Department of Mechanical Engineering, Pardis Branch, Islamic Azad University, Pardis, Iran.
Department of Mechanical Engineering, K. N. Toosi University of Technology, Tehran, Iran; Computational Medicine Center, Tehran, Iran; Division of Nuclear Medicine, Department of Radiology and Radiological Science, School of Medicine, Johns Hopkins University, MD, USA; Department of Earth & Environmental Sciences, University of Waterloo, Ontario, Canada; Cancer Biology Research Centre, Cancer Institute of Iran, Tehran University of Medical Sciences, Tehran, Iran.
Microvasc Res. 2018 Sep;119:105-116. doi: 10.1016/j.mvr.2018.05.001. Epub 2018 May 6.
The mechanisms involved in tumor growth mainly occur at the microenvironment, where the interactions between the intracellular, intercellular and extracellular scales mediate the dynamics of tumor. In this work, we present a multi-scale model of solid tumor dynamics to simulate the avascular and vascular growth as well as tumor-induced angiogenesis. The extracellular and intercellular scales are modeled using partial differential equations and cellular Potts model, respectively. Also, few biochemical and biophysical rules control the dynamics of intracellular level. On the other hand, the growth of melanoma tumors is modeled in an animal in-vivo study to evaluate the simulation. The simulation shows that the model successfully reproduces a completed image of processes involved in tumor growth such as avascular and vascular growth as well as angiogenesis. The model incorporates the phenotypes of cancerous cells including proliferating, quiescent and necrotic cells, as well as endothelial cells during angiogenesis. The results clearly demonstrate the pivotal effect of angiogenesis on the progression of cancerous cells. Also, the model exhibits important events in tumor-induced angiogenesis like anastomosis. Moreover, the computational trend of tumor growth closely follows the observations in the experimental study.
肿瘤生长涉及的机制主要发生在微环境中,细胞内、细胞间和细胞外尺度之间的相互作用介导了肿瘤的动力学。在这项工作中,我们提出了一个实体瘤动力学的多尺度模型,以模拟无血管和血管生长以及肿瘤诱导的血管生成。分别使用偏微分方程和细胞 Potts 模型对细胞外和细胞间尺度进行建模。此外,一些生化和生物物理规则控制着细胞内水平的动力学。另一方面,在动物体内研究中对黑色素瘤肿瘤的生长进行建模,以评估模拟结果。模拟表明,该模型成功地再现了肿瘤生长过程中涉及的完整图像,如无血管和血管生长以及血管生成。该模型包含了癌细胞的表型,包括增殖、静止和坏死细胞,以及血管生成过程中的内皮细胞。结果清楚地表明了血管生成对癌细胞进展的关键影响。此外,该模型还表现出了肿瘤诱导血管生成中的重要事件,如吻合。此外,肿瘤生长的计算趋势与实验研究中的观察结果密切相关。