肿瘤整合素表达的PET显像

W. Cai, Xiaoyuan Chen
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引用次数: 0

摘要

整合素/spl α //sub v//spl β //sub 3/在新生毛细血管细胞上的表达及其与特异性细胞外基质配体的相互作用在肿瘤血管生成和转移中起关键作用。在一些恶性肿瘤中,整合素/spl α //sub v//spl β //sub 3/的肿瘤表达与肿瘤进展密切相关。整合素/spl α //sub v//spl β //sub 3/在体内表达的非侵入性成像方法对于靶向整合素的抗血管生成治疗的成功至关重要。针对小动物的PET、SPECT和近红外荧光成像,开发了相应标记的RGD肽(强效整合素/spl α //sub v//spl β //sub 3/拮抗剂)和抗体。由于PET的高灵敏度和足够的空间和时间分辨率,开发用于整合素表达成像的PET探针一直是活跃研究的支柱。我们利用多价效应和设计的/sup 18/F-和/sup 64/ cu标记的二聚体和多聚体RGD肽,提高肿瘤靶向疗效和体内药代动力学,用于成像和成像引导的内放疗应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
PET imaging of tumor integrin expression
The expression of integrin /spl alpha//sub v//spl beta//sub 3/ on sprouting capillary cells and their interaction with specific extracellular matrix ligands play a key role in tumor angiogenesis and metastasis. In several malignancies, tumor expression of integrin /spl alpha//sub v//spl beta//sub 3/ correlates well with tumor progression. Non-invasive imaging methods to visualize and quantify integrin /spl alpha//sub v//spl beta//sub 3/ expression in vivo are crucial for the success of anti-angiogenic therapy targeting integrin. Suitably labeled RGD peptides (potent integrin /spl alpha//sub v//spl beta//sub 3/ antagonists) and antibodies have been developed for PET, SPECT and NIR fluorescence imaging of small animals. Due to the high sensitivity and adequate spatial and temporal resolution of PET, development of PET probes for integrin expression imaging has been the mainstay of active research. We improved the tumor targeting efficacy and in vivo pharmacokinetics by applying polyvalency effect and designed /sup 18/F- and /sup 64/Cu-labeled dimeric and multimeric RGD peptides for both imaging and imaging-guided internal radiotherapy applications.
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