In vitro and in vivo evaluation of ⁶⁴Cu-radiolabeled KCCYSL peptides for targeting epidermal growth factor receptor-2 in breast carcinomas.

Abstract

Epidermal growth factor receptor-2 (EGFR-2) has been implicated in the pathogenesis of breast and other carcinomas. In this report, we tested the ability of a bacteriophage selected peptide KCCYSL, radiolabeled with ⁶⁴Cu, to image EGFR-2 expressing breast tumors in vivo by positron emission tomography (PET). We evaluated and compared the in vivo tissue distribution and imaging properties of ⁶⁴Cu-X-(Gly-Ser-Gly)-KCCYSL peptide (X = 1,4,7,10, tetraazacyclododecane-N,N',N'',N'''-tetracetic acid, [DOTA] 1,4,8,11-tetraazabicyclo[6.6.2]hexadecane-4,11-diacetic acid [CB-TE2A], and 1,4,7-triazacyclononane-1,4,7-triacetic acid [NOTA] chelators) in a human breast cancer xenograft mouse model using dual modality PET and computed tomography (CT). The synthesized peptides DO3A-GSG-KCCYSL, CB-TE2A-GSG-KCCYSL, and NO2A-GSG-KCCYSL were purified, radiolabeled with ⁶⁴Cu, and evaluated for human breast cancer cell (MDA-MB-435) binding, 50% inhibitory concentration, and serum stability. In vivo pharmacokinetic and small animal PET/CT imaging studies were performed using SCID mice bearing MDA-MB-435 xenografts. The radiolabeled peptides bound with an 50% inhibitory concentration of 42.0 ± 10.2 nM (DO3A), 31 ± 7.9 nM (CB-TE2A), and 44.2 ± 6.6 nM (NO2A) to cultured MDA-MB-435 cells. All of the radiolabeled peptides were stable in vitro. The tumor uptake of DO3A, CB-TE2A, and NO2A peptides were 0.73 ± 0.15 percent injected dose per gram (%ID/g), 0.64 ± 0.08%ID/g, and 0.52 ± 0.04%ID/g, respectively at 1 hour. Liver uptake for the ⁶⁴Cu-DO3A-peptide (1.68 ± 0.42%ID/g) was more than that of the ⁶⁴Cu-CB-TE2A-peptide (0.52 ± 0.02% ID/g) and ⁶⁴Cu-NO2A-peptide (0.48 ± 0.05%ID/g) at 2 hours. PET/CT studies revealed successful tumor uptake of ⁶⁴Cu-peptides at 2 hours postinjection. In vivo kidney retention was observed with all of the radiolabeled peptides. The optimization of bifunctional chelators improves the pharmacokinetic properties of the ⁶⁴Cu-labeled GSG-KCCYSL peptide, which enables the selection of a suitable peptide homolog as a PET imaging agent for EGFR-2 expressing breast carcinomas.

• Authors: Senthil R Kumar, Fabio A Gallazzi, Riccardo Ferdani, Carolyn J Anderson, Thomas P Quinn, Susan L Deutscher
• Journal: Cancer biotherapy & radiopharmaceuticals (Cancer Biother Radiopharm) Vol. 25 Issue 6 Pg. 693-703 (Dec 2010) ISSN: 1557-8852 [Electronic] United States
• PMID: 21204764 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, U.S. Gov't, Non-P.H.S.)

Chemical References

• (4,11-bis(carboxymethyl)-1,4,8,11-tetraazabicyclo(6.6.2)hexadecane)copper(II)
• 1,4,7,10-tetraazacyclododecane-1,4,7-triacetic acid
• 1,4,7-triazacyclononane-1,4-diacetate
• Chelating Agents
• Copper Radioisotopes
• Heterocyclic Compounds
• Heterocyclic Compounds, 1-Ring
• Organometallic Compounds
• Peptides
• Radiopharmaceuticals
• ERBB2 protein, human
• Receptor, ErbB-2

Topics

• Animal Structures (metabolism)
• Animals
• Breast Neoplasms (diagnostic imaging, metabolism)
• Cell Line, Tumor
• Chelating Agents (chemistry)
• Copper Radioisotopes (administration & dosage, chemistry)
• Drug Stability
• Epithelial Cells (metabolism)
• Female
• Heterocyclic Compounds (chemistry)
• Heterocyclic Compounds, 1-Ring (chemistry)
• Humans
• Kidney (metabolism)
• Mice
• Mice, SCID
• Molecular Structure
• Organometallic Compounds (chemistry)
• Peptides (chemistry, metabolism)
• Positron-Emission Tomography
• Radiopharmaceuticals (chemical synthesis, metabolism, pharmacokinetics)
• Receptor, ErbB-2 (metabolism)
• Tissue Distribution