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Sypercompetitor Status of Drosophila Myc Cells Requires p53 as a Fitness Sensor to Reprogram Metabolism and Promote Viability

机译:果蝇Myc细胞的超级竞争者状态需要p53作为适应性传感器来重新编程代谢和促进活力

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In growing tissues, cell fitness disparities can provoke interactions that promote stronger cells at the expense of the weaker in a process called cell competition. The mechanistic definition of cell fitness is not understood, nor is it understood how fitness differences are recognized. Drosophila cells with extra Myc activity acquire "supercompetitor" status upon confrontation with wild-type (WT) cells, prompting the latter's elimination via apoptosis. Here we show that such confrontation enhances glycolytic flux in Myc cells and promotes their fitness and proliferation in a p53-dependent manner. Whereas p53 loss in noncompeting Myc cells is inconsequential, its loss impairs metabolism, reduces viability, and prevents the killing activity of Myc supercompetitor cells. We propose that p53 acts as a general sensor of competitive confrontation to enhance the fitness of the "winner" population. Our findings suggest that the initial confrontation between precancerous and WT cells could enhance cancer cell fitness and promote tumor progression.
机译:在生长中的组织中,细胞适应性差异可能会引发相互作用,从而促进更强壮的细胞,而在称为细胞竞争的过程中却以较弱的细胞为代价。不了解细胞适应性的机制定义,也不了解如何识别适应性差异。果蝇具有额外Myc活性的果蝇细胞在与野生型(WT)细胞对抗时获得“超级竞争者”状态,促使后者通过细胞凋亡消除。在这里,我们表明这种对抗增强了Myc细胞中的糖酵解通量,并以p53依赖性的方式促进了它们的适应性和增殖。尽管在非竞争性Myc细胞中p53丢失是无关紧要的,但其丢失会损害新陈代谢,降低生存能力并阻止Myc超级竞争者细胞的杀伤活性。我们建议p53充当竞争对抗的一般传感器,以增强“优胜者”人群的适应性。我们的发现表明,癌前细胞与野生型细胞之间的最初对抗可以增强癌细胞的适应性并促进肿瘤的进展。

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