Biochemical effects of piceatannol in human HL-60 promyelocytic leukemia cells - Synergism with Ara-C

被引:24
作者
Fritzer-Szekeres, Monika [1 ,2 ]
Savinc, Ivo [1 ,2 ]
Horvath, Zsuzsanna [1 ,2 ]
Saiko, Philipp [1 ,2 ]
Pemberger, Michael [1 ,2 ]
Graser, Geraldine [1 ,2 ]
Bernhaus, Astrid [1 ,2 ]
Ozsvar-Kozma, Maria [1 ,2 ]
Grusch, Michael [3 ]
Jaeger, Walter [4 ]
Szekeres, Thomas [1 ,2 ]
机构
[1] Med Univ Vienna, Gen Hosp Vienna, Inst Clin Med, A-1090 Vienna, Austria
[2] Med Univ Vienna, Gen Hosp Vienna, Chem Lab Diagnost, A-1090 Vienna, Austria
[3] Med Univ Vienna, Div Canc Res, Dept Med 1, A-1090 Vienna, Austria
[4] Univ Vienna, Fac Hlth Sci, Dept Clin Pharmaceut & Diagnost, A-1090 Vienna, Austria
关键词
resveratrol; piceatannol; Ara-C; leukemia; ribonucleotide reductase; apoptosis;
D O I
10.3892/ijo_00000077
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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 C-14-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.
引用
收藏
页码:887 / 892
页数:6
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