PathSynergy: a deep learning model for predicting drug synergy in liver cancer

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.

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Publication Details

Journal
Briefings in Bioinformatics
Published
2025-03-01
DOI
https://doi.org/10.1093/bib/bbaf192
Citations
6
Primary Topic
Computational Drug Discovery Methods
Type
article
Field-Weighted Citation Impact
9.03

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article

PathSynergy: a deep learning model for predicting drug synergy in liver cancer

Fengyue Zhang, Jinrui Wei, Lichuan Wu, Xuqi Zhao
6 citations
Briefings in Bioinformatics
Computational Drug Discovery Methods
9.03
article

PathSynergy: a deep learning model for predicting drug synergy in liver cancer

Fengyue Zhang, Jinrui Wei, Lichuan Wu, Xuqi Zhao
article en
6 citations

Abstract

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.

Briefings in BioinformaticsVol. 26(2)
Guangxi University (CN), Guangxi University of Chinese Medicine (CN)
Guangxi University
Good health and well-being
Openalex Percentile: Top 2%
Computational Drug Discovery Methods
9.03
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PathSynergy: a deep learning model for predicting drug synergy in liver cancer — Fengyue Zhang, Jinrui Wei, et al. · Briefings in Bioinformatics (2025) | TGRS Research Map | TGRS