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Contrast-enhanced microCT Imaging in a Tumor Angiogenesis Murine Model

机译:肿瘤血管生成鼠模型中的对比增强微分成像

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Angiogenesis is the formation of new blood vessels from the pre-existing vasculature, it is essential for tumor growth and development. Quantitative evaluation of vascular parameters that allow to identify angiogenesis in early stages of tumor development could have an impact on lesion detection, cancer treatment, and patient outcome. The aim of this study was to define the factors related to contrast medium administration and image acquisition that allow to quantify vascular parameters from contrast-enhanced micro-computed tomography (CE-microCT) images. Type of contrast-medium, dose and image acquisition time were determined for single-energy (SE) and dual-energy (DE) CE-microCT imaging protocols using a tumor angiogenesis murine model. Enhancement and relative blood volume (rBV) were quantified from SE and DE images in muscle, tumor core, tumor periphery and the whole tumor. The differences in enhancement between muscle and the tumor regions quantified in SE images were not statistically significant. A statistically significant difference was found for rBV between muscle and tumor periphery in SE images, but the differences with tumor core and the whole tumor were not significant. For the DE protocol, more animals need to be included in the study in order to evaluate the differences in enhancement and rBV. Validation studies are also required to evaluate the correlation between rBV and angiogenesis biomarkers. Despite these limitations, rBV quantified from CE-microCT images seems to be a promising vascular parameter that could help to describe the angiogenic status of a tumor during cancer progression.
机译:血管生成是从预先存在的血管系统中形成新的血管,对肿瘤生长和发育至关重要。允许识别肿瘤发育早期血管生成的血管参数的定量评估可能对病变检测,癌症治疗和患者结果产生影响。本研究的目的是定义与造影介质管理和图像采集相关的因素,其允许量化来自对比增强的微计算机断层扫描(CE-Microct)图像的血管参数。使用肿瘤血管生成鼠模型确定对比度介质,剂量和图像采集时间,用于单能(SE)和双能(DE)CE-MicroCT成像协议。从肌肉,肿瘤核心,肿瘤周边和整个肿瘤中的SE和DE图像量化增强和相对血液体积(RBV)。在SE图像中量化的肌肉和肿瘤区域之间增强的差异在统计学上没有统计学意义。在SE图像中的肌肉和肿瘤周边之间的RBV发现统计学上显着差异,但与肿瘤核心和整个肿瘤的差异不显着。对于DE协议,需要将更多的动物纳入研究,以评估增强和RBV的差异。还需要验证研究来评估RBV和血管生成生物标志物之间的相关性。尽管这些限制,从CE-MicroCT图像量化的RBV似乎是一个有前途的血管参数,可以帮助描述癌症进展期间肿瘤的血管生成状态。

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