A Constrained Probabilistic Matrix Decomposition Method for Predicting miRNA-disease Associations

被引:5
作者
Lu, Xinguo [1 ]
Gao, Yan [1 ]
Zhu, Zhenghao [1 ]
Ding, Li [1 ]
Wang, Xinyu [1 ]
Liu, Fang [1 ]
Li, Jinxin [1 ]
机构
[1] Hunan Univ, Coll Comp Sci & Elect Engn, Changsha 410082, Peoples R China
基金
中国国家自然科学基金;
关键词
Matrix decomposition; miRNA-disease association; disease similarity; miRNA similarity; MICRORNAS; GENOMICS; DATABASE;
D O I
10.2174/1574893615999200801014239
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Background: MicroRNA is a type of non-coding RNA molecule whose length is about 22 nucleotides. The growing evidence shows that microRNA makes critical regulations in the development of complex diseases, such as cancers, and cardiovascular diseases. Predicting potential microRNA-disease associations can provide a new perspective to achieve a better scheme of disease diagnosis and prognosis. However, there is a challenge to predict some potential essential microRNAs only with few known associations. Objective: In this paper, we propose a novel method, named as a constrained strategy for predicting microRNA-disease associations called CPMDA, which can predict some potential essential microRNAs only with few known associations. Methods: We firstly construct a disease similarity network and microRNA similarity network to preprocess the microRNAs with none available associations. Then, we apply probabilistic factorization to obtain two feature matrices of microRNA and disease. Meanwhile, we formulate a similarity feature matrix as constraints in the factorization process. Finally, we utilize obtained feature matrixes to identify potential associations for all diseases. Result and Conclusion: The results indicate that CPMDA is superior over other methods in predicting potential microRNA-disease associations. Moreover, the evaluation shows that CPMDA has a strong effect on microRNAs with few known associations. In case studies, CPMDA also demonstrated the effectiveness to infer unknown microRNA-disease associations for those novel diseases and microRNAs.
引用
收藏
页码:524 / 533
页数:10
相关论文
共 35 条
[1]   The functions of animal microRNAs [J].
Ambros, V .
NATURE, 2004, 431 (7006) :350-355
[2]   Metazoan MicroRNAs [J].
Bartel, David P. .
CELL, 2018, 173 (01) :20-51
[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]   Predicting miRNA-disease association based on inductive matrix completion [J].
Chen, Xing ;
Wang, Lei ;
Qu, Jia ;
Guan, Na-Na ;
Li, Jian-Qiang .
BIOINFORMATICS, 2018, 34 (24) :4256-4265
[5]   WBSMDA: Within and Between Score for MiRNA-Disease Association prediction [J].
Chen, Xing ;
Yan, Chenggang Clarence ;
Zhang, Xu ;
You, Zhu-Hong ;
Deng, Lixi ;
Liu, Ying ;
Zhang, Yongdong ;
Dai, Qionghai .
SCIENTIFIC REPORTS, 2016, 6
[6]   Semi-supervised learning for potential human microRNA-disease associations inference [J].
Chen, Xing ;
Yan, Gui-Ying .
SCIENTIFIC REPORTS, 2014, 4
[7]   SemFunSim: A New Method for Measuring Disease Similarity by Integrating Semantic and Gene Functional Association [J].
Cheng, Liang ;
Li, Jie ;
Ju, Peng ;
Peng, Jiajie ;
Wang, Yadong .
PLOS ONE, 2014, 9 (06)
[8]   miRTarBase update 2018: a resource for experimentally validated microRNA-target interactions [J].
Chou, Chih-Hung ;
Shrestha, Sirjana ;
Yang, Chi-Dung ;
Chang, Nai-Wen ;
Lin, Yu-Ling ;
Liao, Kuang-Wen ;
Huang, Wei-Chi ;
Sun, Ting-Hsuan ;
Tu, Siang-Jyun ;
Lee, Wei-Hsiang ;
Chiew, Men-Yee ;
Tai, Chun-San ;
Wei, Ting-Yen ;
Tsai, Tzi-Ren ;
Huang, Hsin-Tzu ;
Wang, Chung-Yu ;
Wu, Hsin-Yi ;
Ho, Shu-Yi ;
Chen, Pin-Rong ;
Chuang, Cheng-Hsun ;
Hsieh, Pei-Jung ;
Wu, Yi-Shin ;
Chen, Wen-Liang ;
Li, Meng-Ju ;
Wu, Yu-Chun ;
Huang, Xin-Yi ;
Ng, Fung Ling ;
Buddhakosai, Waradee ;
Huang, Pei-Chun ;
Lan, Kuan-Chun ;
Huang, Chia-Yen ;
Weng, Shun-Long ;
Cheng, Yeong-Nan ;
Liang, Chao ;
Hsu, Wen-Lian ;
Huang, Hsien-Da .
NUCLEIC ACIDS RESEARCH, 2018, 46 (D1) :D296-D302
[9]   miRTarBase 2016: updates to the experimentally validated miRNA-target interactions database [J].
Chou, Chih-Hung ;
Chang, Nai-Wen ;
Shrestha, Sirjana ;
Hsu, Sheng-Da ;
Lin, Yu-Ling ;
Lee, Wei-Hsiang ;
Yang, Chi-Dung ;
Hong, Hsiao-Chin ;
Wei, Ting-Yen ;
Tu, Siang-Jyun ;
Tsai, Tzi-Ren ;
Ho, Shu-Yi ;
Jian, Ting-Yan ;
Wu, Hsin-Yi ;
Chen, Pin-Rong ;
Lin, Nai-Chieh ;
Huang, Hsin-Tzu ;
Yang, Tzu-Ling ;
Pai, Chung-Yuan ;
Tai, Chun-San ;
Chen, Wen-Liang ;
Huang, Chia-Yen ;
Liu, Chun-Chi ;
Weng, Shun-Long ;
Liao, Kuang-Wen ;
Hsu, Wen-Lian ;
Huang, Hsien-Da .
NUCLEIC ACIDS RESEARCH, 2016, 44 (D1) :D239-D247
[10]   A path-based measurement for human miRNA functional similarities using miRNA-disease associations [J].
Ding, Pingjian ;
Luo, Jiawei ;
Xiao, Qiu ;
Chen, Xiangtao .
SCIENTIFIC REPORTS, 2016, 6