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Efficient framework for predicting MiRNA-disease associations based on improved hybrid collaborative filtering

BACKGROUND: Accumulating studies indicates that microRNAs (miRNAs) play vital roles in the process of development and progression of many human complex diseases. However, traditional biochemical experimental methods for identifying disease-related miRNAs cost large amount of time, manpower, material...

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Autores principales: Nie, Ru, Li, Zhengwei, You, Zhu-hong, Bao, Wenzheng, Li, Jiashu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8406577/
https://www.ncbi.nlm.nih.gov/pubmed/34461870
http://dx.doi.org/10.1186/s12911-021-01616-5
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author Nie, Ru
Li, Zhengwei
You, Zhu-hong
Bao, Wenzheng
Li, Jiashu
author_facet Nie, Ru
Li, Zhengwei
You, Zhu-hong
Bao, Wenzheng
Li, Jiashu
author_sort Nie, Ru
collection PubMed
description BACKGROUND: Accumulating studies indicates that microRNAs (miRNAs) play vital roles in the process of development and progression of many human complex diseases. However, traditional biochemical experimental methods for identifying disease-related miRNAs cost large amount of time, manpower, material and financial resources. METHODS: In this study, we developed a framework named hybrid collaborative filtering for miRNA-disease association prediction (HCFMDA) by integrating heterogeneous data, e.g., miRNA functional similarity, disease semantic similarity, known miRNA-disease association networks, and Gaussian kernel similarity of miRNAs and diseases. To capture the intrinsic interaction patterns embedded in the sparse association matrix, we prioritized the predictive score by fusing three types of information: similar disease associations, similar miRNA associations, and similar disease-miRNA associations. Meanwhile, singular value decomposition was adopted to reduce the impact of noise and accelerate predictive speed. RESULTS: We then validated HCFMDA with leave-one-out cross-validation (LOOCV) and two types of case studies. In the LOOCV, we achieved 0.8379 of AUC (area under the curve). To evaluate the performance of HCFMDA on real diseases, we further implemented the first type of case validation over three important human diseases: Colon Neoplasms, Esophageal Neoplasms and Prostate Neoplasms. As a result, 44, 46 and 44 out of the top 50 predicted disease-related miRNAs were confirmed by experimental evidence. Moreover, the second type of case validation on Breast Neoplasms indicates that HCFMDA could also be applied to predict potential miRNAs towards those diseases without any known associated miRNA. CONCLUSIONS: The satisfactory prediction performance demonstrates that our model could serve as a reliable tool to guide the following research for identifying candidate miRNAs associated with human diseases.
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spelling pubmed-84065772021-08-31 Efficient framework for predicting MiRNA-disease associations based on improved hybrid collaborative filtering Nie, Ru Li, Zhengwei You, Zhu-hong Bao, Wenzheng Li, Jiashu BMC Med Inform Decis Mak Methodology BACKGROUND: Accumulating studies indicates that microRNAs (miRNAs) play vital roles in the process of development and progression of many human complex diseases. However, traditional biochemical experimental methods for identifying disease-related miRNAs cost large amount of time, manpower, material and financial resources. METHODS: In this study, we developed a framework named hybrid collaborative filtering for miRNA-disease association prediction (HCFMDA) by integrating heterogeneous data, e.g., miRNA functional similarity, disease semantic similarity, known miRNA-disease association networks, and Gaussian kernel similarity of miRNAs and diseases. To capture the intrinsic interaction patterns embedded in the sparse association matrix, we prioritized the predictive score by fusing three types of information: similar disease associations, similar miRNA associations, and similar disease-miRNA associations. Meanwhile, singular value decomposition was adopted to reduce the impact of noise and accelerate predictive speed. RESULTS: We then validated HCFMDA with leave-one-out cross-validation (LOOCV) and two types of case studies. In the LOOCV, we achieved 0.8379 of AUC (area under the curve). To evaluate the performance of HCFMDA on real diseases, we further implemented the first type of case validation over three important human diseases: Colon Neoplasms, Esophageal Neoplasms and Prostate Neoplasms. As a result, 44, 46 and 44 out of the top 50 predicted disease-related miRNAs were confirmed by experimental evidence. Moreover, the second type of case validation on Breast Neoplasms indicates that HCFMDA could also be applied to predict potential miRNAs towards those diseases without any known associated miRNA. CONCLUSIONS: The satisfactory prediction performance demonstrates that our model could serve as a reliable tool to guide the following research for identifying candidate miRNAs associated with human diseases. BioMed Central 2021-08-30 /pmc/articles/PMC8406577/ /pubmed/34461870 http://dx.doi.org/10.1186/s12911-021-01616-5 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 Methodology
Nie, Ru
Li, Zhengwei
You, Zhu-hong
Bao, Wenzheng
Li, Jiashu
Efficient framework for predicting MiRNA-disease associations based on improved hybrid collaborative filtering
title Efficient framework for predicting MiRNA-disease associations based on improved hybrid collaborative filtering
title_full Efficient framework for predicting MiRNA-disease associations based on improved hybrid collaborative filtering
title_fullStr Efficient framework for predicting MiRNA-disease associations based on improved hybrid collaborative filtering
title_full_unstemmed Efficient framework for predicting MiRNA-disease associations based on improved hybrid collaborative filtering
title_short Efficient framework for predicting MiRNA-disease associations based on improved hybrid collaborative filtering
title_sort efficient framework for predicting mirna-disease associations based on improved hybrid collaborative filtering
topic Methodology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8406577/
https://www.ncbi.nlm.nih.gov/pubmed/34461870
http://dx.doi.org/10.1186/s12911-021-01616-5
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