Leonidova Anna, Foerster Christian, Zarschler Kristof, Schubert Maik, Pietzsch Hans-Jürgen, Steinbach Jörg, Bergmann Ralf, Metzler-Nolte Nils, Stephan Holger, Gasser Gilles
Department of Chemistry , University of Zurich , Winterthurerstrasse 190 , CH-8057 Zurich , Switzerland . Email:
Helmholtz-Zentrum Dresden - Rossendorf , Institute of Radiopharmaceutical Cancer Research , Bautzner Landstraße 400 , D-01328 Dresden , Germany . Email:
Chem Sci. 2015 Oct 1;6(10):5601-5616. doi: 10.1039/c5sc00951k. Epub 2015 Jun 17.
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 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 Tc-labeled PNA. studies on tumor bearing mice demonstrated a rapid and efficient 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).
一种用于癌症诊断和治疗的新颖且有前景的策略是采用预靶向方法。为此,非天然DNA/RNA类似物肽核酸(PNA)是理想的识别单元候选物,因为它们具有高代谢稳定性且缺乏非特异性积累。在预靶向方法中,未标记的、高度特异性的抗体 - PNA缀合物在施用与肿瘤部位的抗体 - PNA缀合物杂交的小的快速清除的放射性标记互补PNA之前,有足够的时间靶向肿瘤。在此,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(西妥昔单抗)和互补Tc标记的PNA首次成功应用此多步骤过程。对荷瘤小鼠的研究表明,放射性标记的PNA与抗体 - PNA缀合物快速且有效地杂交。决定性的是,观察到肿瘤与肌肉的比率>8,具有高特异性肿瘤积累,通过单光子发射计算机断层扫描(SPECT)实现了肿瘤的清晰可视化。