Fiche publication
Date publication
mars 2026
Journal
Hepatology (Baltimore, Md.)
Auteurs
Membres identifiés du Cancéropôle Est :
Pr BAUMERT Thomas
,
Dr LUPBERGER Joachim
,
Dr CROUCHET Emilie
Tous les auteurs :
Slović N, Mishra S, Paul S, Oudot MA, Jühling F, Kanzaki H, Moehlin J, Charlot A, Denos M, Durand SC, Katz C, Gadenne C, Felli E, Ono A, Oka S, Higashi T, Nakagawa S, Akuta N, Goossens N, Chayama K, Lupberger J, Crouchet E, Hoshida Y, Baumert TF
Lien Pubmed
Résumé
Hepatocellular carcinoma (HCC) is the most common form of liver cancer and is a major global health burden, ranking sixth in incidence and third in cancer-related mortality. Despite therapeutic advances, treatment options for advanced liver disease and HCC are limited and strategies to prevent HCC development are lacking. To address the urgent need for preventive strategies, we identified aripiprazole, an oral atypical antipsychotic, as a candidate for HCC chemoprevention. Analyses of clinical liver tissues showed that aripiprazole targets are expressed in different liver cell compartments including fibroblasts, macrophages and epithelial cancer cells, and that target gene expression is associated with fibrotic liver diseases and HCC. In a rat model of MASH-induced HCC induced by choline-deficient L-amino acid-defined and high-fat diet, aripiprazole prevents liver disease progression and HCC development by modulating fibrogenesis related pathways and inflammation. Mechanistically, aripiprazole exerts antifibrogenic and anti-inflammatory effects by modulating the phenotype of liver fibroblasts and macrophages. Moreover, perturbation studies in cancer cell models showed that aripiprazole prevents tumor initiation and reduces cell proliferation via inhibition of the cMET and ERK pathways and perturbation of mitochondrial functions. Finally, treatment of patient-derived tumorspheroids demonstrated that aripiprazole modulates immune responses in the tumor microenvironment. Collectively, these findings suggest that treatment with aripiprazole is a clinically relevant approach for HCC chemoprevention.
Mots clés
HCC risk, drug repurposing, gene signature, liver fibrosis, serotonin receptors
Référence
Hepatology. 2026 03 13;: