In vivo imaging of prostate cancer using an anti-PSMA scFv fragment as a probe

体内 前列腺癌 LNCaP公司 谷氨酸羧肽酶Ⅱ 癌症研究 前列腺 分子成像 临床前影像学 抗体 荧光 化学 体外 荧光寿命成像显微镜 分子生物学 病理 癌症 医学 生物 免疫学 生物化学 内科学 物理 生物技术 量子力学
作者
Claire Mazzocco,Giulio Fracasso,Coralie Genevois,Nathalie Dugot‐Senant,Mariangela Figini,Marco Colombatti,N. Grenier,Franck Couillaud
出处
期刊:Scientific Reports [Springer Nature]
卷期号:6 (1) 被引量:35
标识
DOI:10.1038/srep23314
摘要

Abstract We aimed to evaluate a fluorescent-labeled single chain variable fragment (scFv) of the anti-PSMA antibody as a specific probe for the detection of prostate cancer by in vivo fluorescence imaging. An orthotopic model of prostate cancer was generated by injecting LNCaP cells into the prostate lobe. ScFvD2B, a high affinity anti-PSMA antibody fragment, was labeled using a near-infrared fluorophore to generate a specific imaging probe (X770-scFvD2B). PSMA-unrelated scFv-X770 was used as a control. Probes were injected intravenously into mice with prostate tumors and fluorescence was monitored in vivo by fluorescence molecular tomography (FMT). In vitro assays showed that X770-scFvD2B specifically bound to PSMA and was internalized in PSMA-expressing LNCaP cells. After intravenous injection, X770-scFvD2B was detected in vivo by FMT in the prostate region. On excised prostates the scFv probe co-localized with the cancer cells and was found in PSMA-expressing cells. The PSMA-unrelated scFv used as a control did not label the prostate cancer cells. Our data demonstrate that scFvD2B is a high affinity contrast agent for in vivo detection of PSMA-expressing cells in the prostate. NIR-labeled scFvD2B could thus be further developed as a clinical probe for imaging-guided targeted biopsies.

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