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EpCAM 靶向适体放射性探针用于肿瘤特异性 PET 成像。

EpCAM-Targeting Aptamer Radiotracer for Tumor-Specific PET Imaging.

出版信息

Bioconjug Chem. 2021 Jun 16;32(6):1139-1145. doi: 10.1021/acs.bioconjchem.1c00188. Epub 2021 May 20.

Abstract

Noninvasive in vivo imaging to measure the expression of EpCAM, a biomarker overexpressed in the majority of carcinoma tumors and metastatic lesions, is highly desirable for accurate tumor staging and therapy evaluation. Here, we report the use of an aptamer radiotracer to enable tumor-specific EpCAM-targeting PET imaging. Oligonucleotide aptamers are small molecular ligands that specifically bind with high affinity to their target molecules. For specific tumor imaging, an aptamer radiotracer was formulated by chelating a Cu isotope and DOTA-PEGylated aptamer sequence to target EpCAM. In vitro cell uptake assays demonstrated that the aptamer radiotracer specifically bound EpCAM-expressing breast cancer cells but did not react with off-target tumor cells. For in vivo tumor imaging, aptamer radiotracer was systemically administered into xenograft mice. MicroPET/CT scans revealed that the aptamer radiotracer rapidly highlighted xenograft tumors derived from MDA-MB-231 breast cancer cells (EpCAM positive) as early as 2 h postadministration with a gradually increasing tumor uptake signal that peaked at 24 h but not in lymphoma 937 tumors (EpCAM negative). In contrast, nonspecific background signals in the liver and kidneys were rapidly decreased postadministration. This proof-of-concept study demonstrates the utility of aptamer radiotracers for tumor-specific PET imaging.

摘要

非侵入性活体成像技术可用于测量 EpCAM 的表达,EpCAM 在大多数癌肿瘤和转移性病变中过表达,这种技术对于准确的肿瘤分期和治疗评估非常理想。在此,我们报告了使用适体放射性示踪剂进行肿瘤特异性 EpCAM 靶向 PET 成像。寡核苷酸适体是能够与靶分子特异性结合的小分子配体,亲和力高。对于特定的肿瘤成像,通过螯合 Cu 同位素和 DOTA-PEG 化适体序列来靶向 EpCAM,来制备适体放射性示踪剂。体外细胞摄取实验表明,适体放射性示踪剂特异性地与表达 EpCAM 的乳腺癌细胞结合,但不与非靶肿瘤细胞反应。对于体内肿瘤成像,将适体放射性示踪剂系统地给予异种移植小鼠。MicroPET/CT 扫描显示,适体放射性示踪剂在给药后 2 小时内迅速突出了源自 MDA-MB-231 乳腺癌细胞(EpCAM 阳性)的异种移植肿瘤,肿瘤摄取信号逐渐增加,在 24 小时达到峰值,但在淋巴瘤 937 肿瘤(EpCAM 阴性)中没有。相比之下,给药后肝和肾中的非特异性背景信号迅速下降。这项概念验证研究证明了适体放射性示踪剂用于肿瘤特异性 PET 成像的效用。

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