Recent developments have established molecular imaging of mouse models with small-animal PET and bioluminescence imaging (BLI) as an important tool in cancer research. One of the disadvantag'/> Multimodality Imaging of Tumor Xenografts and Metastases in Mice with Combined Small-Animal PET, Small-Animal CT, and Bioluminescence Imaging
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Multimodality Imaging of Tumor Xenografts and Metastases in Mice with Combined Small-Animal PET, Small-Animal CT, and Bioluminescence Imaging

机译:结合小动物PET,小动物CT和生物发光成像对小鼠肿瘤异种移植和转移进行多模态成像

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id="p-1">Recent developments have established molecular imaging of mouse models with small-animal PET and bioluminescence imaging (BLI) as an important tool in cancer research. One of the disadvantages of these imaging modalities is the lack of anatomic information. We combined small-animal PET and BLI technology with small-animal CT to obtain fusion images with both molecular and anatomic information. >Methods: We used small-animal PET/CT and BLI to detect xenografts of different cell lines and metastases of a melanoma cell line (A375M-3F) that had been transduced with a lentiviral vector containing a trimodality imaging reporter gene encoding a fusion protein with Renilla luciferase, monomeric red fluorescent protein, and a mutant herpes simplex virus type 1 thymidine kinase. >Results: Validation studies in mouse xenograft models showed a good coregistration of images from both PET and CT. Melanoma metastases were detected by 18F-FDG PET, 9-[4-18F-fluoro-3-(hydroxymethyl)butyl]guanine (18F-FHBG) PET, CT, and BLI and confirmed by ex vivo assays of Renilla luciferase and mutant thymidine kinase expression. 18F-FHBG PET/CT allowed detection and localization of lesions that were not seen on CT because of poor contrast resolution and were not seen on 18F-FDG PET because of higher background uptake relative to 18F-FHBG. >Conclusion: The combination of 18F-FHBG PET, small-animal CT, and BLI allows a sensitive and improved quantification of tumor burden in mice. This technique is potentially useful for the study of the biologic determinants of metastasis and for the evaluation of novel cancer treatments.
机译:id =“ p-1”>最近的发展已经建立了具有小动物PET的小鼠模型分子成像和生物发光成像(BLI)作为癌症研究的重要工具。这些成像方式的缺点之一是缺乏解剖学信息。我们将小动物PET和BLI技术与小动物CT结合使用,以获得具有分子和解剖学信息的融合图像。 >方法:我们使用小动物PET / CT和BLI检测不同细胞系的异种移植物和已通过包含三峰成像的慢病毒载体转导的黑素瘤细胞系(A375M-3F)的转移报告基因编码与 Renilla 荧光素酶,单体红色荧光蛋白和突变型单纯疱疹病毒1型胸苷激酶的融合蛋白。 >结果:在小鼠异种移植模型中的验证研究表明,PET和CT图像均具有良好的配准性。用 18 F-FDG PET,9- [4- 18 F-氟-3-(羟甲基)丁基]鸟嘌呤( 18 F-FHBG)PET,CT和BLI,并且通过 Renilla 荧光素酶和突变型胸苷激酶表达的离体测定得到证实。 18 F-FHBG PET / CT可以检测和定位病变,这些病变在CT上由于对比分辨率差而看不到,而在 18 F-FDG PET上则因为相对于 18 F-FHBG,本底吸收更高。 >结论: 18 F-FHBG PET,小动物CT和BLI的组合可对小鼠的肿瘤负荷进行灵敏且改进的定量。该技术可能用于研究转移的生物学决定因素和评估新型癌症治疗方法。

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