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Targeting Prostate Cancer Cells In Vivo Using a Rapidly Internalizing Novel Human Single-Chain Antibody Fragment

机译:使用快速内在化的新型人单链抗体片段体内靶向前列腺癌细胞

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摘要

Human antibodies targeting prostate cancer cell surface epitopes may be useful for imaging and therapy. The objective of this study was to evaluate the tumor targeting of an internalizing human antibody fragment, a small-size platform, to provide high contrast in a mouse model of human prostate carcinoma.MethodsA prostate tumor-targeting single-chain antibody fragment (scFv), UA20, along with a nonbinding control scFv, N3M2, were labeled with 99mTc and evaluated for binding and rapid internalization into human prostate tumor cells in vitro and tumor homing in vivo using xenograft models. For the in vitro studies, the labeled UA20 scFv was incubated at 37°C for 1 h with metastatic prostate cancer cells (DU145) to assess the total cellular uptake versus intracellular uptake. For the animal studies, labeled UA20 and N3M2 scFvs were administered to athymic mice implanted subcutaneously with DU145 cells. Mice were imaged with small-animal SPECT/CT with concomitant biodistribution at 1 and 3 h after injection.
机译:靶向前列腺癌细胞表面表位的人抗体可能对成像和治疗有用。这项研究的目的是评估内在化的人类抗体片段(一种小型平台)的肿瘤靶向性,以在人类前列腺癌的小鼠模型中提供高对比。方法靶向前列腺肿瘤的单链抗体片段(scFv) ,UA20和非结合性对照scFv N3M2用 99m Tc标记,并在体外和体内异种移植模型中评估其在人前列腺肿瘤细胞中的结合和快速内在化。对于体外研究,将标记的UA20 scFv与转移性前列腺癌细胞(DU145)在37°C孵育1小时,以评估总细胞摄取与细胞内摄取的关系。对于动物研究,将标记的UA20和N3M2 scFvs施用至皮下植入DU145细胞的无胸腺小鼠。小鼠在注射后1和3小时用小动物SPECT / CT成像,并伴随生物分布。

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