A deep generative model for deciphering cellular dynamics and in silico drug discovery in complex diseases
- PMID: 40542107
- DOI: 10.1038/s41551-025-01423-7
A deep generative model for deciphering cellular dynamics and in silico drug discovery in complex diseases
Abstract
Human diseases are characterized by intricate cellular dynamics. Single-cell transcriptomics provides critical insights, yet a persistent gap remains in computational tools for detailed disease progression analysis and targeted in silico drug interventions. Here we introduce UNAGI, a deep generative neural network tailored to analyse time-series single-cell transcriptomic data. This tool captures the complex cellular dynamics underlying disease progression, enhancing drug perturbation modelling and screening. When applied to a dataset from patients with idiopathic pulmonary fibrosis, UNAGI learns disease-informed cell embeddings that sharpen our understanding of disease progression, leading to the identification of potential therapeutic drug candidates. Validation using proteomics reveals the accuracy of UNAGI's cellular dynamics analysis, and the use of the fibrotic cocktail-treated human precision-cut lung slices confirms UNAGI's predictions that nifedipine, an antihypertensive drug, may have anti-fibrotic effects on human tissues. UNAGI's versatility extends to other diseases, including COVID, demonstrating adaptability and confirming its broader applicability in decoding complex cellular dynamics beyond idiopathic pulmonary fibrosis, amplifying its use in the quest for therapeutic solutions across diverse pathological landscapes.
© 2025. The Author(s).
Conflict of interest statement
Competing interests: N.K. served as a consultant to Pliant, Astra Zeneca, Veracyte, Augmanity, CSL Behring, Splisense, Galapagos, Fibrogen, GSK and Merck over the past 3 years, reports Equity in Pliant and Thyron, and grants from Veracyte, Boehringer Ingelheim, BMS and Astra Zeneca. The other authors declare no competing interests.
Update of
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Unagi: Deep Generative Model for Deciphering Cellular Dynamics and In-Silico Drug Discovery in Complex Diseases.Res Sq [Preprint]. 2023 Dec 18:rs.3.rs-3676579. doi: 10.21203/rs.3.rs-3676579/v1. Res Sq. 2023. Update in: Nat Biomed Eng. 2025 Jun 20. doi: 10.1038/s41551-025-01423-7. PMID: 38196613 Free PMC article. Updated. Preprint.
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Grants and funding
- PTJ-180505/Gouvernement du Canada | Canadian Institutes of Health Research (Instituts de Recherche en Santé du Canada)
- 295298; 295299/Fonds de Recherche du Québec-Société et Culture (FRQSC)
- SCHU3147/4-1/Deutsche Forschungsgemeinschaft (German Research Foundation)
- W81XWH-19-1-0131/U.S. Department of Defense (United States Department of Defense)
- EKFS 2021_EKEA.16; 2020_EKSP.78/Else Kröner-Fresenius-Stiftung (Else Kroner-Fresenius Foundation)
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