Resistance to phorbol ester-induced differentiation in human myeloid leukemia cells:: A hypothetic role for the mRNA stabilization process

被引:7
作者
Champelovier, Pierre
Pautre, Virginie
ElAtifi, Michele
Dupre, Isabelle
Rostaing, Beatrice
Michoud, Annick
Berger, Francois
Seigneurin, Daniel
机构
[1] Ctr Hosp Univ Grenoble, INSERM, U318,Dept Biol & Pathol Cellule, Equipe Transcriptome,Lab Hematol, F-38043 Grenoble 09, France
[2] Univ Grenoble 1, CNRS, UMR 5525, EPHE,Lab Dynam Cellulaire, F-38000 Grenoble, France
[3] Univ Grenoble 1, INSERM, U318, Lab Neurosci Preclin,Equipe Transcriptome, F-38000 Grenoble, France
关键词
TPA resistance; microarray; mRNA stabilization; ARE-BP;
D O I
10.1016/j.leukres.2006.04.006
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
UM384 cells, derived from the human myeloid leukemia U937 cell line, fail to differentiate in response to 12-O-tetradecanoylphorbol-13-acetate (TPA). Using cDNA microarray and real-time quantitative PCR (RT-QPCR) approaches, we observed a difference in the response to TPA treatment: all the genes from U937 cells were continuously modulated from 2 to 24 h. In UM384 cells, 60% of the genes were transiently modulated at 2 h, then returned to control levels at 24 h. Moreover, HuR, an AU-rich element-binding protein (ARE-BP), was differentially located in the two cell lines. Therefore, a defect of mRNA stabilization could be responsible for the resistance of UM384 cells to TPA-induced differentiation, suggesting a possible role for the post-transcriptional regulation in the leukemogenesis. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1407 / 1416
页数:10
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