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First published online October 16, 2008
J Nucl Med 2008, doi:10.2967/jnumed.108.053041
© 2008 by Society of Nuclear Medicine
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Peptide-Based Probes for Cancer Imaging

Jean Claude Reubi 1* and Helmut R. Maecke 2

1 University of Berne, Berne, Switzerland
2 University Hospital, Basel, Switzerland

* To whom correspondence should be addressed. E-mail: reubi{at}pathology.unibe.ch.


   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.

Key Words: PET/CT, peptide-based probes, SPECT/CT, cholecystokinin/gastrin, somatostatin analogs




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B. Waser, M.-L. Tamma, R. Cescato, H. R. Maecke, and J. C. Reubi
Highly Efficient In Vivo Agonist-Induced Internalization of sst2 Receptors in Somatostatin Target Tissues
J. Nucl. Med., June 1, 2009; 50(6): 936 - 941.
[Abstract] [Full Text] [PDF]




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