视网膜母细胞瘤蛋白:一种主要的肿瘤抑制因子,是细胞周期和细胞粘附之间的联系。

Brienne E. Engel, Cress Wd, Pedro G Santiago-Cardona
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引用次数: 28

摘要

RB1是第一个发现的肿瘤抑制基因。四十多年来的研究表明,Rb蛋白(pRb)是生物学途径的主要调节剂,影响细胞内在命运的几乎每个方面,包括细胞生长、细胞周期检查点、分化、衰老、自我更新、复制、基因组稳定性和凋亡。虽然这些过程可能是RB1作为肿瘤抑制因子效力的重要部分,但越来越多的证据表明,RB1也显著影响细胞与环境的相互作用,包括细胞与细胞和细胞与细胞外基质的相互作用。本文将重点介绍pRb在控制细胞粘附中的作用,以及肿瘤细胞粘附特性的改变如何驱动致命的转移过程。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
THE RETINOBLASTOMA PROTEIN: A MASTER TUMOR SUPPRESSOR ACTS AS A LINK BETWEEN CELL CYCLE AND CELL ADHESION.
RB1 was the first tumor suppressor gene discovered. Over four decades of work have revealed that the Rb protein (pRb) is a master regulator of biological pathways influencing virtually every aspect of intrinsic cell fate including cell growth, cell-cycle checkpoints, differentiation, senescence, self-renewal, replication, genomic stability and apoptosis. While these many processes may account for a significant portion of RB1's potency as a tumor suppressor, a small, but growing stream of evidence suggests that RB1 also significantly influences how a cell interacts with its environment, including cell-to-cell and cell-to-extracellular matrix interactions. This review will highlight pRb's role in the control of cell adhesion and how alterations in the adhesive properties of tumor cells may drive the deadly process of metastasis.
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