Department of Cell Biology and Physiology, Washington University School of Medicine, St. Louis, MO, USA.
Department of Medicine, Washington University School of Medicine, St. Louis, MO, USA.
Nat Rev Cancer. 2019 Aug;19(8):439-453. doi: 10.1038/s41568-019-0156-2. Epub 2019 Jun 24.
Cellular senescence plays a critical role in tumorigenesis. Once thought of as a tissue culture artefact by some researchers, senescence is now a major field of study. Although there are common molecular mechanisms that enforce the growth arrest that characterizes the phenotype, the impact of senescence is varied and can, in some instances, have opposite effects on tumorigenesis. It has become clearer that the cell of origin and the tissue in question dictate the impact of senescence on tumorigenesis. In this Review, we unravel this complexity by focusing on how senescence impacts tumorigenesis when it arises within incipient tumour cells versus stromal cells, and how these roles can change in different stages of disease progression. In addition, we highlight the diversity of the senescent phenotype and its functional output beyond growth arrest: the senescence-associated secretory phenotype (SASP). Fortunately, a number of new genetic and pharmacologic tools have been developed that are now allowing the senescence phenotype to be parsed further.
细胞衰老在肿瘤发生中起着关键作用。衰老曾被一些研究人员认为是组织培养的一种人为假象,但现在已成为一个主要的研究领域。尽管存在共同的分子机制来强制执行特征为生长停滞的表型,但衰老的影响是多种多样的,在某些情况下,对肿瘤发生可能会产生相反的影响。现在已经越来越清楚,起源细胞和所涉及的组织决定了衰老对肿瘤发生的影响。在这篇综述中,我们通过关注衰老在起源于早期肿瘤细胞与基质细胞的肿瘤发生中所产生的影响,以及这些作用如何在疾病进展的不同阶段发生变化,来揭示这种复杂性。此外,我们还强调了衰老表型的多样性及其除生长停滞之外的功能输出:衰老相关分泌表型(SASP)。幸运的是,现在已经开发出了许多新的遗传和药理学工具,可以进一步解析衰老表型。