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Latent disease similarities and therapeutic repurposing possibilities uncovered by multi-modal generative topic modeling of human diseases

MOTIVATION: Human diseases are characterized by multiple features such as their pathophysiological, molecular and genetic changes. The rapid expansion of such multi-modal disease-omics space provides an opportunity to re-classify diverse human diseases and to uncover their latent molecular similarit...

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Autores principales: Kozawa, Satoshi, Yokoyama, Hirona, Urayama, Kyoji, Tejima, Kengo, Doi, Hotaka, Takagi, Shunki, Sato, Thomas N
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10133403/
https://www.ncbi.nlm.nih.gov/pubmed/37123453
http://dx.doi.org/10.1093/bioadv/vbad047
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author Kozawa, Satoshi
Yokoyama, Hirona
Urayama, Kyoji
Tejima, Kengo
Doi, Hotaka
Takagi, Shunki
Sato, Thomas N
author_facet Kozawa, Satoshi
Yokoyama, Hirona
Urayama, Kyoji
Tejima, Kengo
Doi, Hotaka
Takagi, Shunki
Sato, Thomas N
author_sort Kozawa, Satoshi
collection PubMed
description MOTIVATION: Human diseases are characterized by multiple features such as their pathophysiological, molecular and genetic changes. The rapid expansion of such multi-modal disease-omics space provides an opportunity to re-classify diverse human diseases and to uncover their latent molecular similarities, which could be exploited to repurpose a therapeutic-target for one disease to another. RESULTS: Herein, we probe this underexplored space by soft-clustering 6955 human diseases by multi-modal generative topic modeling. Focusing on chronic kidney disease and myocardial infarction, two most life-threatening diseases, unveiled are their previously underrecognized molecular similarities to neoplasia and mental/neurological-disorders, and 69 repurposable therapeutic-targets for these diseases. Using an edit-distance-based pathway-classifier, we also find molecular pathways by which these targets could elicit their clinical effects. Importantly, for the 17 targets, the evidence for their therapeutic usefulness is retrospectively found in the pre-clinical and clinical space, illustrating the effectiveness of the method, and suggesting its broader applications across diverse human diseases. AVAILABILITY AND IMPLEMENTATION: The code reported in this article is available at: https://github.com/skozawa170301ktx/MultiModalDiseaseModeling SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics Advances online.
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spelling pubmed-101334032023-04-28 Latent disease similarities and therapeutic repurposing possibilities uncovered by multi-modal generative topic modeling of human diseases Kozawa, Satoshi Yokoyama, Hirona Urayama, Kyoji Tejima, Kengo Doi, Hotaka Takagi, Shunki Sato, Thomas N Bioinform Adv Original Paper MOTIVATION: Human diseases are characterized by multiple features such as their pathophysiological, molecular and genetic changes. The rapid expansion of such multi-modal disease-omics space provides an opportunity to re-classify diverse human diseases and to uncover their latent molecular similarities, which could be exploited to repurpose a therapeutic-target for one disease to another. RESULTS: Herein, we probe this underexplored space by soft-clustering 6955 human diseases by multi-modal generative topic modeling. Focusing on chronic kidney disease and myocardial infarction, two most life-threatening diseases, unveiled are their previously underrecognized molecular similarities to neoplasia and mental/neurological-disorders, and 69 repurposable therapeutic-targets for these diseases. Using an edit-distance-based pathway-classifier, we also find molecular pathways by which these targets could elicit their clinical effects. Importantly, for the 17 targets, the evidence for their therapeutic usefulness is retrospectively found in the pre-clinical and clinical space, illustrating the effectiveness of the method, and suggesting its broader applications across diverse human diseases. AVAILABILITY AND IMPLEMENTATION: The code reported in this article is available at: https://github.com/skozawa170301ktx/MultiModalDiseaseModeling SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics Advances online. Oxford University Press 2023-04-12 /pmc/articles/PMC10133403/ /pubmed/37123453 http://dx.doi.org/10.1093/bioadv/vbad047 Text en © The Author(s) 2023. Published by Oxford University Press. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Paper
Kozawa, Satoshi
Yokoyama, Hirona
Urayama, Kyoji
Tejima, Kengo
Doi, Hotaka
Takagi, Shunki
Sato, Thomas N
Latent disease similarities and therapeutic repurposing possibilities uncovered by multi-modal generative topic modeling of human diseases
title Latent disease similarities and therapeutic repurposing possibilities uncovered by multi-modal generative topic modeling of human diseases
title_full Latent disease similarities and therapeutic repurposing possibilities uncovered by multi-modal generative topic modeling of human diseases
title_fullStr Latent disease similarities and therapeutic repurposing possibilities uncovered by multi-modal generative topic modeling of human diseases
title_full_unstemmed Latent disease similarities and therapeutic repurposing possibilities uncovered by multi-modal generative topic modeling of human diseases
title_short Latent disease similarities and therapeutic repurposing possibilities uncovered by multi-modal generative topic modeling of human diseases
title_sort latent disease similarities and therapeutic repurposing possibilities uncovered by multi-modal generative topic modeling of human diseases
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10133403/
https://www.ncbi.nlm.nih.gov/pubmed/37123453
http://dx.doi.org/10.1093/bioadv/vbad047
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