[64Cu]Cu-NOTA-Trastuzumab and [89Zr]Zr-DFO-Trastuzumab in Xenografts with Varied HER2 Expression.

IF 4.5 2区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL Molecular Pharmaceutics Pub Date : 2024-12-02 Epub Date: 2024-10-29 DOI:10.1021/acs.molpharmaceut.4c00777
Cristina Simó, Shayla Shmuel, Alex Vanover, Patrícia M R Pereira
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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 (89Zr) and copper-64 (64Cu) 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 89Zr- and 64Cu-labeled trastuzumab effectively monitor HER2 expression levels in xenografts exhibiting varying HER2 expression. No significant difference in tumor uptake was observed between 89Zr- or 64Cu-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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[64Cu]Cu-NOTA-曲妥珠单抗和[89Zr]Zr-DFO-曲妥珠单抗在不同 HER2 表达的异种移植物中的作用。
正电子发射断层扫描(PET)作为生物标记分析的一种补充技术具有潜力,特别是对于具有高度异质性的人类表皮生长因子受体 2(HER2)表达肿瘤。本研究采用锆-89(89Zr)和铜-64(64Cu)标记的曲妥珠单抗来监测不同水平的肿瘤 HER2 表达。此外,我们还研究了使用去胆固醇的洛伐他汀作为一种药理方法来提高中低HER2水平肿瘤的细胞表面HER2表达,目的是增加抗体在这些类型肿瘤中的积累。89Zr和64Cu标记的曲妥珠单抗都能有效监测不同HER2表达水平的异种移植中的HER2表达水平。89Zr-或64Cu标记的曲妥珠单抗在肿瘤摄取量上没有明显差异,两种放射免疫结合物的肿瘤摄取量与HER2蛋白水平呈正相关。这些发现强调了 PET 监测异质肿瘤中 HER2 蛋白水平的潜力。此外,我们的研究结果表明,进一步优化他汀类药物的剂量和时间可提供一种有前景的策略,以增强曲妥珠单抗在HER2高、HER2中等和HER2低肿瘤中的蓄积。
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来源期刊
Molecular Pharmaceutics
Molecular Pharmaceutics 医学-药学
CiteScore
8.00
自引率
6.10%
发文量
391
审稿时长
2 months
期刊介绍: Molecular Pharmaceutics publishes the results of original research that contributes significantly to the molecular mechanistic understanding of drug delivery and drug delivery systems. The journal encourages contributions describing research at the interface of drug discovery and drug development. Scientific areas within the scope of the journal include physical and pharmaceutical chemistry, biochemistry and biophysics, molecular and cellular biology, and polymer and materials science as they relate to drug and drug delivery system efficacy. Mechanistic Drug Delivery and Drug Targeting research on modulating activity and efficacy of a drug or drug product is within the scope of Molecular Pharmaceutics. Theoretical and experimental peer-reviewed research articles, communications, reviews, and perspectives are welcomed.
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