控制增殖和凋亡平衡的分子开关。

B Schutte, F C Ramaekers
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引用次数: 31

摘要

胚胎发生期间的组织建模和成人生活期间的组织稳态是由生长和程序性细胞死亡(凋亡)之间的动态平衡所控制的。生长控制和细胞凋亡是密切相关的,这两个过程之间的平衡受到干扰通常会导致病理情况,例如癌症中的细胞积聚。迄今为止,许多控制生长和细胞凋亡的分子机制是已知的,而控制这两种途径之间的决定的开关仍然是难以捉摸的。细胞持续暴露于多个对立的“死亡”和“生存”触发器。一个具有挑战性的问题是细胞如何感知这些信号并决定生存或死亡。一个有利于生存的决定应该自动导致死亡途径的关闭。另一种选择是,死亡的决定应该导致对生存的徒劳尝试的抑制。控制这种信号平衡的分子事件将被讨论,特别强调周期蛋白依赖激酶和泛素依赖和蛋白酶体介导的蛋白质降解途径的作用。
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Molecular switches that govern the balance between proliferation and apoptosis.

Tissue modelling during embryogenesis and tissue homeostasis during adult life is governed by a dynamic equilibrium between growth and programmed cell death (apoptosis). Growth control and apoptosis are intimately associated, and a disturbance of the balance between these two processes often leads to pathological situations, such as for example cell accumulations in cancer. To date many of the molecular mechanisms controlling growth control on the one hand, and apoptosis on the other hand are known, whereas the switch that controls the decision between both pathways remains elusive. A cell is continuously exposed to multiple opposing "death" and "survival" triggers. A challenging question is how a cell senses these signals and decides to live or die. A decision in favour of survival should automatically result in a shut down of the death pathways. Alternatively, a decision for death should result in inhibition of futile attempts to survive. The molecular events controlling this balance of signals will be discussed with special emphasis on the role of cyclin-dependent kinases and the ubiquitin-dependent and proteasome-mediated protein degradation pathway.

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