Univ Lyon, Université Claude Bernard Lyon 1, INSERM 1052, CNRS 5286, Centre Léon Bérard, Cancer Research Center of Lyon, Equipe labellisée Ligue Contre le Cancer "EMT and Cancer Cell Plasticity", Lyon 69008, France; LabEx DEVweCAN, Université de Lyon, 69000 Lyon, France.
Univ Lyon, Université Claude Bernard Lyon 1, INSERM 1052, CNRS 5286, Centre Léon Bérard, Cancer Research Center of Lyon, Equipe labellisée Ligue Contre le Cancer "EMT and Cancer Cell Plasticity", Lyon 69008, France; LabEx DEVweCAN, Université de Lyon, 69000 Lyon, France.
Cancer Cell. 2018 Feb 12;33(2):164-172. doi: 10.1016/j.ccell.2018.01.007.
Completion of early stages of tumorigenesis relies on the dynamic interplay between the initiating oncogenic event and the cellular context. Here, we review recent findings indicating that each differentiation stage within a defined cellular lineage is associated with a unique susceptibility to malignant transformation when subjected to a specific oncogenic insult. This emerging notion, named cellular pliancy, provides a rationale for the short delay in the development of pediatric cancers of prenatal origin. It also highlights the critical role of cellular reprogramming in early steps of malignant transformation of adult differentiated cells and its impact on the natural history of tumorigenesis.
肿瘤发生的早期阶段依赖于起始致癌事件和细胞环境之间的动态相互作用。在这里,我们回顾了最近的发现,表明在特定的致癌损伤下,当一个特定的细胞谱系中的每个分化阶段受到影响时,其具有独特的易患恶性转化的倾向。这一新兴概念被称为细胞顺应性,为产前起源的儿科癌症的短暂延迟发展提供了一个合理的解释。它还强调了细胞重编程在成人分化细胞恶性转化早期步骤中的关键作用及其对肿瘤发生自然史的影响。