ImmunoPETImaging of Trop2 Expression in Bladder CancerUsing [<sup>64</sup>Cu]Cu-NOTA-Trodelvy

Trop2 exhibits significantly elevated expression in numerous solid malignancies, playing a crucial role in tumor advancement, whereas its presence in healthy tissues is minimal. In this study, we investigated Trop2 expression in bladder cancer models using [<sup>64</sup>Cu]Cu-NOTA-Trodelvy for immunoPET imaging. In HT-1376 models, [<sup>64</sup>Cu]Cu-NOTA-Trodelvy effectively visualized tumor as early as 12 h p.i. (10.30 ± 1.45% ID/g), with tumor uptake increasing and peaking at 48 h p.i. (13.73 ± 1.16% ID/g), highlighting its potential for tumor imaging. Control groups also demonstrated low tumor uptake (5.27 ± 1.14% ID/g at 48 h in the blocking group; 6.33 ± 0.74% ID/g at 48 h in UM-UC-3; 4.50 ± 0.30% ID/g at 48 h in the [<sup>64</sup>Cu]Cu-NOTA-IgG group). Long-term fluorescence imaging further confirmed the tumor uptake rate in the IRDye 800CW-Trodelvy group was significantly higher than in the IRDye 800CW-Trodelvy blockade group (<i>P</i> < 0.001). Our findings demonstrated that [<sup>64</sup>Cu]Cu-NOTA-Trodelvy enables specific and prolonged tumor accumulation in bladder cancer models, providing precise and noninvasive monitoring of Trop2 expression.

Publication Details

Journal
Figshare
Published
2025-03-10
DOI
https://doi.org/10.1021/acs.molpharmaceut.5c00069.s001
Primary Topic
Bladder and Urothelial Cancer Treatments
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article
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article

ImmunoPETImaging of Trop2 Expression in Bladder CancerUsing [64Cu]Cu-NOTA-Trodelvy

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Bladder and Urothelial Cancer Treatments
article

ImmunoPETImaging of Trop2 Expression in Bladder CancerUsing [64Cu]Cu-NOTA-Trodelvy

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Abstract

Trop2 exhibits significantly elevated expression in numerous solid malignancies, playing a crucial role in tumor advancement, whereas its presence in healthy tissues is minimal. In this study, we investigated Trop2 expression in bladder cancer models using [<sup>64</sup>Cu]Cu-NOTA-Trodelvy for immunoPET imaging. In HT-1376 models, [<sup>64</sup>Cu]Cu-NOTA-Trodelvy effectively visualized tumor as early as 12 h p.i. (10.30 ± 1.45% ID/g), with tumor uptake increasing and peaking at 48 h p.i. (13.73 ± 1.16% ID/g), highlighting its potential for tumor imaging. Control groups also demonstrated low tumor uptake (5.27 ± 1.14% ID/g at 48 h in the blocking group; 6.33 ± 0.74% ID/g at 48 h in UM-UC-3; 4.50 ± 0.30% ID/g at 48 h in the [<sup>64</sup>Cu]Cu-NOTA-IgG group). Long-term fluorescence imaging further confirmed the tumor uptake rate in the IRDye 800CW-Trodelvy group was significantly higher than in the IRDye 800CW-Trodelvy blockade group (<i>P</i> < 0.001). Our findings demonstrated that [<sup>64</sup>Cu]Cu-NOTA-Trodelvy enables specific and prolonged tumor accumulation in bladder cancer models, providing precise and noninvasive monitoring of Trop2 expression.

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