All trans retinoic acid induces apoptosis in acute promyelocytic NB4 cells when combined with isoquinolinediol, a poly(ADP-ribose) polymerase inhibitor

被引:12
作者
Berry, DM
Williams, K
Meckling-Gill, KA [1 ]
机构
[1] Univ Guelph, Dept Human Biol & Nutr Sci, Guelph, ON N1G 2W1, Canada
[2] Hosp Sick Children, Arthur & Sonia LaBatt Brain Tumor Res Ctr, Toronto, ON M5G 1X8, Canada
关键词
apoptosis; all-trans retinoic acid; 1; alpha; 25 dihydroxyvitamin D-3; differentiation; NB4; poly(ADP-ribose) polymerase;
D O I
10.1016/S0145-2126(99)00188-5
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
NB4 cells, a model of acute promyelocytic leukemia have been shown to undergo granulocytic differentiation in response to all trans retinoic acid (ATRA), or monocytic differentiation in response to 1 alpha,25 dihydroxyvitamin D-3 (1,25 D-3) and phorbol ester. We have shown previously that the expression of poly(ADP-ribose) polymerase (PARP) is dramatically increased during monocytic differentiation and completely down-regulated during neutrophilic differentiation. Here we show that NB4 cells simultaneously treated with ATRA and isoquinolinediol (Iso-Q), a specific PARP inhibitor, fail to differentiate into neutrophils. Nitroblue tetrazolium (NBT) dye reduction was inhibited by 48% and neutrophil formation was reduced by 75%. NB4 cells treated with ATRA and Iso-Q instead showed features of apoptosis including nuclear condensation, DNA fragmentation, and PARP cleavage yielding a 85 kDa fragment. NB4 cells treated with ATRA in combination with 1,25 D-3, a monocytic differentiation inducer, while continuing to reduce NET also failed to mature into neutrophils or monocytes and again showed features of apoptosis. Down-regulation of Bcl-2 protein expression was evident in NB4 cells treated with ATRA and ATRA in combination with Iso-Q or 1,25 D-3, but not in cells treated with a classic chemotherapeutic agent, arabinosycytosine, suggesting that Bcl-2 down-regulation is neither necessary, nor specific for apoptosis in this model. (C) 2000 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:307 / 316
页数:10
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