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A non-equilibrium thermodynamic model for tumor extracellular matrix with enzymatic degradation

机译:具有酶促降解作用的肿瘤细胞外基质的非平衡热力学模型

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摘要

The extracellular matrix (ECM) of a solid tumor not only affords scaffolding to support tumor architecture and integrity but also plays an essential role in tumor growth, invasion, metastasis, and therapeutics. In this paper, a non-equilibrium thermodynamic theory is established to study the chemo-mechanical behaviors of tumor ECM, which is modeled as a poroelastic polyelectrolyte consisting of a collagen network and proteoglycans. By using the principle of maximum energy dissipation rate, we deduce a set of governing equations for drug transport and mechanosensitive enzymatic degradation in ECM. The results reveal that osmosis is primarily responsible for the compression resistance of ECM. It is suggested that a well-designed ECM degradation can effectively modify the tumor microenvironment for improved efficiency of cancer therapy. The theoretical predictions show a good agreement with relevant experimental observations. This study aimed to deepen our understanding of tumor ECM may be conducive to novel anticancer strategies.
机译:实体瘤的细胞外基质(ECM)不仅提供支撑肿瘤结构和完整性的支架,而且在肿瘤生长,侵袭,转移和治疗中起着至关重要的作用。在本文中,建立了一种非平衡热力学理论来研究肿瘤ECM的化学力学行为,该模型被建模为由胶原蛋白网络和蛋白聚糖组成的多孔弹性聚电解质。利用最大能量耗散率的原理,我们推导了一套关于ECM中药物转运和机械敏感酶促降解的控制方程。结果表明,渗透主要是ECM的抗压性。有人提出,精心设计的ECM降解可以有效地修饰肿瘤微环境,从而提高癌症治疗的效率。理论预测与相关的实验观察结果吻合良好。这项研究旨在加深我们对肿瘤ECM的了解,可能有助于新的抗癌策略。

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