Predicting miRNA-disease association from heterogeneous information network with GraRep embedding model

被引:55
作者
Ji, Bo-Ya [1 ,2 ]
You, Zhu-Hong [1 ,2 ]
Cheng, Li [1 ]
Zhou, Ji-Ren [1 ]
Alghazzawi, Daniyal [3 ]
Li, Li-Ping [1 ]
机构
[1] Chinese Acad Sci, Xinjiang Tech Inst Phys & Chem, Urumqi 830011, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[3] King Abdulaziz Univ, Dept Informat Syst, Jeddah, Saudi Arabia
基金
美国国家科学基金会; 中国科学院西部之光基金;
关键词
UPDATED DATABASE; HUMAN MICRORNA; BREAST-CANCER; COLON-CANCER; CELL; EXPRESSION; TARGET; RNA; MESSENGER; GROWTH;
D O I
10.1038/s41598-020-63735-9
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
In recent years, accumulating evidences have shown that microRNA (miRNA) plays an important role in the exploration and treatment of diseases, so detection of the associations between miRNA and disease has been drawn more and more attentions. However, traditional experimental methods have the limitations of high cost and time- consuming, a computational method can help us more systematically and effectively predict the potential miRNA-disease associations. In this work, we proposed a novel network embedding-based heterogeneous information integration method to predict miRNA-disease associations. More specifically, a heterogeneous information network is constructed by combining the known associations among lncRNA, drug, protein, disease, and miRNA. After that, the network embedding method Learning Graph Representations with Global Structural Information (GraRep) is employed to learn embeddings of nodes in heterogeneous information network. In this way, the embedding representations of miRNA and disease are integrated with the attribute information of miRNA and disease (e.g. miRNA sequence information and disease semantic similarity) to represent miRNA-disease association pairs. Finally, the Random Forest (RF) classifier is used for predicting potential miRNA-disease associations. Under the 5-fold cross validation, our method obtained 85.11% prediction accuracy with 80.41% sensitivity at the AUC of 91.25%. In addition, in case studies of three major Human diseases, 45 (Colon Neoplasms), 42 (Breast Neoplasms) and 44 (Esophageal Neoplasms) of top-50 predicted miRNAs are respectively verified by other miRNA-disease association databases. In conclusion, the experimental results suggest that our method can be a powerful and useful tool for predicting potential miRNA-disease associations.
引用
收藏
页数:12
相关论文
共 57 条
[21]   Oncomirs - microRNAs with a role in cancer [J].
Esquela-Kerscher, A ;
Slack, FJ .
NATURE REVIEWS CANCER, 2006, 6 (04) :259-269
[22]   The let-7 microRNA reduces tumor growth in mouse models of lung cancer [J].
Esquela-Kerscher, Aurora ;
Trang, Phong ;
Wiggins, Jason F. ;
Patrawala, Lubna ;
Cheng, Angie ;
Ford, Lance ;
Weidhaas, Joanne B. ;
Brown, David ;
Bader, Andreas G. ;
Slack, Frank J. .
CELL CYCLE, 2008, 7 (06) :759-764
[23]   Decision tree classification of land cover from remotely sensed data [J].
Friedl, MA ;
Brodley, CE .
REMOTE SENSING OF ENVIRONMENT, 1997, 61 (03) :399-409
[24]   Integrated analysis of gene expression signatures associated with colon cancer from three datasets [J].
Gao, Ping ;
He, Miao ;
Zhang, Chunling ;
Geng, Changhui .
GENE, 2018, 654 :95-102
[25]   HMDD v3.0: a database for experimentally supported human microRNA-disease associations [J].
Huang, Zhou ;
Shi, Jiangcheng ;
Gao, Yuanxu ;
Cui, Chunmei ;
Zhang, Shan ;
Li, Jianwei ;
Zhou, Yuan ;
Cui, Qinghua .
NUCLEIC ACIDS RESEARCH, 2019, 47 (D1) :D1013-D1017
[26]  
Javle Milind, 2006, J Support Oncol, V4, P365
[27]   Prioritization of disease microRNAs through a human phenome-microRNAome network [J].
Jiang, Qinghua ;
Hao, Yangyang ;
Wang, Guohua ;
Juan, Liran ;
Zhang, Tianjiao ;
Teng, Mingxiang ;
Liu, Yunlong ;
Wang, Yadong .
BMC SYSTEMS BIOLOGY, 2010, 4
[28]   miR2Disease: a manually curated database for microRNA deregulation in human disease [J].
Jiang, Qinghua ;
Wang, Yadong ;
Hao, Yangyang ;
Juan, Liran ;
Teng, Mingxiang ;
Zhang, Xinjun ;
Li, Meimei ;
Wang, Guohua ;
Liu, Yunlong .
NUCLEIC ACIDS RESEARCH, 2009, 37 :D98-D104
[29]   Encountering microRNAs in cell fate signaling [J].
Karp, X ;
Ambros, V .
SCIENCE, 2005, 310 (5752) :1288-1289
[30]   miRBase: from microRNA sequences to function [J].
Kozomara, Ana ;
Birgaoanu, Maria ;
Griffiths-Jones, Sam .
NUCLEIC ACIDS RESEARCH, 2019, 47 (D1) :D155-D162