Evidence map›Paper›PMID 39312682›Full record

ArticleBioinformatics (Oxford, England)2024

Causal enhanced drug-target interaction prediction based on graph generation and multi-source information fusion.

Guanyu Qiao, Guohua Wang, Yang Li

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Article in Bioinformatics (Oxford, England), 2024. 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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8citing papers in PubMed
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1 · What the graph read from it

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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

3 authors.

Guanyu QiaoSchool of Computer Science and Technology, Harbin Institute of Technology, Harbin 150001, China.ORCID 0009-0004-8128-0047
Guohua WangSchool of Computer Science and Technology, Harbin Institute of Technology, Harbin 150001, China.ORCID 0000-0001-7381-2374
Yang LiCollege of Computer and Control Engineering, Northeast Forestry University, Harbin 150040, China.ORCID 0000-0002-0403-7287

Funding

National Key R&D Program of China 2022YFF1202101National Natural Science Foundation of China 62225109
6 · The paper itself

Abstract

motivationThe prediction of drug-target interaction is a vital task in the biomedical field, aiding in the discovery of potential molecular targets of drugs and the development of targeted therapy methods with higher efficacy and fewer side effects. Although there are various methods for drug-target interaction (DTI) prediction based on heterogeneous information networks, these methods face challenges in capturing the fundamental interaction between drugs and targets and ensuring the interpretability of the model. Moreover, they need to construct meta-paths artificially or a lot of feature engineering (prior knowledge), and graph generation can fuse information more flexibly without meta-path selection.

resultsWe propose a causal enhanced method for drug-target interaction (CE-DTI) prediction that integrates graph generation and multi-source information fusion. First, we represent drugs and targets by modeling the fusion of their multi-source information through automatic graph generation. Once drugs and targets are combined, a network of drug-target pairs is constructed, transforming the prediction of drug-target interactions into a node classification problem. Specifically, the influence of surrounding nodes on the central node is separated into two groups: causal and non-causal variable nodes. Causal variable nodes significantly impact the central node's classification, while non-causal variable nodes do not. Causal invariance is then used to enhance the contrastive learning of the drug-target pairs network. Our method demonstrates excellent performance compared with other competitive benchmark methods across multiple datasets. At the same time, the experimental results also show that the causal enhancement strategy can explore the potential causal effects between DTPs, and discover new potential targets. Additionally, case studies demonstrate that this method can identify potential drug targets. AVAILABILITY AND IMPLEMENTATION: The source code of AdaDR is available at: https://github.com/catly/CE-DTI.

Indexed as

AlgorithmsComputational BiologyHumansPharmaceutical PreparationsPharmaceutical Preparations

Identifiers

PMID39312682
PMCPMC11639159

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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.