肿瘤血管系统对实体肿瘤中流体流动的影响:数学模型研究。

Moath Alamer, Xiao Yun Xu
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引用次数: 4

摘要

肿瘤的血管系统是异常的,弯曲的和不稳定的,这可能对流体流动有重要的影响。肿瘤组织中的流体动力学在肿瘤的生长、转移和治疗药物的传递中起着重要的作用。数学模型越来越多地用于阐明肿瘤脉管系统和流体流动的各个方面之间复杂的相互作用。以前的模型通常假设一个均匀分布的血管系统,而没有明确地描述它的结构,或者在没有考虑网络的真实几何特征的情况下纳入血管系统的分布。在这项研究中,通过在整个肿瘤血管网络的单个毛细血管水平上解析流体流动,开发了一个集成的计算模型。它包括一个血管生成模型和一个流体流动模型,该模型通过耦合肿瘤组织的血管内流动和间质流动来解决流动作为外显血管系统的功能。利用综合模型研究了微血管分布、坏死和血管修剪对流体流动的影响,以及非均匀血管通透性的影响。我们的研究结果揭示了肿瘤间质液压力(IFP)的不均匀性水平,在坏死和非坏死肿瘤之间IFP谱有很大的变化。血管网络显微特征的变化可以显著影响肿瘤内的液体流动,其中已发现切除血管盲端可减少IFP并促进间质液体流动。我们的结果表明,在预测肿瘤组织中的流体流动时,结合肿瘤血管和血管内流动的微观特性的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The influence of tumour vasculature on fluid flow in solid tumours: a mathematical modelling study.

The influence of tumour vasculature on fluid flow in solid tumours: a mathematical modelling study.

The influence of tumour vasculature on fluid flow in solid tumours: a mathematical modelling study.

The influence of tumour vasculature on fluid flow in solid tumours: a mathematical modelling study.

Tumour vasculature is known to be aberrant, tortuous and erratic which can have significant implications for fluid flow. Fluid dynamics in tumour tissue plays an important part in tumour growth, metastasis and the delivery of therapeutics. Mathematical models are increasingly employed to elucidate the complex interplay between various aspects of the tumour vasculature and fluid flow. Previous models usually assume a uniformly distributed vasculature without explicitly describing its architecture or incorporate the distribution of vasculature without accounting for real geometric features of the network. In this study, an integrated computational model is developed by resolving fluid flow at the single capillary level across the whole tumour vascular network. It consists of an angiogenesis model and a fluid flow model which resolves flow as a function of the explicit vasculature by coupling intravascular flow and interstitial flow in tumour tissue. The integrated model has been used to examine the influence of microvascular distribution, necrosis and vessel pruning on fluid flow, as well as the effect of heterogeneous vessel permeability. Our results reveal the level of nonuniformity in tumour interstitial fluid pressure (IFP), with large variations in IFP profile between necrotic and non-necrotic tumours. Changes in microscopic features of the vascular network can significantly influence fluid flow in the tumour where removal of vessel blind ends has been found to reduce IFP and promote interstitial fluid flow. Our results demonstrate the importance of incorporating microscopic properties of the tumour vasculature and intravascular flow when predicting fluid flow in tumour tissue.

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