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In vivo demonstration of an active tumor pretargeting approach with peptide nucleic acid bioconjugates as complementary system

机译:以肽核酸生物共轭物为互补系统的主动肿瘤预靶向方法的体内演示

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摘要

A novel, promising strategy for cancer diagnosis and therapy is the use of a pretargeting approach. For this purpose, the non-natural DNA/RNA analogues Peptide Nucleic Acids (PNAs) are ideal candidates as in vivo recognition units due to their high metabolic stability and lack of unspecific accumulation. In the pretargeting approach, an unlabeled, highly specific antibody–PNA conjugate has sufficient time to target a tumor before administration of a small fast-clearing radiolabeled complementary PNA that hybridizes with the antibody–PNA conjugate at the tumor site. Herein, we report the first successful application of this multistep process using a PNA-modified epidermal growth factor receptor (EGFR) specific antibody (cetuximab) and a complementary 99mTc-labeled PNA. In vivo studies on tumor bearing mice demonstrated a rapid and efficient in vivo hybridization of the radiolabeled PNA with the antibody–PNA conjugate. Decisively, a high specific tumor accumulation was observed with a tumor-to-muscle ratio of >8, resulting in a clear visualization of the tumor by single photon emission computed tomography (SPECT).
机译:一种用于癌症诊断和治疗的新颖,有前途的策略是使用预靶向方法。为此,非天然DNA / RNA类似物肽核酸(PNA)由于其高代谢稳定性和缺乏非特异性积累,因此是体内识别单位的理想候选者。在预靶向方法中,未标记的高度特异性抗体-PNA缀合物在给予小快速清除的放射性标记的互补PNA之前有足够的时间靶向肿瘤,该互补性PNA在肿瘤部位与抗体-PNA缀合物杂交。本文中,我们报道了使用PNA修饰的表皮生长因子受体(EGFR)特异性抗体(cetuximab)和互补的 99m Tc标记的PNA进行此多步骤过程的首次成功应用。对荷瘤小鼠的体内研究表明,放射性标记的PNA与抗体-PNA缀合物可进行快速有效的体内杂交。决定性地,观察到高的特异性肿瘤蓄积,肿瘤与肌肉的比率> 8,从而通过单光子发射计算机断层扫描(SPECT)清晰地看到了肿瘤。

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