Glycogen synthase kinase 3 beta inhibitors induce apoptosis in ovarian cancer cells and inhibit in-vivo tumor growth

作者：Hilliard Tyvette S; Gaisina Irina N; Muehlbauer Amanda G; Gaisin Arsen M; Gallier Franck; Burdette Joanna E^*

来源：Anti-Cancer Drugs, 2011, 22(10): 978-985.

DOI：10.1097/CAD.0b013e32834ac8fc

• drug discovery
• GSK3 beta
• ovarian cancer
• Wnt
• xenograft

Ovarian cancer is the most lethal gynecological malignancy among US women. Paclitaxel/carboplatin is the current drug therapy used to treat ovarian cancer, but most women develop drug resistance and recurrence of the disease, necessitating alternative strategies for treatment. A possible molecular target for cancer therapy is glycogen synthase kinase 3 beta (GSK3 beta), a downstream kinase in the Wnt signaling pathway that is overexpressed in serous ovarian cancer. Novel maleimide-based GSK3b inhibitors (GSK3 beta i) were synthesized, selected, and tested in vitro using SKOV3 and OVCA432 serous ovarian cancer cell lines. From a panel of 10 inhibitors, GSK3 beta i 9ING41 was found to be the most effective in vitro. 9ING41 induced apoptosis as indicated by 4',6-diamidino-2-phenylindole-positive nuclear condensation, poly (ADP-ribose) polymerase cleavage, and terminal deoxynucleotidyl transferase dUTP nick end labeling staining. The mechanism for apoptosis was through caspase-3 cleavage. GSK3 beta i upregulated phosphorylation of the inhibitory serine residue of GSK3 beta in OVCA432 and SKOV3 cell lines and also inhibited phosphorylation of the downstream target glycogen synthase. An in-vivo xenograft study using SKOV3 cells demonstrated that tumor progression was hindered by 9ING41 in vivo. The maximum tolerated dose for 9ING41 was greater than 500 mg/kg in rats. Pharmacokinetic analysis showed 9ING41 to have a bioavailability of 4.5% and to be well distributed in tissues. Therefore, GSK3 beta inhibitors alone or in combination with existing drugs may hinder the growth of serous ovarian cancers.

• 出版日期2011-11