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Construction and Evaluation of the Tumor-Targeting Cell-Penetrating Multifunctional Molecular Probe iCREKA

机译:靶向肿瘤的可穿透细胞的多功能分子探针iCREKA的构建和评价

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摘要

A novel tumor stroma targeting and membrane-penetrating cyclic peptide, named iCREKA, was designed and labeled by fluorescein isothiocyanate (FITC) and positron emitter 18F 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 in vitro. 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 in vivo 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.
机译:设计了一种新型的靶向肿瘤基质和膜穿透的环状肽iCREKA,并用异硫氰酸荧光素(FITC)和正电子发射体 18 F进行标记,以构建靶向肿瘤的示踪剂。通过体外细胞荧光试验证明,在存在激活的MMP-2的情况下,FITC-iCREKA在胶质瘤U87细胞中的细胞摄取明显高于在不存在激活的MMP-2的情况下。肿瘤组织荧光显微镜成像显示,FITC-iCREKA在静脉注射后1 h聚集在胶质瘤肿瘤的血管壁和周围基质中。注射后3小时,发现FITC-iCREKA被肿瘤细胞摄取。但是,无论注射后1?h还是3?h,对照FITC-CREKA只能在肿瘤基质中发现,而在肿瘤细胞中则没有。整个动物的荧光成像显示神经胶质瘤肿瘤可以清晰地以高荧光信号可视化。 microPET / CT成像进一步证明18F-iCREKA可以在注射后30分钟至2小时内体内靶向U87MG肿瘤。本研究表明,iCREKA具有靶向肿瘤基质和穿透膜的能力。它有可能被开发为用于肿瘤成像的荧光和PET示踪剂。

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