[64Cu-NOTA-8-Aoc-BBN(7-14)NH2] targeting vector for positron-emission tomography imaging of gastrin-releasing peptide receptor-expressing tissues

Proc Natl Acad Sci U S A. 2007 Jul 24;104(30):12462-7. doi: 10.1073/pnas.0705347104. Epub 2007 Jul 12.

Abstract

Radiolabeled peptides hold promise as diagnostic/therapeutic targeting vectors for specific human cancers. We report the design and development of a targeting vector, [(64)Cu-NOTA-8-Aoc-BBN(7-14)NH(2)] (NOTA = 1,4,7-triazacyclononane-1,4,7-triacetic acid, 8-Aoc = 8-aminooctanoic acid, and BBN = bombesin), having very high selectivity and affinity for the gastrin-releasing peptide receptor (GRPr). GRPrs are expressed on a variety of human cancers, including breast, lung, pancreatic, and prostate, making this a viable approach toward site-directed localization or therapy of these human diseases. In this study, [NOTA-X-BBN(7-14)NH(2)] conjugates were synthesized, where X = a specific pharmacokinetic modifier. The IC(50) of [NOTA-8-Aoc-BBN(7-14)NH(2)] was determined by a competitive displacement cell-binding assay in PC-3 human prostate cancer cells using (125)I-[Tyr(4)]-BBN as the displacement ligand. An IC(50) of 3.1 +/- 0.5 nM was obtained, demonstrating high binding affinity of [NOTA-8-Aoc-BBN] for the GRPr. [(64)Cu-NOTA-X-BBN] conjugates were prepared by the reaction of (64)CuCl(2) with peptides in buffered aqueous solution. In vivo studies of [(64)Cu-NOTA-8-Aoc-BBN(7-14)NH(2)] in tumor-bearing PC-3 mouse models indicated very high affinity of conjugate for the GRPr. Uptake of conjugate in tumor was 3.58 +/- 0.70% injected dose (ID) per g at 1 h postintravenous injection (p.i.). Minimal accumulation of radioactivity in liver tissue (1.58 +/- 0.40% ID per g, 1 h p.i.) is indicative of rapid renal-urinary excretion and suggests very high in vivo kinetic stability of [(64)Cu-NOTA-8-Aoc-BBN(7-14)NH(2)] with little or no in vivo dissociation of (64)Cu(2+) from the NOTA chelator. Kidney accumulation at 1 h p.i. was 3.79 +/- 1.09% ID per g. Molecular imaging studies in GRPr-expressing tumor models produced high-contrast, high-quality micro-positron-emission tomography images.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Boron Compounds
  • Cell Line, Tumor
  • Heterocyclic Compounds, 1-Ring* / chemistry
  • Heterocyclic Compounds, 1-Ring* / isolation & purification
  • Heterocyclic Compounds, 1-Ring* / pharmacokinetics
  • Humans
  • Methacrylates
  • Methylmethacrylates
  • Mice
  • Mice, SCID
  • Molecular Structure
  • Neoplasms / diagnosis
  • Neoplasms / metabolism
  • Organ Specificity / drug effects
  • Peptide Fragments* / chemistry
  • Peptide Fragments* / isolation & purification
  • Peptide Fragments* / pharmacokinetics
  • Positron-Emission Tomography / methods*
  • Receptors, Bombesin / metabolism*
  • Xenograft Model Antitumor Assays

Substances

  • 64Cu-1,4,7-triazacyclononane-1,4,7-triacetic acid-8-aminooctanoic acid-bombesin(7-14)amide
  • Boron Compounds
  • Heterocyclic Compounds, 1-Ring
  • Methacrylates
  • Methylmethacrylates
  • Peptide Fragments
  • Receptors, Bombesin
  • Super-bond