Fatehi D, Baral T N, Abulrob A
J Nanosci Nanotechnol. 2014 Jul;14(7):5355-62. doi: 10.1166/jnn.2014.9076.
Diagnosis of glioblastoma multiform (GBM) with MRI lacks molecular information and requires a biopsy for pathologic confirmation. The EGFRvIII, is a constitutively active mutant of the EGF receptor, identified in a high percentage of brain cancers and associated with increased invasiveness and resistance, making it a good target to improve imaging and diagnosis. The present study shows that conjugation of near-infrared quantum dot (Qd800) to an anti-EGFRvIII single domain antibody, made of the variable region with an extra cysteine for site-specific conjugation (EG2-Cys), increased its internalization in U87MG-EGFRvIII cells in vitro compared to Qd800 conjugated with the Fc region of the antibody (EG2-hFc) or unconjugated. EG2-Cys also improved the contrast in Near-Infrared Imaging of mice bearing orthotopic glioblastoma. The increased accumulation was confirmed by fluorescence microscopy of brain sections. The specificity of EG2-Cys in brain tumor expressing the EGFRvIII mutant receptor may provide an accurate less invasive diagnosis and determine the level of tumor aggressiveness and resistance.
通过磁共振成像(MRI)诊断多形性胶质母细胞瘤(GBM)缺乏分子信息,需要进行活检以获得病理证实。表皮生长因子受体变异体III(EGFRvIII)是表皮生长因子受体的一种组成型活性突变体,在高比例的脑癌中被发现,且与侵袭性增加和耐药性相关,这使其成为改善成像和诊断的良好靶点。本研究表明,将近红外量子点(Qd800)与抗EGFRvIII单域抗体偶联,该抗体由带有用于位点特异性偶联的额外半胱氨酸的可变区制成(EG2-Cys),与与抗体Fc区偶联的Qd800(EG2-hFc)或未偶联的Qd800相比,在体外可增加其在U87MG-EGFRvIII细胞中的内化。EG2-Cys还改善了原位胶质母细胞瘤小鼠近红外成像的对比度。通过脑切片的荧光显微镜检查证实了积累增加。EG2-Cys在表达EGFRvIII突变受体的脑肿瘤中的特异性可能提供一种准确的、侵入性较小的诊断,并确定肿瘤侵袭性和耐药性水平。