Related Experiment Video
Updated: Sep 20, 2025

Harnessing the Bioorthogonal Inverse Electron Demand Diels-Alder Cycloaddition for Pretargeted PET Imaging
Published on: February 3, 2015
Preclinical ImmunoPET Imaging of Thyroid-Stimulating Hormone Receptor Expression in Thyroid Cancer using
Wenhui Fu1, Ephraim E Parent1, Justyna J Gleba2
1Department of Radiology, Mayo Clinic, Jacksonville, Florida 32224, United States.
Abstract:
Advanced thyroid cancers are aggressive and often refractory to the current standard of care. The thyroid-stimulating hormone receptor (TSHR) is highly expressed in thyroid cancers and rarely expressed outside the thyroid, making it a viable target for developing radiotheranostics for imaging and therapy of advanced thyroid cancer. This study reports the radiosynthesis and preclinical evaluation of a 64Cu-labeled human antibody for positron emission tomography (PET) imaging of TSHR expression in advanced thyroid cancer mouse models. Human anti-TSHR recombinant antibody K1-70 (TSHR-Ab) was labeled with copper-64, yielding [64Cu]Cu-NOTA-TSHR-Ab with a radiochemical yield of 46.89 ± 3.74%, radiochemical purity of 98.77 ± 0.89%, and specific activity >212 GBq/μmol (n = 5). In vitro studies on TSHR-positive (THJ529TTSHR+) and wild-type (THJ529TWT) cells demonstrated the radiotracer's high specificity and nanomolar binding affinity for THJ529TTSHR+ cells, with a dissociation constant (Kd) of 4.74 nM and an inhibition constant (Ki) of 0.92 nM. ImmunoPET imaging in mice bearing dual-flank tumors (THJ529TWT and THJ529TTSHR+) at multiple time points (1, 2, 4, 18, 24, and 48 h) postinjection (p.i.) revealed rapid tumor targeting and high uptake in TSHR-positive thyroid tumors (SUVmax: 3.63 ± 0.42, 3.82 ± 0.44, and 4.09 ± 0.56 at 18, 24, and 48 h p.i., respectively). Co-injection studies with varying doses of unlabeled TSHR-Ab (0, 25, 50, 100 μg) demonstrated that the coinjection significantly reduced background signals, especially in the spleen, liver, and bone, with a dose of 25 μg effectively reducing off-target signals without affecting tumor uptake. Biodistribution and immunohistochemistry analyses supported these immunoPET imaging results. Furthermore, a comparison study with traditional [18F]FDG PET imaging showed that [64Cu]Cu-NOTA-TSHR outperformed [18F]FDG in tumor detection. In conclusion, [64Cu]Cu-NOTA-TSHR-Ab is a promising radiotracer for PET imaging of TSHR-positive advanced thyroid cancers, with the potential to guide and monitor TSHR-targeted therapies. Further clinical evaluation of [64Cu]Cu-NOTA-TSHR-Ab could provide valuable insights for patient stratification and optimization of anti-TSHR treatments.
Insights
A novel Copper-64 labeled antibody ([64Cu]Cu-NOTA-TSHR-Ab) shows promise for imaging advanced thyroid cancers by targeting the thyroid-stimulating hormone receptor (TSHR). This radiotracer demonstrates high specificity and superior tumor detection compared to [18F]FDG PET imaging.
Area of Science:
- Nuclear medicine
- Oncology
- Radiopharmaceutical chemistry
Background:
- Advanced thyroid cancers are aggressive and often resistant to conventional treatments.
- The thyroid-stimulating hormone receptor (TSHR) is a promising target due to its high expression in thyroid cancers and limited expression elsewhere.
- Radiotheranostics offer a dual approach for imaging and therapy.
Purpose of the Study:
- To develop and evaluate a Copper-64 labeled antibody for positron emission tomography (PET) imaging of TSHR expression in advanced thyroid cancer.
- To assess the specificity, binding affinity, and tumor targeting capabilities of the novel radiotracer in preclinical models.
- To compare the diagnostic performance of the novel radiotracer with established PET imaging agents.
Main Methods:
- Radiosynthesis of human anti-TSHR recombinant antibody K1-70 labeled with Copper-64 ([64Cu]Cu-NOTA-TSHR-Ab).
- In vitro characterization of radiotracer specificity and binding affinity using TSHR-positive and wild-type cells.
- In vivo immunoPET imaging in mouse models bearing thyroid cancer xenografts, including biodistribution and blocking studies.
- Comparative analysis with [18F]FDG PET imaging.
Main Results:
- Successful radiosynthesis of [64Cu]Cu-NOTA-TSHR-Ab with high radiochemical yield and purity.
- Demonstrated high specificity and nanomolar binding affinity for TSHR-positive cells in vitro.
- ImmunoPET imaging revealed rapid and specific tumor targeting in TSHR-positive thyroid tumors in vivo.
- Blocking studies confirmed reduced off-target signals, and [64Cu]Cu-NOTA-TSHR-Ab outperformed [18F]FDG in tumor detection.
Conclusions:
- [64Cu]Cu-NOTA-TSHR-Ab is a highly promising radiotracer for PET imaging of TSHR-positive advanced thyroid cancers.
- The radiotracer has the potential to guide and monitor TSHR-targeted therapies.
- Further clinical evaluation is warranted for patient stratification and treatment optimization.
Related Concept Videos
Imaging Studies II: Positron Emission Tomography and Scintigraphy
Fundamental Principles of PET
Positron Emission Tomography
One of the main requirements of a PET scan is a positron-emitting radioisotope, which is produced in a cyclotron and then attached to a substance used by the part of the body...

