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通过[F]FDG-PET/MRI对胆管癌同基因原位模型的表征

Characterization of a Syngeneic Orthotopic Model of Cholangiocarcinoma by [F]FDG-PET/MRI.

作者信息

Zachhuber Lena, Filip Thomas, Mozayani Behrang, Löbsch Mathilde, Scheiner Stefan, Vician Petra, Stanek Johann, Hacker Marcus, Helbich Thomas H, Wanek Thomas, Berger Walter, Kuntner Claudia

机构信息

Preclinical Imaging Lab (PIL), Department of Biomedical Imaging and Image-Guided Therapy, Medical University of Vienna, 1090 Vienna, Austria.

Division of Nuclear Medicine, Department of Biomedical Imaging and Image-Guided Therapy, Medical University of Vienna, 1090 Vienna, Austria.

出版信息

Cancers (Basel). 2024 Jul 19;16(14):2591. doi: 10.3390/cancers16142591.

DOI:10.3390/cancers16142591
PMID:39061229
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11275149/
Abstract

Cholangiocarcinoma (CCA) is a type of primary liver cancer originating from the biliary tract epithelium, characterized by limited treatment options for advanced cases and low survival rates. This study aimed to establish an orthotopic mouse model for CCA and monitor tumor growth using PET/MR imaging. Murine CCA cells were implanted into the liver lobe of male C57BL/6J mice. The imaging groups included contrast-enhanced (CE) MR, CE-MR with static [F]FDG-PET, and dynamic [F]FDG-PET. Tumor volume and FDG uptake were measured weekly over four weeks. Early tumor formation was visible in CE-MR images, with a gradual increase in volume over time. Dynamic FDG-PET revealed an increase in the metabolic glucose rate (MRGlu) over time. Blood analysis showed pathological changes in liver-related parameters. Lung metastases were observed in nearly all animals after four weeks. The study concludes that PET-MR imaging effectively monitors tumor progression in the CCA mouse model, providing insights into CCA development and potential treatment strategies.

摘要

胆管癌(CCA)是一种起源于胆道上皮的原发性肝癌,其特点是晚期病例的治疗选择有限且生存率低。本研究旨在建立一种CCA的原位小鼠模型,并使用PET/MR成像监测肿瘤生长。将小鼠CCA细胞植入雄性C57BL/6J小鼠的肝叶。成像组包括对比增强(CE)MR、静态[F]FDG-PET的CE-MR和动态[F]FDG-PET。在四周内每周测量肿瘤体积和FDG摄取。在CE-MR图像中可见早期肿瘤形成,随着时间的推移体积逐渐增加。动态FDG-PET显示代谢葡萄糖率(MRGlu)随时间增加。血液分析显示肝脏相关参数的病理变化。四周后几乎所有动物都观察到肺转移。该研究得出结论,PET-MR成像可有效监测CCA小鼠模型中的肿瘤进展,为CCA的发展和潜在治疗策略提供见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b4d/11275149/274458239f8e/cancers-16-02591-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b4d/11275149/130587c8275e/cancers-16-02591-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b4d/11275149/3d43dd30ee01/cancers-16-02591-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b4d/11275149/462cc200b134/cancers-16-02591-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b4d/11275149/786b2bfcb0b1/cancers-16-02591-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b4d/11275149/4c1a5d52dde9/cancers-16-02591-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b4d/11275149/af0d7c0d470a/cancers-16-02591-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b4d/11275149/27784d5a6977/cancers-16-02591-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b4d/11275149/274458239f8e/cancers-16-02591-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b4d/11275149/130587c8275e/cancers-16-02591-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b4d/11275149/3d43dd30ee01/cancers-16-02591-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b4d/11275149/462cc200b134/cancers-16-02591-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b4d/11275149/786b2bfcb0b1/cancers-16-02591-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b4d/11275149/4c1a5d52dde9/cancers-16-02591-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b4d/11275149/af0d7c0d470a/cancers-16-02591-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b4d/11275149/27784d5a6977/cancers-16-02591-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b4d/11275149/274458239f8e/cancers-16-02591-g008.jpg

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本文引用的文献

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