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Multi-modality PET-CT imaging of breast cancer in an animal model using nanoparticle x-ray contrast agent and 18F-FDG

机译:使用纳米粒子X射线造影剂和18F-FDG在动物模型中对乳腺癌进行多模态PET-CT成像

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Multi-modality PET-CT imaging is playing an important role in the field of oncology. While PET imaging facilitates functional interrogation of tumor status, the use of CT imaging is primarily limited to anatomical reference. In an attempt to extract comprehensive information about tumor cells and its microenvironment, we used a nanoparticle x-ray contrast agent to image tumor vasculature and vessel 'leakiness' and 18F-FDG to investigate the metabolic status of tumor cells. In vivo PET/CT studies were performed in mice implanted with 4T1 mammary breast cancer cells.Early-phase micro-CT imaging enabled visualization 3D vascular architecture of the tumors whereas delayed-phase micro-CT demonstrated highly permeable vessels as evident by nanoparticle accumulation within the tumor. Both imaging modalities demonstrated the presence of a necrotic core as indicated by a hypo-enhanced region in the center of the tumor. At early time-points, the CT-derived fractional blood volume did not correlate with 18F-FDG uptake. At delayed time-points, the tumor enhancement in 18F-FDG micro-PET images correlated with the delayed signal enhanced due to nanoparticle extravasation seen in CT images. The proposed hybrid imaging approach could be used to better understand tumor angiogenesis and to be the basis for monitoring and evaluating anti-angiogenic and nano-chemotherapies.
机译:多模态PET-CT成像在肿瘤学领域发挥着重要作用。尽管PET成像有助于对肿瘤状态进行功能检查,但CT成像的使用主要限于解剖参考。为了提取有关肿瘤细胞及其微环境的全面信息,我们使用了纳米粒子X射线造影剂对肿瘤脉管和血管“渗出”进行成像,并使用18F-FDG来研究肿瘤细胞的代谢状态。体内PET / CT研究是在植入了4T1乳腺癌细胞的小鼠中进行的。早期微CT成像可实现肿瘤的3D血管结构可视化,而延迟相微CT则显示出高渗透性的血管,其表现为纳米颗粒在血管内的蓄积肿瘤。两种成像方式均显示出坏死核心的存在,如肿瘤中心的低增强区域所示。在早期时间点,CT衍生的部分血容量与18F-FDG摄取无关。在延迟的时间点,在18F-FDG micro-PET图像中的肿瘤增强与在CT图像中看到的纳米颗粒外渗引起的延迟信号增强相关。提出的混合成像方法可用于更好地理解肿瘤血管生成,并成为监测和评估抗血管生成和纳米化学疗法的基础。

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