Marseille Cancer Research Centre (CRCM), U1068 Inserm, UMR7258, CNRS, Aix-Marseille Université, Institut Paoli-Calmettes, Equipe labellisée Ligue, Marseille, 13273, France.
Centre de Recherche des Cordeliers, UMR 1162, Inserm, Université Paris Descartes, 75006, Paris, France.
Curr Genet. 2019 Oct;65(5):1081-1088. doi: 10.1007/s00294-019-00967-x. Epub 2019 Apr 11.
Ploidy is stably maintained in most human somatic cells by a sequential and tight coordination of cell cycle events. Undesired whole genome doublings or duplications are frequent in tumours and have been quite recently described as macro-evolutionary events associated with poor prognosis. In vitro and in vivo studies suggest that polyploidy can favour genome instability, facilitate the formation and progression of tumours, and modify their sensitivity to chemotherapeutic agents. Stress is strongly related to changes in ploidy and whole genome doublings. In this review, we summarize different mechanisms that promote polyploidization, describe a new type of stress able to trigger WGDs in S. cerevisiae, histone stress, and provide some examples and theoretical scenarios that support that cancer cells might suffer from this type of stress. We finally highlight some results showing that the kinase Swe1 (Wee1 in humans) has a role in sensing histone levels before cells enter mitosis, thereby avoiding their undesired consequences on chromosome segregation and ploidy control.
在大多数人类体细胞中,通过细胞周期事件的顺序和紧密协调,可以稳定地维持倍性。在肿瘤中,不期望的全基因组加倍或重复是很常见的,并且最近被描述为与预后不良相关的宏观进化事件。体外和体内研究表明,多倍体可以促进基因组不稳定性,促进肿瘤的形成和进展,并改变它们对化疗药物的敏感性。应激与倍性变化和全基因组加倍密切相关。在这篇综述中,我们总结了促进多倍体形成的不同机制,描述了一种新型应激,能够在酿酒酵母中触发全基因组加倍,即组蛋白应激,并提供了一些支持癌细胞可能遭受这种应激的例子和理论情景。最后,我们强调了一些结果,表明激酶 Swe1(人类中的 Wee1)在细胞进入有丝分裂之前在感知组蛋白水平方面具有作用,从而避免了它们对染色体分离和倍性控制的不良后果。