Abstract:LncRNA-protein interactions play important roles in post-transcriptional gene regulation, poly-adenylation, splicing and translation. Identification of lncRNA-protein interactions helps to understand lncRNA-related activities. Existing computational methods utilize multiple lncRNA features or multiple protein features to predict lncRNA-protein interactions, but features are not available for all lncRNAs or proteins; most of existing methods are not capable of predicting interacting proteins (or lncRNAs) for ne… Show more
“…RWNS fused different biological information related to small molecules and miRNAs. However, it may be improved by integrating more data, for example, functional associations between microRNAs and long non-coding RNAs (Zhang et al, 2018b). More importantly, how to integrate these data is still an ongoing challenge.…”
Section: Conclusion and Further Researchmentioning
Recently, many studies have demonstrated that microRNAs (miRNAs) are new small molecule drug targets. Identifying small molecule-miRNA associations (SMiRs) plays an important role in finding new clues for various human disease therapy. Wet experiments can discover credible SMiR associations; however, this is a costly and time-consuming process. Computational models have therefore been developed to uncover possible SMiR associations. In this study, we designed a new SMiR association prediction model, RWNS. RWNS integrates various biological information, credible negative sample selections, and random walk on a triple-layer heterogeneous network into a unified framework. It includes three procedures: similarity computation, negative sample selection, and SMiR association prediction based on random walk on the constructed small molecule-disease-miRNA association network. To evaluate the performance of RWNS, we used leave-one-out cross-validation (LOOCV) and 5-fold cross validation to compare RWNS with two state-of-the-art SMiR association methods, namely, TLHNSMMA and SMiR-NBI. Experimental results showed that RWNS obtained an AUC value of 0.9829 under LOOCV and 0.9916 under 5-fold cross validation on the SM2miR1 dataset, and it obtained an AUC value of 0.8938 under LOOCV and 0.9899 under 5fold cross validation on the SM2miR2 dataset. More importantly, RWNS successfully captured 9, 17, and 37 SMiR associations validated by experiments among the predicted top 10, 20, and 50 SMiR candidates with the highest scores, respectively. We inferred that enoxacin and decitabine are associated with mir-21 and mir-155, respectively. Therefore, RWNS can be a powerful tool for SMiR association prediction.
“…RWNS fused different biological information related to small molecules and miRNAs. However, it may be improved by integrating more data, for example, functional associations between microRNAs and long non-coding RNAs (Zhang et al, 2018b). More importantly, how to integrate these data is still an ongoing challenge.…”
Section: Conclusion and Further Researchmentioning
Recently, many studies have demonstrated that microRNAs (miRNAs) are new small molecule drug targets. Identifying small molecule-miRNA associations (SMiRs) plays an important role in finding new clues for various human disease therapy. Wet experiments can discover credible SMiR associations; however, this is a costly and time-consuming process. Computational models have therefore been developed to uncover possible SMiR associations. In this study, we designed a new SMiR association prediction model, RWNS. RWNS integrates various biological information, credible negative sample selections, and random walk on a triple-layer heterogeneous network into a unified framework. It includes three procedures: similarity computation, negative sample selection, and SMiR association prediction based on random walk on the constructed small molecule-disease-miRNA association network. To evaluate the performance of RWNS, we used leave-one-out cross-validation (LOOCV) and 5-fold cross validation to compare RWNS with two state-of-the-art SMiR association methods, namely, TLHNSMMA and SMiR-NBI. Experimental results showed that RWNS obtained an AUC value of 0.9829 under LOOCV and 0.9916 under 5-fold cross validation on the SM2miR1 dataset, and it obtained an AUC value of 0.8938 under LOOCV and 0.9899 under 5fold cross validation on the SM2miR2 dataset. More importantly, RWNS successfully captured 9, 17, and 37 SMiR associations validated by experiments among the predicted top 10, 20, and 50 SMiR candidates with the highest scores, respectively. We inferred that enoxacin and decitabine are associated with mir-21 and mir-155, respectively. Therefore, RWNS can be a powerful tool for SMiR association prediction.
