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Chemo-Elastic Modeling of Invasive Carcinoma Development Accompanied by Oncogenic Epithelial-Mesenchymal Transition

机译:肿瘤间充质转换伴随泌乳癌发展的化学弹性建模

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We present a further development of a multiscale chemo-mechanical model of carcinoma growth in the epithelium tissue proposed earlier. The epithelium is represented by an elastic 2D array of polygonal cells, each with its own gene regulation dynamics. The model allows the simulation of evolution of multiple cells interacting via the chemical signaling or mechanically induced strain. The algorithm takes into account the division and intercalation of cells. The latter is most important since, first of all, carcinoma cells lose cell-cell adhesion and polarity via the oncogenic variant of the epithelial-mesenchymal transition (EMT) at which cells gain migratory and invasive properties. This process is mediated by E-cadherin repression and requires the differentiation of tumor cells with respect to the edge of the tumor that means that front cells should be most mobile. Taking into account this suggestion, we present the results of simulations demonstrating different patterns of carcinoma invasion. The comparison of our results with recent experimental observations is given and discussed.
机译:我们在先前提出的上皮组织中进一步发展了多尺度的癌细胞生长的化学机械模型。上皮用弹性2D多边形细胞阵列表示,每个电池阵列具有其自身基因调节动态。该模型允许通过化学信号传导或机械诱导的应变进行仿真多电池的演变。该算法考虑了小区的划分和嵌入。后者最重要的是,首先,癌细胞通过上皮 - 间充质转换(EMT)的致癌变体丧失细胞 - 细胞粘附性和极性,在这种情况下,细胞增益迁移和侵入性。该方法由E-Cadherin抑制介导,并且需要肿瘤细胞相对于肿瘤的边缘的分化,这意味着前电池应该是最移动的。考虑到这一建议,我们展示了模拟结果,展示了癌症侵袭的不同模式。对我们最近的实验观察结果进行了比较并讨论。

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