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Pharmacological evaluation and mechanistic study of compound Xishu Granule in hepatocellular carcinoma

机译:肝细胞癌复方番禺颗粒的药理评价与机械研究

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ObjectiveIn this study, we used HepG2 human hepatocellular carcinoma cells to study the effects of Compound Xishu Granule (CXG) on cell proliferation, apoptosis, and the cell cyclein?vitro. We also used a xenograft tumor model to study the anti-tumor effects of CXG and related mechanismsin?vivo.MethodsThe effect of CXG on cell viability was measured using Cell Counting Kit-8 and a colony formation assay. The effect of CXG on apoptosis and the cell cycle was analyzed using flow cytometry. Thein?vivoanti-tumor effect of CXG was assessed by measuring the volume change in xenograft tumors after drug administration. The CXG anti-tumor mechanism was studied using western blotting assay to detect cell cycle and apoptotic associated proteins.ResultsCXG suppressed HepG2 cell proliferation in a time- and dose-dependent mannerin?vitro. Colony formation experiments showed that CXG administration for 24?h significantly reduced HepG2 cell formations (P?
机译:目的鉴定本研究,我们使用Hepg2人肝细胞癌细胞来研究复方番禺颗粒(CXG)对细胞增殖,细胞凋亡和细胞周期素的影响。我们还使用了异种移植肿瘤模型来研究CXG和相关机制的抗肿瘤作用ΔVivo.M使用细胞计数试剂盒-8和菌落形成测定测量CXG对细胞活力的影响。用流式细胞术分析CXG对细胞凋亡和细胞周期的影响。通过测量药物施用后的异种移植肿瘤的体积变化来评估CXG的蛋白质的诱发效果。使用蛋白质印迹测定来研究CXG抗肿瘤机制,以检测细胞周期和凋亡相关蛋白质。抑制时间和剂量依赖的典型抑制HepG2细胞增殖。菌落形成实验表明,CXG施用24μm,显着降低了HepG2细胞形成(p≤101)。流式细胞术分析表明,CXG处理48〜H促进细胞凋亡并在G2 / M相中阻断了HepG2细胞。 Western印迹结果表明,在CXG给药后,BCCR-2在接枝肿瘤组织和HepG2细胞中下调,增加了Bax / Bcl-2的比例。 PLK1,CDC25C,CDK1和细胞周期蛋白B1表达被上调。 CXG对接枝肿瘤生长症具有良好的抑制作用?Vivo.conclusioncxg具有良好的抗肿瘤作用?vivoandinα体外,CXG促进Hepg2细胞凋亡并诱导G2 / M期捕获.IVIVO,CXG显着抑制接枝肿瘤生长。治疗肝细胞癌的CXG机制可能是CXG可以诱导异常的凋亡和细胞周期相关的蛋白质表达,导致有丝分裂灾难和凋亡。

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