Gong CuiCui, Chen Junyang, Zou Pingjin, Fang Zengyi, Quan Li, Wang Jing, Yin Jie, Lin Bing, Lang Jinyi, Chen Meihua
School of Clinical Medicine, Chengdu University of Traditional Chinese Medicine, Chengdu, Sichuan, 610032, People's Republic of China.
Department of Radiation Oncology, Radiation Oncology Key Laboratory of Sichuan Province, Sichuan Clinical Research Center for Cancer, Sichuan Cancer Hospital & Institute, Sichuan Cancer Center, University of Electronic Science and Technology of China, Chengdu, 610041, People's Republic of China.
Drug Des Devel Ther. 2025 Jan 27;19:627-644. doi: 10.2147/DDDT.S490844. eCollection 2025.
Radiation-induced pulmonary fibrosis (RIPF) is a serious complication of radiotherapy that lacks effective treatment options. The Huaxian formula (HXF), a traditional Chinese herbal remedy, shows promise in alleviating RIPF; however, its active ingredients and underlying mechanisms remain poorly understood.
Through serum pharmacochemistry, network pharmacology, molecular docking, and experimental validation, we investigate the potential mechanisms of HXF in the prevention and treatment of radiation-induced pulmonary fibrosis (RIPF).
Histological examination and non-invasive computed tomography (CT) scans in animal experiments revealed that HXF improved extracellular matrix collagen deposition in the lung tissue of irradiated mice and reduced fibrosis manifestations on CT images. Analysis of post-HXF administration serum samples identified 21 enriched compounds as potential active compounds, with 430 corresponding prospective targets. Overlapping these compounds with 991 RIPF-related genes yielded 127 genes primarily associated with the PI3K-Akt signaling pathway, EGFR tyrosine kinase inhibitor resistance, and the MAPK signaling pathway. Molecular docking indicated that key compounds in HXF serum, 5,7,8-trimethoxyflavone, and hyperoside, exhibited strong affinity with key targets. Finally, animal experiments confirmed that HXF significantly inhibited the expression of p-Akt and p-PI3K proteins in the lung tissue of irradiated mice.
Our research results indicate that HXF may exert its effects on the prevention and treatment of radiation-induced pulmonary fibrosis (RIPF) through multiple pathways and targets, with the PI3K-Akt signaling pathway likely playing the most crucial role in this process.
放射性肺纤维化(RIPF)是放射治疗的一种严重并发症,缺乏有效的治疗选择。化仙方(HXF)是一种传统中药方剂,在缓解RIPF方面显示出前景;然而,其活性成分和潜在机制仍知之甚少。
通过血清药物化学、网络药理学、分子对接和实验验证,我们研究了HXF预防和治疗放射性肺纤维化(RIPF)的潜在机制。
动物实验中的组织学检查和非侵入性计算机断层扫描(CT)显示,HXF改善了受照射小鼠肺组织中细胞外基质胶原蛋白的沉积,并减少了CT图像上的纤维化表现。对给予HXF后的血清样本分析确定了21种富集化合物为潜在活性化合物,有430个相应的潜在靶点。将这些化合物与991个RIPF相关基因进行比对,得到127个主要与PI3K-Akt信号通路、EGFR酪氨酸激酶抑制剂耐药性和MAPK信号通路相关的基因。分子对接表明,HXF血清中的关键化合物5,7,8-三甲氧基黄酮和金丝桃苷与关键靶点表现出很强的亲和力。最后,动物实验证实HXF显著抑制了受照射小鼠肺组织中p-Akt和p-PI3K蛋白的表达。
我们的研究结果表明,HXF可能通过多种途径和靶点对放射性肺纤维化(RIPF)发挥预防和治疗作用,其中PI3K-Akt信号通路可能在此过程中起最关键的作用。