Evidence map›Paper›PMID 42352374›Full record

ArticleBiomolecules2026

A Node-Adaptive Feature Fusion Network for Drug-Target Interaction Prediction Based on Multi-View Graphs.

Lin Xie, Hongmei Xu, Pinglu Zhang, Jianshe Xiong, Jing Li

Abstract read
In one paragraph

Article in Biomolecules, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Lin XieCollege of Electronic Engineering, Faculty of Information Science and Engineering, Ocean University of China, Qingdao 266404, China.ORCID 0009-0000-2479-6988
Hongmei XuCollege of Electronic Engineering, Faculty of Information Science and Engineering, Ocean University of China, Qingdao 266404, China.
Pinglu ZhangCollege of Electronic Engineering, Faculty of Information Science and Engineering, Ocean University of China, Qingdao 266404, China.
Jianshe XiongCollege of Electronic Engineering, Faculty of Information Science and Engineering, Ocean University of China, Qingdao 266404, China.
Jing LiKey Laboratory of Marine Drugs, Chinese Ministry of Education, School of Medicine and Pharmacy, Ocean University of China, Qingdao 266003, China.

Funding

National Key R&D Program of China 2024YFC2815900
6 · The paper itself

Abstract

Existing drug-target interaction (DTI) prediction methods still face challenges caused by sparse interaction data, complex multi-source relationships, and imbalanced information contributions among different nodes. In this study, we propose NAFF-DTI, a node-level adaptive feature fusion network based on multi-view graphs. The model uniformly represents drug similarity, target similarity, and known drug-target interactions as multiple relational views, and learns node representations through graph encoding and cross-view representation learning. To more effectively utilize heterogeneous relational information, NAFF-DTI introduces cross-view feature discrepancy modeling and a node-level adaptive fusion mechanism to dynamically adjust the contribution of different views according to node structural characteristics. Experimental results show that NAFF-DTI achieves the best AUC and AUPR on all five benchmark datasets. Compared with the strongest baseline for each dataset and metric, NAFF-DTI achieves average relative improvements of 3.81% in AUC and 3.23% in AUPR. It can also improve the utilization of multi-source information, maintain relatively stable prediction under different data distributions, and prioritize biologically plausible candidate drug-target associations from the unannotated candidate space. These results indicate that NAFF-DTI can provide computational support for DTI candidate prioritization and repurposing-oriented hypothesis generation.

Indexed as

Drug DesignAlgorithmsdrug–target interaction predictiongraph representation learningmulti-view graphnode-level adaptive fusion

Identifiers

PMID42352374
PMCPMC13297179

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