Particle automata model of renal cancer progression

M. Panuszewska, B. Minch, W. Dzwinel
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引用次数: 2

Abstract

Even though the cancer mortality rate is slowly decreasing, it is still one of the leading causes of morbidity and mortality worldwide. One of the most common types of this disease is renal cancer, occurring in kidneys. A total of 63,340 new renal cancer cases (42,680 in men and 22,660 in women) and 14,970 deaths from renal cancer (10,010 men and 4,960 women) are projected to occur only in the US in 2018, with 1 in 48 lifetime risk for developing kidney cancer for men and 1 in 83 for women. Tumor growth is a complex, multiscale phenomena with many coupled microscopic and macroscopic factors that have to be accounted for while studying the disease. Despite a tremendous amount of work on understanding cancerogenesis and developing an effective anticancer therapies we still do not fully understand the mechanics of the malignant tissue development. Even though it is impossible to fully simulate and control cancer growth, numerical model allows for identification and investigation of the most crucial tumor growth factors and possible scenarios of its proliferation. The purpose of this article is to create model of renal tumor that uses the particle automata model[1,2]. We would also like to clarify if smooth particle hydrodynamics (SPH) method can be used to improve modelling of this particular biological process[3]. In the particle automata model both cancerous and healthy tissues are made of particles interacting with each other via spring harmonic forces and in SPH model we assume that biological tissues are represented as viscous fluids. In each model healthy tissue serves as an environment in which the renal tumor develops. Both healthy and cancerous cells have a life cycle in which they can be proliferating, dormant or necrotic. We use oxygen concentration, external pressure and time as restrictive factors for tissue growth. Herein we hope to reproduce in vivo tumor growth results inside in silico model and gain more insight into the rules governing the spread of the disease.
肾癌进展的粒子自动机模型
尽管癌症死亡率正在缓慢下降,但它仍然是全世界发病率和死亡率的主要原因之一。这种疾病最常见的类型之一是肾癌,发生在肾脏。预计2018年仅在美国就会有63340例新的肾癌病例(男性42680例,女性22660例)和14970例死于肾癌(10010名男性和4960名女性),男性患肾癌的终生风险为1 / 48,女性为1 / 83。肿瘤生长是一个复杂的、多尺度的现象,有许多微观和宏观的耦合因素,在研究疾病时必须考虑这些因素。尽管在了解癌症发生和开发有效的抗癌疗法方面做了大量的工作,但我们仍然没有完全了解恶性组织发展的机制。尽管不可能完全模拟和控制肿瘤的生长,但数值模型可以识别和研究最关键的肿瘤生长因子及其增殖的可能情况。本文的目的是利用粒子自动机模型(particle automata model)建立肾脏肿瘤模型[1,2]。我们还想澄清是否可以使用光滑粒子流体动力学(SPH)方法来改进这一特定生物过程的建模[3]。在粒子自动机模型中,癌变组织和健康组织都是由粒子通过弹簧调和力相互作用构成的,在SPH模型中,我们假设生物组织被表示为粘性流体。在每个模型中,健康组织作为肾肿瘤发展的环境。健康细胞和癌细胞都有一个生命周期,它们可以增殖、休眠或坏死。我们使用氧气浓度、外部压力和时间作为组织生长的限制因素。在此,我们希望在硅模型中重现体内肿瘤生长的结果,并对控制疾病传播的规则有更多的了解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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