Multiscale and multi-modality visualization of angiogenesis in a human breast cancer model

被引:27
|
作者
Cebulla, Jana [1 ]
Kim, Eugene [2 ]
Rhie, Kevin [3 ]
Zhang, Jiangyang [3 ]
Pathak, Arvind P. [3 ,4 ]
机构
[1] Norwegian Univ Sci & Technol, Dept Circulat & Med Imaging, N-7034 Trondheim, Norway
[2] Johns Hopkins Univ, Sch Med, Dept Biomed Engn, Baltimore, MD 21205 USA
[3] Johns Hopkins Univ, Sch Med, Russell H Morgan Dept Radiol & Radiol Sci, Div Canc Imaging Res, Baltimore, MD 21205 USA
[4] Johns Hopkins Univ, Sch Med, Sidney Kimmel Comprehens Canc Ctr, Baltimore, MD 21205 USA
关键词
Breast cancer; Imaging; Multiscale; MRI; Micro-CT; MR microscopy; TUMOR ANGIOGENESIS; BLOOD-FLOW; COMPUTED-TOMOGRAPHY; IMAGING REVEALS; MRI; CONTRAST; MICROVASCULATURE; MICROENVIRONMENT; QUANTIFICATION; VASCULATURE;
D O I
10.1007/s10456-014-9429-2
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Angiogenesis in breast cancer helps fulfill the metabolic demands of the progressing tumor and plays a critical role in tumor metastasis. Therefore, various imaging modalities have been used to characterize tumor angiogenesis. While micro-CT (mu CT) is a powerful tool for analyzing the tumor microvascular architecture at micron-scale resolution, magnetic resonance imaging (MRI) with its sub-millimeter resolution is useful for obtaining in vivo vascular data (e.g. tumor blood volume and vessel size index). However, integration of these microscopic and macroscopic angiogenesis data across spatial resolutions remains challenging. Here we demonstrate the feasibility of 'multiscale' angiogenesis imaging in a human breast cancer model, wherein we bridge the resolution gap between ex vivo mu CT and in vivo MRI using intermediate resolution ex vivo MR microscopy (mu MRI). To achieve this integration, we developed suitable vessel segmentation techniques for the ex vivo imaging data and co-registered the vascular data from all three imaging modalities. We showcase two applications of this multiscale, multi-modality imaging approach: (1) creation of co-registered maps of vascular volume from three independent imaging modalities, and (2) visualization of differences in tumor vasculature between viable and necrotic tumor regions by integrating mu CT vascular data with tumor cellularity data obtained using diffusion-weighted MRI. Collectively, these results demonstrate the utility of 'mesoscopic' resolution mu MRI for integrating macroscopic in vivo MRI data and microscopic mu CT data. Although focused on the breast tumor xenograft vasculature, our imaging platform could be extended to include additional data types for a detailed characterization of the tumor microenvironment and computational systems biology applications.
引用
收藏
页码:695 / 709
页数:15
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