Hu Leihao, He Canfeng, Mo Aier, Zhan Xingkai, Yang Caizhi, Guo Wei, Sun Lingling, Su Weiwei, Lin Lizhu
School of the First Clinical Medicine, Guangzhou University of Chinese Medicine, Guangzhou, Guangdong, China.
Dongguan Hospital of Integrated Chinese and Western Medicine, Dongguan, Guangdong, China.
Evid Based Complement Alternat Med. 2023 Jan 9;2023:3436814. doi: 10.1155/2023/3436814. eCollection 2023.
Non-small-cell lung cancer (NSCLC) is one of the most prevalent cancers worldwide. A Yi-Fei-San-Jie formula (YFSJF), widely used in NSCLC treatment in south China, has been validated in clinical studies. However, the pharmacological mechanism behind it remains unclear. In this study, 73 compounds were identified using ultraperformance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS), with 58 enrolled in network pharmacology. The protein-protein interaction network, functional enrichment analysis, and compound-target-pathway network were constructed using 74 overlapping targets from 58 drugs and NSCLC. YFSJF has many targets and pathways in the fight against NSCLC. PIK3R1, PIK3CA, and AKT1 were identified as key targets, and the PI3K/AKT pathway was identified as the key pathway. According to the Human Protein Atlas (THPA) database and the Kaplan-Meier Online website, the three key targets had varying expression levels in normal and abnormal tissues and were linked to prognosis. Molecular docking and dynamics simulations verified that hub compounds have a strong affinity with three critical targets. This study revealed multiple compounds, targets, and pathways for YFSJF against NSCLC and suggested that YFSJF might inhibit PIK3R1, PIK3CA, and AKT1 to suppress the PI3K/AKT pathway and play its pharmacological role.
非小细胞肺癌(NSCLC)是全球最常见的癌症之一。在中国南方广泛用于NSCLC治疗的益肺散结方(YFSJF)已在临床研究中得到验证。然而,其背后的药理机制仍不清楚。在本研究中,使用超高效液相色谱-串联质谱法(UPLC-MS/MS)鉴定了73种化合物,其中58种纳入网络药理学研究。利用58种药物与NSCLC的74个重叠靶点构建了蛋白质-蛋白质相互作用网络、功能富集分析和化合物-靶点-途径网络。YFSJF在对抗NSCLC中有许多靶点和途径。PIK3R1、PIK3CA和AKT1被确定为关键靶点,PI3K/AKT途径被确定为关键途径。根据人类蛋白质图谱(THPA)数据库和Kaplan-Meier在线网站,这三个关键靶点在正常组织和异常组织中的表达水平不同,且与预后相关。分子对接和动力学模拟验证了枢纽化合物与三个关键靶点具有很强的亲和力。本研究揭示了YFSJF对抗NSCLC的多种化合物、靶点和途径,并表明YFSJF可能通过抑制PIK3R1、PIK3CA和AKT1来抑制PI3K/AKT途径并发挥其药理作用。