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Therapeutic effects of Euphorbia Pekinensis and Glycyrrhiza glabra on Hepatocellular Carcinoma Ascites Partially Via Regulating the Frk-Arhgdib-Inpp5d-Avpr2-Aqp4 Signal Axis

机译:一品红和甘草对肝癌腹水的治疗作用部分通过调节Frk-Arhgdib-Inpp5d-Avpr2-Aqp4信号轴

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摘要

To clarify unknown rationalities of herbaceous compatibility of Euphorbia Pekinensis (DJ) and Glycyrrhiza glabra (GC) acting on hepatocellular carcinoma (HCC) ascites, peritoneum transcriptomics profiling of 15 subjects, including normal control (Con), HCC ascites mouse model (Mod), DJ-alone, DJ/GC-synergy and DJ/GC-antagonism treatment groups were performed on OneArray platform, followed by differentially expressed genes (DEGs) screening. DEGs between Mod and Con groups were considered as HCC ascites-related genes, and those among different drug treatment and Mod groups were identified as DJ/GC-combination-related genes. Then, an interaction network of HCC ascites-related gene-DJ/GC combination-related gene-known therapeutic target gene for ascites was constructed. Based on nodes’ degree, closeness, betweenness and k-coreness, the Frk-Arhgdib-Inpp5d-Avpr2-Aqp4 axis with highly network topological importance was demonstrated to be a candidate target of DJ/GC combination acting on HCC ascites. Importantly, both qPCR and western blot analyses verified this regulatory effects based on HCC ascites mice in vivo and M-1 collecting duct cells in vitro. Collectively, different combination designs of DJ and GC may lead to synergistic or antagonistic effects on HCC ascites partially via regulating the Frk-Arhgdib-Inpp5d-Avpr2-Aqp4 axis, implying that global gene expression profiling combined with network analysis can offer an effective way to understand pharmacological mechanisms of traditional Chinese medicine prescriptions.
机译:为了阐明作用于肝细胞癌(HCC)腹水的大戟(DJ)和甘草(GC)的草本相容性的未知合理性,包括正常对照(Con),HCC腹水小鼠模型(Mod)在内的15位受试者的腹膜转录组谱,在OneArray平台上进行单独DJ,DJ / GC协同作用和DJ / GC拮抗作用治疗组,然后筛选差异表达基因(DEG)。 Mod组和Con组之间的DEG被认为是HCC腹水相关基因,而不同药物治疗组和Mod组之间的DEG被认为是DJ / GC组合相关基因。然后,构建了HCC腹水相关基因-DJ / GC结合相关基因-已知的腹水治疗靶基因的相互作用网络。基于节点的程度,紧密度,中间度和k核,具有高度网络拓扑重要性的Frk-Arhgdib-Inpp5d-Avpr2-Aqp4轴被证明是DJ / GC组合作用于HCC腹水的候选目标。重要的是,基于体内HCC腹水小鼠和体外M-1收集导管细胞,qPCR和Western blot分析均证实了这种调节作用。总体而言,DJ和GC的不同组合设计可能部分通过调节Frk-Arhgdib-Inpp5d-Avpr2-Aqp4轴而对HCC腹水产生协同或拮抗作用,这意味着与网络分析相结合的全局基因表达谱分析可以提供一种有效的方法来了解中药处方的药理机制。

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