NHC Key Laboratory of Carcinogenesis, Hunan Provincial Cancer Hospital and the Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University, Changsha, 410013, Hunan, China.
Department of Dermatology, Xiangya Hospital, Central South University, Changsha, 410008, Hunan, China.
Cell Mol Life Sci. 2020 Nov;77(21):4325-4346. doi: 10.1007/s00018-020-03539-2. Epub 2020 May 23.
Squamous cell carcinoma (SCC) is an aggressive malignancy that can originate from various organs. TP63 is a master regulator that plays an essential role in epidermal differentiation. It is also a lineage-dependent oncogene in SCC. ΔNp63α is the prominent isoform of TP63 expressed in epidermal cells and SCC, and overexpression promotes SCC development through a variety of mechanisms. Recently, ΔNp63α was highlighted to act as an epidermal-specific pioneer factor that binds closed chromatin and enhances chromatin accessibility at epidermal enhancers. ΔNp63α coordinates chromatin-remodeling enzymes to orchestrate the tissue-specific enhancer landscape and three-dimensional high-order architecture of chromatin. Moreover, ΔNp63α establishes squamous-like enhancer landscapes to drive oncogenic target expression during SCC development. Importantly, ΔNp63α acts as an upstream regulator of super enhancers to activate a number of oncogenic transcripts linked to poor prognosis in SCC. Mechanistically, ΔNp63α activates genes transcription through physically interacting with a number of epigenetic modulators to establish enhancers and enhance chromatin accessibility. In contrast, ΔNp63α also represses gene transcription via interacting with repressive epigenetic regulators. ΔNp63α expression is regulated at multiple levels, including transcriptional, post-transcriptional, and post-translational levels. In this review, we summarize recent advances of p63 in epigenomic and transcriptional control, as well as the mechanistic regulation of p63.
鳞状细胞癌(SCC)是一种侵袭性恶性肿瘤,可起源于多种器官。TP63 是一种主调控因子,在表皮分化中发挥重要作用。它也是 SCC 中的谱系依赖性癌基因。ΔNp63α 是在表皮细胞和 SCC 中表达的 TP63 的主要异构体,过表达通过多种机制促进 SCC 的发展。最近,ΔNp63α 被强调为一种表皮特异性的先驱因子,它可以结合封闭的染色质,并增强表皮增强子的染色质可及性。ΔNp63α 协调染色质重塑酶,以协调组织特异性增强子景观和染色质的三维高级结构。此外,ΔNp63α 建立鳞状样增强子景观,以在 SCC 发展过程中驱动致癌靶基因的表达。重要的是,ΔNp63α 作为超级增强子的上游调节剂,激活与 SCC 预后不良相关的许多致癌转录本。从机制上讲,ΔNp63α 通过与许多表观遗传调节剂相互作用来激活基因转录,从而建立增强子并增强染色质可及性。相反,ΔNp63α 还通过与抑制性表观遗传调节剂相互作用来抑制基因转录。ΔNp63α 的表达受多个水平的调节,包括转录、转录后和翻译后水平。在这篇综述中,我们总结了 p63 在表观基因组学和转录控制以及 p63 的机制调节方面的最新进展。