Building Multi-Source Semantic Knowledge Graph for Drug Repositioning

被引:0
|
作者
Han Z. [1 ]
Xinyu A. [1 ]
Chunhe L. [1 ]
机构
[1] School of Health Management, China Medical University, Shenyang
关键词
Drug Repositioning; Knowledge Discovery; Knowledge Graph; Semantic Model;
D O I
10.11925/infotech.2096-3467.2021.1364
中图分类号
学科分类号
摘要
[Objective] This paper constructs a cross-platform semantic knowledge graph with whole datasets, which helps us find novel drug knowledge. [Methods] First, we developed a new model for the proposed knowledge graph, which integrated semantic relations from PubMed, DrugBank and CTD, as well as knowledge fusion and attribute definition. Then, we conducted drug repositioning with pathway identification and link predication to discover new treatments for cancers. [Results] The F-score of pathway identification (0.57) was better than that of the linkage predication (0.56). The more pathways existing between drugs and indications, the greater possibility of predicting positively. [Limitations] Since the reasoning mechanism was based on the existing associations among knowledge units, it is hard to discover the novel indications for drugs without the known targets. It is difficult to update knowledge graph dynamically due to the huge data volume. [Conclusions] The proposed knowledge graph could effectively find new drug indications as well as improve the efficiency for drug research and development. © 2022, Chinese Academy of Sciences. All rights reserved.
引用
收藏
页码:87 / 98
页数:11
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共 56 条
  • [1] Hu Zhengyin, Liu Leilei, Dai Bing, Et al., Discovering Subject Knowledge in Life and Medical Sciences with Knowledge Graph, Data Analysis and Knowledge Discovery, 4, 11, pp. 1-14, (2020)
  • [2] Swanson D R., Fish Oil, Raynaud’s Syndrome, and Undiscovered Public Knowledge, Perspectives in Biology and Medicine, 30, 1, pp. 7-18, (1986)
  • [3] Li Dongqiao, Chen Fang, Han Tao, Et al., Research on the Tacit Knowledge Discovery Based on Two-Mode Complex Network—Take Mining Potential Drug Targets as an Example, Library and Information Service, 64, 21, pp. 120-129, (2020)
  • [4] Ma J, Wang J, Ghoraie L S, Et al., A Comparative Study of Cluster Detection Algorithms in Protein-Protein Interaction for Drug Target Discovery and Drug Repurposing, Frontiers in Pharmacology, 10, (2019)
  • [5] Hristovski D, Kastrin A, Dinevski D, Et al., Using Literature-Based Discovery to Explain Adverse Drug Effects, Journal of Medical Systems, 40, 8, (2016)
  • [6] Shang N, Xu H, Rindflesch T C, Et al., Identifying Plausible Adverse Drug Reactions Using Knowledge Extracted from the Literature, Journal of Biomedical Informatics, 52, pp. 293-310, (2014)
  • [7] Xu R, Wang Q Q., Toward Creation of a Cancer Drug Toxicity Knowledge Base: Automatically Extracting Cancer Drug—Side Effect Relationships from the Literature, Journal of the American Medical Informatics Association, 21, 1, pp. 90-96, (2013)
  • [8] Fan Xinyue, Cui Lei, Using Text Mining to Discover Drug Side Effects: Case Study of PubMed, Data Analysis and Knowledge Discovery, 2, 3, pp. 79-86, (2018)
  • [9] Zhang R, Cairelli M J, Fiszman M, Et al., Using Semantic Predications to Uncover Drug-Drug Interactions in Clinical Data, Journal of Biomedical Informatics, 49, pp. 134-147, (2014)
  • [10] Du J, Li X Y., A Knowledge Graph of Combined Drug Therapies Using Semantic Predications from Biomedical Literature: Algorithm Development[J], JMIR Medical Informatics, 8, 4, (2020)