肝细胞癌
生物信息学
波形蛋白
下调和上调
生物
微阵列分析技术
体内
微阵列
中医药
转移
癌症研究
基因
生物信息学
基因表达
肿瘤科
医学
癌症
内科学
遗传学
病理
免疫组织化学
替代医学
作者
Tianqi Gao,Rui-Sheng Zhou,Dan Huang,Dailin Wu,Yong Gao,Yi Yuan,Jing Li,Shangyi Huang,Yanfang Xian,Ying Tang,Zhi‐Xiu Lin,Dai-Han Zhou,S. J. Wang
标识
DOI:10.1142/s0192415x24500964
摘要
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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