MFH-LPI: based on multi-view similarity networks fusion and hypergraph learning for long non-coding RNA-protein interactions prediction

Studies demonstrate that long non-coding RNAs (lncRNAs) and their protein interactions (LPIs) play crucial roles in regulating gene expression and participating in diverse biological processes. Aberrant expression of these interactions is closely associated with the initiation and progression of various diseases. Therefore, investigating LPI prediction is critical for elucidating disease mechanisms and identifying potential biomarkers and therapeutic targets. Given the high costs and limited efficiency of traditional biological methods, developing cost-effective and accurate computational models for LPI prediction becomes essential. Inspired by similarity network fusion and hypergraph learning, this study proposes a computational framework named MFH-LPI. First, we construct separate similarity networks for lncRNAs and proteins, then employ an attention mechanism to extract and fuse key features from these multi-view networks. Subsequently, we introduce a hypernode (randomly generated node) to establish a heterogeneous hypergraph integrating lncRNAs and proteins, thereby capturing richer node representations. Finally, we predict LPIs using a multilayer graph convolutional network (GCN) combined with a fully connected (FC) layer. We conduct several experiments on three datasets to validate the method's effectiveness. The experimental findings indicate that the suggested model is effective compared to existing processes and outperforms other approaches.

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Publication Details

Journal
BMC Genomics
Published
2025-07-01
DOI
https://doi.org/10.1186/s12864-025-11774-9
Citations
2
Primary Topic
Cancer-related molecular mechanisms research
Type
article
Field-Weighted Citation Impact
1.87

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article

MFH-LPI: based on multi-view similarity networks fusion and hypergraph learning for long non-coding RNA-protein interactions prediction

Stephen Shaoyi Liao, Shaoyou Yu, Richard C. Wang, Zheng Xing et al.
2 citations
BMC Genomics
Cancer-related molecular mechanisms research
1.87
article

MFH-LPI: based on multi-view similarity networks fusion and hypergraph learning for long non-coding RNA-protein interactions prediction

Stephen Shaoyi Liao, Shaoyou Yu, Richard C. Wang, Zheng Xing, Bo Liao
article en
2 citations

Abstract

Studies demonstrate that long non-coding RNAs (lncRNAs) and their protein interactions (LPIs) play crucial roles in regulating gene expression and participating in diverse biological processes. Aberrant expression of these interactions is closely associated with the initiation and progression of various diseases. Therefore, investigating LPI prediction is critical for elucidating disease mechanisms and identifying potential biomarkers and therapeutic targets. Given the high costs and limited efficiency of traditional biological methods, developing cost-effective and accurate computational models for LPI prediction becomes essential. Inspired by similarity network fusion and hypergraph learning, this study proposes a computational framework named MFH-LPI. First, we construct separate similarity networks for lncRNAs and proteins, then employ an attention mechanism to extract and fuse key features from these multi-view networks. Subsequently, we introduce a hypernode (randomly generated node) to establish a heterogeneous hypergraph integrating lncRNAs and proteins, thereby capturing richer node representations. Finally, we predict LPIs using a multilayer graph convolutional network (GCN) combined with a fully connected (FC) layer. We conduct several experiments on three datasets to validate the method's effectiveness. The experimental findings indicate that the suggested model is effective compared to existing processes and outperforms other approaches.

BMC GenomicsVol. 26(1)
Hainan Normal University (CN)
National Natural Science Foundation of China, Natural Science Foundation of Hainan Province, National Key Research and Development Program of China, Division of Graduate Education
Openalex Percentile: Top 14%
Cancer-related molecular mechanisms research
1.87
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