Mol Imaging. 2013 Jun;12(4):244-56.
Imaging tumors and their response to treatment could be a valuable biomarker toward early assessment of therapy in patients with cancer. Phosphatidylserine (PS) is confined to the inner leaflet of the plasma membrane in normal cells but is externalized on tumor vascular endothelial cells (ECs) and tumor cells, and PS exposure is further enhanced in response to radiation and chemotherapy. In the present study, we evaluated the potential of a PS-targeting human F(ab')2 antibody fragment, PGN650, to detect exposure of PS in tumor-bearing mice. Tumor uptake of PGN650 was measured by near-infrared optical imaging in human tumor xenografts in immunodeficient mice. PGN650 specifically targeted tumors and was shown to target CD31-positive ECs and tumor cells. Tumor uptake of PGN650 was significantly higher in animals pretreated with docetaxel. The peak tumor to normal tissue (T/N) ratio of probe was observed at 24 hours postinjection of probe, and tumor binding was detected for at least 120 hours. In repeat dose studies, PGN650 uptake in tumors was significantly higher following pretreatment with docetaxel compared to baseline uptake prior to treatment. PGN650 may be a useful probe to detect PS exposed in tumors and to monitor enhanced PS exposure to optimize therapeutic agents to treat tumors.
成像肿瘤及其对治疗的反应可能是癌症患者早期评估治疗的有价值的生物标志物。磷脂酰丝氨酸(PS)在正常细胞中局限于质膜的内小叶,但在外化在肿瘤血管内皮细胞(EC)和肿瘤细胞上,并且 PS 的暴露在辐射和化疗的反应中进一步增强。在本研究中,我们评估了 PS 靶向人 F(ab')2 抗体片段 PGN650 检测荷瘤小鼠 PS 暴露的潜力。通过近红外光学成像测量免疫缺陷小鼠人肿瘤异种移植物中的 PGN650 摄取。PGN650 特异性靶向肿瘤,并显示靶向 CD31 阳性 EC 和肿瘤细胞。在预先用多西紫杉醇处理的动物中,PGN650 的肿瘤摄取显著增加。在探针注射后 24 小时观察到探针的峰值肿瘤与正常组织(T/N)比,并且肿瘤结合至少可检测 120 小时。在重复剂量研究中,与治疗前基线摄取相比,多西紫杉醇预处理后肿瘤中 PGN650 的摄取显著增加。PGN650 可能是一种有用的探针,用于检测肿瘤中暴露的 PS,并监测增强的 PS 暴露以优化治疗剂来治疗肿瘤。