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首页> 外文期刊>International journal of molecular medicine >Zanthoxylum avicennae extracts inhibit cell proliferation through protein phosphatase 2A activation in HA22T human hepatocellular carcinoma cells in vitro and in vivo
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Zanthoxylum avicennae extracts inhibit cell proliferation through protein phosphatase 2A activation in HA22T human hepatocellular carcinoma cells in vitro and in vivo

机译:花椒提取物通过蛋白磷酸酶2A活化在体外和体内抑制HA22T人肝癌细胞中的细胞增殖

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Hepatocellular carcinoma is a common type of cancer that is usually associated with poor prognosis. In this study, we examined the in vitro and in vivo mechanisms of the traditional Vietnamese herb Zanthoxylum avicennae on the inhibition of HA22T human hepatocellular carcinoma cell proliferation. HA22T cells were treated with different concentrations of Zanthoxylum avicennae extracts (YBBEs) and analyzed with the MTT assay, western blot analysis, flow cytometry, siRNA transfection assays and co-immunoprecipitation assay. Additionally, the HA22T-implanted xenograft nude mouse model was applied to confirm the cellular effects. YBBEs showed a strong inhibition of HA22T cell viability in a dose-dependent manner and significantly reduced cell proliferation-related proteins as well as induced cell cycle arrest in the G2/M phase. Protein phosphatase 2A (PP2A) siRNA or okadaic acid totally blocked YBBE-mediated cell proliferation inhibition. In addition, an HA22T-implanted nude mouse model further confirmed that YBBEs inhibit HA22T tumor cell growth and downregulate the survival and cell cycle regulating proteins, as well as activate the PP2A protein. Our findings indicate that the inhibition of HA22T cell proliferation by YBBEs is mediated through PP2A activation.
机译:肝细胞癌是常见的癌症类型,通常与不良预后相关。在这项研究中,我们研究了传统越南草药花椒(Zanthoxylum avicennae)抑制HA22T人肝癌细胞增殖的体外和体内机制。用不同浓度的花椒提取物(YBBEs)处理HA22T细胞,并用MTT分析,western印迹分析,流式细胞仪,siRNA转染分析和免疫共沉淀分析进行分析。另外,将HA22T植入的异种移植裸鼠模型应用于证实细胞效应。 YBBEs以剂量依赖的方式显示出对HA22T细胞活力的强烈抑制,并显着降低了与细胞增殖相关的蛋白,并诱导了G2 / M期的细胞周期停滞。蛋白磷酸酶2A(PP2A)siRNA或冈田酸完全阻断了YBBE介导的细胞增殖抑制作用。此外,植入HA22T的裸鼠模型进一步证实YBBE抑制HA22T肿瘤细胞的生长并下调存活和细胞周期调节蛋白,并激活PP2A蛋白。我们的发现表明,YBBEs对HA22T细胞增殖的抑制作用是通过PP2A激活介导的。

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