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February 8, 2026Journal of Medicinal Chemistry0 citations

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

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ZLZhihan LiuKLKairui LyuYLYa Li

Key Points

  • This research aims to develop a predictive model for drug response using multi-omics data and spatial features of drug molecules.
  • Developed a multiomics fusion model named MTEGDRP.
  • Employed a transformer to extract features from drug and cancer cell data.
  • Utilized an equivariant graph neural network to capture spatial drug structures.
  • Conducted regression tasks to assess model performance.
  • Performed ablation studies to evaluate multiomics integration and spatial information.
  • MTEGDRP outperformed current state-of-the-art models in drug response prediction.
  • Ablation studies confirmed the effectiveness of multiomics integration.
  • Visualization of feature weights enhanced interpretability of predictions.

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.

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Cite This Study

Liu et al. (2026) studied this question.

synapsesocial.com/papers/698827570fc35cd7a8845f51https://doi.org/10.1021/acs.jmedchem.5c03438
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