Naive Bayes classifier predicts functional microRNA target interactions in colorectal cancer

被引:21
作者
Amirkhah, Raheleh [1 ]
Farazmand, Ali [1 ]
Gupta, Shailendra K. [2 ,3 ]
Ahmadi, Hamed [4 ]
Wolkenhauer, Olaf [2 ,5 ]
Schmitz, Ulf [2 ]
机构
[1] Univ Tehran, Coll Sci, Sch Biol, Dept Cell & Mol Biol, Tehran, Iran
[2] Univ Rostock, Inst Comp Sci, Dept Syst Biol & Bioinformat, D-18055 Rostock, Germany
[3] CSIR, Indian Inst Toxicol Res, Dept Bioinformat, Lucknow, Uttar Pradesh, India
[4] Univ Tehran, Sch Elect & Comp Engn, Coll Engn, Multimedia Proc Lab, Tehran, Iran
[5] Univ Stellenbosch, Stellenbosch Inst Adv Study STIAS, Wallenberg Res Ctr, ZA-7600 Stellenbosch, South Africa
关键词
MIRNA; IDENTIFICATION; NETWORKS; DATABASE; CERNA;
D O I
10.1039/c5mb00245a
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Alterations in the expression of miRNAs have been extensively characterized in several cancers, including human colorectal cancer (CRC). Recent publications provide evidence for tissue-specific miRNA target recognition. Several computational methods have been developed to predict miRNA targets; however, all of these methods assume a general pattern underlying these interactions and therefore tolerate reduced prediction accuracy and a significant number of false predictions. The motivation underlying the presented work was to unravel the relationship between miRNAs and their target mRNAs in CRC. We developed a novel computational algorithm for miRNA-target prediction in CRC using a Naive Bayes classifier. The algorithm, which is referred to as CRCmiRTar, was trained with data from validated miRNA target interactions in CRC and other cancer entities. Furthermore, we identified a set of position-based, sequence, structural, and thermodynamic features that identify CRC-specific miRNA target interactions. Evaluation of the algorithm showed a significant improvement of performance with respect to AUC, and sensitivity, compared to other widely used algorithms based on machine learning. Based on miRNA and gene expression profiles in CRC tissues with similar clinical and pathological features, our classifier predicted 204 functional interactions, which involve 11 miRNAs and 41 mRNAs in this cancer entity. While the approach is here validated for CRC, the implementation of disease-specific miRNA target prediction algorithms can be easily adopted for other applications too. The identification of disease-specific miRNA target interactions may also facilitate the identification of potential drug targets.
引用
收藏
页码:2126 / 2134
页数:9
相关论文
共 40 条
[1]
MicroRNA-mRNA Interactions in Colorectal Cancer and Their Role in Tumor Progression [J].
Amirkhah, Raheleh ;
Schmitz, Ulf ;
Linnebacher, Michael ;
Wolkenhauer, Olaf ;
Farazmand, Ali .
GENES CHROMOSOMES & CANCER, 2015, 54 (03) :129-141
[2]
MBSTAR: multiple instance learning for predicting specific functional binding sites in microRNA targets [J].
Bandyopadhyay, Sanghamitra ;
Ghosh, Dip ;
Mitra, Ramkrishna ;
Zhao, Zhongming .
SCIENTIFIC REPORTS, 2015, 5
[3]
TargetMiner: microRNA target prediction with systematic identification of tissue-specific negative examples [J].
Bandyopadhyay, Sanghamitra ;
Mitra, Ramkrishna .
BIOINFORMATICS, 2009, 25 (20) :2625-2631
[4]
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
[5]
Pleiotropic actions of miR-21 highlight the critical role of deregulated stromal microRNAs during colorectal cancer progression [J].
Bullock, M. D. ;
Pickard, K. M. ;
Nielsen, B. S. ;
Sayan, A. E. ;
Jenei, V. ;
Mellone, M. ;
Mitter, R. ;
Primrose, J. N. ;
Thomas, G. J. ;
Packham, G. K. ;
Mirenzami, A. H. .
CELL DEATH & DISEASE, 2013, 4 :e684-e684
[6]
Wnt5a-mediated non-canonical Wnt signalling regulates human endothelial cell proliferation and migration [J].
Cheng, Ching-wen ;
Yeh, Ju-ching ;
Fan, Tai-Ping ;
Smith, Stephen K. ;
Charnock-Jones, D. Stephen .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2008, 365 (02) :285-290
[7]
Argonaute CLIP-Seq reveals miRNA targetome diversity across tissue types [J].
Clark, Peter M. ;
Loher, Phillipe ;
Quann, Kevin ;
Brody, Jonathan ;
Londin, Eric R. ;
Rigoutsos, Isidore .
SCIENTIFIC REPORTS, 2014, 4
[8]
Assessing the ceRNA Hypothesis with Quantitative Measurements of miRNA and Target Abundance [J].
Denzler, Remy ;
Agarwal, Vikram ;
Stefano, Joanna ;
Bartel, David P. ;
Stoffel, Markus .
MOLECULAR CELL, 2014, 54 (05) :766-776
[9]
Identification and functional screening of microRNAs highly deregulated in colorectal cancer [J].
Faltejskova, Petra ;
Svoboda, Marek ;
Srutova, Klara ;
Mlcochova, Jitka ;
Besse, Andrej ;
Nekvindova, Jana ;
Radova, Lenka ;
Fabian, Pavel ;
Slaba, Katerina ;
Kiss, Igor ;
Vyzula, Rostislav ;
Slaby, Ondrej .
JOURNAL OF CELLULAR AND MOLECULAR MEDICINE, 2012, 16 (11) :2655-2666
[10]
Data mining in bioinformatics using Weka [J].
Frank, E ;
Hall, M ;
Trigg, L ;
Holmes, G ;
Witten, IH .
BIOINFORMATICS, 2004, 20 (15) :2479-2481