Chang Chih-Hsien, Fan Kuo-Hsien, Chen Te-Jung, Hsu Wei-Chun, Jan Mei-Ling, Tsai Tung-Hu, Kao Pan-Fu, Chen Chieh-Fu, Fu Ying-Kai, Lee Te-Wei
Institute of Pharmacology, National Yang-Ming University, Taipei, Taiwan.
J Formos Med Assoc. 2004 Nov;103(11):876-81.
Fluorine-18-2-deoxy-D-glucose (18F-FDG) has been used in the clinic as a diagnostic radiotracer for monitoring many kinds of tumors, but its value for monitoring fibrosarcoma is not well established.
In this study, the uptake of 18F-FDG in a fibrosarcoma-bearing mouse model was evaluated using the high resolution positron emission tomography (PET) system microPET. Tumor cells were implanted in 3 FVB/N mice, and static microPET scanning was performed on day 1, 7, 12 and 15 after implantation. A dynamic microPET image was scanned on day 12 to determine the 18F-FDG uptake in 3 other tumor-bearing mice. Time-activity curves were plotted by drawing regions of interest in the tumor, liver, kidneys and muscles. The mice were sacrificed after dynamic microPET imaging and whole-body autoradiography (WBAR) was performed. For biodistribution study, 9 tumor-bearing mice, 3 per experimental group, were studied at 3 time points and the results were compared with the static microPET images.
MicroPET images suggested that 18F-FDG could be used to monitor the growth of tumors 7 days after implantation. Dynamic scans of 18F-FDG uptake reached a plateau in the tumor after 20 minutes on day 12 after implantation. Both microPET and WBAR revealed evidence of tumor necrosis. The results of biodistribution and WBAR agreed with those from microPET images.
MicroPET was useful for monitoring the growth of fibrosarcoma and determination of the maximal uptake time point of 18F-FDG in tumors in this tumor-bearing mouse model.
氟-18-2-脱氧-D-葡萄糖(18F-FDG)已在临床上用作诊断放射性示踪剂以监测多种肿瘤,但其对监测纤维肉瘤的价值尚未明确确立。
在本研究中,使用高分辨率正电子发射断层扫描(PET)系统microPET评估18F-FDG在荷纤维肉瘤小鼠模型中的摄取情况。将肿瘤细胞植入3只FVB/N小鼠体内,并在植入后第1、7、12和15天进行静态microPET扫描。在第12天对另外3只荷瘤小鼠进行动态microPET成像扫描以确定18F-FDG摄取情况。通过在肿瘤、肝脏、肾脏和肌肉中绘制感兴趣区域来绘制时间-活性曲线。在动态microPET成像后处死小鼠并进行全身放射自显影(WBAR)。对于生物分布研究,在3个时间点研究9只荷瘤小鼠,每组3只,并将结果与静态microPET图像进行比较。
MicroPET图像表明18F-FDG可用于监测植入后7天肿瘤的生长情况。植入后第12天,18F-FDG摄取的动态扫描在20分钟后肿瘤中达到平台期。MicroPET和WBAR均显示有肿瘤坏死的证据。生物分布和WBAR的结果与microPET图像的结果一致。
在该荷瘤小鼠模型中,MicroPET有助于监测纤维肉瘤的生长并确定肿瘤中18F-FDG的最大摄取时间点。