Network Insights into Improving Drug Target Inference Algorithms

biorxiv(2020)

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摘要
To improve the efficacy of drug research and development (R&D), a better understanding of drug mechanisms of action (MoA) is needed to improve drug discovery. Computational algorithms, such as ProTINA, that integrate protein-protein interactions (PPIs), protein-gene interactions (PGIs) and gene expression data have shown promising performance on drug target inference. In this work, we evaluated how network and gene expression data affect ProTINA’s accuracy. Network data predominantly determines the accuracy of ProTINA instead of gene expression, while the size of an interaction network or selecting cell/tissue-specific networks have limited effects on the accuracy. However, we found that protein network betweenness values showed high accuracy in predicting drug targets. Therefore, we suggested a new algorithm, TREAP (), that combines betweenness values and adjusted -values for target inference. This algorithm has resulted in higher accuracy than ProTINA using the same datasets.
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关键词
drug target inference,network topology,gene expression,protein-protein interactions,betweenness centrality
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