Biochemical effects of piceatannol in human HL-60 promyelocytic leukemia cells--synergism with Ara-C
Fritzer-Szekeres, M.; Savinc, I.; Horvath, Z.; Saiko, P.; Pemberger, M.; Graser, G.; Bernhaus, A.; Ozsvar-Kozma, M.; Grusch, M.; Jaeger, W.; Szekeres, T.
International Journal of Oncology 33(4): 887-892
2008
ISSN/ISBN: 1019-6439 PMID: 18813804 Document Number: 622124
Piceatannol (3,3',4,5'-tetrahydroxy-trans-stilbene; PCA) is a naturally occurring metabolite of resveratrol (3,4',5-trihydroxy-trans-stilbene; RV). In this study, we identified additional biochemical targets of PCA in human HL-60 promyelocytic leukemia cells. Incubation with PCA led to a significant proportion of apoptotic cells and caused an arrest in the G2-M phase of the cell cycle. PCA depleted intracellular dCTP and dGTP pools, and inhibited the incorporation of 14C-labeled cytidine into DNA. PCA significantly abolished all NTP pools, and sequential treatment with PCA and Ara-C yielded synergistic growth inhibitory effects because of remarkably increased Ara-CTP formation after PCA preincubation. Due to these promising results, PCA may support conventional chemotherapy of human malignancies and therefore, deserves further preclinical and in vivo testing.