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P120 和 E-钙黏蛋白:肿瘤转移的双刃剑。

P120 and E-cadherin: Double-edged swords in tumor metastasis.

机构信息

Department of Cell Biology, RIMLS, Radboud University Medical Center, Nijmegen, the Netherlands.

Radiotherapy & OncoImmunology laboratory, Department of Radiation Oncology, RIMLS, Radboud University Medical Center, Nijmegen, the Netherlands.

出版信息

Semin Cancer Biol. 2020 Feb;60:107-120. doi: 10.1016/j.semcancer.2019.07.020. Epub 2019 Jul 29.

Abstract

Cell-cell adhesion by adherens junctions controls proliferation and cell polarization and is crucial to maintain epithelial architecture and homeostasis. Downregulation of two of the main components of adherens junctions, E-cadherin and p120, is an often recurring hallmark of carcinomas, causing loss of polarity and increased proliferation, survival and invasion of epithelial cells. On the other hand, tumor-promoting effects of both E-cadherin and p120 have been reported, substantiated by sustained, or even elevated expression of these molecules in many cancers. In this review, we will discuss how expression regulation by EMT, E-cadherin cleavage or p120 isoform expression can contribute to either tumor-supressing or tumor-promoting processes. Furthermore, we will focus on the contradictory functions of E-cadherin and p120 in the different phases of tumor progression, from carcinoma in situ up to the formation of distant metastasis. Finally, we will discuss the possibilities and challenges when using either protein as a biomarker.

摘要

细胞-细胞黏附通过黏附连接控制增殖和细胞极化,对于维持上皮组织的结构和稳态至关重要。黏附连接的两个主要成分 E-钙黏蛋白和 p120 的下调是癌的常见特征,导致极性丧失以及上皮细胞增殖、存活和侵袭增加。另一方面,E-钙黏蛋白和 p120 都具有促进肿瘤的作用,这一点得到了许多癌症中这些分子持续甚至升高表达的支持。在这篇综述中,我们将讨论 EMT、E-钙黏蛋白切割或 p120 异构体表达的表达调控如何有助于肿瘤抑制或促进过程。此外,我们将重点讨论 E-钙黏蛋白和 p120 在肿瘤进展的不同阶段(从原位癌到远处转移的形成)中的矛盾功能。最后,我们将讨论将这两种蛋白中的任一种作为生物标志物的可能性和挑战。

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