Ahmadi Peni, Muguruma Kyohei, Chang Tsung-Che, Tamura Satoru, Tsubokura Kazuki, Egawa Yasuko, Suzuki Takehiro, Dohmae Naoshi, Nakao Yoichi, Tanaka Katsunori
Biofunctional Synthetic Chemistry, RIKEN Cluster for Pioneering Research 2-1 Hirosawa Wako Saitama 351-0198 Japan
Department of Chemical Science and Engineering, School of Materials and Chemical Technology, Tokyo Institute of Technology 2-12-1 Ookayama Meguro Tokyo 152-8552 Japan.
Chem Sci. 2021 Sep 2;12(37):12266-12273. doi: 10.1039/d1sc01784e. eCollection 2021 Sep 29.
Selective cell tagging (SeCT) therapy is a strategy for labeling a targeted cell with certain chemical moieties a catalytic chemical transformation in order to elicit a therapeutic effect. Herein, we report a cancer therapy based on targeted cell surface tagging with proapoptotic peptides (Ac-GGKLFG-X; X = reactive group) that induce apoptosis when attached to the cell surface. Using either Au-catalyzed amidation or Ru-catalyzed alkylation, these proapoptotic peptides showed excellent therapeutic effects both and . In particular, co-treatment with proapoptotic peptide and the carrier-Ru complex significantly and synergistically inhibited tumor growth and prolonged survival rate of tumor-bearing mice after only a single injection. This is the first report of Ru catalyst application , and this approach could be used in SeCT for cancer therapy.
选择性细胞标记(SeCT)疗法是一种通过特定化学基团对靶向细胞进行标记以引发催化化学转化从而产生治疗效果的策略。在此,我们报道了一种基于用促凋亡肽(Ac-GGKLFG-X;X = 反应基团)对细胞表面进行靶向标记的癌症治疗方法,该促凋亡肽附着于细胞表面时可诱导细胞凋亡。使用金催化的酰胺化反应或钌催化的烷基化反应,这些促凋亡肽在体内和体外均显示出优异的治疗效果。特别是,促凋亡肽与载体-钌配合物联合治疗在仅单次注射后就能显著且协同地抑制肿瘤生长并延长荷瘤小鼠的存活率。这是关于钌催化剂应用的首次报道,并且这种方法可用于癌症治疗的选择性细胞标记疗法。