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用于癌症成像的肽基探针。

Peptide-based probes for cancer imaging.

作者信息

Reubi Jean Claude, Maecke Helmut R

机构信息

University of Berne, Berne, Switzerland.

出版信息

J Nucl Med. 2008 Nov;49(11):1735-8. doi: 10.2967/jnumed.108.053041. Epub 2008 Oct 16.

DOI:10.2967/jnumed.108.053041
PMID:18927341
Abstract

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 sst2-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.

摘要

调节肽受体在多种人类癌症中过度表达。它们是用放射性标记肽探针进行体内成像的分子基础。设计用于对过表达sst2的神经内分泌肿瘤进行成像的生长抑素衍生示踪剂,已经历了近20年的成功研发和广泛的临床应用。最近的进展包括第二代和第三代生长抑素类似物,它们具有更广泛的受体亚型谱或拮抗特性。目前也在研发用于其他肽受体的新型示踪剂,包括用于神经内分泌肿瘤的胆囊收缩素/胃泌素和GLP-1类似物、用于前列腺癌或乳腺癌的蛙皮素和神经肽Y类似物,或用于新生血管标记的精氨酸-甘氨酸-天冬氨酸肽。应用领域包括SPECT/CT和PET/CT。

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