Wang Kezheng, Wang Kai, Li Weihual, Huang Tao, Li Renfei, Wang Dan, Shen Baozhong, Chen Xiaoyuan
Department of Medical Imaging and Nuclear Medicine, Fourth Affiliated Hospital, Harbin Medical University, Harbin, China.
Acta Radiol. 2009 Dec;50(10):1095-103. doi: 10.3109/02841850903008800.
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.
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.
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.
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.
Erbitux-Cy5.5 may be used as a specific NIR contrast agent for the noninvasive characterization of EGFR expression level in breast cancer xenografts.
表皮生长因子受体(EGFR)的过表达与癌症发生和发展的几个关键特征相关。因此,EGFR是肿瘤诊断和抗癌治疗中一个非常有前景的生物学靶点。EGFR表达的特征对于临床医生选择适合EGFR靶向治疗的患者以及评估治疗效果非常重要。
采用体内近红外成像方法,研究近红外(NIR)荧光染料Cy5.5标记的抗EGFR单克隆抗体爱必妥是否能表征MDA-MB-231和MCF-7乳腺癌异种移植瘤中的EGFR表达水平。
通过酰化反应将Cy5.5与爱必妥偶联,设计一种荧光染料探针,并用荧光光谱法表征爱必妥-Cy5.5偶联物的荧光特性。采用流式细胞术和激光共聚焦显微镜在体外检测抗体探针的EGFR特异性。将爱必妥-Cy5.5静脉注射到携带MDA-MB-231或MCF-7肿瘤的免疫缺陷小鼠体内。采集并分析全身和感兴趣区域的荧光图像。还通过免疫组织化学分析对EGFR表达进行分析和确认。
爱必妥-Cy5.5探针的最大激发/发射波长为674/697 nm,与游离Cy5.5(674/712 nm)相似。共聚焦显微镜证实了MDA-MB-231和MCF-7细胞中受体特异性摄取。在流式细胞术探针特异性分析中,爱必妥-Cy5.5对MDA-MB-231的亲和力比对MCF-7细胞高9.32倍。体内近红外成像也表明在EGFR阳性肿瘤中有特异性摄取。MDA-MB-231中的探针摄取率和最大摄取剂量显著高于MCF-7异种移植瘤(P < 0.001)。免疫组织化学染色证实了体内成像结果,显示MDA-MB-231(+++)和MCF-7(+)肿瘤组织中EGFR表达存在差异。
爱必妥-Cy5.5可作为一种特异性近红外造影剂,用于无创表征乳腺癌异种移植瘤中的EGFR表达水平。