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首页> 外文期刊>Cancer Cell International >Three steps to the immortality of cancer cells: senescence, polyploidy and self-renewal
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Three steps to the immortality of cancer cells: senescence, polyploidy and self-renewal

机译:癌细胞永生的三个步骤:衰老,多倍性和自我更新

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摘要

Metastatic cancer is rarely cured by current DNA damaging treatments, apparently due to the development of resistance. However, recent data indicates that tumour cells can elicit the opposing processes of senescence and stemness in response to these treatments, the biological significance and molecular regulation of which is currently poorly understood. Although cellular senescence is typically considered a terminal cell fate, it was recently shown to be reversible in a small population of polyploid cancer cells induced after DNA damage. Overcoming genotoxic insults is associated with reversible polyploidy, which itself is associated with the induction of a stemness phenotype, thereby providing a framework linking these separate phenomena. In keeping with this suggestion, senescence and autophagy are clearly intimately involved in the emergence of self-renewal potential in the surviving cells that result from de-polyploidisation. Moreover, subsequent analysis indicates that senescence may paradoxically be actually required to rejuvenate cancer cells after genotoxic treatments. We propose that genotoxic resistance is thereby afforded through a programmed life-cycle-like process which intimately unites senescence, polyploidy and stemness.
机译:显然,由于耐药性的发展,目前的DNA损伤治疗很少能治愈转移性癌症。然而,最近的数据表明,肿瘤细胞可以响应于这些治疗而引起衰老和干性的相反过程,其生物学意义和分子调控目前尚不清楚。尽管通常认为细胞衰老是终末细胞的命运,但最近发现在DNA损伤后诱导的少数多倍体癌细胞中它是可逆的。克服遗传毒性侮辱与可逆的多倍体有关,其本身与茎表型的诱导有关,从而提供了连接这些独立现象的框架。与该建议一致,衰老和自噬显然与去多倍体化导致的存活细胞中自我更新潜能的出现密切相关。而且,随后的分析表明,在遗传毒性治疗后,实际上可能需要衰老才能使癌细胞再生。我们建议通过程序化的类似于生命周期的过程提供遗传毒性抗性,该过程将衰老,多倍性和茎干紧密结合在一起。

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