Fiche publication
Date publication
mars 2018
Journal
International journal of oncology
Auteurs
Membres identifiés du Cancéropôle Est :
Dr BOISBRUN Michel
,
Pr FLAMENT Stéphane
,
Dr GRILLIER-VUISSOZ Isabelle
,
Dr KUNTZ Sandra
Tous les auteurs :
Colin C, Meyer M, Cerella C, Kleinclauss A, Monard G, Boisbrun M, Diederich M, Flament S, Grillier-Vuissoz I, Kuntz S
Lien Pubmed
Résumé
15-Deoxy-∆12,14-prostaglandin J2 (15d‑PGJ2) is a natural agonist of peroxisome proliferator-activated receptor γ (PPARγ) that displays anticancer activity. Various studies have indicated that the effects of 15d‑PGJ2 are due to both PPARγ-dependent and -independent mechanisms. In the present study, we examined the effects of a biotinylated form of 15d‑PGJ2 (b‑15d‑PGJ2) on hormone-dependent MCF‑7 and triple‑negative MDA‑MB‑231 breast cancer cell lines. b‑15d‑PGJ2 inhibited cell proliferation more efficiently than 15d‑PGJ2 or the synthetic PPARγ agonist, efatutazone. b‑15d‑PGJ2 was also more potent than its non-biotinylated counterpart in inducing apoptosis. We then analyzed the mechanisms underlying this improved efficiency. It was found not to be the result of biotin receptor-mediated increased incorporation, since free biotin in the culture medium did not decrease the anti-proliferative activity of b‑15d‑PGJ2 in competition assays. Of note, b‑15d‑PGJ2 displayed an improved PPARγ agonist activity, as measured by transactivation experiments. Molecular docking analyses revealed a similar insertion of b‑15d‑PGJ2 and 15d‑PGJ2 into the ligand binding domain of PPARγ via a covalent bond with Cys285. Finally, PPARγ silencing markedly decreased the cleavage of the apoptotic markers, poly(ADP-ribose) polymerase 1 (PARP‑1) and caspase‑7, that usually occurs following b‑15d‑PGJ2 treatment. Taken together, our data indicate that biotinylation enhances the anti-proliferative and pro-apoptotic activity of 15d‑PGJ2, and that this effect is partly mediated via a PPARγ-dependent pathway. These results may aid in the development of novel therapeutic strategies for breast cancer treatment.
Mots clés
Binding Sites, genetics, Biotinylation, methods, Breast Neoplasms, chemistry, Cell Line, Tumor, Cell Proliferation, drug effects, Cell Survival, drug effects, Female, Gene Expression Regulation, Neoplastic, drug effects, Humans, MCF-7 Cells, Models, Molecular, Molecular Docking Simulation, PPAR gamma, agonists, Prostaglandin D2, analogs & derivatives, Thiazolidinediones, pharmacology
Référence
Int. J. Oncol.. 2018 Mar 28;:
