Evidence map›Paper›PMID 42057106›Full record

ArticleBMC biology2026

Embedding multilayer RNA networks for lncRNA-miRNA interaction prediction via LMI-MHGAT.

Jing Chen, Peimeng Zhen, Zhengxuan Liu, Yongtian Wang, Jiajie Peng, Yifu Xiao, Tao Wang

Abstract read
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Article in BMC biology, 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

7 authors.

Jing ChenSchool of Automation (School of Artificial Intelligence), Beijing Information Science and Technology University, Beijing, China.
Peimeng ZhenSchool of Computer Science, Northwestern Polytechnical University, 1 Dongxiang Rd., 710072, Xi'an, China.
Zhengxuan LiuSchool of Computer Science, Northwestern Polytechnical University, 1 Dongxiang Rd., 710072, Xi'an, China.
Yongtian WangSchool of Computer Science, Northwestern Polytechnical University, 1 Dongxiang Rd., 710072, Xi'an, China.
Jiajie PengSchool of Computer Science, Northwestern Polytechnical University, 1 Dongxiang Rd., 710072, Xi'an, China.
Yifu XiaoSchool of Computer Science, Northwestern Polytechnical University, 1 Dongxiang Rd., 710072, Xi'an, China. xiaoyifu@csu.edu.cn.
Tao WangSchool of Computer Science, Northwestern Polytechnical University, 1 Dongxiang Rd., 710072, Xi'an, China. twang@nwpu.edu.cn.

Funding

National Key R&D Program of China 2025YFC3410200National Natural Science Foundation of China 62102319National Natural Science Foundation of China 62572391, 62402382
6 · The paper itself

Abstract

backgroundThe identification of lncRNA-miRNA interactions (LMIs) is crucial for deciphering post-transcriptional regulatory networks and their roles in development and disease. While computational methods have been developed to predict LMIs, existing approaches are often limited by an inability to effectively integrate multimodal biological data and to handle the severe class imbalance inherent to biological networks.

resultsTo overcome these limitations, we present LMI-MHGAT, a novel deep learning framework for LMI prediction based on a Multilayer Heterogeneous Graph Attention network. Our model integrates diverse data-including RNA sequences, expression profiles, and known molecular interactions-into a unified graph representation. A key innovation is the use of a graph attention mechanism that dynamically learns to weight information from different relational layers, enabling the model to learn robust embeddings for lncRNAs and miRNAs. LMI-MHGAT significantly outperforms 14 existing methods on human LMI data, demonstrating exceptional robustness under severe class imbalance (positive-to-negative ratio 1:60). The model generalizes effectively, achieving state-of-the-art performance on rat and plant datasets. Case studies confirm its ability to recover disease-associated regulatory axes and predict novel, biologically plausible interactions.

conclusionsLMI-MHGAT provides a more powerful and robust framework for LMI prediction by simultaneously addressing key limitations in data utilization and integration. The tool is freely accessible at https://github.com/Zhenpm/LMI-MHGAT .

Indexed as

Computational BiologyDeep LearningGene Regulatory NetworksMicroRNAsRNA, Long NoncodingAnimalsGraph Neural NetworksHumansRatsMicroRNAsRNA, Long NoncodingDeep learningImbalanced networkLncRNA-miRNA interactionMultilayer heterogeneous RNA network

Identifiers

PMID42057106
PMCPMC13277062

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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.