Abstract
Considering the limited efficacy of existing pharmacotherapies for brain tumors, the development of accurate predictive models is essential for advancing neuro-oncology treatment strategies. In this article, we introduce a drug response prediction model, DeepMoDRP, specifically designed for brain cancer. This model integrates genomic, transcriptomic, and epigenomic data from various brain tumor cell lines, including low-grade glioma, glioblastoma multiforme, and diffuse large B-cell lymphoma. To address the high-dimensional complexity inherent in gene expression and copy number variations within cell line data, we have integrated sparse autoencoders (AEs) and denoising AEs to reduce noise and redundancy. Meanwhile, one-dimensional convolutional neural networks are utilized to process the low-dimensional mutation and DNA methylation data. Additionally, a multiscale graph neural network is implemented to handle the drug-related data. Finally, fully connected networks are employed to generate predictions of drug responses. A series of experiments were conducted utilizing a brain tumor dataset that was extracted and curated from public databases. The experimental results demonstrate that the proposed DeepMoDRP outperforms the performance of state-of-the-art pan-cancer baseline models in predicting drug responses for brain tumors. The downstream analysis indicates that the DeepMoDRP holds significant promise for the treatment of brain tumors.
| Original language | English |
|---|---|
| Article number | e70020 |
| Journal | Molecular Informatics |
| Volume | 45 |
| Issue number | 2 |
| DOIs | |
| Publication status | Published - Feb 2026 |
| Externally published | Yes |
Keywords
- brain cancer
- denoising autoencoder
- drug response prediction
- graph neural network
- muti-omics
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