Mechanism of Guishao Yigong decoction in treating colorectal cancer based on network pharmacology and experimental validation

克隆形成试验 蛋白激酶B 结直肠癌 细胞周期 流式细胞术 MAPK/ERK通路 药理学 汤剂 PI3K/AKT/mTOR通路 细胞生长 信号转导 癌症研究 生物 细胞 化学 癌症 细胞生物学 医学 生物化学 内科学 免疫学
作者
Yuwen Fan,Quyi Wang,Yun Zhang,Yu Wang,Wenwen Li,Shu Jiang,Jinao Duan
出处
期刊:Journal of Pharmacy and Pharmacology [Oxford University Press]
标识
DOI:10.1093/jpp/rgae045
摘要

Abstract Objectives To explore the effective components of Guishao Yigong decoction (GYD) in the treatment of colorectal cancer and reveal its potential mechanism of action. Methods Through network pharmacology, the main target and signaling pathway of GYD therapy for colorectal cancer (CRC) were found. Subsequently, the effect of GYD was verified by in vitro cell viability measurements, colony formation, and scratch healing tests. The effects of GYD on metabolic pathways in vivo were found through plasma metabolomics. Finally, flow cytometry and qPCR experiments were used to verify the cycle-blocking effect of GYD on CRC cells. Key findings Based on the network pharmacological analysis and molecular docking technology, it was found that GYD could restrain the growth of CRC cells by affecting lipid metabolic pathways and mitogen-activated protein kinase (MAPK) signaling pathways. A series of cell experiments showed that GYD could inhibit the proliferation, migration and clonogenic ability of CRC cells. Furthermore, the plasma metabolomics results showed that GYD could affect the production of unsaturated fatty acids in mice. Flow cytometry and qPCR experiments further proved that GYD blocked the CRC cells in the G1 phase and modulated the expression of cell cycle-related targets, such as AKT, TP53, CDKN1A, and CDK2. Conclusions All the results indicated that GYD could regulate the related metabolism of unsaturated fatty acids. Thus, the cell cycle was blocked and the expressions of the key proteins such as AKT and TP53 were regulated, which achieved the purpose of intervention in colorectal cancer.

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