The differentiation state of small intestinal organoid models influences prediction of drug-induced toxicity.
Ontology highlight
ABSTRACT: Drug-induced intestinal toxicity (GIT) is a frequent dose-limiting adverse event that can impact patient compliance and treatment outcomes. In vivo, there are proliferative and differentiated cell types critical to maintaining intestinal homeostasis. Traditional in vitro models using transformed cell lines do not capture this cellular complexity, and often fail to predict intestinal toxicity. Primary tissue-derived intestinal organoids, on the other hand, are a scalable Complex in vitro Model (CIVM) that recapitulates major intestinal cell lineages and function. Intestinal organoid toxicity assays have been shown to correlate with clinical incidence of drug-induced diarrhea, however existing studies do not consider how differentiation state of the organoids impacts ass
SUBMITTER: Klein JA
PROVIDER: S-EPMC11799252 | biostudies-literature | 2025
REPOSITORIES: biostudies-literature
ACCESS DATA