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A new biomimetic assay reveals the temporal role of matrix stiffening in cancer cell invasion

机译:一种新的仿生测定揭示了基质硬化在癌细胞侵袭中的暂时作用

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摘要

Tumor initiation and growth is associated with significant changes in the surrounding tissue. During carcinoma progression, a global stiffening of the extracellular matrix is observed and is interpreted as a signature of aggressive invasive tumors. However, it is still unknown whether this increase in matrix rigidity promotes invasion and whether this effect is constant along the course of invasion. Here we have developed a biomimetic in vitro assay that enabled us to address the question of the importance of tissue rigidity in the chronology of tumor invasion. Using low concentrations of the sugar threose, we can effectively stiffen reconstituted collagen I matrices and control the stiffening in time with no direct effect on residing cells. Our findings demonstrate that, depending on the timing of its stiffening, the extracellular matrix could either inhibit or promote cancer cell invasion and subsequent metastasis: while matrix stiffening after the onset of invasion promotes cancer cell migration and tumor spreading, stiff matrices encapsulate the tumor at an early stage and prevent cancer cell invasion. Our study suggests that adding a temporal dimension in in vitro models to analyze biological processes in four dimensions is necessary to fully capture their complexity.
机译:肿瘤的发生和生长与周围组织的显着变化有关。在癌症进展期间,观察到细胞外基质的整体变硬,并被解释为侵袭性侵袭性肿瘤的标志。但是,仍然不清楚基质刚度的这种提高是否促进了侵袭,并且这种影响在侵袭过程中是否恒定。在这里,我们开发了一种仿生体外测定法,使我们能够解决组织刚度在肿瘤侵袭时间顺序中的重要性的问题。使用低浓度的糖苏糖,我们可以有效地使重构的胶原蛋白I基质变硬,并控制时间的变硬,而对驻留细胞没有直接影响。我们的研究结果表明,取决于其变硬的时间,细胞外基质可能抑制或促进癌细胞的侵袭和随后的转移:尽管侵袭后的基质变硬促进了癌细胞的迁移和肿瘤的扩散,但僵硬的基质将肿瘤包裹在及早预防癌细胞入侵。我们的研究表明,在体外模型中添加时间维度以分析四个维度的生物过程对于充分捕获其复杂性是必要的。

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