Suppr超能文献

使用异硫氰酸荧光素标记的上皮细胞粘附分子(EpCAM)和表皮生长因子受体(EGF-R)抗体,在细胞系和肿瘤活检中对头颈部恶性肿瘤进行共聚焦激光内镜检查。

Confocal laser endomicroscopy in head and neck malignancies using FITC-labelled EpCAM- and EGF-R-antibodies in cell lines and tumor biopsies.

作者信息

Englhard Anna S, Palaras Alexander, Volgger Veronika, Stepp Herbert, Mack Brigitte, Libl Darko, Gires Olivier, Betz Christian S

机构信息

Department of Otorhinolaryngology-Head and Neck Surgery, Klinikum der Universität München, Marchioninistr. 15, 81377, Munich, Germany.

Laser-Forschungslabor, LIFE-Zentrum, Klinikum der Universität München, Feodor-Lynen-Str. 19, 81377, Munich, Germany.

出版信息

J Biophotonics. 2017 Oct;10(10):1365-1376. doi: 10.1002/jbio.201600238. Epub 2017 Jan 20.

Abstract

Intraoperative detection of residual malignant cells at tumor margins following excision of primary tumors could help improving surgery and thus patients' outcome. The feasibility of the tumor antigens epidermal growth factor receptor (EGF-R) and epithelial cell adhesion molecule (EpCAM) for antibody-dependent confocal laser scanning endomicroscopy (CLE)-mediated visualization of malignant cells was addressed. Both tumor antigens are highly and frequently expressed in the majority of carcinomas, including head and neck squamous cell carcinomas (HNSCC), and represent prognostic and therapeutic tumor target molecules. FITC-conjugated EGF-R- and EpCAM-specific antibodies served as molecular tools for the detection of antigen-positive cells using the CLE technology. Specificity of both antibodies and their ability to discriminate tumor from non-tumor cells were assessed in vitro with human fibroblasts and PCI-1 HNSCC cell lines, and ex vivo on primary HNSCC samples (n = 11) and healthy mucosa (n = 5). Antigen specificity of the used EpCAM-specific antibody was superior to that of the EGF-R-specific antibody both in vitro and ex vivo (100% vs. 31.25%), and allowed visualization of cellular structures in CLE measurements. These results hold promise for possible future applications in humans.

摘要

在原发性肿瘤切除后术中检测肿瘤边缘残留的恶性细胞有助于改善手术效果,从而提高患者的预后。本研究探讨了肿瘤抗原表皮生长因子受体(EGF-R)和上皮细胞黏附分子(EpCAM)用于抗体依赖性共聚焦激光扫描内镜(CLE)介导的恶性细胞可视化的可行性。这两种肿瘤抗原在大多数癌症中均高表达且表达频率高,包括头颈部鳞状细胞癌(HNSCC),并且代表预后和治疗的肿瘤靶分子。异硫氰酸荧光素(FITC)偶联的EGF-R和EpCAM特异性抗体用作利用CLE技术检测抗原阳性细胞的分子工具。在体外使用人成纤维细胞和PCI-1 HNSCC细胞系,以及在原发性HNSCC样本(n = 11)和健康黏膜(n = 5)上进行离体实验,评估了两种抗体的特异性及其区分肿瘤细胞与非肿瘤细胞的能力。所用EpCAM特异性抗体的抗原特异性在体外和离体实验中均优于EGF-R特异性抗体(100%对31.25%),并能在CLE测量中可视化细胞结构。这些结果为未来在人体中的可能应用带来了希望。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验