首页|匹伐他汀治疗肝细胞癌机制的网络药理学研究

匹伐他汀治疗肝细胞癌机制的网络药理学研究

扫码查看
目的 通过网络药理学、分子对接及体外细胞实验验证匹伐他汀治疗肝细胞癌的药效及其分子机制.方法 使用PharmMapper网站预测匹伐他汀的作用靶点.通过GeneCards、OMIM及DisGeNet数据库获得肝细胞癌的潜在靶点.采用STRING数据库获得匹伐他汀与肝细胞癌交集靶点的蛋白相互作用网络(PPI),并通过Cytoscape软件筛选关键靶点.使用分子对接评估匹伐他汀与关键靶点间的亲和力.在体外肝癌细胞系中验证匹伐他汀对细胞存活率的影响.结果 共筛选得到匹伐他汀靶点286个,肝细胞癌靶点609个,二者交集靶点37个.通过PPI共筛选得到EGFR、ALB、HSP90AA1靶点.匹伐他汀与3个关键靶点均有较强的亲和力.40 pmol·L-1匹伐他汀处理24 h可抑制HepG2肿瘤细胞的生长.结论 匹伐他汀具一定的抗肝癌作用,可能与调控EGFR、ALB、HSP90AA1多种靶点有关.
Study on the mechanism of Pitavastatin treatment for hepatocellular carcinoma based on Network pharmacology
OBJECTIVE To validate the efficacy of Pitavastatin in treating hepatocellular carcinoma and its molecular mechanism through Network pharmacology,molecular docking,and experiment on cells in vitro.METHODS Targets of Pitavastatin were predicted using PharmMapper.The potential targets of hepatocellular carcinoma were obtained from GeneCards,OMIM,and DisGeNet databases.The STRING database was used to obtain protein-protein interaction networks(PPI)of intersecting targets between Pitavastatin and hepatocellular carcinoma,and Cytoscape was used to obtain key targets from PPI.The affinity between Pitavastatin and the key targets was assessed using molecular docking.Finally,the effect of Pitavastatin on hepatocellular carcinoma was verified in HepG2 cells in vitro.RESULTS A total of 289 Pitavastatin targets,609 hepatocellular carcinoma targets,and 37 intersecting targets were screened.Three key targets including EGFR,ALB,and HSP90AA1 were identified by PPI.Pitavastatin had a strong affinity with the three key targets.40 μmol·L-1 Pitavastatin treatment for 24 h could inhibit the growth of HepG2 cells.CONCLUSION Pitavastatin has certain anti-hepatocellular carcinoma effects,and the mechanism may be related to EGFR,ALB,and HSP90AA1.

PitavastatinHepatocellular carcinomaNetwork pharmacologyMolecular dockingCell assay verificationEGFRALBHSP90AA1

梁中旭、蒋学华、王凌

展开 >

四川大学华西药学院,四川成都 610041

匹伐他汀 肝细胞癌 网络药理学 分子对接 细胞实验 表皮生长因子受体 白蛋白 热休克蛋白

2024

华西药学杂志
四川大学,四川省药学会

华西药学杂志

CSTPCD北大核心
影响因子:0.624
ISSN:1006-0103
年,卷(期):2024.39(6)