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人类血管系统的几何学:它是量化抗血管生成疗法的障碍吗?

Geometry of human vascular system: is it an obstacle for quantifying antiangiogenic therapies?

作者信息

Grizzi Fabio, Colombo Piergiuseppe, Taverna Gianluigi, Chiriva-Internati Maurizio, Cobos Everardo, Graziotti Pierpaolo, Muzzio Pier Carlo, Dioguardi Nicola

机构信息

Laboratories of Quantitative Medicine, Istituto Clinico Humanitas, IRCCS, Via Manzoni 56 20089 Rozzano, Milan, Italy.

出版信息

Appl Immunohistochem Mol Morphol. 2007 Jun;15(2):134-9. doi: 10.1097/01.pai.0000213105.18569.fa.

Abstract

It is now recognized that all human natural and diseased anatomic systems are characterized by irregular shapes and very complex behaviors. In geometrical terms, tumor vascularity (which is the result of a nonlinear dynamic process called angiogenesis) is an archetypal anatomic system that irregularly fills a 3-dimensional Euclidean space. This characteristic, together with the highly variable nature of vessel shapes and surfaces, leads to considerable spatial and temporal heterogeneity in the delivery of oxygen, nutrients, and drugs, and the removal of metabolites. Although these biologic features have been well established, the quantitative analysis of neovascularity in 2-dimensional histologic sections still fails to view its architecture as a non-Euclidean geometrical object, thus allowing errors in visual interpretation and discordant results concerning the same tumor from different laboratories. We discuss here the tumor-induced vascular system as a fractal object, and what changes this new way of observing may bring to the quantification of effective antiangiogenic therapies.

摘要

现在人们认识到,所有人类正常和患病的解剖系统都具有不规则的形状和非常复杂的行为。从几何学角度来看,肿瘤血管生成(这是一个称为血管生成的非线性动态过程的结果)是一个典型的解剖系统,它不规则地填充三维欧几里得空间。这种特征,连同血管形状和表面的高度可变性质,导致在氧气、营养物质和药物的输送以及代谢产物的清除方面存在相当大的空间和时间异质性。尽管这些生物学特征已经得到充分证实,但二维组织学切片中新血管生成的定量分析仍然未能将其结构视为非欧几里得几何对象,从而在视觉解释中产生误差,并导致不同实验室对同一肿瘤的结果不一致。我们在此讨论肿瘤诱导的血管系统作为分形对象,以及这种新的观察方式可能给有效抗血管生成疗法的量化带来哪些变化。

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