing mice was prolonged after Birinapant treatment (<0.01).

CONCLUSIONS

Birinapant can inhibit the expression of cIAP-1, cIAP-2 and the proteins of Ras-Raf-MEK-ERK signal pathways, so as to activate the mitochondria mediated endogenous apoptosis pathway.Birinapant shows a certain inhibitory effect on liver cancer.

摘要

目的

探讨比瑞那潘对肝癌细胞的作用及其相关分子机制。

方法

将人肝癌细胞QGY-7701分别用0、1、5、25和125 nmol/L的比瑞那潘处理24、48和72小时,每个实验设3个孔。分析细胞的增殖活性、凋亡水平、细胞核型、线粒体膜电位、基因的转录和表达水平以及比瑞那潘的细胞毒性。同时,将4周龄雄性BALB/C小鼠随机分为5组,每组20只。小鼠腹股沟注射QGY-7701细胞,两天后每组皮下注射比瑞那潘(浓度分别为0、1、5、25、125 μg/kg),每隔一天注射一次。自首次注射比瑞那潘后的第18天,每组处死10只小鼠称取肿瘤组织重量,并记录其余10只小鼠的生存时间。观察比瑞那潘对肿瘤生长及荷瘤小鼠生存时间的影响。

结果

与阴性对照组(NC)相比,比瑞那潘处理后QGY-7701的增殖活性显著受到抑制,凋亡水平显著升高(P<0.01)。细胞线粒体膜电位降低,核型改变(P<0.01)。同时,凋亡抑制蛋白1(cIAP-1)、凋亡抑制蛋白2(cIAP-2)、ras、raf、mek和erk基因的转录和表达水平显著降低(P<0.01),而半胱天冬酶-3(caspase-3)和半胱天冬酶-9(caspase-9)基因的表达水平上调(P<0.01)。与模型组(MG)相比,比瑞那潘处理后肿瘤生长显著受到抑制,荷瘤小鼠的生存时间延长(P<0.01)。

结论

比瑞那潘可抑制cIAP-1、cIAP-2的表达以及Ras-Raf-MEK-ERK信号通路的蛋白表达,从而激活线粒体介导内源凋亡途径。比瑞那潘对肝癌显示出一定的抑制作用。

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