Prednisolone exerts late mitogenic and biphasic effects on resistant acute lymphoblastic leukemia cells: Relation to early gene expression

被引:28
作者
Lambrou, George I. [1 ]
Vlahopoulos, Spiros [1 ]
Papathanasiou, Chrisanthi [1 ]
Papanikolaou, Maria [1 ]
Karpusas, Michael
Zoumakis, Emmanouil [2 ]
Tzortzatou-Stathopoulou, Fotini [1 ]
机构
[1] Univ Athens, Sch Med, Aghia Sophia Childrens Hosp, Hematol Oncol Unit,Dept Pediat 1, GR-11527 Athens, Greece
[2] Univ Athens, Sch Med, Aghia Sophia Childrens Hosp, Choremeio Res Lab,Dept Pediat 1, GR-11527 Athens, Greece
关键词
Prednisolone; Biphasic; CCRF-CEM; Mitogenic; Differential gene expression; NF-KAPPA-B; GLUCOCORTICOID-RECEPTOR GENE; INDUCED APOPTOSIS; MICROARRAY DATA; IN-VIVO; TRANSCRIPTION FACTOR; EVOKED APOPTOSIS; DNA HISTOGRAMS; T-CELLS; C-MYB;
D O I
10.1016/j.leukres.2009.04.018
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Resistance or sensitivity to glucocorticoids is considered to be of crucial importance for disease prognosis in childhood acute lymphoblastic leukemia. Prednisolone exerted a delayed biphasic effect on the resistant CCRF-CEM leukemic cell line, necrotic at low doses and apoptotic at higher doses. At low doses, prednisolone exerted a pre-dominant mitogenic effect despite its induction on total cell death, while at higher doses, prednisolone's mitogenic and cell death effects were counterbalanced. Early gene microarray analysis revealed notable differences in 40 genes. The mitogenic/biphasic effects of prednisolone are of clinical importance in the case of resistant leukemic cells. This approach might lead to the identification of gene candidates for future molecular drug targets in combination therapy with glucocorticoids, along with early markers for glucocorticoid resistance. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1684 / 1695
页数:12
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