[Inhibitory effect of Fuzheng Huaji Decoction against non-small cell lung cancer cells in vitro and the possible molecular mechanism].

Q3 Medicine
Lijun He, Xiaofei Chen, Chenxin Yan, Lin Shi
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引用次数: 0

Abstract

Objectives: To investigate the inhibitory effect of Fuzheng Huaji Decoction against non-small cell lung cancer (NSCLC) cells in vitro and explore the underlying mechanism.

Methods: The active ingredients and targets of Fuzheng Huaji Decoction were identified using TCMSP and SwissTargetPrediction databases. NSCLC-related targets from GeneCards and PharmGKB were intersected with the targets of the Decoction, and a protein-protein interaction (PPI) network was constructed to identify the core targets, which were analyzed with GO and KEGG pathway enrichment analysis. Cultured A549 cells were treated with different concentrations of Fuzheng Huaji Decoction-medicated serum, and the changes in cell proliferation, apoptosis, and protein expressions were examined using CCK-8 assay, annexin V-FITC/PI staining and Western blotting.

Results: Fuzheng Huaji Decoction contained 140 active ingredients, and 707 drug-disease intersecting targets were identified. Among these targets, TP53, AKT1, HIF1A, GAPDH, ALB, EGFR, CTNNB1, and TNF were identified as the core targets which were involved in the biological processes related to kinases and receptors and the PI3K-AKT, Ras, calcium, and MAPK pathways. Molecular docking studies indicated strong binding affinity of the active ingredients with TP53, AKT1, and HIF1A. In cultured A549 cells, treatment with 2.5%, 5%, and 10% Fuzheng Huaji Decoction-medicated serum significantly inhibited cell proliferation, promoted cell apoptosis, and downregulated the expression levels of HIF1A, p-AKT (Thr308), and TP53 proteins.

Conclusions: Fuzheng Huaji Decoction inhibits proliferation of NSCLC cells possibly by downregulating the expressions of HIF1A, p-AKT (Thr308), and TP53.

扶正化瘀汤对非小细胞肺癌细胞的体外抑制作用及可能的分子机制
目的:观察扶正化瘀汤对非小细胞肺癌(NSCLC)细胞的体外抑制作用,并探讨其作用机制。方法:采用TCMSP和SwissTargetPrediction数据库对扶正化瘀汤的有效成分和靶点进行鉴定。将GeneCards和PharmGKB中的nsclc相关靶点与汤的靶点相交,构建蛋白-蛋白相互作用(PPI)网络,鉴定核心靶点,并通过GO和KEGG途径富集分析对其进行分析。采用不同浓度扶正化机煎剂血清处理A549细胞,采用CCK-8法、annexin V-FITC/PI染色及Western blotting检测细胞增殖、凋亡及蛋白表达的变化。结果:扶正化瘀汤含有效成分140种,鉴定出药病交叉靶点707个。在这些靶点中,TP53、AKT1、HIF1A、GAPDH、ALB、EGFR、CTNNB1和TNF被确定为参与激酶和受体以及PI3K-AKT、Ras、钙和MAPK通路相关的生物学过程的核心靶点。分子对接研究表明,活性成分与TP53、AKT1和HIF1A具有较强的结合亲和力。在A549细胞培养中,2.5%、5%、10%扶正化机煎剂血清处理A549细胞可显著抑制细胞增殖,促进细胞凋亡,下调HIF1A、p-AKT (Thr308)、TP53蛋白表达水平。结论:扶正化瘀汤抑制非小细胞肺癌细胞增殖可能通过下调HIF1A、p-AKT (Thr308)、TP53的表达来实现。
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来源期刊
南方医科大学学报杂志
南方医科大学学报杂志 Medicine-Medicine (all)
CiteScore
1.50
自引率
0.00%
发文量
208
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