Evidence map›Paper›PMID 40596835›Full record

ArticleBMC genomics2025

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

Zengwei Xing, Shaoyou Yu, Shuzu Liao, Peng Wang, Bo Liao

Abstract read
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Article in BMC genomics, 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

Authors and funding

5 authors.

Zengwei Xing *School of Mathematics and Statistics, Hainan Normal University, Hainan Haikou, 571158, China.
Shaoyou Yu *School of Mathematics and Statistics, Hainan Normal University, Hainan Haikou, 571158, China.
Shuzu LiaoZhangjiajie People's Hospital, Hunan Zhangjiajie, 427000, China.
Peng WangSchool of Mathematics and Statistics, Hainan Normal University, Hainan Haikou, 571158, China.
Bo LiaoSchool of Mathematics and Statistics, Hainan Normal University, Hainan Haikou, 571158, China. dragonbw@163.com.

Funding

National Key Research and Development Program of China No. 2020YFB2104400National Natural Science Foundation of China NO.62362027 and NO.62362028Natural Science Foundation of Hainan Province No. 122MS055, NO. 824MS063 and NO. 824MS062Program of Graduate Education and Teaching Reform in Hainan, China No. Hnjg2023-54
6 · The paper itself

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.

Indexed as

Computational BiologyRNA, Long NoncodingAlgorithmsHumansMachine LearningRNA, Long NoncodingGraph convolutional networksHypergraphLncRNA-protein interactionMulti-view similarity networks

Identifiers

PMID40596835
PMCPMC12210599

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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.