AE-RW: Predicting miRNA-disease associations by using autoencoder and random walk on miRNA-gene-disease heterogeneous network

被引:4
作者
Lu, Pengli [1 ]
Jiang, Jicheng [1 ]
机构
[1] Lanzhou Univ Technol, Sch Comp & Commun, Lanzhou 730050, Gansu, Peoples R China
基金
中国国家自然科学基金;
关键词
MiRNA-disease association; Autoencoder; Random walk; MiRNA-gene-disease heterogeneous network; DECISION TREE; MICRORNAS; GROWTH; INHIBITION; SURVIVAL;
D O I
10.1016/j.compbiolchem.2024.108085
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Since scientific investigations have demonstrated that aberrant expression of miRNAs brings about the incidence of numerous intricate diseases, precise determination of miRNA-disease relationships greatly contributes to the advancement of human medical progress. To tackle the issue of inefficient conventional experimental approaches, numerous computational methods have been proposed to predict miRNA-disease association with enhanced accuracy. However, constructing miRNA-gene-disease heterogeneous network by incorporating gene information has been relatively under-explored in existing computational techniques. Accordingly, this paper puts forward a technique to predict miRNA-disease association by applying autoencoder and implementing random walk on miRNA-gene-disease heterogeneous network(AE-RW). Firstly, we integrate association information and similarities between miRNAs, genes, and diseases to construct a miRNA-genedisease heterogeneous network. Subsequently, we consolidate two network feature representations extracted independently via an autoencoder and a random walk procedure. Finally, deep neural network(DNN) are utilized to conduct association prediction. The experimental results demonstrate that the AE-RW model achieved an AUC of 0.9478 through 5-fold CV on the HMDD v3.2 dataset, outperforming the five most advanced existing models. Additionally, case studies were implemented for breast and lung cancer, further validated the superior predictive capabilities of our model.
引用
收藏
页数:9
相关论文
共 44 条
[1]   The functions of animal microRNAs [J].
Ambros, V .
NATURE, 2004, 431 (7006) :350-355
[2]   MicroRNAs: Target Recognition and Regulatory Functions [J].
Bartel, David P. .
CELL, 2009, 136 (02) :215-233
[3]   MicroRNAs: Genomics, biogenesis, mechanism, and function (Reprinted from Cell, vol 116, pg 281-297, 2004) [J].
Bartel, David P. .
CELL, 2007, 131 (04) :11-29
[4]   Random forests [J].
Breiman, L .
MACHINE LEARNING, 2001, 45 (01) :5-32
[5]   XGBoost: A Scalable Tree Boosting System [J].
Chen, Tianqi ;
Guestrin, Carlos .
KDD'16: PROCEEDINGS OF THE 22ND ACM SIGKDD INTERNATIONAL CONFERENCE ON KNOWLEDGE DISCOVERY AND DATA MINING, 2016, :785-794
[6]   MicroRNAs and complex diseases: from experimental results to computational models [J].
Chen, Xing ;
Xie, Di ;
Zhao, Qi ;
You, Zhu-Hong .
BRIEFINGS IN BIOINFORMATICS, 2019, 20 (02) :515-539
[7]   Antisense inhibition of human miRNAs and indications for an involvement of miRNA in cell growth and apoptosis [J].
Cheng, AM ;
Byrom, MW ;
Shelton, J ;
Ford, LP .
NUCLEIC ACIDS RESEARCH, 2005, 33 (04) :1290-1297
[8]   MDA-CF: Predicting MiRNA-Disease associations based on a cascade forest model by fusing multi-source information [J].
Dai, Qiuying ;
Chu, Yanyi ;
Li, Zhiqi ;
Zhao, Yusong ;
Mao, Xueying ;
Wang, Yanjing ;
Xiong, Yi ;
Wei, Dong-Qing .
COMPUTERS IN BIOLOGY AND MEDICINE, 2021, 136
[9]   Predicting miRNA-Disease Associations Based On Multi-View Variational Graph Auto-Encoder With Matrix Factorization [J].
Ding, Yulian ;
Lei, Xiujuan ;
Liao, Bo ;
Wu, Fang-Xiang .
IEEE JOURNAL OF BIOMEDICAL AND HEALTH INFORMATICS, 2022, 26 (01) :446-457
[10]  
Fung Glenn, 2002, Advances in Neural Information Processing Systems, V15