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
相关论文
共 33 条
[21]   Antioxidant prooxidant and cytotoxic activity of hydroxylated resveratrol analogues:: structure-activity relationship [J].
Murias, M ;
Jäger, W ;
Handler, N ;
Erker, T ;
Horvath, Z ;
Szekeres, T ;
Nohl, H ;
Gille, L .
BIOCHEMICAL PHARMACOLOGY, 2005, 69 (06) :903-912
[22]   Resveratrol analogues as selective cyclooxygenase-2 inhibitors:: synthesis and structure-activity relationship [J].
Murias, M ;
Handler, N ;
Erker, T ;
Pleban, K ;
Ecker, G ;
Saiko, P ;
Szekeres, T ;
Jäger, W .
BIOORGANIC & MEDICINAL CHEMISTRY, 2004, 12 (21) :5571-5578
[23]   Properties of DNA fragmentation activity generated by ATP depletion [J].
Nakamura, N ;
Wada, Y .
CELL DEATH AND DIFFERENTIATION, 2000, 7 (05) :477-484
[24]   HLA-G expression is associated with an unfavorable outcome and immunodeficiency in chronic lymphocytic leukemia [J].
Nückel, H ;
Rebmann, V ;
Dürig, J ;
Dührsen, U ;
Grosse-Wilde, H .
BLOOD, 2005, 105 (04) :1694-1698
[25]  
Palmieri L, 1999, DRUG EXP CLIN RES, V25, P79
[26]   The cancer preventative agent resveratrol is converted to the anticancer agent piceatannol by the cytochrome P450 enzyme CYPIBI [J].
Potter, GA ;
Patterson, LH ;
Wanogho, E ;
Perry, PJ ;
Butler, PC ;
Ijaz, T ;
Ruparelia, KC ;
Lamb, JH ;
Farmer, PB ;
Stanley, LA ;
Burke, MD .
BRITISH JOURNAL OF CANCER, 2002, 86 (05) :774-778
[27]   WINE, ALCOHOL, PLATELETS, AND THE FRENCH PARADOX FOR CORONARY HEART-DISEASE [J].
RENAUD, S ;
DELORGERIL, M .
LANCET, 1992, 339 (8808) :1523-1526
[28]   Effects of resveratrol, piceatannol, triacetoxystilbene, and genistein on the inflammatory response of human peripheral blood leukocytes [J].
Richard, N ;
Porath, D ;
Radspieler, A ;
Schwager, J .
MOLECULAR NUTRITION & FOOD RESEARCH, 2005, 49 (05) :431-442
[29]   Distinct mechanisms of STAT phosphorylation via the interferon-α/β receptor -: Selective inhibition of STAT3 and STAT5 by piceatannol [J].
Su, L ;
David, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (17) :12661-12666
[30]   Pterostilbene and 3′-hydroxypterostilbene are effective apoptosis-inducing agents in MDR and BCR-ABL-expressing leukemia cells [J].
Tolomeo, M ;
Grimaudo, S ;
Di Cristina, A ;
Roberti, M ;
Pizzirani, D ;
Meli, M ;
Dusonchet, L ;
Gebbia, N ;
Abbadessa, V ;
Crosta, L ;
Barucchello, R ;
Grisolia, G ;
Invidiata, F ;
Simoni, D .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2005, 37 (08) :1709-1726