Melanocortin-1 receptor-targeting with radiolabeled cyclic α-melanocyte-stimulating hormone analogs for melanoma imaging

Biopolymers. 2010;94(6):820-9. doi: 10.1002/bip.21490.

Abstract

Melanoma is a type of skin cancer known for its high aggressiveness, early dissemination of metastases, and poor prognosis once metastasized. Thus, early diagnosis of melanoma is a key issue for increasing patient survival. The overexpression of melanocortin-1 receptors (MC1R) in isolated melanoma cells and melanoma tissues led to the radiolabeling of several linear and cyclic MC analogs for melanoma imaging or therapy. Cyclization of α-melanocyte stimulating hormone (α-MSH) peptides has been successfully used to improve binding affinity and in vivo stability of peptides. Herein, we describe the different peptide cyclization strategies recently reported for radiolabeled α-MSH analogs and discuss how such strategies affect MC1R binding affinity, pharmacokinetic profile, and MC1R-melanoma imaging. This review also highlights how the nature of the radiometal and labeling approach influence those properties. Among the cyclized α-MSH peptides reported, (99m)Tc/(111)In-labeled metal-cyclized and lactam bridge-cyclized peptides displayed the highest melanoma and lowest renal uptake values in B16/F1 melanoma-bearing mice and became the most promising tools to be further explored as potential melanoma imaging probes.

MeSH terms

  • Animals
  • Cell Line, Tumor
  • Humans
  • Melanoma / metabolism*
  • Melanoma / pathology*
  • Mice
  • Molecular Imaging*
  • Neoplasms, Experimental / metabolism
  • Neoplasms, Experimental / pathology
  • Peptides, Cyclic* / chemistry
  • Peptides, Cyclic* / pharmacokinetics
  • Peptides, Cyclic* / pharmacology
  • Protein Binding
  • Receptor, Melanocortin, Type 1 / chemistry
  • Receptor, Melanocortin, Type 1 / metabolism*
  • alpha-MSH* / chemistry
  • alpha-MSH* / pharmacokinetics
  • alpha-MSH* / pharmacology

Substances

  • Peptides, Cyclic
  • Receptor, Melanocortin, Type 1
  • alpha-MSH