| Literature DB >> 30304690 |
Chi Xu1, Daosheng Ai2, Dawei Shi2, Shengbao Suo2, Xingwei Chen1, Yizhen Yan1, Yaqiang Cao1, Rui Zhang2, Na Sun2, Weizhong Chen2, Joseph McDermott2, Shiqiang Zhang1, Yingying Zeng1, Jing-Dong Jackie Han3.
Abstract
Experimental large-scale screens for drug repositioning are limited by restriction to in vitro conditions and lack of applicability to real human conditions. Here, we developed an in silico screen in human in vivo conditions using a reference of single gene mutations' non-tissue-specific "core transcriptome signatures" (CSs) of 8,476 genes generated from the TCGA database. We developed the core-signature drug-to-gene (csD2G) software to scan 3,546 drug treatment profiles against the reference signatures. csD2G significantly outperformed conventional cell line-based gene perturbation signatures and existing drug-repositioning methods in both coverage and specificity. We highlight this with 3 demonstrated applications: (1) repositioned category of psychiatric drugs to inhibit the TGF-β pathway; (2) antihypertensive calcium channel blockers predicted to activate AMPK and inhibit AKT pathways, and validated by clinical electronic medical records; and (3) 7 drugs predicted and validated to selectively target the AKT-FOXO and AMPK pathways and thus regulate worm lifespan.Entities:
Keywords: cancer genomics; data integrative analysis; drug repositioning; drug target
Year: 2018 PMID: 30304690 DOI: 10.1016/j.celrep.2018.09.031
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423