SGAEMDA: Predicting miRNA-Disease Associations Based on Stacked Graph Autoencoder

被引:9
作者
Wang, Shudong [1 ]
Lin, Boyang [1 ]
Zhang, Yuanyuan [1 ,2 ]
Qiao, Sibo [1 ]
Wang, Fuyu [1 ]
Wu, Wenhao [1 ]
Ren, Chuanru [1 ]
机构
[1] China Univ Petr, Qingdao Inst Software, Coll Comp Sci & Technol, Qingdao 266580, Peoples R China
[2] Qingdao Univ Technol, Sch Informat & Control Engn, Qingdao 266525, Peoples R China
基金
中国国家自然科学基金;
关键词
miRNA; disease; association prediction; stacked graph autoencoder; higher-order features; MICRORNA; SIMILARITY; CANCER; ROLES; PCR;
D O I
10.3390/cells11243984
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
MicroRNA (miRNA)-disease association (MDA) prediction is critical for disease prevention, diagnosis, and treatment. Traditional MDA wet experiments, on the other hand, are inefficient and costly.Therefore, we proposed a multi-layer collaborative unsupervised training base model called SGAEMDA (Stacked Graph Autoencoder-Based Prediction of Potential miRNA-Disease Associations). First, from the original miRNA and disease data, we defined two types of initial features: similarity features and association features. Second, stacked graph autoencoder is then used to learn unsupervised low-dimensional representations of meaningful higher-order similarity features, and we concatenate the association features with the learned low-dimensional representations to obtain the final miRNA-disease pair features. Finally, we used a multilayer perceptron (MLP) to predict scores for unknown miRNA-disease associations. SGAEMDA achieved a mean area under the ROC curve of 0.9585 and 0.9516 in 5-fold and 10-fold cross-validation, which is significantly higher than the other baseline methods. Furthermore, case studies have shown that SGAEMDA can accurately predict candidate miRNAs for brain, breast, colon, and kidney neoplasms.
引用
收藏
页数:18
相关论文
共 47 条
[1]   The functions of animal microRNAs [J].
Ambros, V .
NATURE, 2004, 431 (7006) :350-355
[2]   Breast cancer in young women: an overview [J].
Anastasiadi, Zoi ;
Lianos, Georgios D. ;
Ignatiadou, Eleftheria ;
Harissis, Haralampos V. ;
Mitsis, Michail .
UPDATES IN SURGERY, 2017, 69 (03) :313-317
[3]  
Bray F, 2018, CA-CANCER J CLIN, V68, P394, DOI [10.3322/caac.21492, 10.3322/caac.21609]
[4]   NCMCMDA: miRNA-disease association prediction through neighborhood constraint matrix completion [J].
Chen, Xing ;
Sun, Lian-Gang ;
Zhao, Yan .
BRIEFINGS IN BIOINFORMATICS, 2021, 22 (01) :485-496
[5]   Epidemiology and risk factors for kidney cancer [J].
Chow, Wong-Ho ;
Dong, Linda M. ;
Devesa, Susan S. .
NATURE REVIEWS UROLOGY, 2010, 7 (05) :245-257
[6]   Salivary microR-153 and microR-223 Levels as Potential Diagnostic Biomarkers of Idiopathic Parkinson's Disease [J].
Cressatti, Marisa ;
Juwara, Lamin ;
Galindez, Julia M. ;
Velly, Ana M. ;
Nkurunziza, Eva S. ;
Marier, Sara ;
Canie, Olivia ;
Gornistky, Mervyn ;
Schipper, Hyman M. .
MOVEMENT DISORDERS, 2020, 35 (03) :468-477
[7]   Non-coding RNAs in human disease [J].
Esteller, Manel .
NATURE REVIEWS GENETICS, 2011, 12 (12) :861-874
[8]   Heterogeneous graph inference based on similarity network fusion for predicting lncRNA-miRNA interaction [J].
Fan, Yongxian ;
Cui, Juan ;
Zhu, QingQi .
RSC ADVANCES, 2020, 10 (20) :11634-11642
[9]   Stem cells and brain cancer [J].
Galderisi, U ;
Cipollaro, M ;
Giordano, A .
CELL DEATH AND DIFFERENTIATION, 2006, 13 (01) :5-11
[10]   NPCMF: Nearest Profile-based Collaborative Matrix Factorization method for predicting miRNA-disease associations [J].
Gao, Ying-Lian ;
Cui, Zhen ;
Liu, Jin-Xing ;
Wang, Juan ;
Zheng, Chun-Hou .
BMC BIOINFORMATICS, 2019, 20 (1)