Kurz Felix T, Hahn Artur
Division of Radiology, German Cancer Research Center, Heidelberg, Germany.
, Hamburg, Germany.
Methods Mol Biol. 2023;2660:283-294. doi: 10.1007/978-1-0716-3163-8_20.
During tumor growth, the complex composition of vasculature is prone to dynamic changes due to mechanic and biochemical challenges. Perivascular invasion of tumor cells to co-opt existing vasculature, but also formation of de-novo vasculature and other effects on the vascular network, may lead to altered geometric vessel properties as well as changes in vascular network topology, which is defined by vascular multifurcations and connections between vessel segments. The intricate organization and heterogeneity of the vascular network can be analyzed with advanced computational methods to uncover vascular network signatures that may allow differentiating between pathological and physiological vessel regions. Herein, we present a protocol to evaluate vascular heterogeneity in whole vascular networks, using morphological and topological measures. The protocol was developed for single plane illumination microscopy images of mice brain vasculature but can be applied to any vascular network.
在肿瘤生长过程中,由于机械和生化挑战,血管的复杂组成容易发生动态变化。肿瘤细胞的血管周围浸润不仅会利用现有的血管,还会导致新生血管的形成以及对血管网络的其他影响,这可能会改变血管的几何特性以及血管网络拓扑结构的变化,血管网络拓扑结构由血管分支和血管段之间的连接定义。血管网络的复杂组织和异质性可以通过先进的计算方法进行分析,以揭示可能有助于区分病理和生理血管区域的血管网络特征。在此,我们提出了一种使用形态学和拓扑学测量方法来评估整个血管网络中血管异质性的方案。该方案是针对小鼠脑血管系统的单平面照明显微镜图像开发的,但可应用于任何血管网络。