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Choline Molecular Imaging with Small-animal PET for Monitoring Tumor Cellular Response to Photodynamic Therapy of Cancer

机译:小动物宠物的胆碱分子成像,用于监测肿瘤细胞反应对癌症的光动力治疗

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We are developing and evaluating choline molecular imaging with positron emission tomography (PET) for monitoring tumor response to photodynamic therapy (PDT) in animal models. Human prostate cancer (PC-3) was studied in athymic nude mice. A second-generation photosensitizer Pc 4 was used for PDT in tumor-bearing mice. MicroPET images with ~(11)C-choline were acquired before PDT and 48 h after PDT. Time-activity curves of ~(11)C-choline uptake were analyzed before and after PDT. For treated tumors, normalized choline uptake decreased significantly 48 h after PDT, compared to the same tumors pre-PDT (p < 0.001). However, for the control tumors, normalized choline uptake increased significantly (p < 0.001). PET imaging with ~(11)C-choline is sensitive to detect early tumor response to PDT in the animal model of human prostate cancer.
机译:我们正在通过正电子发射断层扫描(PET)开发和评估胆碱分子成像,用于监测动物模型中对光动力治疗(PDT)的肿瘤反应。在无胸腺裸鼠中研究了人类前列腺癌(PC-3)。第二代光敏剂PC 4用于携带肿瘤小鼠中的PDT。在PDT和48小时之前获得了〜(11)C-胆碱的Micropet图像。在PDT之前和之后分析〜(11)C-胆碱摄取的时间活性曲线。对于经过处理的肿瘤,与PDT相比,归一化的胆碱摄取在PDT预接收PDT(p <0.001)相比下降48小时。然而,对于对照肿瘤,标准化的胆碱摄取显着增加(P <0.001)。用〜(11)C-胆碱的宠物成像对人道前列腺癌动物模型中的PDT检测早期肿瘤反应敏感。

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