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p63:上皮干细胞调节中的关键因子。

p63: a crucial player in epithelial stemness regulation.

机构信息

Department of Experimental Medicine, TOR, University of Rome Tor Vergata, 00133, Rome, Italy.

The Third Affiliated Hospital of Soochow University, Institutes for Translational Medicine, Soochow University, Suzhou, 215000, China.

出版信息

Oncogene. 2023 Nov;42(46):3371-3384. doi: 10.1038/s41388-023-02859-4. Epub 2023 Oct 17.

Abstract

Epithelial tissue homeostasis is closely associated with the self-renewal and differentiation behaviors of epithelial stem cells (ESCs). p63, a well-known marker of ESCs, is an indispensable factor for their biological activities during epithelial development. The diversity of p63 isoforms expressed in distinct tissues allows this transcription factor to have a wide array of effects. p63 coordinates the transcription of genes involved in cell survival, stem cell self-renewal, migration, differentiation, and epithelial-to-mesenchymal transition. Through the regulation of these biological processes, p63 contributes to, not only normal epithelial development, but also epithelium-derived cancer pathogenesis. In this review, we provide an overview of the role of p63 in epithelial stemness regulation, including self-renewal, differentiation, proliferation, and senescence. We describe the differential expression of TAp63 and ΔNp63 isoforms and their distinct functional activities in normal epithelial tissues and in epithelium-derived tumors. Furthermore, we summarize the signaling cascades modulating the TAp63 and ΔNp63 isoforms as well as their downstream pathways in stemness regulation.

摘要

上皮组织稳态与上皮干细胞 (ESCs) 的自我更新和分化行为密切相关。p63 是 ESCs 的一个著名标志物,是其在上皮发育过程中生物活性所必需的因素。在不同组织中表达的 p63 异构体的多样性使该转录因子具有广泛的作用。p63 协调参与细胞存活、干细胞自我更新、迁移、分化和上皮-间充质转化的基因的转录。通过对这些生物学过程的调节,p63 不仅有助于正常的上皮发育,也有助于上皮来源的癌症发病机制。在这篇综述中,我们概述了 p63 在调节上皮干细胞特性中的作用,包括自我更新、分化、增殖和衰老。我们描述了 TAp63 和 ΔNp63 异构体的差异表达及其在正常上皮组织和上皮来源的肿瘤中的不同功能活性。此外,我们总结了调节 TAp63 和 ΔNp63 异构体及其下游途径在干细胞特性调节中的信号级联。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f680/10638092/40128743e49f/41388_2023_2859_Fig1_HTML.jpg

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