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基于网络药理学、分子对接和体外实验探讨补骨脂定抗鼻咽癌的作用机制 被引量:3
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作者 覃柳洁 周守常 +4 位作者 白先愚 郭兴喆 杨江平 焦爱军 林文珍 《广西医科大学学报》 CAS 2023年第5期822-829,共8页
目的:基于网络药理学和生物信息学探讨补骨脂定(PSO)治疗鼻咽癌的作用及分子机制。方法:将鼻咽癌5-8F细胞分为5-8F组(0μmol/L PSO),PSO低剂量组(10μmol/L组)、中剂量组(20μmol/L组)、高剂量组(30μmol/L组)。通过CCK-8、平板克隆探究... 目的:基于网络药理学和生物信息学探讨补骨脂定(PSO)治疗鼻咽癌的作用及分子机制。方法:将鼻咽癌5-8F细胞分为5-8F组(0μmol/L PSO),PSO低剂量组(10μmol/L组)、中剂量组(20μmol/L组)、高剂量组(30μmol/L组)。通过CCK-8、平板克隆探究PSO对鼻咽癌5-8F细胞增殖、克隆形成的影响;Pubchem、Pharmmapper、GeneCards数据库得到PSO治疗鼻咽癌的潜在靶点;DAVID数据库进行GO、KEGG分析;STRING、GEPIA数据库和Cytoscape软件构建网络图并得到核心靶点;分子对接、western blotting对核心靶点及主要通路进行验证。结果:PSO呈浓度依赖性抑制5-8F细胞的增殖;与5-8F组比较,PSO各剂量组细胞克隆形成能力降低(P<0.05);PSO治疗鼻咽癌的潜在靶点共有66个,KEGG分析显示,与PI3K-Akt信号通路密切相关;核心靶点为ALB、HSP90AA1、SRC、EGFR、CASP3、ANXA5、MAPK1,其中ALB、HSP90AA1、ANXA5为生存相关靶点;PSO与核心靶点ALB、HSP90AA1、ANXA5具有良好的结合能力;与5-8F组比较,PSO高剂量组细胞中PI3K、p-PI3K、Akt、pAkt蛋白水平的表达降低(P<0.05)。结论:PSO可有效抑制鼻咽癌5-8F细胞的增殖、克隆形成,其抗鼻咽癌机制主要与抑制PI3K-Akt信号通路活性有关。 展开更多
关键词 补骨脂定 鼻咽癌 网络药理学 分子对接 PI3K-AKT信号通路
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Sanguinarine suppresses cell proliferation, migration and invasion in nasopharyngeal carcinoma via inhibiting mTOR signaling
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作者 YANG Mengzhe ZHANG Beibei +8 位作者 LIANG Zhenqiang CHENG Nannan LüAnqiao YANG Jianyu GUO Xingzhe BAI Xianyu HUANG Yuanjiao jiao aijun XU Ning 《Journal of Traditional Chinese Medicine》 SCIE CSCD 2022年第5期687-692,共6页
OBJECTIVE: To confirm the anti-NPC effect of sanguinarine(SA) through a series of wet experiments.METHODS: NPC cell viability was determined by proliferation experiment. Cell clone formation experiment, cell scratch t... OBJECTIVE: To confirm the anti-NPC effect of sanguinarine(SA) through a series of wet experiments.METHODS: NPC cell viability was determined by proliferation experiment. Cell clone formation experiment, cell scratch test, transwell migration and invasion experiment and flow cytometry-based cell apoptosis assay were further performed. In addition, Western blotting was performed to investigate the cell signaling pathway. All the relevant experimental data were statistically processed using SPSS 16.0 software.RESULTS: The results showed that sanguinarine represented a time and dose dependent inhibition effects on NPC cell proliferation including the low differentiated CNE2 cells and high metastatic 5-8F cells, along with the cell cloning ability reduction. In addition, sanguinarine has a certain inhibitory effect on the invasion and migration of NPC cells. Mechanistically, sanguinarine displayed the anti-NPC effects mainly involved into the suppression of m TOR signaling and cell apoptosis, which is closely associated with the tumor growth and metastatic malignancy. CONCLUSIONS: Collectively, we discover that sanguinarine is a new high-efficiency anti-NPC monomer of Chinese medicine, with a value for the follow-up preclinical research. 展开更多
关键词 nasopharyngeal carcinoma SANGUINARINE TOR serine-threonine kinases apoptosis
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