期刊
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES
卷 160, 期 -, 页码 -出版社
ELSEVIER
DOI: 10.1016/j.ejps.2021.105742
关键词
Bioinformatics; Drug-drug interaction; Feature extraction; Gene expression; Tensor decomposition; Unsupervi s e d learning
资金
- KAKENHI [19H05270,20H04848, 20K12067]
- Deanship of Scientific Research (DSR) at King Abdulaziz University, Jeddah [KEP861138]
- Grants-in-Aid for Scientific Research [20K12067] Funding Source: KAKEN
Accurately predicting new drug interactions is crucial for preventing adverse reactions. A recent study highlights the importance of understanding non-linear effects of DDIs and introduces a new unsupervised learning approach. The analysis of gene expression data suggests that non-linear dose-dependence is not always a result of DDIs.
The accurate prediction of new interactions between drugs is important for avoiding unknown (mil d or severe) adverse reactions to drug combinations. The development of effective in silico methods for evaluating drug in-teractions based on gene expression data requires an understanding of how various drugs alter gene expression. Current computational methods for the prediction of drug-drug interactions (DDIs) utilize data for known DDIs to predict unknown interactions. However, these methods are limited in the absence of known predictive DDIs. To improve DDIs interpretation, a recent study has demonstrated strong non-linear (i.e., dose-dependent ) effects of DDIs. In this study, we present a new unsupervised learnin g approach involving tensor decomposition (TD)-based unsupervised feature extraction (FE) in 3D. We utilize ou r approach to reanalyze available gene expression profiles for Saccharomyces cerevisiae. We found that non-linearity is possible, even for single drugs. Thus, non-linear dose-dependence cannot always be attributed to DDIs. Ou r analysis provides a basis for the design of effective methods for evaluating DDIs.
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