“…Recently, one broad theme is that lncRNAs can drive the assembly of RNA-protein complexes by facilitating the regulation of gene expression (Rinn and Chang, 2012;Chen and Yan, 2013;Hentze et al, 2018;Munschauer et al, 2018;Nozawa and Gilbert, 2019). lncRNAs achieve their specific functions by interacting with multiple proteins and thus regulating multiple cellular processes (Zhang et al, 2018c;Pyfrom et al, 2019). Studies reported that lncRNAs can activate post-transcriptional gene regulation, splicing, and translation by binding to proteins (Zhang et al,.…”
Section: Introductionmentioning
confidence: 99%
“…lncRNAs achieve their specific functions by interacting with multiple proteins and thus regulating multiple cellular processes (Zhang et al, 2018c;Pyfrom et al, 2019). Studies reported that lncRNAs can activate post-transcriptional gene regulation, splicing, and translation by binding to proteins (Zhang et al,. 2018c;Li et al, 2019a) Therefore, identifying possible lncRNA-protein interactions (LPIs) is essential for unraveling lncRNA-related activities (Qian et al, 2018;Zhang et al, 2018c;Zhao et al, 2018c).…”
Section: Introductionmentioning
confidence: 99%
“…Studies reported that lncRNAs can activate post-transcriptional gene regulation, splicing, and translation by binding to proteins (Zhang et al,. 2018c;Li et al, 2019a) Therefore, identifying possible lncRNA-protein interactions (LPIs) is essential for unraveling lncRNA-related activities (Qian et al, 2018;Zhang et al, 2018c;Zhao et al, 2018c). Wet experiments validated parts of LPIs, but experimental methods remain costly and time-consuming.…”
Identifying lncRNA-protein interactions (LPIs) is vital to understanding various key biological processes. Wet experiments found a few LPIs, but experimental methods are costly and time-consuming. Therefore, computational methods are increasingly exploited to capture LPI candidates. We introduced relevant data repositories, focused on two types of LPI prediction models: network-based methods and machine learning-based methods. Machine learning-based methods contain matrix factorization-based techniques and ensemble learning-based techniques. To detect the performance of computational methods, we compared parts of LPI prediction models on Leave-One-Out cross-validation (LOOCV) and fivefold cross-validation. The results show that SFPEL-LPI obtained the best performance of AUC. Although computational models have efficiently unraveled some LPI candidates, there are many limitations involved. We discussed future directions to further boost LPI predictive performance.Keywords: lncRNA-protein interaction, computational method, network-based method, machine learning-based method, data repositories
“…As a powerful complementary tool for biological and clinical experiments, many computational approaches have been developed to effectively predict the lncRNA-disease associations (Zou et al, 2016;Chen et al, 2017;Zhang et al, 2018c;Gong et al, 2019;Yue et al, 2019). Under the assumption that similar diseases are more likely to be associated with functionally similar lncRNAs, Chen et al proposed Laplacian regularized least squares for lncRNA-disease association in terms of a semi-supervised learning framework (Chen and Yan, 2013).…”
Long noncoding RNAs (lncRNAs) are a class of noncoding RNA molecules longer than 200 nucleotides. Recent studies have uncovered their functional roles in diverse cellular processes and tumorigenesis. Therefore, identifying novel disease-related lncRNAs might deepen our understanding of disease etiology. However, due to the relatively small number of verified associations between lncRNAs and diseases, it remains a challenging task to reliably and effectively predict the associated lncRNAs for given diseases. In this paper, we propose a novel multiview consensus graph learning method to infer potential disease-related lncRNAs. Specifically, we first construct a set of similarity matrices for lncRNAs and diseases by taking advantage of the known associations. We then iteratively learn a consensus graph from the multiple input matrices and simultaneously optimize the predicted association probability based on a multi-label learning framework. To convey the utility of our method, three state-of-the-art methods are compared with our method on three widely used datasets. The experiment results illustrate that our method could obtain the best prediction performance under different cross validation schemes. The case study analysis implemented for uterine cervical neoplasms further confirmed the utility of our method in identifying lncRNAs as potential prognostic biomarkers in practice.
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