A peptide nucleic acid-based pretargeting approach using (161)Tb for radionuclide therapy in a murine tumor model

在小鼠肿瘤模型中,利用肽核酸预靶向方法,以(161)Tb进行放射性核素治疗。

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Abstract

BACKGROUND: Although molecular tumor-targeting peptides modified with albumin-binding domains can enhance tumor probe uptake and prolong tumor retention time, the prolonged systemic circulation resulting from this modification also increases radiation exposure to normal tissues. This study aims to validate that peptide nucleic acid (PNA)-mediated pretargeted (161)Tb radionuclide therapy can slow tumor growth and reduce systemic radiation exposure. RESULTS: (68)Ga-EB-RGD, (68)Ga-cPNA-PNA-EB-RGD, (161)Tb-EB-RGD, and (161)Tb-cPNA-PNA-EB-RGD all demonstrated labeling efficiencies exceeding 80% and exhibited high stability in phosphate-buffered saline. (161)Tb-EB-RGD and (161)Tb-cPNA-PNA-EB-RGD showed comparable tumor cell uptake and apoptosis induction (0.95-fold). The binding capability between the pretargeting receptor PNA-EB-RGD and the ligand cPNA reached 80%. The blood biodistribution of the pretargeting group ((161)Tb-cPNA-PNA-EB-RGD) was 32-fold lower than that of the conventional group ((161)Tb-EB-RGD) (0.37 ± 0.05%ID/g vs. 11.93 ± 0.62%ID/g, P < 0.05). The biodistribution of (161)Tb-EB-RGD and (161)Tb-cPNA-PNA-EB-RGD in 4T1 tumor cells was 8.77 ± 0.16%ID/g and 3.86 ± 0.21%ID/g, respectively. The conventional treatment group ((161)Tb-EB-RGD) showed superior therapeutic efficacy compared to the pretargeting group ((161)Tb-cPNA-PNA-EB-RGD), which in turn outperformed the control group (345.09 ± 4.93 vs. 100.76 ± 12.20 vs. 183.02 ± 12.94 mm(3), P < 0.05). No significant pathological changes were detected in the vital organs of treated animals. Ex vivo tumor analysis supported the treatment trends. CONCLUSIONS: Compared to conventional non-pretargeted radionuclide therapy, PNA-based pretargeted (161)Tb radionuclide therapy reduced systemic radiation exposure, significantly decreased hematotoxicity, and suppressed tumor growth in tumor-bearing mice.

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