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OSW-1 Induced Apoptosis in Hepatocellular Carcinoma through Generation of ROS, Cytochrome C and Noxa Activation Independent of p53 with Non-Activation of Caspase-3

机译:OSW-1通过产生ROS,细胞色素C和NOXA活化在肝细胞癌中诱导肝细胞癌的细胞凋亡,与P53无关,无活化Caspase-3

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Aim: To study the antitumor mechanism of OSW-1 in hepatocellular carcinoma. Materials and Methods: The expression profiling microarray was carried out to extract RNA from SK-Hep-1 which suffered from OSW-1. ρ0-SK-Hep-1 was maintained SK-Hep-1 in MEM containing 100 μg/L ethidium bromide (EB), 1 mM sodium pyruvate and 50 μg/ml uridine for 40 days. Then confirmed COX-I and COX-II of mitochondrial DNA were knocked out. Cells suffered from OSW-1 or doxorubicin. Then cells were washed twice with cold PBS and incubated with DCFH-DA. Fluorescent signal was recorded by using Infinite 200 Pro multimode Plate readers. Results: OSW-1 elevates generation of ROS and Cytochrome C which are associated with the induction of apoptosis in SK-Hep-1 cells. We also demonstrate that OSW-1 does not depend on p53 to up-regulate the BH3-only protein Noxa. What is more noteworthy that the Caspase-9 and FADD are down-regulated in above process. Conclusion: OSW-1 induced special apoptosis is different from the mitochondrial death pathway and the death receptor pathway and final result is not Caspase family’s activating. This provides a novel theory that nonmalignant cells are significantly less sensitive to OSW-1 than cancer cell lines.
机译:目的:研究肝细胞癌OSW-1的抗肿瘤机制。材料和方法:进行表达分析微阵列,以从患OSW-1患者中提取来自SK-HEP-1的RNA。 ρ0-sk-hep-1在MEM中保持含有100μg/ l溴化乙锭(EB),1mM丙酮酸钠和50μg/ ml尿苷的40天。然后被证实的COX-I和COX-II的线粒体DNA被淘汰。患OSW-1或多柔比星的细胞。然后用冷PBS洗涤细胞两次,并与DCFH-DA温育。使用无限200 Pro多模板读数器记录荧光信号。结果:OSW-1升高了ROS和细胞色素C的产生,其与SK-HEP-1细胞中凋亡的诱导相关。我们还证明OSW-1不依赖于P53来上调BH3蛋白NOXA。更值得注意的是,Caspase-9和FADD在上述过程中受到了下调。结论:OSW-1诱导的特殊细胞凋亡与线粒体死亡途径不同,死亡受体途径和最终结果不是Caspase系列的激活。这提供了一种新颖的理论,即非开始细胞显着对OSW-1敏感而不是癌细胞系。

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