[Cu]Cu-NOTA-Trastuzumab and [Zr]Zr-DFO-Trastuzumab in Xenografts with Varied HER2 Expression.

Mol Pharm

Department of Radiology, Mallinckrodt Institute of Radiology, Washington University School of Medicine, St. Louis, Missouri 63110, United States.

Published: December 2024

AI Article Synopsis

  • Positron emission tomography (PET) can be a useful tool alongside biomarker analysis for monitoring HER2 levels in diverse tumors, especially those with high variability.
  • In the study, Zr-89 and Cu-64 labeled trastuzumab were used to track HER2 expression in tumors, showing that both methods effectively measure HER2 protein levels.
  • The research also indicates that lovastatin may enhance HER2 expression in tumors that have moderate to low HER2, potentially increasing the effectiveness of trastuzumab treatment.

Article Abstract

Positron emission tomography (PET) has potential as a complementary technique to biomarker analysis, especially for human epidermal growth factor receptor 2 (HER2)-expressing tumors characterized by high heterogeneity. In this study, zirconium-89 (Zr) and copper-64 (Cu) labeled trastuzumab were employed to monitor varying levels of tumoral HER2 expression. Additionally, we studied the use of the cholesterol-depleting lovastatin as a pharmacological approach to enhance cell-surface HER2 expression in tumors with moderate to low HER2 levels, aiming to increase antibody accumulation in these tumor types. Both Zr- and Cu-labeled trastuzumab effectively monitor HER2 expression levels in xenografts exhibiting varying HER2 expression. No significant difference in tumor uptake was observed between Zr- or Cu-labeled trastuzumab, and tumor uptake for both radioimmunoconjugates positively correlated with HER2 protein levels. These findings underscore the potential of PET to monitor HER2 protein levels across heterogeneous tumors. Furthermore, our results suggest that further optimization of statin dosing and timing could offer a promising strategy to enhance trastuzumab accumulation in HER2-high, HER2-moderate, and HER2-low tumors.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11611601PMC
http://dx.doi.org/10.1021/acs.molpharmaceut.4c00777DOI Listing

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