基于综合生物信息学和实验验证的含人参中药方剂治疗肝细胞癌的药理作用

The American journal of Chinese medicine Pub Date : 2024-01-01 Epub Date: 2024-12-24 DOI:10.1142/S0192415X24500964
Tianqi Gao, Ruisheng Zhou, Dan Huang, Dailin Wu, Yong Gao, Yi Yuan, Jing Li, Shangyi Huang, Yanfang Xian, Ying Tang, Zhixiu Lin, Daihan Zhou, Shutang Wang
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引用次数: 0

摘要

含人参的参道软肝颗粒(STR)是中国治疗肝细胞癌(HCC)的知名中药处方。本研究旨在建立一个计算机实验框架,以破译STR治疗HCC的潜在机制。通过微阵列分析、网络药理学、rna测序(RNA-seq)、生物信息学分析和体内外实验等综合手段,揭示了STR的作用和作用机制。STR的引入可显著抑制HepG2和Huh7细胞的增殖和转移。STR治疗明显抑制移植Huh7肿瘤的生长。此外,STR降低了各种上皮-间质转化(EMT)相关蛋白的表达,包括N-cadherin、vimentin和catenin。通过采用系统生物学方法,从RNA-seq数据、TCGA-HCC数据集和网络药理学分析中鉴定出21个常见基因。最后,在TCGA队列中,这些基因中有9个被发现与HCC患者的OS和PFS相关。通过qPCR和WB验证候选基因发现,随着STR浓度的增加,pGSK3[公式:见文]和RELA蛋白的表达显著下调,这些结果阐明了STR抑制肿瘤生长和肝癌EMT的机制可能与GSK3[公式:见文]/RELA通路有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pharmacological Effects of a Ginseng-Containing Chinese Medicine Formula in Treating Hepatocellular Carcinoma Based on Comprehensive Bioinformatics and Experimental Validation.

Ginseng-containing Shentao Ruangan granules (STR) have been a well-known Chinese medicine prescription for the treatment of hepatocellular carcinoma (HCC) in China for decades. This study aimed to establish an in silico experimental framework to decipher the underlying mechanism of STR in the treatment of HCC. Microarray analysis, network pharmacology, RNA-sequencing (RNA-seq), bioinformatics analysis, and in vivo and in vitro experiments were used as integrated approaches to uncover the effects and mechanisms of action of STR. The introduction of STR significantly suppresses the proliferation and metastasis of HepG2 and Huh7 cells. STR treatment notably suppressed the growth of transplanted Huh7 tumors. Furthermore, STR administration reduced the expression of various epithelial-to-mesenchymal transition (EMT)-related proteins including N-cadherin, vimentin, and [Formula: see text]-catenin. By employing a systems biology approach, 21 common genes were identified across RNA-seq data, TCGA-HCC dataset, and network pharmacology analysis. Finally, of these genes nine were found to be associated with both OS and PFS in patients with HCC within the TCGA cohort. Validation of candidate genes by qPCR and WB identified a significant downregulation in the expression of pGSK3[Formula: see text] and RELA protein with increasing concentrations of STR. These results elucidated the mechanism by which STR inhibits tumor growth and EMT of HCC may be related to the GSK3[Formula: see text]/RELA pathway.

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