College of Life Science, Zhejiang Chinese Medical University, Zhejiang, Hangzhou, China.
J Cell Mol Med. 2024 Apr;28(8):e18211. doi: 10.1111/jcmm.18211.
Chaihu Shugan San (CSS) is a well-known traditional herbal formula that has the potential to ameliorate hepatocellular carcinoma (HCC); however, its mechanism of action remains unknown. Here, we identified the key targets of CSS against HCC and developed a prognostic model to predict the survival of patients with HCC. The effect of CSS plus sorafenib on HCC cell proliferation was evaluated using the MTT assay. LASSO-Cox regression was used to establish a three-gene signature model targeting CSS. Correlations between immune cells, immune checkpoints and risk score were determined to evaluate the immune-related effects of CSS. The interactions between the components and targets were validated using molecular docking and Surface Plasmon Resonance (SPR) assays. CSS and sorafenib synergistically inhibited HCC cell proliferation. Ten core compounds and 224 targets were identified using a drug compound-target network. The prognostic model of the three CSS targets (AKT1, MAPK3 and CASP3) showed predictive ability. Risk scores positively correlated with cancer-promoting immune cells and high expression of immune checkpoint proteins. Molecular docking and SPR analyses confirmed the strong binding affinities of the active components and the target genes. Western blot analysis confirmed the synergistic effect of CSS and sorafenib in inhibiting the expression of these three targets. In conclusion, CSS may regulate the activity of immune-related factors in the tumour microenvironment, reverse immune escape, enhance immune responses through AKT1, MAPK3, and CASP3, and synergistically alleviate HCC. The co-administration of sorafenib with CSS has a strong clinical outlook against HCC.
柴胡疏肝散(CSS)是一种著名的传统草药配方,具有改善肝细胞癌(HCC)的潜力;然而,其作用机制尚不清楚。在这里,我们确定了 CSS 针对 HCC 的关键靶标,并开发了一个预测 HCC 患者生存的预后模型。使用 MTT 法评估 CSS 加索拉非尼对 HCC 细胞增殖的影响。LASSO-Cox 回归用于建立针对 CSS 的三基因特征模型。确定免疫细胞、免疫检查点与风险评分之间的相关性,以评估 CSS 的免疫相关作用。使用分子对接和表面等离子体共振(SPR)实验验证了成分与靶点之间的相互作用。CSS 和索拉非尼协同抑制 HCC 细胞增殖。使用药物化合物-靶标网络鉴定了 10 种核心化合物和 224 个靶标。三个 CSS 靶标(AKT1、MAPK3 和 CASP3)的预后模型显示出预测能力。风险评分与癌症促进免疫细胞呈正相关,并且免疫检查点蛋白表达较高。分子对接和 SPR 分析证实了活性成分和靶基因具有很强的结合亲和力。Western blot 分析证实了 CSS 和索拉非尼协同抑制这三个靶标表达的作用。总之,CSS 可能通过 AKT1、MAPK3 和 CASP3 调节肿瘤微环境中免疫相关因子的活性,逆转免疫逃逸,增强免疫反应,并协同缓解 HCC。CSS 与索拉非尼联合使用具有很强的 HCC 临床前景。