SynergyX: a multi-modality mutual attention network for interpretable drug synergy prediction

Author:

Guo Yue1ORCID,Hu Haitao12,Chen Wenbo12,Yin Hao12,Wu Jian3,Hsieh Chang-Yu45,He Qiaojun16748,Cao Ji16748ORCID

Affiliation:

1. Institute of Pharmacology and Toxicology, Zhejiang Province Key Laboratory of Anti-Cancer Drug Research, College of Pharmaceutical Sciences, Zhejiang University , 866 Yuhangtang Road, 310058, Hangzhou, Zhejiang , China

2. Polytechnic Institute, Zhejiang University , 269 Shixiang Road,310000, Hangzhou, Zhejiang , China

3. Second Affiliated Hospital School of Medicine, School of Public Health, Zhejiang University , 866 Yuhangtang Road, 310058, Hangzhou, Zhejiang , China

4. The Innovation Institute for Artificial Intelligence in Medicine, Zhejiang University , 291 Fucheng Road, 310018, Hangzhou, Zhejiang , China

5. College of Pharmaceutical Sciences, Zhejiang University , 866 Yuhangtang Road, 310058, Hangzhou, Zhejiang , China

6. Engineering Research Center of Innovative Anticancer Drugs, Ministry of Education , 866 Yuhangtang Road, 310058, Hangzhou, Zhejiang , China

7. Center for Medical Research and Innovation in Digestive System Tumors, Ministry of Education , 310020, Hangzhou, Zhejiang , China

8. Cancer Center, Zhejiang University , 866 Yuhangtang Road, 310058, Hangzhou, Zhejiang , China

Abstract

Abstract Discovering effective anti-tumor drug combinations is crucial for advancing cancer therapy. Taking full account of intricate biological interactions is highly important in accurately predicting drug synergy. However, the extremely limited prior knowledge poses great challenges in developing current computational methods. To address this, we introduce SynergyX, a multi-modality mutual attention network to improve anti-tumor drug synergy prediction. It dynamically captures cross-modal interactions, allowing for the modeling of complex biological networks and drug interactions. A convolution-augmented attention structure is adopted to integrate multi-omic data in this framework effectively. Compared with other state-of-the-art models, SynergyX demonstrates superior predictive accuracy in both the General Test and Blind Test and cross-dataset validation. By exhaustively screening combinations of approved drugs, SynergyX reveals its ability to identify promising drug combination candidates for potential lung cancer treatment. Another notable advantage lies in its multidimensional interpretability. Taking Sorafenib and Vorinostat as an example, SynergyX serves as a powerful tool for uncovering drug-gene interactions and deciphering cell selectivity mechanisms. In summary, SynergyX provides an illuminating and interpretable framework, poised to catalyze the expedition of drug synergy discovery and deepen our comprehension of rational combination therapy.

Funder

Key Projects of Hangzhou Agricultural and Social Development Program

National Natural Science Foundation of China

Zhejiang Provincial Natural Science Foundation

Fundamental Research Funds for the Central Universities

Zhejiang Key R&D Program of China

Publisher

Oxford University Press (OUP)

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