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A radiogallium-DOTA-based bivalent peptidic ligand targeting a chemokine receptor, CXCR4, for tumor imaging

机译:基于放射性镓-DOTA的二价肽配体,靶向趋化因子受体CXCR4,用于肿瘤成像

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摘要

We have developed a novel radiogallium (Ga)-DOTA-based bivalent peptidic ligand targeting a chemokine receptor, CXCR4, for tumor imaging. A CXCR4 imaging probe with two CXCR4 antagonists (Ac-TZ14011) on Ga-DOTA core, Ga-DOTA-TZ2, was synthesized, and the affinity and binding to CXCR4 was evaluated in CXCR4 expressing cells in vitro. The affinity of Ga-DOTA-TZ2 for CXCR4 was 20-fold greater than the corresponding monovalent probe, Ga-DOTA-TZ1. 67Ga-DOTA-TZ2 showed the significantly higher accumulation in CXCR4-expressing tumor cells compared with 67Ga-DOTA-TZ1, suggesting the bivalent effect enhances its binding to CXCR4. The incorporation of two CXCR4 antagonists to Ga-DOTA could be effective in detecting CXCR4-expressing tumors.
机译:我们已经开发了靶向肿瘤趋化因子受体CXCR4的新型基于放射性镓(Ga)-DOTA的二价肽配体。合成了在Ga-DOTA核心Ga-DOTA-TZ2上具有两个CXCR4拮抗剂(Ac-TZ14011)的CXCR4成像探针,并在体外表达CXCR4的细胞中评估了对CXCR4的亲和力和结合力。 Ga-DOTA-TZ2对CXCR4的亲和力比相应的单价探针Ga-DOTA-TZ1高20倍。与67Ga-DOTA-TZ1相比,67Ga-DOTA-TZ2在表达CXCR4的肿瘤细胞中显示出明显更高的蓄积,表明二价效应增强了其与CXCR4的结合。将两种CXCR4拮抗剂掺入Ga-DOTA可以有效检测表达CXCR4的肿瘤。

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