Evidence map›Paper›PMID 30598084›Full record

ArticleBMC systems biology2018

Computational drug repositioning using meta-path-based semantic network analysis.

Zhen Tian, Zhixia Teng, Shuang Cheng, Maozu Guo

Abstract read
In one paragraph

Article in BMC systems biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

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0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

8 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Zhen TianSchool of Information Engineering, Zhengzhou University, Zhengzhou, 450001, People's Republic of China.
Zhixia TengSchool of information and computer engineering, Northeast Forestry, Harbin, 150001, People's Republic of China.
Shuang ChengInstitute of Materials, China Academy of Engineering Physics, Jiang You, 621907, Sichuan, China.
Maozu GuoSchool of Electrical and Information Engineering, Beijing University of Civil Engineering and Architecture, Beijing, 100044, People's Republic of China. guomaozu@bucea.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDrug repositioning is a promising and efficient way to discover new indications for existing drugs, which holds the great potential for precision medicine in the post-genomic era. Many network-based approaches have been proposed for drug repositioning based on similarity networks, which integrate multiple sources of drugs and diseases. However, these methods may simply view nodes as the same-typed and neglect the semantic meanings of different meta-paths in the heterogeneous network. Therefore, it is urgent to develop a rational method to infer new indications for approved drugs.

resultsIn this study, we proposed a novel methodology named HeteSim_DrugDisease (HSDD) for the prediction of drug repositioning. Firstly, we build the drug-drug similarity network and disease-disease similarity network by integrating the information of drugs and diseases. Secondly, a drug-disease heterogeneous network is constructed, which combines the drug similarity network, disease similarity network as well as the known drug-disease association network. Finally, HSDD predicts novel drug-disease associations based on the HeteSim scores of different meta-paths. The experimental results show that HSDD performs significantly better than the existing state-of-the-art approaches. HSDD achieves an AUC score of 0.8994 in the leave-one-out cross validation experiment. Moreover, case studies for selected drugs further illustrate the practical usefulness of HSDD.

conclusionsHSDD can be an effective and feasible way to infer the associations between drugs and diseases using on meta-path-based semantic network analysis.

Indexed as

SemanticsComputational BiologyDiseaseDrug RepositioningMachine LearningDrug repositioningHeteSimHSDDMeta-path-basedSemantic network analysis

Identifiers

PMID30598084
PMCPMC6311940

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.