Centre for Vascular Research, University of New South Wales, Sydney 2052 NSW, Australia.
J Oncol. 2010;2010:363106. doi: 10.1155/2010/363106. Epub 2010 Jun 23.
Cell migration contributes to cancer metastasis and involves cell adhesion to the extracellular matrix (ECM), force generation through the cell's cytoskeletal, and finally cell detachment. Both adhesive cues from the ECM and soluble cues from neighbouring cells and tissue trigger intracellular signalling pathways that are essential for cell migration. While the machinery of many signalling pathways is relatively well understood, how hierarchies of different and conflicting signals are established is a new area of cellular cancer research. We examine the recent advances in microfabrication, microfluidics, and nanotechnology that can be utilized to engineer micro- and nanoscaled cellular environments. Controlling both adhesive and soluble cues for migration may allow us to decipher how cells become motile, choose the direction for migration, and how oncogenic transformations influences these decision-making processes.
细胞迁移有助于癌症转移,涉及细胞与细胞外基质(ECM)的黏附、通过细胞的细胞骨架产生力,最后是细胞脱离。ECM 中的黏附线索以及来自相邻细胞和组织的可溶性线索都会触发细胞迁移所必需的细胞内信号通路。虽然许多信号通路的机制相对较好理解,但不同和冲突信号的层次结构是细胞癌症研究的一个新领域。我们研究了微制造、微流控和纳米技术的最新进展,这些技术可用于构建微纳米级别的细胞环境。控制迁移的黏附性和可溶性线索可以帮助我们理解细胞如何变得运动,选择迁移的方向,以及致癌转化如何影响这些决策过程。