AI and network biology for rational polypharmacology in signaling drug design: a review
Xuehao Li1, Zhaoqi Wu2, Te Fang2
1Department of Thoracic Surgery, The First Hospital of China Medical University, Shenyang, China.
Abstract:
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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