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重编程、细胞年轻化及肿瘤发生过程中的细胞可塑性:先驱转录因子视角

Cellular plasticity in reprogramming, rejuvenation and tumorigenesis: a pioneer TF perspective.

作者信息

Huyghe Aurélia, Trajkova Aneta, Lavial Fabrice

机构信息

Cellular Reprogramming, Stem Cells and Oncogenesis Laboratory, Equipe Labellisée la Ligue Contre le Cancer, Labex Dev2Can - Univeristy of Lyon, Université Claude Bernard Lyon 1, INSERM 1052, CNRS 5286, Centre Léon Bérard, Centre de Recherche en Cancérologie de Lyon, 69008 Lyon, France.

Cellular Reprogramming, Stem Cells and Oncogenesis Laboratory, Equipe Labellisée la Ligue Contre le Cancer, Labex Dev2Can - Univeristy of Lyon, Université Claude Bernard Lyon 1, INSERM 1052, CNRS 5286, Centre Léon Bérard, Centre de Recherche en Cancérologie de Lyon, 69008 Lyon, France.

出版信息

Trends Cell Biol. 2024 Mar;34(3):255-267. doi: 10.1016/j.tcb.2023.07.013. Epub 2023 Aug 28.

Abstract

The multistep process of in vivo reprogramming, mediated by the transcription factors (TFs) Oct4, Sox2, Klf4, and c-Myc (OSKM), holds great promise for the development of rejuvenating and regenerative strategies. However, most of the approaches developed so far are accompanied by a persistent risk of tumorigenicity. Here, we review the groundbreaking effects of in vivo reprogramming with a particular focus on rejuvenation and regeneration. We discuss how the activity of pioneer TFs generates cellular plasticity that may be critical for inducing not only reprogramming and regeneration, but also cancer initiation. Finally, we highlight how a better understanding of the uncoupled control of cellular identity, plasticity, and aging during reprogramming might pave the way to the development of rejuvenating/regenerating strategies in a nontumorigenic manner.

摘要

由转录因子Oct4、Sox2、Klf4和c-Myc(OSKM)介导的体内重编程多步骤过程,为开发年轻化和再生策略带来了巨大希望。然而,迄今为止开发的大多数方法都伴随着持续的致瘤风险。在这里,我们回顾了体内重编程的开创性作用,特别关注年轻化和再生。我们讨论了先驱转录因子的活性如何产生细胞可塑性,这不仅对诱导重编程和再生至关重要,而且对癌症起始也可能至关重要。最后,我们强调了更好地理解重编程过程中细胞身份、可塑性和衰老的解耦控制如何可能为以非致瘤方式开发年轻化/再生策略铺平道路。

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