Hernandez Reinier, Sun Haiyan, England Christopher G, Valdovinos Hector F, Barnhart Todd E, Yang Yunan, Cai Weibo
Department of Medical Physics, University of Wisconsin , Madison, Wisconsin 53705, United States.
Department of Radiology, University of Wisconsin , Madison, Wisconsin 53705, United States.
Mol Pharm. 2016 Jul 5;13(7):2563-70. doi: 10.1021/acs.molpharmaceut.6b00372. Epub 2016 Jun 10.
Recently, the overexpression of CD146 and its potential as a therapeutic target in high-grade gliomas, the most lethal type of brain cancer, was uncovered. In this study, we describe the generation of (89)Zr-Df-YY146, a novel (89)Zr-labeled monoclonal antibody (mAb) for the targeting and quantification of CD146 expression in a mouse model of glioblastoma, using noninvasive immunoPET imaging. YY146, a high affinity anti-CD146 mAb, was conjugated to deferoxamine (Df) for labeling with the long-lived positron emitter (89)Zr (t1/2: 78.4 h). In vitro assays, including flow cytometry, immunofluorescence microscopy, and Western blot, were performed with two glioblastoma cell lines, U87MG and U251, to determine their CD146 expression levels. Also, YY146 and Df-YY146's CD146-binding affinities were compared using flow cytometry. In vivo CD146-targeting of (89)Zr-Df-YY146 was evaluated by sequential PET imaging, in athymic nude mice bearing subcutaneously implanted U87MG or U251 tumors. CD146 blocking, ex vivo biodistribution, and histological studies were carried out to confirm (89)Zr-Df-YY146 specificity, as well as the accuracy of PET data. In vitro studies exposed elevated CD146 expression levels in U87MG cells, but negligible levels in U251 cells. Flow cytometry revealed no differences in affinity between YY146 and Df-YY146. (89)Zr labeling of Df-YY146 proceeded with excellent yield (∼80%), radiochemical purity (>95%), and specific activity (∼44 GBq/μmol). Longitudinal PET revealed prominent and persistent (89)Zr-Df-YY146 uptake in mice bearing U87MG tumors that peaked at 14.00 ± 3.28%ID/g (n = 4), 48 h post injection of the tracer. Conversely, uptake was significantly lower in CD146-negative U251 tumors (5.15 ± 0.99%ID/g, at 48 h p.i.; n = 4; P < 0.05). Uptake in U87MG tumors was effectively blocked in a competitive inhibition experiment, corroborating the CD146 specificity of (89)Zr-Df-YY146. Finally, ex vivo biodistribution validated the accuracy of PET data and histological examination successfully correlated tracer uptake with in situ CD146 expression. Prominent, persistent, and specific uptake of (89)Zr-Df-YY146 was observed in brain tumors, demonstrating the potential of this radiotracer for noninvasive PET imaging of CD146 expression. In a future clinical scenario, (89)Zr-Df-YY146 may serve as a tool to guide intervention and assess response to CD146-targeted therapies.
最近,人们发现了CD146的过表达及其作为最致命的脑癌类型——高级别胶质瘤治疗靶点的潜力。在本研究中,我们描述了(89)Zr-Df-YY146的生成,这是一种新型的(89)Zr标记单克隆抗体(mAb),用于通过无创免疫PET成像在胶质母细胞瘤小鼠模型中靶向和定量CD146表达。YY146是一种高亲和力抗CD146 mAb,与去铁胺(Df)偶联,用于用长寿命正电子发射体(89)Zr(半衰期:78.4小时)进行标记。使用两种胶质母细胞瘤细胞系U87MG和U251进行了包括流式细胞术、免疫荧光显微镜和蛋白质印迹在内的体外试验,以确定它们的CD146表达水平。此外,使用流式细胞术比较了YY146和Df-YY146与CD146的结合亲和力。通过连续PET成像评估了(89)Zr-Df-YY146在皮下植入U87MG或U251肿瘤的无胸腺裸鼠体内对CD146的靶向性。进行了CD146阻断、离体生物分布和组织学研究,以确认(89)Zr-Df-YY146的特异性以及PET数据的准确性。体外研究显示U87MG细胞中CD146表达水平升高,但U251细胞中的水平可忽略不计。流式细胞术显示YY146和Df-YY146之间的亲和力没有差异。Df-YY146的(89)Zr标记产率极高(约80%)、放射化学纯度(>95%)和比活度(约44 GBq/μmol)。纵向PET显示,在注射示踪剂后48小时,携带U87MG肿瘤的小鼠体内(89)Zr-Df-YY146摄取显著且持续,峰值为14.00±3.28%ID/g(n = 4)。相反,在CD146阴性的U251肿瘤中摄取显著较低(注射后48小时为5.15±0.99%ID/g;n = 4;P < 0.05)。在竞争性抑制实验中,U87MG肿瘤中的摄取被有效阻断,证实了(89)Zr-Df-YY146对CD146的特异性。最后,离体生物分布验证了PET数据的准确性,组织学检查成功地将示踪剂摄取与原位CD146表达相关联。在脑肿瘤中观察到(89)Zr-Df-YY146有显著、持续和特异性摄取,证明了这种放射性示踪剂用于CD146表达无创PET成像的潜力。在未来的临床场景中,(89)Zr-Df-YY146可能作为一种工具来指导干预并评估对CD146靶向治疗的反应。