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Updated: Jan 19, 2026

Rapid in vivo Drug Response Prediction Using Leukemia Cell Grafts in Zebrafish Embryos
Published on: May 23, 2025
Predicting drug-induced transcriptome responses of a wide range of human cell lines by a novel tensor-train
Michio Iwata1, Longhao Yuan2,3, Qibin Zhao3,4
1Department of Bioscience and Bioinformatics, Faculty of Computer Science and Systems Engineering, Kyushu Institute of Technology, Iizuka, Fukuoka, Japan.
Motivation:
Genome-wide identification of the transcriptomic responses of human cell lines to drug treatments is a challenging issue in medical and pharmaceutical research. However, drug-induced gene expression profiles are largely unknown and unobserved for all combinations of drugs and human cell lines, which is a serious obstacle in practical applications.
Results:
Here, we developed a novel computational method to predict unknown parts of drug-induced gene expression profiles for various human cell lines and predict new drug therapeutic indications for a wide range of diseases. We proposed a tensor-train weighted optimization (TT-WOPT) algorithm to predict the potential values for unknown parts in tensor-structured gene expression data. Our results revealed that the proposed TT-WOPT algorithm can accurately reconstruct drug-induced gene expression data for a range of human cell lines in the Library of Integrated Network-based Cellular Signatures. The results also revealed that in comparison with the use of original gene expression profiles, the use of imputed gene expression profiles improved the accuracy of drug repositioning. We also performed a comprehensive prediction of drug indications for diseases with gene expression profiles, which suggested many potential drug indications that were not predicted by previous approaches.
Supplementary Information:
Supplementary data are available at Bioinformatics online.
Insights
This study introduces a new computational method to predict gene expression profiles for drug treatments in human cell lines. This approach enhances drug repositioning accuracy and identifies novel therapeutic indications for diseases.
Area of Science:
- Computational biology
- Genomics
- Pharmacology
Background:
- Understanding genome-wide transcriptomic responses to drug treatments is crucial but challenging due to incomplete gene expression data.
- Existing data lacks comprehensive profiles for all drug-cell line combinations, hindering practical applications in medicine and pharmaceuticals.
Purpose of the Study:
- To develop a novel computational method for predicting missing drug-induced gene expression profiles.
- To predict new therapeutic indications for diseases using computational modeling.
- To improve the accuracy of drug repositioning.
Main Methods:
- Developed a tensor-train weighted optimization (TT-WOPT) algorithm to predict unknown values in tensor-structured gene expression data.
- Applied the TT-WOPT algorithm to reconstruct drug-induced gene expression data for human cell lines.
- Evaluated the impact of imputed gene expression profiles on drug repositioning accuracy.
Main Results:
- The TT-WOPT algorithm accurately reconstructed drug-induced gene expression data across various human cell lines.
- Imputed gene expression profiles significantly improved the accuracy of drug repositioning compared to original profiles.
- Comprehensive predictions identified numerous potential drug indications for diseases missed by previous methods.
Conclusions:
- The developed TT-WOPT method provides an effective approach for predicting gene expression profiles and uncovering novel drug indications.
- This computational strategy advances drug discovery and personalized medicine by leveraging incomplete biological data.
- The findings suggest a powerful new tool for pharmaceutical research and disease treatment strategies.
Related Concept Videos
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06:40Cost-Efficient Transcriptomic-Based Drug Screening
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