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Two cell cycle blocks caused by iron chelation of neuroblastoma cells: separating cell cycle events associated with each block

机译:由神经母细胞瘤细胞铁螯合引起的两个细胞周期阻滞:分离与每个阻滞相关的细胞周期事件

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摘要

Studies have presented evidence that besides the well described S phase block, treatment of cancer cell lines with the iron chelator deferrioxamine (DFO) also results in an earlier block in G1 phase. In this article, measurements of cell cycle regulatory proteins define this block at a very specific point in G1. DFO treatment results in markedly decreased cyclin A protein levels. Cyclin E levels that accumulate in early to mid‐G1 are increased in cells treated with DFO as compared to the resting cells. The DFO S phase block is shown after cells are arrested at G1/S by (aphidicolin) then released into DFO. The same S phase block occurs with DFO treatment of a neuroblastoma cell line relatively resistant to the G1 DFO block. These experiments clearly differentiate the S phase DFO block from the earlier block pinpointed to a point in mid‐G1, before G1/S when cyclin E protein increases but before increased cyclin A synthesis. Apoptosis was observed in cells inhibited by DFO at both cell cycle arrest points.
机译:研究已经提供了证据,除了充分描述的S期阻滞外,用铁螯合剂去铁胺(DFO)处理癌细胞系也可导致G1期更早的阻滞。在本文中,细胞周期调节蛋白的测量在G1的一个非常特定的点上定义了该阻滞。 DFO处理导致细胞周期蛋白A蛋白水平显着降低。与静息细胞相比,DFO处理的细胞在G1早期至中期积累的细胞周期蛋白E水平升高。图中显示了DFO S相阻滞后,细胞被(aphidicolin)阻滞在G1 / S,然后释放到DFO中。 DFO处理对G1 DFO阻滞相对抗性的神经母细胞瘤细胞系时,会发生相同的S期阻滞。这些实验清楚地区分了S期DFO嵌段与精确定位到G1中点的早期嵌段,后者在G1 / S之前细胞周期蛋白E蛋白增加,而在细胞周期蛋白A合成增加之前。在两个细胞周期停滞点均观察到DFO抑制的细胞凋亡。

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