PET Center, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong 510515, China.
Contrast Media Mol Imaging. 2018 Mar 4;2018:7929617. doi: 10.1155/2018/7929617. eCollection 2018.
A novel tumor stroma targeting and membrane-penetrating cyclic peptide, named iCREKA, was designed and labeled by fluorescein isothiocyanate (FITC) and positron emitter F to build the tumor-targeting tracers. The FITC-iCREKA was proved to have significantly higher cellular uptake in the glioma U87 cells in the presence of activated MMP-2 than that in absence of activated MMP-2 by cells fluorescence test . The tumor tissue fluorescence microscope imaging demonstrated that FITC-iCREKA accumulated in the walls of the blood vessels and the surrounding stroma in the glioma tumor at 1 h after intravenous injection. While at 3 h after injection, FITC-iCREKA was found to be uptaken in the tumor cells. However, the control FITC-CREKA can only be found in the tumor stroma, not in the tumor cells, no matter at 1 h or 3 h after injection. The whole-animal fluorescence imaging showed that the glioma tumor could be visualized clearly with high fluorescence signal. The microPET/CT imaging further demonstrated that 18F-iCREKA could target U87MG tumor from 30 min to 2 h after injection. The present study indicated the iCREKA had the capacity of tumor stroma targeting and the membrane-penetrating. It was potential to be developed as the fluorescent and PET tracers for tumor imaging.
一种新型的肿瘤基质靶向和膜穿透环肽,命名为 iCREKA,被设计并标记上荧光素异硫氰酸酯(FITC)和正电子发射体 F,以构建肿瘤靶向示踪剂。通过细胞荧光试验证明,FITC-iCREKA 在存在激活的 MMP-2 的情况下,在 U87 胶质细胞瘤细胞中的细胞摄取率明显高于不存在激活的 MMP-2 的情况。肿瘤组织荧光显微镜成像显示,在静脉注射后 1 小时,FITC-iCREKA 积聚在胶质瘤肿瘤的血管壁和周围基质中。而在注射后 3 小时,发现 FITC-iCREKA 被摄取到肿瘤细胞中。然而,对照 FITC-CREKA 只能在肿瘤基质中发现,而不能在肿瘤细胞中发现,无论是在注射后 1 小时还是 3 小时。全动物荧光成像显示,胶质瘤肿瘤可以清晰地可视化,具有高荧光信号。MicroPET/CT 成像进一步表明,18F-iCREKA 可以从注射后 30 分钟到 2 小时靶向 U87MG 肿瘤。本研究表明 iCREKA 具有肿瘤基质靶向和膜穿透的能力。它有可能被开发为荧光和 PET 示踪剂用于肿瘤成像。