Molecular targets and the emerging role of copper radionuclides in prostate cancer theranostics
Diana Rodrigues, Alexandra I. Fonseca, João N. Moreira, Célia Gomes, Antero Abrunhosa

TL;DR
This paper reviews the potential of copper-based radiopharmaceuticals for improving prostate cancer diagnosis and treatment through targeted imaging and therapy.
Contribution
The paper highlights the emerging role of copper radionuclides in prostate cancer theranostics and evaluates their clinical potential.
Findings
Copper radioisotopes like Cu-61, Cu-64, and Cu-67 show favorable properties for prostate cancer theranostics.
Agents targeting PSMA and GRPR are the most studied for copper-based radiopharmaceuticals in prostate cancer.
Copper-based radiopharmaceuticals could enable more personalized and effective prostate cancer management.
Abstract
Prostate cancer (PCa) remains one of the most commonly diagnosed malignancies and a leading cause of cancer-related morbidity and mortality among men worldwide. Despite considerable progress in diagnostic and therapeutic modalities, conventional approaches often fall short in capturing disease heterogeneity and managing advanced or treatment-resistant cases. Over the past years, molecular imaging and targeted radionuclide therapy within a theranostic framework have emerged as powerful tools to potentially overcome these limitations. In this context, copper radioisotopes—particularly copper-61 (T1/2 = 3.33 h; 61% β+), copper-64 (T1/2 = 12.7 h; 17% β+, 39% β–), and copper-67 (T1/2 = 2.58 d; 100% β–)—have garnered considerable attention due to their favorable half-lives, straightforward coordination chemistry, and optimal physical decay properties for both imaging and therapy. This review…
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Taxonomy
TopicsRadiopharmaceutical Chemistry and Applications · Prostate Cancer Treatment and Research · Trace Elements in Health
