Synthesis and preclinical evaluation of a Ga-labeled peptide for PET imaging of transferrin receptor 1 in tumor.

PURPOSE

Transferrin receptor 1 (TfR1) is a transmembrane glycoprotein that mediates cellular iron uptake. Despite its potential as a target for tumor diagnosis, the lack of suitable TfR1 ligands has hindered the development of effective TfR1 imaging agents. We labeled a recently discovered TfR1 ligand, TfRB1G3, with Ga-68 and evaluated its potential for TfR1 imaging through preclinical experiments.

METHODS

TfRB1G3 was modified with HBED-CC and radiolabeled with Ga ([Ga]Ga-TfRB1G3). Human glioblastoma (U87MG) cells were transfected with TfR1-targeting siRNA (TfR1-knockdown) or non-targeting siRNA (control), and accumulation of [Ga]Ga-TfRB1G3 was evaluated. The K value of [Ga]Ga-TfRB1G3 for TfR1 was also calculated. Ex vivo biodistribution was conducted in normal and U87MG tumor-bearing mice after injecting [Ga]Ga-TfRB1G3. PET imaging studies were conducted after injecting [Ga]Ga-TfRB1G3, with/without co-injection of 10 nmol TfRB1G3 in mice bearing U87MG tumors.

RESULTS

[Ga]Ga-TfRB1G3 was obtained with high radiochemical purity (> 90%). The accumulation of [Ga]Ga-TfRB1G3 in the TfR1-knockdown cells (22.0 ± 1.1% Dose/mg) was significantly lower than that in the control (308.5 ± 14.3% Dose/mg). The K value was 1.0 nM. Tumor accumulation of [Ga]Ga-TfRB1G3 was higher than in any other organs except the kidneys, and co-injection of TfRB1G3 significantly reduced the tumor accumulation by more than 90%. PET imaging with [Ga]Ga-TfRB1G3 clearly visualized TfR1-positive tumor as early as 20 min post-injection.

CONCLUSION

[Ga]Ga-TfRB1G3 demonstrated excellent affinity and specificity for TfR1 both in vitro and in vivo, providing clear PET images of TfR1-positive tumors shortly after injection. [Ga]Ga-TfRB1G3 would enable sensitive and quantitative imaging of TfR1 expression.