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联合固体肿瘤生长抑制机制:数学研究。

Combining Mechanisms of Growth Arrest in Solid Tumours: A Mathematical Investigation.

机构信息

Wolfson Centre for Mathematical Biology, Mathematical Institute, University of Oxford, Radcliffe Observatory Quarter, Oxford, OX2 6GG, UK.

出版信息

Bull Math Biol. 2022 Jul 1;84(8):80. doi: 10.1007/s11538-022-01034-2.

Abstract

The processes underpinning solid tumour growth involve the interactions between various healthy and tumour tissue components and the vasculature, and can be affected in different ways by cancer treatment. In particular, the growth-limiting mechanisms at play may influence tumour responses to treatment. In this paper, we propose a simple ordinary differential equation model of solid tumour growth to investigate how tumour-specific mechanisms of growth arrest may affect tumour response to different combination cancer therapies. We consider the interactions of tumour cells with the physical space in which they proliferate and a nutrient supplied by the tumour vasculature, with the aim of representing two distinct growth arrest mechanisms. More specifically, we wish to consider growth arrest due to (1) nutrient deficiency, which corresponds to balancing cell proliferation and death rates, and (2) competition for space, which corresponds to cessation of proliferation without cell death. We perform numerical simulations of the model and a steady-state analysis to determine the possible tumour growth scenarios described by the model. We find that there are three distinct growth regimes: the nutrient- and spatially limited regimes and a bi-stable regime, in which both growth arrest mechanisms are simultaneously active. Thus, the proposed model has the features required to investigate and distinguish tumour responses to different cancer treatments.

摘要

实体瘤生长的过程涉及各种健康组织和肿瘤组织成分与脉管系统之间的相互作用,并可能受到癌症治疗的不同影响。特别是,起生长限制作用的机制可能会影响肿瘤对治疗的反应。在本文中,我们提出了一个简单的实体瘤生长常微分方程模型,以研究肿瘤特有的生长抑制机制如何影响不同联合癌症疗法的肿瘤反应。我们考虑了肿瘤细胞与它们增殖的物理空间以及肿瘤脉管系统供应的营养物质之间的相互作用,旨在代表两种不同的生长抑制机制。更具体地说,我们希望考虑由于(1)营养缺乏而导致的生长抑制,这对应于平衡细胞增殖和死亡率,以及(2)由于空间竞争而导致的增殖停止而没有细胞死亡。我们对模型进行数值模拟和稳态分析,以确定模型描述的可能的肿瘤生长情况。我们发现存在三种不同的生长状态:营养和空间受限状态以及双稳态状态,其中两种生长抑制机制同时活跃。因此,所提出的模型具有研究和区分不同癌症治疗方法对肿瘤反应的特征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e241/9246818/18081fa2bc36/11538_2022_1034_Fig1_HTML.jpg

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