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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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Detalles Bibliográficos
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
Descripción
Sumario: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.