Xu Yongfeng, Yang Xiaojuan, Xiong Qunli, Han Junhong, Zhu Qing
Abdominal Oncology Ward, Cancer Center, West China Hospital of Sichuan University, Chengdu, Sichuan, China.
State Key Laboratory of Biotherapy and Cancer Center, Frontiers Science Center for Disease-Related Molecular Network, West China Hospital, Sichuan University, Chengdu, China.
Front Oncol. 2023 Apr 27;13:1116061. doi: 10.3389/fonc.2023.1116061. eCollection 2023.
The p53 family is made up of three transcription factors: p53, p63, and p73. These proteins are well-known regulators of cell function and play a crucial role in controlling various processes related to cancer progression, including cell division, proliferation, genomic stability, cell cycle arrest, senescence, and apoptosis. In response to extra- or intracellular stress or oncogenic stimulation, all members of the p53 family are mutated in structure or altered in expression levels to affect the signaling network, coordinating many other pivotal cellular processes. P63 exists as two main isoforms (TAp63 and ΔNp63) that have been contrastingly discovered; the TA and ΔN isoforms exhibit distinguished properties by promoting or inhibiting cancer progression. As such, p63 isoforms comprise a fully mysterious and challenging regulatory pathway. Recent studies have revealed the intricate role of p63 in regulating the DNA damage response (DDR) and its impact on diverse cellular processes. In this review, we will highlight the significance of how p63 isoforms respond to DNA damage and cancer stem cells, as well as the dual role of TAp63 and ΔNp63 in cancer.
p53家族由三种转录因子组成:p53、p63和p73。这些蛋白质是众所周知的细胞功能调节因子,在控制与癌症进展相关的各种过程中发挥着关键作用,包括细胞分裂、增殖、基因组稳定性、细胞周期停滞、衰老和凋亡。响应细胞外或细胞内应激或致癌刺激,p53家族的所有成员在结构上发生突变或表达水平发生改变,从而影响信号网络,协调许多其他关键的细胞过程。p63以两种主要异构体(TAp63和ΔNp63)的形式存在,它们的发现形成了对比;TA和ΔN异构体通过促进或抑制癌症进展表现出不同的特性。因此,p63异构体构成了一个完全神秘且具有挑战性的调节途径。最近的研究揭示了p63在调节DNA损伤反应(DDR)及其对多种细胞过程的影响方面的复杂作用。在这篇综述中,我们将重点阐述p63异构体如何应对DNA损伤和癌症干细胞的重要性,以及TAp63和ΔNp63在癌症中的双重作用。