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

IF 3.7 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Zengwei Xing, Shaoyou Yu, Shuzu Liao, Peng Wang, Bo Liao
{"title":"MFH-LPI: based on multi-view similarity networks fusion and hypergraph learning for long non-coding RNA-protein interactions prediction.","authors":"Zengwei Xing, Shaoyou Yu, Shuzu Liao, Peng Wang, Bo Liao","doi":"10.1186/s12864-025-11774-9","DOIUrl":null,"url":null,"abstract":"<p><p>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.</p>","PeriodicalId":9030,"journal":{"name":"BMC Genomics","volume":"26 1","pages":"597"},"PeriodicalIF":3.7000,"publicationDate":"2025-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12210599/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"BMC Genomics","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1186/s12864-025-11774-9","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0

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.

MFH-LPI:基于多视图相似网络融合和超图学习的长链非编码rna -蛋白相互作用预测。
研究表明,长链非编码rna (long non-coding rna, lncRNAs)及其蛋白相互作用(protein interaction, lpi)在调控基因表达和参与多种生物过程中起着至关重要的作用。这些相互作用的异常表达与各种疾病的发生和发展密切相关。因此,研究LPI预测对于阐明疾病机制和确定潜在的生物标志物和治疗靶点至关重要。鉴于传统生物方法的高成本和有限的效率,开发具有成本效益和准确的LPI预测计算模型变得至关重要。受相似网络融合和超图学习的启发,本研究提出了一个名为MFH-LPI的计算框架。首先,我们构建了lncrna和蛋白质的独立相似网络,然后采用注意机制从这些多视图网络中提取和融合关键特征。随后,我们引入一个超级节点(随机生成的节点)来建立一个整合lncrna和蛋白质的异构超图,从而捕获更丰富的节点表示。最后,我们使用多层图卷积网络(GCN)结合全连接层(FC)来预测lpi。我们在三个数据集上进行了多次实验来验证该方法的有效性。实验结果表明,该模型与现有方法相比是有效的,并且优于其他方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
BMC Genomics
BMC Genomics 生物-生物工程与应用微生物
CiteScore
7.40
自引率
4.50%
发文量
769
审稿时长
6.4 months
期刊介绍: BMC Genomics is an open access, peer-reviewed journal that considers articles on all aspects of genome-scale analysis, functional genomics, and proteomics. BMC Genomics is part of the BMC series which publishes subject-specific journals focused on the needs of individual research communities across all areas of biology and medicine. We offer an efficient, fair and friendly peer review service, and are committed to publishing all sound science, provided that there is some advance in knowledge presented by the work.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信