Laboratory of Stem Cell Biology and Regenerative Medicine, Department of Biology, Technion Israel Institute of Technology; the Lorry Lokey Interdisciplinary Center for Life Sciences & Engineering, Technion Israel Institute of Technology; and the Technion Integrated Cancer Center, Technion Israel Institute of Technology, Haifa 3200, Israel.
Nat Rev Cancer. 2018 Mar;18(3):187-201. doi: 10.1038/nrc.2017.122. Epub 2018 Jan 19.
In recent years, great strides have been made in our understanding of how stem cells (SCs) govern tissue homeostasis and regeneration. The inherent longevity of SCs raises the possibility that the unique protective mechanisms in these cells might also be involved in tumorigenesis. In this Opinion article, we discuss how SCs are protected throughout their lifespan, focusing on quiescent behaviour, DNA damage response and programmed cell death. We briefly examine the roles of adult SCs and progenitors in tissue repair and tumorigenesis and explore how signals released from dying or dormant cells influence the function of healthy or aberrant SCs. Important insight into the mechanisms that regulate SC death and survival, as well as the 'legacy' imparted by departing cells, may unlock novel avenues for regenerative medicine and cancer therapy.
近年来,人们对干细胞 (SCs) 如何调控组织稳态和再生有了更深入的了解。SCs 具有内在的长寿性,这使得人们提出一个假设,即这些细胞中独特的保护机制也可能参与肿瘤发生。在这篇观点文章中,我们讨论了SCs 如何在其整个生命周期中受到保护,重点关注静止行为、DNA 损伤反应和程序性细胞死亡。我们简要探讨了成年SCs 和祖细胞在组织修复和肿瘤发生中的作用,并探讨了来自死亡或休眠细胞的信号如何影响健康或异常SCs 的功能。对调控SCs 死亡和存活的机制以及离开细胞所赋予的“遗产”的深入了解,可能为再生医学和癌症治疗开辟新途径。