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cFos Mediates cAMP-Dependent Generation of ROS and Rescue of Maturation Program in Retinoid-Resistant Acute Promyelocytic Leukemia Cell Line NB4-LR1

机译:在视黄醇抗急性早幼粒细胞白血病细胞系NB4-LR1 ROs和成熟方案的救援cFos的介导的camp依赖性产生

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摘要

A determining role has been assigned to cAMP in the signaling pathways that relieve resistance to anti-leukemia differentiation therapy. However, the underlying mechanisms have not been elucidated yet. Here, we identify cFos as a critical cAMP effector, able to regulate the re-expression and splicing of epigenetically silenced genes associated with maturation (CD44) in retinoid-resistant NB4-LR1 leukemia cells. Furthermore, using RNA interference approach, we show that cFos mediates cAMP-induced ROS generation, a critical mediator of neutrophil maturation, and in fine differentiation. This study highlights some of the mechanisms by which cAMP acts to overcome resistance, and reveals a new alternative cFos-dependent pathway which, though nonexistent in retinoid-sensitive NB4 cells, is essential to rescue the maturation program of resistant cells.
机译:在减轻对抗白血病分化治疗的抗性的信号传导途径中,cAMP被赋予了决定性的作用。但是,尚未阐明其基本机制。在这里,我们确定cFos为关键的cAMP效应物,能够调节与类维生素A耐药的NB4-LR1白血病细胞中与成熟(CD44)相关的表观遗传沉默基因的重新表达和剪接。此外,使用RNA干扰方法,我们显示cFos介导cAMP诱导的ROS生成,中性粒细胞成熟的关键介体以及精细分化。这项研究强调了cAMP克服抗性的一些机制,并揭示了一种新的替代性cFos依赖性途径,尽管在类维生素A敏感的NB4细胞中不存在,但对挽救抗性细胞的成熟程序至关重要。

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