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DrugRep-HeSiaGraph: when heterogenous siamese neural network meets knowledge graphs for drug repurposing

BACKGROUND: Drug repurposing is an approach that holds promise for identifying new therapeutic uses for existing drugs. Recently, knowledge graphs have emerged as significant tools for addressing the challenges of drug repurposing. However, there are still major issues with constructing and embeddin...

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Autores principales: Ghorbanali, Zahra, Zare-Mirakabad, Fatemeh, Salehi, Najmeh, Akbari, Mohammad, Masoudi-Nejad, Ali
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10548718/
https://www.ncbi.nlm.nih.gov/pubmed/37789314
http://dx.doi.org/10.1186/s12859-023-05479-7
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author Ghorbanali, Zahra
Zare-Mirakabad, Fatemeh
Salehi, Najmeh
Akbari, Mohammad
Masoudi-Nejad, Ali
author_facet Ghorbanali, Zahra
Zare-Mirakabad, Fatemeh
Salehi, Najmeh
Akbari, Mohammad
Masoudi-Nejad, Ali
author_sort Ghorbanali, Zahra
collection PubMed
description BACKGROUND: Drug repurposing is an approach that holds promise for identifying new therapeutic uses for existing drugs. Recently, knowledge graphs have emerged as significant tools for addressing the challenges of drug repurposing. However, there are still major issues with constructing and embedding knowledge graphs. RESULTS: This study proposes a two-step method called DrugRep-HeSiaGraph to address these challenges. The method integrates the drug-disease knowledge graph with the application of a heterogeneous siamese neural network. In the first step, a drug-disease knowledge graph named DDKG-V1 is constructed by defining new relationship types, and then numerical vector representations for the nodes are created using the distributional learning method. In the second step, a heterogeneous siamese neural network called HeSiaNet is applied to enrich the embedding of drugs and diseases by bringing them closer in a new unified latent space. Then, it predicts potential drug candidates for diseases. DrugRep-HeSiaGraph achieves impressive performance metrics, including an AUC-ROC of 91.16%, an AUC-PR of 90.32%, an accuracy of 84.63%, a BS of 0.119, and an MCC of 69.31%. CONCLUSION: We demonstrate the effectiveness of the proposed method in identifying potential drugs for COVID-19 as a case study. In addition, this study shows the role of dipeptidyl peptidase 4 (DPP-4) as a potential receptor for SARS-CoV-2 and the effectiveness of DPP-4 inhibitors in facing COVID-19. This highlights the practical application of the model in addressing real-world challenges in the field of drug repurposing. The code and data for DrugRep-HeSiaGraph are publicly available at https://github.com/CBRC-lab/DrugRep-HeSiaGraph. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12859-023-05479-7.
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spelling pubmed-105487182023-10-05 DrugRep-HeSiaGraph: when heterogenous siamese neural network meets knowledge graphs for drug repurposing Ghorbanali, Zahra Zare-Mirakabad, Fatemeh Salehi, Najmeh Akbari, Mohammad Masoudi-Nejad, Ali BMC Bioinformatics Research BACKGROUND: Drug repurposing is an approach that holds promise for identifying new therapeutic uses for existing drugs. Recently, knowledge graphs have emerged as significant tools for addressing the challenges of drug repurposing. However, there are still major issues with constructing and embedding knowledge graphs. RESULTS: This study proposes a two-step method called DrugRep-HeSiaGraph to address these challenges. The method integrates the drug-disease knowledge graph with the application of a heterogeneous siamese neural network. In the first step, a drug-disease knowledge graph named DDKG-V1 is constructed by defining new relationship types, and then numerical vector representations for the nodes are created using the distributional learning method. In the second step, a heterogeneous siamese neural network called HeSiaNet is applied to enrich the embedding of drugs and diseases by bringing them closer in a new unified latent space. Then, it predicts potential drug candidates for diseases. DrugRep-HeSiaGraph achieves impressive performance metrics, including an AUC-ROC of 91.16%, an AUC-PR of 90.32%, an accuracy of 84.63%, a BS of 0.119, and an MCC of 69.31%. CONCLUSION: We demonstrate the effectiveness of the proposed method in identifying potential drugs for COVID-19 as a case study. In addition, this study shows the role of dipeptidyl peptidase 4 (DPP-4) as a potential receptor for SARS-CoV-2 and the effectiveness of DPP-4 inhibitors in facing COVID-19. This highlights the practical application of the model in addressing real-world challenges in the field of drug repurposing. The code and data for DrugRep-HeSiaGraph are publicly available at https://github.com/CBRC-lab/DrugRep-HeSiaGraph. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12859-023-05479-7. BioMed Central 2023-10-03 /pmc/articles/PMC10548718/ /pubmed/37789314 http://dx.doi.org/10.1186/s12859-023-05479-7 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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
Ghorbanali, Zahra
Zare-Mirakabad, Fatemeh
Salehi, Najmeh
Akbari, Mohammad
Masoudi-Nejad, Ali
DrugRep-HeSiaGraph: when heterogenous siamese neural network meets knowledge graphs for drug repurposing
title DrugRep-HeSiaGraph: when heterogenous siamese neural network meets knowledge graphs for drug repurposing
title_full DrugRep-HeSiaGraph: when heterogenous siamese neural network meets knowledge graphs for drug repurposing
title_fullStr DrugRep-HeSiaGraph: when heterogenous siamese neural network meets knowledge graphs for drug repurposing
title_full_unstemmed DrugRep-HeSiaGraph: when heterogenous siamese neural network meets knowledge graphs for drug repurposing
title_short DrugRep-HeSiaGraph: when heterogenous siamese neural network meets knowledge graphs for drug repurposing
title_sort drugrep-hesiagraph: when heterogenous siamese neural network meets knowledge graphs for drug repurposing
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10548718/
https://www.ncbi.nlm.nih.gov/pubmed/37789314
http://dx.doi.org/10.1186/s12859-023-05479-7
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