系统药理学
计算机科学
系统生物学
药物发现
人工智能
计算生物学
机器学习
生物网络
人工神经网络
深度学习
生成语法
转化医学
冗余(工程)
药物重新定位
药品
计算模型
药物开发
神经科学
数据科学
可解释性
生成模型
生物
图形
疾病
药物靶点
作者
Xuehao Li,Zhaoqi Wu,Te Fang,Jun Li,Danyang Li,Xi Zhang,L liu,Liming Wang
标识
DOI:10.1038/s41698-026-01407-z
摘要
The complexity of disease-causing signaling networks is indicative of the failure of single-target therapeutics to work, particularly because of feedback, redundancy and activation of compensatory responses. The review describes the recent movement to network pharmacology and purposeful polypharmacology facilitated by the emergence of artificial intelligence (AI) and massive biological knowledge graphs. This review explains how machine learning and graph neural networks can be used to characterize molecular interactions systematically, predict targets that are of disease relevance, as well as priorities on multi-target intervention strategies. Generative models and reinforcement-based learning strategies are addressed to create compounds and combinations of drugs designed to modulate networks, and not individual protein inhibition. It describes the experimental validation processes, such as CETSA, NanoBRET, and Perturb-seq, and patient-derived models and MIDD systems to aid the translational evidence. Data quality, bias, interpretability, and reproducibility are taken into consideration. In sum, this review presents a feasible and combined model of AI-assisted network-mediated drug discovery.
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