MTEGDRP: Interpretable Molecular Self-Attention Transformer and Equivariant Graph Neural Network Based on Multi-Omics Fusion for Drug Response Prediction in Cancer Cell Lines

Cancer drug response prediction is crucial for precision medicine, as it can improve treatment outcomes and reduce medical costs. However, existing models often ignore the geometric features of drug molecules and their interactions with cancer cells. To address this, this study proposes a multiomics fusion model named MTEGDRP. The model uses a transformer to extract high-level features from drug and cell data, as well as their interactions, while an equivariant graph neural network captures the spatial structure of drugs. In regression tasks, MTEGDRP performs better than current state-of-the-art methods. Ablation studies show that multiomics integration and molecular spatial information are effective. Visualization of the feature weights provides interpretability for the model. With its excellent prediction performance, MTEGDRP shows great potential as a useful tool for guiding anticancer drug design in precision medicine.

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Publication Details

Journal
Journal of Medicinal Chemistry
Published
2026-02-04
DOI
https://doi.org/10.1021/acs.jmedchem.5c03438
Primary Topic
Computational Drug Discovery Methods
Type
article
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article

MTEGDRP: Interpretable Molecular Self-Attention Transformer and Equivariant Graph Neural Network Based on Multi-Omics Fusion for Drug Response Prediction in Cancer Cell Lines

Xiang Sun, Bin Yu, Zhihan Liu, Kairui Lyu et al.
Journal of Medicinal Chemistry
Computational Drug Discovery Methods
article

MTEGDRP: Interpretable Molecular Self-Attention Transformer and Equivariant Graph Neural Network Based on Multi-Omics Fusion for Drug Response Prediction in Cancer Cell Lines

Xiang Sun, Bin Yu, Zhihan Liu, Kairui Lyu, Ya Li, Xin Gao
article en

Abstract

Cancer drug response prediction is crucial for precision medicine, as it can improve treatment outcomes and reduce medical costs. However, existing models often ignore the geometric features of drug molecules and their interactions with cancer cells. To address this, this study proposes a multiomics fusion model named MTEGDRP. The model uses a transformer to extract high-level features from drug and cell data, as well as their interactions, while an equivariant graph neural network captures the spatial structure of drugs. In regression tasks, MTEGDRP performs better than current state-of-the-art methods. Ablation studies show that multiomics integration and molecular spatial information are effective. Visualization of the feature weights provides interpretability for the model. With its excellent prediction performance, MTEGDRP shows great potential as a useful tool for guiding anticancer drug design in precision medicine.

Journal of Medicinal ChemistryVol. 69(4)
University of Science and Technology of China (CN), Qingdao University of Science and Technology (CN), King Abdullah University of Science and Technology (SA)
Good health and well-being
Openalex Percentile: Top 65%
Computational Drug Discovery Methods
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MTEGDRP: Interpretable Molecular Self-Attention Transformer and Equivariant Graph Neural Network Based on Multi-Omics Fusion for Drug Response Prediction in Cancer Cell Lines — Xiang Sun, Bin Yu, et al. · Journal of Medicinal Chemistry (2026) | TGRS Research Map | TGRS