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In Vivo Assessment of HER2 Receptor Density in HER2-positive Tumors by Near-infrared Imaging Using Repeated Injections of the Fluorescent Probe

机译:使用重复注射的荧光探针通过近红外成像体内评估HER2阳性肿瘤中的HER2受体密度。

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摘要

HER2 overexpression and amplification of the HER2eu gene have been found in approximately 25% of invasive breast carcinomas. They are associated with a poor prognosis and resistance to therapy in breast cancer patients. Up to now, clinical evaluation of human epidermal growth factor receptor 2 (HER2) expression is based on ex vivo methods (immunohistochemistry (IHC) or fluorescence in situ hybridization (FISH) staining of biopsied tissue). Our goal is to realize “image and treat” paradigm using targeted fluorescent probes to evaluate expression levels of cell biomarkers responsible for cancer progression and to monitor the efficacy of corresponding monoclonal antibody treatments. We used fluorescent Affibody-based probes for in vivo analysis of HER2 receptors using near-infrared optical imaging that do not interfere with binding of the therapeutic agents to these receptors. We have analyzed two types of breast carcinoma xenografts with significant differences in HER2 expression (3+ and 2+ according to classification) in the mouse model. Using our kinetic model to analyze the temporal variations of the fluorescence intensity in the tumor area after two subsequent injections allowed us to assess quantitatively the difference in HER2 expression levels for two tumor types (BT-474 and MD-MBA-361). This result was substantiated by ELISA ex vivo assays of HER2 expression in the same tumors.
机译:在大约25%的浸润性乳腺癌中发现了HER2过表达和HER2 / neu基因的扩增。它们与乳腺癌患者的不良预后和对治疗的抵抗力有关。到目前为止,人类表皮生长因子受体2(HER2)表达的临床评估是基于离体方法(活组织的免疫组织化学(IHC)或荧光原位杂交(FISH)染色)。我们的目标是使用靶向的荧光探针来实现“图像和治疗”范式,以评估负责癌症进展的细胞生物标志物的表达水平并监测相应单克隆抗体治疗的疗效。我们使用基于荧光Affibody的探针,使用不影响治疗剂与这些受体结合的近红外光学成像,对HER2受体进行体内分析。我们分析了两种类型的乳腺癌异种移植物,在小鼠模型中HER2表达有显着差异(根据分类,为3+和2+)。使用我们的动力学模型分析两次后续注射后肿瘤区域中荧光强度的时间变化,使我们能够定量评估两种肿瘤类型(BT-474和MD-MBA-361)HER2表达水平的差异。该结果通过在相同肿瘤中HER2表达的ELISA离体测定得到证实。

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