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ABSTRACT: Background
IBD is a chronic inflammatory condition driven by complex genetic and immune interactions, yet preclinical models often fail to fully recapitulate all aspects of the human disease. A systematic comparison of commonly used IBD models is essential to identify conserved molecular mechanisms and improve translational relevance.Objective
We performed a multimodel transcriptomic analysis of 13 widely used IBD mouse models to uncover coregulatory gene networks conserved between preclinical colitis/ileitis and human IBD and to define model-specific and conserved cellular, subcellular and molecular signatures.Design
We employed comparative transcriptomic analyses with curated and a priori statistical correlative methods between mouse models versus IBD patient data
SUBMITTER: Gonzalez-Acera M
PROVIDER: S-EPMC12505074 | biostudies-literature | 2025 Sep
REPOSITORIES: biostudies-literature