整合网络药理和实验验证,以确定肝癌的关键草药成分和标
Fang Wang1,2,3, Shenghao Li3, Xiling Liu1
1Hebei Medical University, Shijiazhuang, China.
Iranian journal of pharmaceutical research : IJPR
|October 17, 2025
概括
传统中医药 (TCM) 在肝癌治疗方面表现有前途. 这项研究确定了关键的草药,比如β-醇等化合物,以及JUN等标,通过网络药理学和体外实验验验证了它们的治疗潜力.
科学领域:
- 综合性瘤学是一种综合性瘤学.
- 网络药理学 网络药理学
- 计算生物学是一种计算生物学.
背景情况:
- 传统中医 (TCM) 提供了一种整体的策略来管理恶性瘤.
- 肝癌仍然是一个重大的全球健康挑战,需要新的治疗方法.
研究的目的:
- 用数据挖掘和网络药理学来预测高频草药,活性化合物和肝癌治疗的核心分子标.
- 建立一个全面的网络,将TCM,活性成分,标和肝癌联系起来.
- 通过分子对接和体外测试来验证已识别的组件和点的治疗潜力.
主要方法:
- 使用Cytoscape构建一个"TCM - 活性成分 - 目标 - 疾病"网络.
- 通过STRING数据库开发蛋白质与蛋白质相互作用 (PPI) 网络,用于核心目标识别.
- 使用AutoDock Vina和PyMOL进行分子对接模拟,以评估结合亲缘关系.
- 在体外实验中评估奎尔素对肝癌细胞迁移,细胞亡和蛋白质表达的影响.
主要成果:
- 识别了50种高频TCM,包括*Atractylodes macrocephala*,*Astragalus membranaceus*,*Scutellaria barbata*和*Cremastra appendiculata*.这些高频TCM的确诊情况包括在内.
- 发现了226个常见的标,其中β-固醇,kaempferol,stigmasterol和luteolin被确定为潜在的核心成分.
- 对8个关键目标 (JUN,MAPK1,RELA,TNF,ESR1,IL-6,TP53,FOS) 的选,涉及417个入口和159个通道.
- 分子对接证实了强烈的结合亲缘关系;体外研究表明,奎尔素通过调节p-c-Jun/c-Jun和c-Fos表达来抑制HepG2细胞迁移和诱导细胞亡.
结论:
- 这项研究为TCM在肝癌治疗中的临床应用提供了数据驱动的基础.
- 确定了核心组件和目标,为肝癌管理提供了潜在的治疗策略.
- 网络药理学和实验验证强调了TCM在癌症治疗中的复杂机制.
关键词:
AP-1 AP-1 AP-1 AP-1 AP-1 AP-1 AP-1 AP-1 AP-1 AP-1 AP-1 AP-1 AP-1 AP-1 AP-1 AP-1 AP-1 AP-1 AP-1 AP-1 AP-1 AP-1 AP-1 AP-1 AP-1 AP-1 AP-1 AP-1 AP-1 AP-1 AP-1 AP-1 AP-1 AP-1 AP-1 AP-1热清除 - 清除热量激发活力的人气.肝癌 肝癌 是一种癌症.传统中国医药 传统中国医药更多相关视频
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