Plasticity in cell adhesion during tumor progression.

Advances in cancer research Pub Date : 2025-01-01 Epub Date: 2025-06-23 DOI:10.1016/bs.acr.2025.06.001
Arka Saha, Avri Ben-Ze'ev
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引用次数: 0

Abstract

Cell adhesion molecules (CAMs) mediate cellular adhesions to neighboring cells and the extracellular matrix (ECM) to regulate tissue homeostasis and morphogenesis. Dysfunctional CAM-mediated signaling is required for a neoplastic cell to gain an invasive and metastatic phenotype. Numerous studies have reported a dynamic plasticity in the function and expression of CAMs that regulates the different stages of tumor progression. As such, CAM-induced changes in cell adhesion and intracellular signaling enable phenotype switching and cellular plasticity in cancer cells that contribute to tumor aggressiveness and metastasis. This review summarizes the properties of cell adhesion molecules and the signaling pathways involved in regulating tumor progression and metastasis.

肿瘤进展过程中细胞粘附的可塑性。
细胞粘附分子(CAMs)介导细胞与邻近细胞和细胞外基质(ECM)的粘附,调节组织稳态和形态发生。功能失调的cam介导的信号是肿瘤细胞获得侵袭性和转移性表型所必需的。许多研究报道了CAMs的功能和表达的动态可塑性,调节肿瘤进展的不同阶段。因此,cam诱导的细胞粘附和细胞内信号的改变使癌细胞的表型转换和细胞可塑性成为可能,从而促进肿瘤的侵袭性和转移。本文就细胞粘附分子的特性及调控肿瘤进展和转移的信号通路作一综述。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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