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肿瘤血管结构在营养物质和药物输送中的作用:基于入侵渗流的网络模型。

Role of tumor vascular architecture in nutrient and drug delivery: an invasion percolation-based network model.

作者信息

Baish J W, Gazit Y, Berk D A, Nozue M, Baxter L T, Jain R K

机构信息

Steele Laboratory, Department of Radiation Oncology, Massachusetts General Hospital, Harvard Medical School, Boston 02114, USA.

出版信息

Microvasc Res. 1996 May;51(3):327-46. doi: 10.1006/mvre.1996.0031.

Abstract

Delivery of diffusible nutrients and drugs in tissues is limited in part by the distance over which substances must diffuse between the vascular space and the surrounding tissues and by upstream losses prior to local delivery by the blood. By examining the fractal behavior of two-dimensional vascular networks in the murine dorsal skinfold chamber preparation, we have identified distinct architectural features of normal and tumor vascular networks that lead to fundamentally different transport behavior. Normal capillaries which are relatively straight and regularly spaced are well modeled by the widely used Krogh cylinder model. In contrast, the fractal dimensions of tumor vascular networks suggest that the tortuous vessels and wide range of avascular spaces found in tumors are better represented by invasion percolation, a well-known statistical growth process governed by local substrate properties. Based on these observations, we have constructed a percolation-based model of tumor vascular growth that enables us to predict the effects of network architecture on transport. We find that the number of avascular spaces in tumors scales with the size of the spaces so that there will exist a few large avascular spaces and many smaller avascular spaces between vessels. We also find that the tortuosity of the vessels, as reflected by the elevated minimum path dimension, produces regions of locally flow-limited transport and reduces flow through the tumor as a whole. Our model helps to explain the long-standing paradox that tumor vasculature has a higher geometrical resistance than normal vasculature despite increases in vessel diameter. A comparison to oxygenation measurements in normal and tumor tissues shows that our model predicts the architectural obstacles to transport in tumors more accurately than the Krogh cylinder model. Our results suggest that clinical interventions that yield more regular vascular geometry may be useful as a supplement to those that improve arterial availability or decrease rates of consumption by the tissue.

摘要

可扩散营养物质和药物在组织中的递送受到一定限制,部分原因在于物质在血管腔隙与周围组织之间扩散所需经过的距离,以及血液在局部递送之前的上游损失。通过研究小鼠背部皮褶腔制备中二维血管网络的分形行为,我们确定了正常和肿瘤血管网络的不同结构特征,这些特征导致了根本不同的传输行为。相对笔直且间距规则的正常毛细血管可以很好地用广泛使用的克罗格圆柱模型来模拟。相比之下,肿瘤血管网络的分形维数表明,肿瘤中发现的曲折血管和广泛的无血管间隙用入侵渗流来更好地表示,入侵渗流是一种由局部底物特性控制的著名统计生长过程。基于这些观察结果,我们构建了一个基于渗流的肿瘤血管生长模型,使我们能够预测网络结构对传输的影响。我们发现肿瘤中无血管间隙的数量与间隙大小成比例,因此血管之间会存在一些大的无血管间隙和许多较小的无血管间隙。我们还发现,由升高的最小路径维数反映的血管曲折度会产生局部流量受限的传输区域,并减少整体通过肿瘤的血流量。我们的模型有助于解释一个长期存在的悖论,即尽管血管直径增加,但肿瘤血管系统的几何阻力比正常血管系统更高。与正常和肿瘤组织中的氧合测量结果进行比较表明,我们的模型比克罗格圆柱模型更准确地预测了肿瘤中传输的结构障碍。我们的结果表明,产生更规则血管几何形状的临床干预措施可能作为改善动脉供应或降低组织消耗率的临床干预措施的补充而有用。

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