Modelling the liver’s regenerative capacity across different clinical conditions

The aim of this study was to identify key transcriptomic, proteomic, and serum biomarkers of regeneration in mouse models under diverse conditions, using systems biology and machine learning approaches. Key molecular drivers of liver regeneration across diverse clinical conditions were identified using innovative deep learning and multi-omics approaches. By identifying conserved cell cycle genes predictive of regenerative outcomes, this study offers a powerful framework to assess and potentially enhance liver recovery in older patients, those with fibrosis or steatosis, and/or those under immunosuppression.

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Institutions

Publication Details

Journal
JHEP Reports
Published
2025-05-30
DOI
https://doi.org/10.1016/j.jhepr.2025.101465
Citations
2
Primary Topic
Liver physiology and pathology
Type
article
Field-Weighted Citation Impact
2.64

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article

Modelling the liver’s regenerative capacity across different clinical conditions

Elisa Pasini, Michael Brudno, Anh Thu Nguyen‐Lefebvre, Bima J. Hasjim et al.
2 citations
JHEP Reports
Liver physiology and pathology
2.64
article

Modelling the liver’s regenerative capacity across different clinical conditions

Elisa Pasini, Michael Brudno, Anh Thu Nguyen‐Lefebvre, Bima J. Hasjim, Mamatha Bhat, Graziano Oldani, Nazia Selzner, Jeffrey L. Wrana, Cristina Baciu, Sara Naimimohasses, Soumita Ghosh
article en
2 citations

Abstract

The aim of this study was to identify key transcriptomic, proteomic, and serum biomarkers of regeneration in mouse models under diverse conditions, using systems biology and machine learning approaches. Key molecular drivers of liver regeneration across diverse clinical conditions were identified using innovative deep learning and multi-omics approaches. By identifying conserved cell cycle genes predictive of regenerative outcomes, this study offers a powerful framework to assess and potentially enhance liver recovery in older patients, those with fibrosis or steatosis, and/or those under immunosuppression.

JHEP ReportsVol. 7(8)
University of Geneva (CH), University Health Network (CA), University of British Columbia (CA), University of Toronto (CA), University of California, Irvine (US), Lunenfeld-Tanenbaum Research Institute (CA), University of California, Irvine Medical Center (US)
Stem Cell Network, Hospital for Sick Children, Scheme for Promotion of Academic and Research Collaboration, University Health Network Foundation, Natural Sciences and Engineering Research Council of Canada
Openalex Percentile: Top 10%
Liver physiology and pathology
2.64
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