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本文引用的文献

1
Imaging of EGFR expression in murine xenografts using site-specifically labelled anti-EGFR 111In-DOTA-Z EGFR:2377 Affibody molecule: aspect of the injected tracer amount.使用特异性标记的抗 EGFR 111In-DOTA-Z EGFR:2377 Affibody 分子对小鼠异种移植中的 EGFR 表达进行成像:注射示踪剂量的方面。
Eur J Nucl Med Mol Imaging. 2010 Mar;37(3):613-22. doi: 10.1007/s00259-009-1283-x. Epub 2009 Oct 17.
2
Optical molecular imaging of epidermal growth factor receptor expression to improve detection of oral neoplasia.表皮生长因子受体表达的光学分子成像以改善口腔肿瘤的检测
Neoplasia. 2009 Jun;11(6):542-51. doi: 10.1593/neo.09188.
3
Affibody molecules for epidermal growth factor receptor targeting in vivo: aspects of dimerization and labeling chemistry.用于体内靶向表皮生长因子受体的亲和体分子:二聚化及标记化学方面
J Nucl Med. 2009 Feb;50(2):274-83. doi: 10.2967/jnumed.108.055525. Epub 2009 Jan 21.
4
beta-Galactosidase activity assay using far-red-shifted fluorescent substrate DDAOG.使用远红移荧光底物DDAOG进行β-半乳糖苷酶活性测定。
Anal Biochem. 2009 Mar 1;386(1):59-64. doi: 10.1016/j.ab.2008.11.031. Epub 2008 Dec 3.
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Multimodal nanoprobes for radionuclide and five-color near-infrared optical lymphatic imaging.用于放射性核素和五色近红外光学淋巴成像的多模态纳米探针。
ACS Nano. 2007 Nov;1(4):258-64. doi: 10.1021/nn700062z.
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Selective molecular imaging of viable cancer cells with pH-activatable fluorescence probes.使用pH可激活荧光探针进行活癌细胞的选择性分子成像。
Nat Med. 2009 Jan;15(1):104-9. doi: 10.1038/nm.1854. Epub 2008 Dec 7.
7
Molecular imaging of therapeutic response to epidermal growth factor receptor blockade in colorectal cancer.结直肠癌中表皮生长因子受体阻断治疗反应的分子成像
Clin Cancer Res. 2008 Nov 15;14(22):7413-22. doi: 10.1158/1078-0432.CCR-08-0239.
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Characterization and performance of a near-infrared 2-deoxyglucose optical imaging agent for mouse cancer models.用于小鼠癌症模型的近红外2-脱氧葡萄糖光学成像剂的表征与性能
Anal Biochem. 2009 Jan 15;384(2):254-62. doi: 10.1016/j.ab.2008.09.050. Epub 2008 Oct 7.
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Glucocorticoids antagonize estrogens by glucocorticoid receptor-mediated activation of estrogen sulfotransferase.糖皮质激素通过糖皮质激素受体介导的雌激素磺基转移酶激活来拮抗雌激素。
Cancer Res. 2008 Sep 15;68(18):7386-93. doi: 10.1158/0008-5472.CAN-08-1545.
10
Molecular imaging in drug development.药物研发中的分子成像
Nat Rev Drug Discov. 2008 Jul;7(7):591-607. doi: 10.1038/nrd2290.

利用近红外荧光染料标记的表皮生长因子受体特异性亲和体分子对异种移植瘤进行体内成像。

In vivo imaging of xenograft tumors using an epidermal growth factor receptor-specific affibody molecule labeled with a near-infrared fluorophore.

机构信息

LI-COR Biosciences, Lincoln, NE, USA.

出版信息

Neoplasia. 2010 Feb;12(2):139-49. doi: 10.1593/neo.91446.

DOI:10.1593/neo.91446
PMID:20126472
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2814352/
Abstract

Overexpression of epidermal growth factor receptor (EGFR) is associated with many types of cancers. It is of great interest to noninvasively image the EGFR expression in vivo. In this study, we labeled an EGFR-specific Affibody molecule (Eaff) with a near-infrared (NIR) dye IRDye800CW maleimide and tested the binding of this labeled molecule (Eaff800) in cell culture and xenograft mouse tumor models. Unlike EGF, Eaff did not activate the EGFR signaling pathway. Results showed that Eaff800 was bound and taken up specifically by EGFR-overexpressing A431 cells. When Eaff800 was intravenously injected into nude mice bearing A431 xenograft tumors, the tumor could be identified 1 hour after injection and it became most prominent after 1 day. Images of dissected tissue sections demonstrated that the accumulation of Eaff800 was highest in the liver, followed by the tumor and kidney. Moreover, in combination with a human EGFR type 2 (HER2)-specific probe Haff682, Eaff800 could be used to distinguish between EGFR- and HER2-overexpressing tumors. Interestingly, the organ distribution pattern and the clearance rate of Eaff800 were different from those of Haff682. In conclusion, Eaff molecule labeled with a NIR fluorophore is a promising molecular imaging agent for EGFR-overexpressing tumors.

摘要

表皮生长因子受体 (EGFR) 的过度表达与多种类型的癌症有关。因此,非侵入性地对体内 EGFR 表达进行成像具有重要意义。在这项研究中,我们用近红外染料 IRDye800CW 马来酰亚胺标记了一种 EGFR 特异性的亲和体分子 (Eaff),并在细胞培养和异种移植小鼠肿瘤模型中测试了这种标记分子 (Eaff800) 的结合情况。与 EGF 不同,Eaff 不会激活 EGFR 信号通路。结果表明,Eaff800 被 EGFR 过表达的 A431 细胞特异性结合和摄取。当 Eaff800 被静脉注射到携带 A431 异种移植肿瘤的裸鼠体内时,肿瘤在注射后 1 小时即可被识别,1 天后最为明显。对组织切片的图像分析表明,Eaff800 在肝脏中的积累最高,其次是肿瘤和肾脏。此外,与一种人表皮生长因子受体 2 (HER2) 特异性探针 Haff682 结合使用时,Eaff800 可用于区分 EGFR 和 HER2 过表达的肿瘤。有趣的是,Eaff800 的器官分布模式和清除率与 Haff682 不同。总之,用近红外荧光染料标记的 Eaff 分子是一种很有前途的用于 EGFR 过表达肿瘤的分子成像剂。