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In vivo imaging of human colorectal cancer using radiolabeled analogs of the uroguanylin peptide hormone.

Publication ,  Journal Article
Liu, D; Overbey, D; Watkinson, LD; Daibes-Figueroa, S; Hoffman, TJ; Forte, LR; Volkert, WA; Giblin, MF
Published in: Anticancer Res
October 2009

BACKGROUND: Uroguanylin is an endogenous peptide agonist that binds to the guanylate cyclase C receptor (GC-C). GC-C is overexpressed in human colorectal cancer (CRC), and exposure of GC-C-expressing cells to GC-C agonists results in cell cycle arrest and/or apoptosis, highlighting the therapeutic potential of such compounds. This study describes the first use of radiolabeled uroguanylin analogs for in vivo detection of CRC. MATERIALS AND METHODS: The peptides uroguanylin and E(3)-uroguanylin were N-terminally labeled with the DOTA chelating group via NHS ester activation and characterized by RP-HPLC, ESI-MS, and GC-C receptor binding assays. The purified conjugates were radiolabeled with In-111 and used for in vivo biodistribution and SPECT imaging studies. In vivo experiments were carried out using SCID mice bearing T84 human colorectal cancer tumor xenografts. RESULTS: Alteration of the position 3 aspartate residue to glutamate resulted in increased affinity for GC-C, with IC(50) values of 5.0+/-0.3 and 9.6+/-2.9 nM for E(3)-uroguanylin and DOTA-E(3)-uroguanylin, respectively. In vivo, (111)In-DOTA-E(3)-uroguanylin demonstrated tumor uptake of 1.17+/-0.23 and 0.61+/-0.07% ID/g at 1 and 4 h post injection, respectively. The specificity of tumor localization was demonstrated by coinjection of 3 mg/kg unlabeled E(3)-uroguanylin, which reduced tumor uptake by 69%. Uptake in kidney, however, was dramatically higher for the uroguanylin peptides than for previously characterized radiolabeled E. coli heat-stable enterotoxin (STh) analogs targeting GC-C, and was also inhibited by coinjection of unlabeled peptide in a fashion not previously observed. CONCLUSION: Use of uroguanylin-targeting vectors for in vivo imaging of colorectal cancers expressing GC-C resulted in tumor uptake that paralleled that of higher affinity heat-stable enterotoxin peptides, but also resulted in increased kidney uptake in vivo.

Duke Scholars

Published In

Anticancer Res

EISSN

1791-7530

Publication Date

October 2009

Volume

29

Issue

10

Start / End Page

3777 / 3783

Location

Greece

Related Subject Headings

  • Transplantation, Heterologous
  • Tomography, Emission-Computed, Single-Photon
  • Tissue Distribution
  • Radiopharmaceuticals
  • Oncology & Carcinogenesis
  • Natriuretic Peptides
  • Molecular Sequence Data
  • Mice, SCID
  • Mice, Inbred ICR
  • Mice
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Liu, D., Overbey, D., Watkinson, L. D., Daibes-Figueroa, S., Hoffman, T. J., Forte, L. R., … Giblin, M. F. (2009). In vivo imaging of human colorectal cancer using radiolabeled analogs of the uroguanylin peptide hormone. Anticancer Res, 29(10), 3777–3783.
Liu, Dijie, Douglas Overbey, Lisa D. Watkinson, Said Daibes-Figueroa, Timothy J. Hoffman, Leonard R. Forte, Wynn A. Volkert, and Michael F. Giblin. “In vivo imaging of human colorectal cancer using radiolabeled analogs of the uroguanylin peptide hormone.Anticancer Res 29, no. 10 (October 2009): 3777–83.
Liu D, Overbey D, Watkinson LD, Daibes-Figueroa S, Hoffman TJ, Forte LR, et al. In vivo imaging of human colorectal cancer using radiolabeled analogs of the uroguanylin peptide hormone. Anticancer Res. 2009 Oct;29(10):3777–83.
Liu, Dijie, et al. “In vivo imaging of human colorectal cancer using radiolabeled analogs of the uroguanylin peptide hormone.Anticancer Res, vol. 29, no. 10, Oct. 2009, pp. 3777–83.
Liu D, Overbey D, Watkinson LD, Daibes-Figueroa S, Hoffman TJ, Forte LR, Volkert WA, Giblin MF. In vivo imaging of human colorectal cancer using radiolabeled analogs of the uroguanylin peptide hormone. Anticancer Res. 2009 Oct;29(10):3777–3783.

Published In

Anticancer Res

EISSN

1791-7530

Publication Date

October 2009

Volume

29

Issue

10

Start / End Page

3777 / 3783

Location

Greece

Related Subject Headings

  • Transplantation, Heterologous
  • Tomography, Emission-Computed, Single-Photon
  • Tissue Distribution
  • Radiopharmaceuticals
  • Oncology & Carcinogenesis
  • Natriuretic Peptides
  • Molecular Sequence Data
  • Mice, SCID
  • Mice, Inbred ICR
  • Mice