Integration Approaches of UPLC-Q-Exactive Orbitrap-MS/MS, Network Pharmacology Molecular Docking, and Molecular Dynamics to Explore the Effective Constituents and Potential Mechanisms of S. vaniniiporus vaninii against Tumor

化学 高良姜素 计算生物学 PI3K/AKT/mTOR通路 小桶 对接(动物) 信号转导 生物化学 药理学 类黄酮 生物 山奈酚 基因表达 医学 基因 转录组 护理部 抗氧化剂
作者
Wenlong Li,Peilu Wang,Yan Xu,Mengyi Shan,Gang Cheng,Yunjie Sheng,Kaohua Liu,Bingqian He,Qi Shi,Huaqiang Li,Xiongyu Meng,Luping Qin
出处
期刊:Current Pharmaceutical Design [Bentham Science Publishers]
卷期号:31 (39): 3139-3168
标识
DOI:10.2174/0113816128365808250413155927
摘要

S. vaninii, a well-established traditional Chinese medicine with potent pharmacological effects against cancer, lacks clarity regarding its mechanism of action. To elucidate the bioactive components in S. vaninii and to elucidate their potential anticancer mechanisms. Firstly, the chemical composition of S. vaninii was characterized using UPLC-Q-Exactive Orbitrap- MS/MS technique. Subsequently, bioinformatics-related techniques were employed to elucidate the bioactive components and potential mechanisms of S. vaninii anti-tumor based on the identified chemical constituents. Finally, molecular dynamics simulation was conducted to validate the obtained results. Our findings revealed the characterization of 226 constituents from S. vaninii including 30 flavonoids, 27 carbohydrates and glycosides, 26 amino acids, peptides and their derivatives, 18 phenylpropanoids, 13terpenes, 12 phenols, 6 organic acids and its derivatives, 4 alkaloids, etc. Subsequently, 195 key tumorrelated active compounds were identified and established in the Drug-Compound-Target-Disease network. The PPI network screened out 85 key targets (TP53, STAT3, EGFR, GAPDH, BCL2, AKT1, CASP3, mTOR, JUN, and TNF) in tumors. Furthermore, functional enrichment analyses using GO and KEGG pathways highlighted the involvement of PI3K-Akt signaling pathways in S. vaninii's anti-tumor effects. Finally, the top ten significant bioactive constituents were selected as key targets for molecular docking studies which revealed Alpinetin, Galangin, and 4',5-Dihydroxyflavone as potential core compounds targeting mTOR, EGFR, and AKT1 respectively; these complexes were further assessed for stability through MD simulations. This study provides insights into the potential active compounds, target proteins, and signaling pathways underlying the clinical application of S. vaninii in treating tumors.
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