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Characterizing Breast Cancer Xenograft Epidermal Growth Factor Receptor Expression by Using Near-Infrared Optical Imaging

机译:通过使用近红外光学成像表征乳腺癌异种移植表皮生长因子受体表达

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Background: Epidermal growth factor receptor (EGFR) overexpression is associated with several key features of cancer development and growth. Therefore, EGFR is a very promising biological target for tumor diagnosis and anticancer therapy. Characterization of EGFR expression is important for clinicians to select patients for EGFR-targeted therapy and evaluate therapeutic effects. Purpose: To investigate whether near-infrared (NIR) fluorescent dye Cy5.5-labeled anti-EGFR monoclonal antibody Erbitux can characterize EGFR expression level in MDA-MB-231 and MCF-7 breast cancer xenografts using an in vivo NIR imaging method. Material and Methods: A fluorochrome probe was designed by coupling Cy5.5 to Erbitux through acidylation, and the fluorescence property of the Erbitux-Cy5.5 conjugate was characterized by fluorospectroscopy. Flow cytometry and laser confocal microscopy were used to test the EGFR specificity of the antibody probe in vitro. Erbitux-Cy5.5 was also injected intravenously into immune-deficient mice bearing MDA-MB-231 or MCF-7 tumors. Whole-body and region-of-interest fluorescence images were acquired and analyzed. The EGFR expression was also analyzed and confirmed by immunohistochemical assay. Results: The maximum excitation/emission wavelength for the Erbitux-Cy5.5 probe was 674/697 nm, similar to that of free Cy5.5 (674/712 nm). Confocal microscopy confirmed receptor-specific uptake in MDA-MB-231 and MCF-7 cells. In flow cytometry probe specificity assay, Erbitux-Cy5.5 showed a 9.32-fold higher affinity for MDA-MB-231 than MCF-7 cells. In vivo NIR imaging also indicated specific uptake in EGFR-positive tumors. Probe uptake rate and maximum intake dose in MDA-MB-231 were significantly higher than those in MCF-7 xenografts (P < 0.001). Immunohistochemical staining confirmed the in vivo imaging results, showing differentiated EGFR expression in MDA-MB-231 (+ + +) and MCF-7 (+) tumor tissues. Conclusion: Erbitux-Cy5.5 may be used as a specific NIR contrast agent for the noninvasive characterization of EGFR expression level in breast cancer xenografts.
机译:背景:表皮生长因子受体(EGFR)的过度表达与癌症发生和发展的几个关键特征有关。因此,EGFR是用于肿瘤诊断和抗癌治疗的非常有希望的生物学靶标。 EGFR表达的表征对于临床医生选择患者进行EGFR靶向治疗并评估治疗效果非常重要。目的:利用体内NIR成像方法,研究近红外(NIR)荧光染料Cy5.5标记的抗EGFR单克隆抗体爱必妥(Erbitux)是否可以表征MDA-MB-231和MCF-7乳腺癌异种移植物中的EGFR表达水平。材料与方法:通过酸化将Cy5.5与Erbitux偶联来设计荧光染料探针,并通过荧光光谱法表征Erbitux-Cy5.5共轭物的荧光性质。流式细胞仪和激光共聚焦显微镜用于测试抗体探针的EGFR特异性。还将Erbitux-Cy5.5静脉注射到携带MDA-MB-231或MCF-7肿瘤的免疫缺陷小鼠中。采集并分析了全身和感兴趣区域的荧光图像。还通过免疫组织化学测定法分析并确认了EGFR表达。结果:Erbitux-Cy5.5探针的最大激发/发射波长为674/697 nm,类似于游离Cy5.5的最大激发/发射波长(674/712 nm)。共聚焦显微镜证实了MDA-MB-231和MCF-7细胞中的受体特异性摄取。在流式细胞仪探针特异性测定中,Erbitux-Cy5.5对MDA-MB-231的亲和力比MCF-7细胞高9.32倍。体内NIR成像也表明在EGFR阳性肿瘤中有特异性摄取。 MDA-MB-231的探针摄取率和最大摄取剂量显着高于MCF-7异种移植物(P <0.001)。免疫组织化学染色证实了体内成像结果,显示在MDA-MB-231(+ + +)和MCF-7(+)肿瘤组织中EGFR表达差异。结论:Erbitux-Cy5.5可以作为特异性NIR造影剂用于乳腺癌异种移植物中EGFR表达水平的非侵入性表征。

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