GDC-0152

Fluorescence polarization-based competition assay

Inhibition constants ( Ki ) for the antagonists are determined by adding the IAP protein constructs to wells containing serial dilutions of the antagonists or the peptide AVPW, and the Hid-FAM probe or AVP-diPhe-FAM probe, as appropriate, in the polarization buffer. Samples are read after a 30-min incubation. Fluorescence polarization values are plotted as a function of the antagonist concentration, and the IC50 values are obtained by fitting the data to a 4-parameter equation using KaleidaGraph software. Ki values for the antagonists are determined from the IC50 values.

Cell lines

U87MG, GL261, GBM6, GBM9 cell lines, and MDA-MB-231 breast carcinoma cells

Preparation method

The solubility of this compound in DMSO is >10 mM. General tips for obtaining a higher concentration: Please warm the tube at 37℃ for 10 minutes and/or shake it in the ultrasonic bath for a while. Stock solution can be stored below -20℃ for several months.

Reacting condition

1μM or 100μM; 72h or 8 days; 10 nM-10μM; 3h-24h

Applications

GDC-0152 treatment triggered apoptosis and decreased IAP protein expression in glioblastoma cell lines. Moreover, GDC-0152 (10 nM-10μM) dose-dependently promoted degradation of cIAP1, induced caspase-3/7 activation, and lead to decreased viability of breast cancer cells.

Animal models

100 000 U87MG-iRFP cells were injected into the corpus callosum of athymic nude mice; MDA-MB-231 breast cancer xenograft model;

Dosage form

10, 20, 50, and 100 mg/kg; intravenous injection or oral gavage; weekly for 2 months

Applications

GDC-0152 (10 mg/kg or 20 mg/kg) dose-dependently increased survival and slowed down tumor growth of mice bearing intracranial tumors. Moreover, GDC-0152 (10, 50, and 100 mg/kg) suppressed tumor growth in dose-dependent manner in the MDA-MB-231 breast cancer xenograft model.

Other notes

Please test the solubility of all compounds indoor, and the actual solubility may slightly differ with the theoretical value. This is caused by an experimental system error and it is normal.

References:

1. Flygare, J. A., Beresini, M., Budha, N., Chan, H., Chan, I. T., Cheeti, S., Cohen, F., Deshayes, K., Doerner, K., Eckhardt, S. G., Elliott, L. O., Feng, B., Franklin, M. C., Reisner, S. F., Gazzard, L., Halladay, J., Hymowitz, S. G., La, H., LoRusso, P., Maurer, B., Murray, L., Plise, E., Quan, C., Stephan, J. P., Young, S. G., Tom, J., Tsui, V., Um, J., Varfolomeev, E., Vucic, D., Wagner, A. J., Wallweber, H. J., Wang, L., Ware, J., Wen, Z., Wong, H., Wong, J. M., Wong, M., Wong, S., Yu, R., Zobel, K. and Fairbrother, W. J. (2012) Discovery of a potent small-molecule antagonist of inhibitor of apoptosis (IAP) proteins and clinical candidate for the treatment of cancer (GDC-0152). J Med Chem. 55, 4101-41132

2. Tchoghandjian, A., Souberan, A., Tabouret, E., Colin, C., Denicolai, E., Jiguet-Jiglaire, C., El-Battari, A., Villard, C., Baeza-Kallee, N. and Figarella-Branger, D. (2016) Inhibitor of apoptosis protein expression in glioblastomas and their in vitro and in vivo targeting by SMAC mimetic GDC-0152. Cell Death Dis. 7, e2325