Zhang Fengyue, Zhao Xuqi, Wei Jinrui, Wu Lichuan
Guangxi Key Laboratory of Special Biomedicine, School of Medicine, Guangxi University, No. 100, East Daxue Road, Xixiangtang District, Nanning 530004, Guangxi, China.
Guangxi Key Laboratory of Efficacy Study on Chinese Materia Medica, Guangxi Scientific Research Center of Traditional Chinese Medicine, Guangxi University of Chinese Medicine, No. 13 Wuhe Avenue, Nanning 530200, Guangxi, China.
Brief Bioinform. 2025 Mar 4;26(2). doi: 10.1093/bib/bbaf192.
Cancer is a major public health problem while liver cancer is the main cause of global cancer-related deaths. The previous study demonstrates that the 5-year survival rate for advanced liver cancer is only 30%. Few of the first-line targeted drugs including sorafenib and lenvatinib are available, which often develop resistance. Drug combination therapy is crucial for improving the efficacy of cancer therapy and overcoming resistance. However, traditional methods for discovering drug synergy are costly and time consuming. In this study, we developed a novel predicting model PathSynergy by integrating drug feature data, cell line data, drug-target interactions, and signaling pathways. PathSynergy combined the advantages of graph neural networks and pathway map mapping. Comparing with other baseline models, PathSynergy showed better performance in model classification, accuracy, and precision. Excitingly, six Food and Drug Administration (FDA)-approved drugs including pimecrolimus, topiramate, nandrolone_decanoate, fluticasone propionate, zanubrutinib, and levonorgestrel were predicted and validated to show synergistic effects with sorafenib or lenvatinib against liver cancer for the first time. In general, the PathSynergy model provides a new perspective to discover synergistic combinations of drugs and has broad application potential in the fields of drug discovery and personalized medicine.
癌症是一个重大的公共卫生问题,而肝癌是全球癌症相关死亡的主要原因。先前的研究表明,晚期肝癌的5年生存率仅为30%。包括索拉非尼和仑伐替尼在内的一线靶向药物很少,而且这些药物常常会产生耐药性。联合药物疗法对于提高癌症治疗效果和克服耐药性至关重要。然而,传统的发现药物协同作用的方法既昂贵又耗时。在本研究中,我们通过整合药物特征数据、细胞系数据、药物-靶点相互作用和信号通路,开发了一种新型预测模型PathSynergy。PathSynergy结合了图神经网络和通路图谱映射的优点。与其他基线模型相比,PathSynergy在模型分类、准确性和精确性方面表现更佳。令人兴奋的是,首次预测并验证了包括吡美莫司、托吡酯、癸酸诺龙、丙酸氟替卡松、泽布替尼和左炔诺孕酮在内的六种美国食品药品监督管理局(FDA)批准的药物与索拉非尼或仑伐替尼联合使用时对肝癌具有协同作用。总的来说,PathSynergy模型为发现药物协同组合提供了新的视角,在药物发现和个性化医疗领域具有广泛的应用潜力。