Peptide-Based Probes for Cancer Imaging

被引:231
作者
Reubi, Jean Claude [1 ]
Maecke, Helmut R. [2 ]
机构
[1] Univ Bern, Inst Pathol, Div Cell Biol & Expt Canc Res, CH-3010 Bern, Switzerland
[2] Univ Hosp, Basel, Switzerland
关键词
PET/CT; peptide-based probes; SPELT/CT; cholecystokinin/gastrin; somatostatin analogs;
D O I
10.2967/jnumed.108.053041
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Receptors for regulatory peptides are overexpressed in a variety of human cancers. They represent the molecular basis for in vivo imaging with radiolabeled peptide probes. Somatostatin-derived tracers, designed to image the sst(2)-overexpressing neuroendocrine tumors, have enjoyed almost 2 decades of successful development and extensive clinical applications. More recent developments include second- and third-generation somatostatin analogs, with a broader receptor subtype profile or with antagonistic properties. Emerging tracers for other peptide receptors, including cholecystokinin/gastrin and GLP-1 analogs for neuroendocrine tumors, bombesin and neuropeptide-Y analogs for prostate or breast cancers, or Arg-Gly-Asp peptides for neoangiogenesis labeling, are also in current development. Application fields include both SPECT/CT and PET/CT.
引用
收藏
页码:1735 / 1738
页数:4
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