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Identifying circRNA-miRNA interaction based on multi-biological interaction fusion

CircRNA is a new type of non-coding RNA with a closed loop structure. More and more biological experiments show that circRNA plays important roles in many diseases by regulating the target genes of miRNA. Therefore, correct identification of the potential interaction between circRNA and miRNA not on...

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Autores principales: Yao, Dunwei, Nong, Lidan, Qin, Minzhen, Wu, Shengbin, Yao, Shunhan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9815023/
https://www.ncbi.nlm.nih.gov/pubmed/36620017
http://dx.doi.org/10.3389/fmicb.2022.987930
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author Yao, Dunwei
Nong, Lidan
Qin, Minzhen
Wu, Shengbin
Yao, Shunhan
author_facet Yao, Dunwei
Nong, Lidan
Qin, Minzhen
Wu, Shengbin
Yao, Shunhan
author_sort Yao, Dunwei
collection PubMed
description CircRNA is a new type of non-coding RNA with a closed loop structure. More and more biological experiments show that circRNA plays important roles in many diseases by regulating the target genes of miRNA. Therefore, correct identification of the potential interaction between circRNA and miRNA not only helps to understand the mechanism of the disease, but also contributes to the diagnosis, treatment, and prognosis of the disease. In this study, we propose a model (IIMCCMA) by using network embedding and matrix completion to predict the potential interaction of circRNA-miRNA. Firstly, the corresponding adjacency matrix is constructed based on the experimentally verified circRNA-miRNA interaction, circRNA-cancer interaction, and miRNA-cancer interaction. Then, the Gaussian kernel function and the cosine function are used to calculate the circRNA Gaussian interaction profile kernel similarity, circRNA functional similarity, miRNA Gaussian interaction profile kernel similarity, and miRNA functional similarity. In order to reduce the influence of noise and redundant information in known interactions, this model uses network embedding to extract the potential feature vectors of circRNA and miRNA, respectively. Finally, an improved inductive matrix completion algorithm based on the feature vectors of circRNA and miRNA is used to identify potential interactions between circRNAs and miRNAs. The 10-fold cross-validation experiment is utilized to prove the predictive ability of the IIMCCMA. The experimental results show that the AUC value and AUPR value of the IIMCCMA model are higher than other state-of-the-art algorithms. In addition, case studies show that the IIMCCMA model can correctly identify the potential interactions between circRNAs and miRNAs.
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spelling pubmed-98150232023-01-06 Identifying circRNA-miRNA interaction based on multi-biological interaction fusion Yao, Dunwei Nong, Lidan Qin, Minzhen Wu, Shengbin Yao, Shunhan Front Microbiol Microbiology CircRNA is a new type of non-coding RNA with a closed loop structure. More and more biological experiments show that circRNA plays important roles in many diseases by regulating the target genes of miRNA. Therefore, correct identification of the potential interaction between circRNA and miRNA not only helps to understand the mechanism of the disease, but also contributes to the diagnosis, treatment, and prognosis of the disease. In this study, we propose a model (IIMCCMA) by using network embedding and matrix completion to predict the potential interaction of circRNA-miRNA. Firstly, the corresponding adjacency matrix is constructed based on the experimentally verified circRNA-miRNA interaction, circRNA-cancer interaction, and miRNA-cancer interaction. Then, the Gaussian kernel function and the cosine function are used to calculate the circRNA Gaussian interaction profile kernel similarity, circRNA functional similarity, miRNA Gaussian interaction profile kernel similarity, and miRNA functional similarity. In order to reduce the influence of noise and redundant information in known interactions, this model uses network embedding to extract the potential feature vectors of circRNA and miRNA, respectively. Finally, an improved inductive matrix completion algorithm based on the feature vectors of circRNA and miRNA is used to identify potential interactions between circRNAs and miRNAs. The 10-fold cross-validation experiment is utilized to prove the predictive ability of the IIMCCMA. The experimental results show that the AUC value and AUPR value of the IIMCCMA model are higher than other state-of-the-art algorithms. In addition, case studies show that the IIMCCMA model can correctly identify the potential interactions between circRNAs and miRNAs. Frontiers Media S.A. 2022-12-22 /pmc/articles/PMC9815023/ /pubmed/36620017 http://dx.doi.org/10.3389/fmicb.2022.987930 Text en Copyright © 2022 Yao, Nong, Qin, Wu and Yao. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Yao, Dunwei
Nong, Lidan
Qin, Minzhen
Wu, Shengbin
Yao, Shunhan
Identifying circRNA-miRNA interaction based on multi-biological interaction fusion
title Identifying circRNA-miRNA interaction based on multi-biological interaction fusion
title_full Identifying circRNA-miRNA interaction based on multi-biological interaction fusion
title_fullStr Identifying circRNA-miRNA interaction based on multi-biological interaction fusion
title_full_unstemmed Identifying circRNA-miRNA interaction based on multi-biological interaction fusion
title_short Identifying circRNA-miRNA interaction based on multi-biological interaction fusion
title_sort identifying circrna-mirna interaction based on multi-biological interaction fusion
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9815023/
https://www.ncbi.nlm.nih.gov/pubmed/36620017
http://dx.doi.org/10.3389/fmicb.2022.987930
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