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The actin cytoskeleton in cancer cell motility

机译:肌动蛋白细胞骨架与癌细胞运动

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Cancer cell metastasis is a multi-stage process involving invasion into surrounding tissue, intravasation, transit in the blood or lymph, extravasation, and growth at a new site. Many of these steps require cell motility, which is driven by cycles of actin polymerization, cell adhesion and acto-myosin contraction. These processes have been studied in cancer cells in vitro for many years, often with seemingly contradictory results. The challenge now is to understand how the multitude of in vitro observations relates to the movement of cancer cells in living tumour tissue. In this review we will concentrate on actin protrusion and acto-myosin contraction. We will begin by presenting some general principles summarizing the widely-accepted mechanisms for the co-ordinated regulation of actin polymerization and contraction. We will then discuss more recent studies that investigate how experimental manipulation of actin dynamics affects cancer cell invasion in complex environments and in vivo.
机译:癌细胞转移是一个多阶段的过程,涉及侵入周围组织,血管内介入,血液或淋巴中的转运,血管外渗以及新部位的生长。这些步骤中的许多步骤都要求细胞运动,这是由肌动蛋白聚合,细胞粘附和肌动蛋白-肌动蛋白收缩的周期驱动的。这些过程已经在体外癌细胞中进行了多年研究,结果往往相矛盾。现在的挑战是要了解大量的体外观察结果如何与活肿瘤组织中癌细胞的运动有关。在这篇综述中,我们将集中讨论肌动蛋白的突出和肌动蛋白的收缩。我们将从介绍一些普遍的原则开始,总结一些广泛接受的肌动蛋白聚合和收缩协调调控机制。然后,我们将讨论更多最新研究,这些研究调查肌动蛋白动力学的实验性操作如何影响复杂环境和体内癌细胞的侵袭。

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