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EOESGC: predicting miRNA-disease associations based on embedding of embedding and simplified graph convolutional network

BACKGROUND: A large number of biological studies have shown that miRNAs are inextricably linked to many complex diseases. Studying the miRNA-disease associations could provide us a root cause understanding of the underlying pathogenesis in which promotes the progress of drug development. However, tr...

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Autores principales: Pang, Shanchen, Zhuang, Yu, Wang, Xinzeng, Wang, Fuyu, Qiao, Sibo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8597227/
https://www.ncbi.nlm.nih.gov/pubmed/34789236
http://dx.doi.org/10.1186/s12911-021-01671-y
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author Pang, Shanchen
Zhuang, Yu
Wang, Xinzeng
Wang, Fuyu
Qiao, Sibo
author_facet Pang, Shanchen
Zhuang, Yu
Wang, Xinzeng
Wang, Fuyu
Qiao, Sibo
author_sort Pang, Shanchen
collection PubMed
description BACKGROUND: A large number of biological studies have shown that miRNAs are inextricably linked to many complex diseases. Studying the miRNA-disease associations could provide us a root cause understanding of the underlying pathogenesis in which promotes the progress of drug development. However, traditional biological experiments are very time-consuming and costly. Therefore, we come up with an efficient models to solve this challenge. RESULTS: In this work, we propose a deep learning model called EOESGC to predict potential miRNA-disease associations based on embedding of embedding and simplified convolutional network. Firstly, integrated disease similarity, integrated miRNA similarity, and miRNA-disease association network are used to construct a coupled heterogeneous graph, and the edges with low similarity are removed to simplify the graph structure and ensure the effectiveness of edges. Secondly, the Embedding of embedding model (EOE) is used to learn edge information in the coupled heterogeneous graph. The training rule of the model is that the associated nodes are close to each other and the unassociated nodes are far away from each other. Based on this rule, edge information learned is added into node embedding as supplementary information to enrich node information. Then, node embedding of EOE model training as a new feature of miRNA and disease, and information aggregation is performed by simplified graph convolution model, in which each level of convolution can aggregate multi-hop neighbor information. In this step, we only use the miRNA-disease association network to further simplify the graph structure, thus reducing the computational complexity. Finally, feature embeddings of both miRNA and disease are spliced into the MLP for prediction. On the EOESGC evaluation part, the AUC, AUPR, and F1-score of our model are 0.9658, 0.8543 and 0.8644 by 5-fold cross-validation respectively. Compared with the latest published models, our model shows better results. In addition, we predict the top 20 potential miRNAs for breast cancer and lung cancer, most of which are validated in the dbDEMC and HMDD3.2 databases. CONCLUSION: The comprehensive experimental results show that EOESGC can effectively identify the potential miRNA-disease associations.
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spelling pubmed-85972272021-11-17 EOESGC: predicting miRNA-disease associations based on embedding of embedding and simplified graph convolutional network Pang, Shanchen Zhuang, Yu Wang, Xinzeng Wang, Fuyu Qiao, Sibo BMC Med Inform Decis Mak Research BACKGROUND: A large number of biological studies have shown that miRNAs are inextricably linked to many complex diseases. Studying the miRNA-disease associations could provide us a root cause understanding of the underlying pathogenesis in which promotes the progress of drug development. However, traditional biological experiments are very time-consuming and costly. Therefore, we come up with an efficient models to solve this challenge. RESULTS: In this work, we propose a deep learning model called EOESGC to predict potential miRNA-disease associations based on embedding of embedding and simplified convolutional network. Firstly, integrated disease similarity, integrated miRNA similarity, and miRNA-disease association network are used to construct a coupled heterogeneous graph, and the edges with low similarity are removed to simplify the graph structure and ensure the effectiveness of edges. Secondly, the Embedding of embedding model (EOE) is used to learn edge information in the coupled heterogeneous graph. The training rule of the model is that the associated nodes are close to each other and the unassociated nodes are far away from each other. Based on this rule, edge information learned is added into node embedding as supplementary information to enrich node information. Then, node embedding of EOE model training as a new feature of miRNA and disease, and information aggregation is performed by simplified graph convolution model, in which each level of convolution can aggregate multi-hop neighbor information. In this step, we only use the miRNA-disease association network to further simplify the graph structure, thus reducing the computational complexity. Finally, feature embeddings of both miRNA and disease are spliced into the MLP for prediction. On the EOESGC evaluation part, the AUC, AUPR, and F1-score of our model are 0.9658, 0.8543 and 0.8644 by 5-fold cross-validation respectively. Compared with the latest published models, our model shows better results. In addition, we predict the top 20 potential miRNAs for breast cancer and lung cancer, most of which are validated in the dbDEMC and HMDD3.2 databases. CONCLUSION: The comprehensive experimental results show that EOESGC can effectively identify the potential miRNA-disease associations. BioMed Central 2021-11-16 /pmc/articles/PMC8597227/ /pubmed/34789236 http://dx.doi.org/10.1186/s12911-021-01671-y Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Pang, Shanchen
Zhuang, Yu
Wang, Xinzeng
Wang, Fuyu
Qiao, Sibo
EOESGC: predicting miRNA-disease associations based on embedding of embedding and simplified graph convolutional network
title EOESGC: predicting miRNA-disease associations based on embedding of embedding and simplified graph convolutional network
title_full EOESGC: predicting miRNA-disease associations based on embedding of embedding and simplified graph convolutional network
title_fullStr EOESGC: predicting miRNA-disease associations based on embedding of embedding and simplified graph convolutional network
title_full_unstemmed EOESGC: predicting miRNA-disease associations based on embedding of embedding and simplified graph convolutional network
title_short EOESGC: predicting miRNA-disease associations based on embedding of embedding and simplified graph convolutional network
title_sort eoesgc: predicting mirna-disease associations based on embedding of embedding and simplified graph convolutional network
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8597227/
https://www.ncbi.nlm.nih.gov/pubmed/34789236
http://dx.doi.org/10.1186/s12911-021-01671-y
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