The Walter and Eliza Hall Institute of Medical Research, Melbourne, Australia.
Department of Medical Biology, University of Melbourne, Melbourne, Australia.
J Mol Cell Biol. 2019 Mar 1;11(3):212-223. doi: 10.1093/jmcb/mjy077.
Activation of the tumour suppressor p53 upon cellular stress can induce a number of different cellular processes. The diverse actions of these processes are critical for the protective function of p53 in preventing the development of cancer. However, it is still not fully understood which process(es) activated by p53 is/are critical for tumour suppression and how this might differ depending on the type of cells undergoing neoplastic transformation and the nature of the drivers of oncogenesis. Moreover, it is not clear why upon activation of p53 some cells undergo cell cycle arrest and senescence whereas others die by apoptosis. Here we discuss some of the cellular processes that are crucial for p53-mediated tumour suppression and the factors that could impact cell fate upon p53 activation. Finally, we describe therapies aimed either at activating wild-type p53 or at changing the behaviour of mutant p53 to unleash tumour growth suppressive processes for therapeutic benefit in malignant disease.
细胞应激时肿瘤抑制因子 p53 的激活可以诱导多种不同的细胞过程。这些过程的多样化作用对于 p53 防止癌症发展的保护功能至关重要。然而,目前仍不完全清楚 p53 激活的哪些过程对于肿瘤抑制是至关重要的,以及这可能因发生癌变的细胞类型和致癌驱动因素的性质而有所不同。此外,目前尚不清楚为什么 p53 激活后,一些细胞经历细胞周期停滞和衰老,而另一些细胞则通过细胞凋亡死亡。在这里,我们讨论了对 p53 介导的肿瘤抑制至关重要的一些细胞过程,以及可能影响 p53 激活后细胞命运的因素。最后,我们描述了旨在激活野生型 p53 或改变突变型 p53 行为以释放肿瘤生长抑制过程的治疗方法,以在恶性疾病中获得治疗益处。