Abstract

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.

Highlights

  • The diagnosis and treatment of malignant tumors remain extremely difficult

  • high-performance liquid chromatography (HPLC) analysis demonstrated that the purity of iCREKA, fluorescein isothiocyanate (FITC)-iCREKA, and FITC-CREKA was 98.27%, 98.23%, and 98.66%, respectively, after purification

  • The present study showed that the addition of MMP-2 to the medium during incubation of tumor cells with FITC-iCREKA allowed FITC-iCREKA to penetrate into tumor cells

Read more

Summary

Introduction

The diagnosis and treatment of malignant tumors remain extremely difficult. The construction of molecular probes that are capable of recognizing specific molecular targets in tumor tissues and possess the ability to penetrate into tumor cells is of great significance for the specific diagnosis of tumors. Constructing such molecular probes is even more important for specific targeted therapies that need to overcome the biological barrier effect of the cell membrane. Cell-penetrating peptides (CPPs), known as protein transduction domains (PTDs), are a special class of polypeptides that have the ability to overcome the physiological barrier imposed by the cell membrane. In general, broad-spectrum tumorspecific targeting is extremely difficult to achieve

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call