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首页> 外文期刊>Cancer research: The official organ of the American Association for Cancer Research, Inc >Coevolution of solid stress and interstitial fluid pressure in tumors during progression: Implications for vascular collapse
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Coevolution of solid stress and interstitial fluid pressure in tumors during progression: Implications for vascular collapse

机译:进展过程中肿瘤中固体压力和间质液压力的共同演化:对血管塌陷的影响

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The stress harbored by the solid phase of tumors is known as solid stress. Solid stress can be either applied externally by the surrounding normal tissue or induced by the tumor itself due to its growth. Fluid pressure is the isotropic stress exerted by the fluid phase. We recently showed that growth-induced solid stress is on the order of 1.3 to 13.0 kPa (10-100 mmHg) - high enough to cause compression of fragile blood vessels, resulting in poor perfusion and hypoxia. However, the evolution of growth-induced stress with tumor progression and its effect on cancer cell proliferation in vivo is not understood. To this end, we developed a mathematical model for tumor growth that takes into account all three types of stresses: growth-induced stress, externally applied stress, and fluid pressure. First, we conducted in vivo experiments and found that growth-induced stress is related to tumor volume through a biexponential relationship. Then, we incorporated this information into our mathematical model and showed that due to the evolution of growth-induced stress, total solid stress levels are higher in the tumor interior and lower in the periphery. Elevated compressive solid stress in the interior of the tumor is sufficient to cause the collapse of blood vessels and results in a lower growth rate of cancer cells compared with the periphery, independently from that caused by the lack of nutrients due to vessel collapse. Furthermore, solid stress in the periphery of the tumor causes blood vessels in the surrounding normal tissue to deform to elliptical shapes. We present histologic sections of human cancers that show such vessel deformations. Finally, we found that fluid pressure increases with tumor growth due to increased vascular permeability and lymphatic impairment, and is governed by the microvascular pressure. Crucially, fluid pressure does not cause vessel compression of tumor vessels.
机译:肿瘤的固相所隐含的应力称为固相应力。固体应力可以由周围的正常组织外部施加,也可以由于肿瘤的生长而由肿瘤本身引起。流体压力是流体相施加的各向同性应力。我们最近发现,生长诱导的固体压力约为1.3至13.0 kPa(10-100 mmHg)-足以引起脆弱血管的压缩,从而导致灌注不足和缺氧。然而,尚不了解生长诱导的应激随肿瘤进展的演变及其对体内癌细胞增殖的影响。为此,我们开发了一种针对肿瘤生长的数学模型,该模型考虑了所有三种类型的压力:生长诱导的压力,外部施加的压力和流体压力。首先,我们进行了体内实验,发现通过双指数关系,生长诱导的应激与肿瘤体积有关。然后,我们将此信息整合到我们的数学模型中,结果表明,由于生长诱导应力的演变,肿瘤内部的总固体应力水平较高,而周围的较低。肿瘤内部较高的压缩固体应力足以引起血管萎缩,并导致癌细胞的生长速度比周围环境低,这与由血管萎缩引起的营养缺乏引起的增长无关。此外,肿瘤周围的固体应力导致周围正常组织中的血管变形为椭圆形。我们提出了显示这种血管变形的人类癌症的组织学切片。最后,我们发现由于血管通透性增加和淋巴损伤,流体压力随着肿瘤的生长而增加,并受微血管压力的控制。至关重要的是,流体压力不会引起肿瘤血管的压缩。

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