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Cited 40 time in webofscience Cited 48 time in scopus
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Biomedical knowledge graph learning for drug repurposing by extending guilt-by-association to multiple layersopen access

Authors
Bang, DongminLim, SangsooLee, SangseonKim, Sun
Issue Date
Jun-2023
Publisher
Nature Portfolio
Keywords
Alpha2b Interferon; Armodafinil; Atomoxetine; Brexpiprazole; Caffeine; Clomipramine; Cortisone Acetate; Dactinomycin; Dexamphetamine; Duloxetine; Escitalopram; Etoposide; Fluoxetine; Guanfacine; Hydralazine; Hydroxyurea; Irinotecan; Levetiracetam; Lisdexamfetamine; Maprotiline; Metformin; Mitoxantrone; Sertraline; Teniposide; Vinblastine; Vindesine; Alpha2b Interferon; Armodafinil; Atomoxetine; Brexpiprazole; Caffeine; Clomipramine; Cortisone Acetate; Dactinomycin; Dexamphetamine; Duloxetine; Escitalopram; Etoposide; Fluoxetine; Guanfacine; Hydralazine; Hydroxyurea; Irinotecan; Levetiracetam; Lisdexamfetamine; Maprotiline; Metformin; Mitoxantrone; Omega 3 Fatty Acid; Sertraline; Teniposide; Vinblastine; Vindesine; Dominance; Drug; Gene Expression; Knowledge; Medical Geography; Mental Disorder; Prediction; Alzheimer Disease; Article; Biomedicine; Breast Carcinoma; Drug Repositioning; Embedding; Human; Random Walk; Automated Pattern Recognition; Learning; Drug Repositioning; Learning; Pattern Recognition, Automated
Citation
Nature Communications, v.14, no.1, pp 1 - 17
Pages
17
Indexed
SCIE
SCOPUS
Journal Title
Nature Communications
Volume
14
Number
1
Start Page
1
End Page
17
URI
https://scholarworks.dongguk.edu/handle/sw.dongguk/19995
DOI
10.1038/s41467-023-39301-y
ISSN
2041-1723
2041-1723
Abstract
Computational drug repurposing aims to identify new indications for existing drugs by utilizing high-throughput data, often in the form of biomedical knowledge graphs. However, learning on biomedical knowledge graphs can be challenging due to the dominance of genes and a small number of drug and disease entities, resulting in less effective representations. To overcome this challenge, we propose a "semantic multi-layer guilt-by-association" approach that leverages the principle of guilt-by-association - "similar genes share similar functions", at the drug-gene-disease level. Using this approach, our model DREAMwalk: Drug Repurposing through Exploring Associations using Multi-layer random walk uses our semantic information-guided random walk to generate drug and disease-populated node sequences, allowing for effective mapping of both drugs and diseases in a unified embedding space. Compared to state-of-the-art link prediction models, our approach improves drug-disease association prediction accuracy by up to 16.8%. Moreover, exploration of the embedding space reveals a well-aligned harmony between biological and semantic contexts. We demonstrate the effectiveness of our approach through repurposing case studies for breast carcinoma and Alzheimer's disease, highlighting the potential of multi-layer guilt-by-association perspective for drug repurposing on biomedical knowledge graphs.
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