Evidence map›Paper›PMID 39806287›Full record

ArticleBMC bioinformatics2025

MDFGNN-SMMA: prediction of potential small molecule-miRNA associations based on multi-source data fusion and graph neural networks.

Jianwei Li, Xukun Zhang, Bing Li, Ziyu Li, Zhenzhen Chen

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Article in BMC bioinformatics, 2025. 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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5 · Who and what money

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5 authors.

Jianwei LiSchool of Artificial Intelligence, Hebei University of Technology, Tianjin, 300401, China.
Xukun ZhangSchool of Artificial Intelligence, Hebei University of Technology, Tianjin, 300401, China.
Bing LiSchool of Artificial Intelligence, Hebei University of Technology, Tianjin, 300401, China.
Ziyu LiSchool of Artificial Intelligence, Hebei University of Technology, Tianjin, 300401, China.
Zhenzhen ChenBeijing Institute of Heart Lung and Blood Vessel Diseases, Beijing Anzhen Hospital of Capital Medical University, Beijing, 101100, China. chenzhenzhen@bjmu.edu.cn.

Funding

Hebei Province Key Research and Development Plan Project 22342001DNational Natural Science Foundation of China 62202330National Natural Science Foundation of China,China 62072154
6 · The paper itself

Abstract

backgroundMicroRNAs (miRNAs) are pivotal in the initiation and progression of complex human diseases and have been identified as targets for small molecule (SM) drugs. However, the expensive and time-intensive characteristics of conventional experimental techniques for identifying SM-miRNA associations highlight the necessity for efficient computational methodologies in this field.

resultsIn this study, we proposed a deep learning method called Multi-source Data Fusion and Graph Neural Networks for Small Molecule-MiRNA Association (MDFGNN-SMMA) to predict potential SM-miRNA associations. Firstly, MDFGNN-SMMA extracted features of Atom Pairs fingerprints and Molecular ACCess System fingerprints to derive fusion feature vectors for small molecules (SMs). The K-mer features were employed to generate the initial feature vectors for miRNAs. Secondly, cosine similarity measures were computed to construct the adjacency matrices for SMs and miRNAs, respectively. Thirdly, these feature vectors and adjacency matrices were input into a model comprising GAT and GraphSAGE, which were utilized to generate the final feature vectors for SMs and miRNAs. Finally, the averaged final feature vectors were utilized as input for a multilayer perceptron to predict the associations between SMs and miRNAs.

conclusionsThe performance of MDFGNN-SMMA was assessed using 10-fold cross-validation, demonstrating superior compared to the four state-of-the-art models in terms of both AUC and AUPR. Moreover, the experimental results of an independent test set confirmed the model's generalization capability. Additionally, the efficacy of MDFGNN-SMMA was substantiated through three case studies. The findings indicated that among the top 50 predicted miRNAs associated with Cisplatin, 5-Fluorouracil, and Doxorubicin, 42, 36, and 36 miRNAs, respectively, were corroborated by existing literature and the RNAInter database.

Indexed as

Computational BiologyDeep LearningMicroRNAsNeural Networks, ComputerSmall Molecule LibrariesGraph Neural NetworksHumansMicroRNAsSmall Molecule LibrariesGraph neural networksMultilayer perceptronMulti-source data fusionSmall molecule-miRNA association

Identifiers

PMID39806287
PMCPMC11730471

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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.