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Indexed by:Journal Papers

Date of Publication:2020-08-01

Journal:BIOORGANIC CHEMISTRY

Included Journals:SCIE

Volume:101

ISSN No.:0045-2068

Key Words:Oleanolic acid derivatives; Anticancer; PI3K/AKT/mTOR signaling pathway; Cell apoptosis induction; S phase arrest

Abstract:Oleanolic acid (OA) and its semi-synthetic derivatives have been reported to have a wide range of biological activities. The introduction of electrophilic Michael acceptor group can increase the reactivity of OA to cellular targets and thus improve the anti-tumor activity. In this work, a series of novel alpha,beta-unsaturated carbonyl de-rivatives of OA were designed and synthesized. Their in vitro cytotoxic activity against MCF-7, HepG2 and HeLa cells were tested. Most derivatives exhibited improved cell growth inhibitory activity, especially for 3d with an IC50 of 0.77 mu M in MCF-7 cells. Moreover, 3d inhibited the migration of MCF-7 and HeLa cells at the con-centration of 4 mu M. Flow cytometric analysis revealed that 3d induced cell apoptosis and S phase arrest in a concentration-dependent manner. Western blotting experiment demonstrated that 3d inhibited the phosphor-ylation of AKT and mTOR. These results suggest that this series of OA derivatives bearing exocyclic methylene ketone pharmacophore are promising anticancer agents as potential PI3K/AKT/mTOR pathway inhibitors.