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首页> 外文期刊>Journal of biomedical nanotechnology >Mechanism of Action of Periplogenin on Nasopharyngeal Carcinoma Based on Network Pharmacology and Experimental Study of Vitamin E Coupled with Periplogenin Self-Assembled Nano-Prodrug for Nasopharyngeal Carcinoma
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Mechanism of Action of Periplogenin on Nasopharyngeal Carcinoma Based on Network Pharmacology and Experimental Study of Vitamin E Coupled with Periplogenin Self-Assembled Nano-Prodrug for Nasopharyngeal Carcinoma

机译:基于网络药理学的鼻咽癌对鼻咽癌的作用机制及维生素E与鼻咽癌自组装纳米前药的鼻咽癌

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Periplogenin is a compound extracted from cortex periplocae. In the monomers' screening for inhibiting nasopharyngeal carcinoma, we found that periplogenin can inhibit nasopharyngeal carcinoma; however, its mechanism is still unclear. In this study, the chemical structure of periplogenin was uploaded to the PubChem database in order to obtain the target of periplogenin. The NPC's differential genes were obtained by analyzing the nasopharyngeal carcinoma data in the GEO database by R software. The common target of periplogenin and nasopharyngeal carcinoma was obtained through Cytoscape. Through R software analysis, ALB, epidermal growth factor receptor (EGFR), MAPK1, ESR1, MAPK8, SRC, CASP3, HSP90AA1, AR, MAPK14 may be the main targets of periplogenin in NPC. Through go enrichment analysis, it was found that periplogenin acted mainly on nasopharyngeal carcinoma through response to steroid metabolic process, cellular response to steroid hormone stimulus, hormone-mediated, and steroid hormone signaling pathway. After enrichment analysis on the Kyoto Encyclopedia of Genes and Genomes pathway, it was found that periplocan may inhibit NPC through the MAPK signaling pathway (the main signaling pathway), and the signaling pathway of proteoglycans in cancer, and the PI3K/AKT signaling pathway as well. In this study, we also carried out the experimental study of vitamin E together with periplogenin self-assembled nano-prodrugs in the treatment of NPC, and the results showed that tumor weight of PBS group was 0.531 +/- 0.039 g, while that of PPG group and MPSSV-NPs group was 0.258 +/- 0.059 g and 0.169 +/- 0.033 g, respectively, which was lower than PBS group. And the tumor inhibition rate of MPSSV-NPs was 69.41%, which was significantly higher than that of the PPG group (51.38%). This study demonstrated the mechanism of inhibition of nasopharyngeal carcinoma (NPC) by the monomer of periplogenin based on network pharmacology. We preliminarily confirmed that vitamin E coupled w
机译:香加素是从香加皮中提取的化合物。在抑制鼻咽癌的单体筛选中,我们发现外周血素可以抑制鼻咽癌;然而,其机制尚不清楚。在本研究中,为了获得外周素的靶点,外周素的化学结构被上传到PubChem数据库。通过R软件分析GEO数据库中的鼻咽癌数据,获得NPC的差异基因。通过Cytoscape获得了外周血原蛋白与鼻咽癌的共同靶点。通过R软件分析,ALB、表皮生长因子受体(EGFR)、MAPK1、ESR1、MAPK8、SRC、CASP3、HSP90AA1、AR、MAPK14可能是鼻咽癌外周蛋白的主要靶点。通过go富集分析发现,外周素主要通过对类固醇代谢过程的反应、细胞对类固醇激素刺激的反应、激素介导的反应和类固醇激素信号通路作用于鼻咽癌。通过对京都基因和基因组途径百科全书的浓缩分析,发现杠柳聚糖可能通过MAPK信号通路(主要信号通路)、癌症中蛋白多糖的信号通路以及PI3K/AKT信号通路抑制NPC。在本研究中,我们还进行了维生素E与外周血素自组装纳米前体药物联合治疗鼻咽癌的实验研究,结果显示,PBS组的肿瘤重量为0.531+/-0.039 g,而PPG组和MPSSV NPs组的肿瘤重量分别为0.258+/-0.059 g和0.169+/-0.033 g,低于PBS组。MPSSV-NPs的抑瘤率为69.41%,明显高于PPG组(51.38%)。本研究以网络药理学为基础,探讨了外周素单体对鼻咽癌的抑制机制。我们初步证实,维生素E与w

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