Bombesin receptor-mediated imaging and cytotoxicity: review and current status.

Curr Drug Deliv

Digestive Diseases Branch, National Institutes of Diabetes, Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD 20892, USA.

Published: January 2011

AI Article Synopsis

  • The three mammalian bombesin receptors (GRP, NMB, BRS-3) are often over-expressed in major cancers, making them significant targets for research.
  • Recent clinical advancements in somatostatin receptor imaging for neuroendocrine tumors have sparked interest in applying similar techniques to bombesin receptors.
  • The paper reviews over 200 studies focusing on Bn receptor-mediated imaging and cytotoxicity, highlighting both in vitro, in vivo results, and human study findings using various Bn-based ligands.

Article Abstract

The three mammalian bombesin (Bn) receptors (gastrin-releasing peptide [GRP] receptor, neuromedin B [NMB] receptor, BRS-3) are one of the classes of G protein-coupled receptors that are most frequently over-express/ectopically expressed by common, important malignancies. Because of the clinical success of somatostatin receptor-mediated imaging and cytotoxicity with neuroendocrine tumors, there is now increasing interest in pursuing a similar approach with Bn receptors. In the last few years then have been more than 200 studies in this area. In the present paper, the in vitro and in vivo results, as well as results of human studies from many of these studies are reviewed and the current state of Bn receptor-mediated imaging or cytotoxicity is discussed. Both Bn receptor-mediated imaging studies as well as Bn receptor-mediated tumoral cytotoxic studies using radioactive and non-radioactive Bn-based ligands are covered.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3058932PMC
http://dx.doi.org/10.2174/156720111793663624DOI Listing

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