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

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Confocal laser endomicroscopy in head and neck malignancies using FITC-labelled EpCAM- and EGF-R-antibodies in cell lines and tumor biopsies. / Englhard, Anna S; Palaras, Alexander; Volgger, Veronika; Stepp, Herbert; Mack, Brigitte; Libl, Darko; Gires, Olivier; Betz, Christian S.

In: J BIOPHOTONICS, Vol. 10, No. 10, 10.2017, p. 1365-1376.

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@article{bd04e7efa797432c92ebcaa4d8ae04ee,
title = "Confocal laser endomicroscopy in head and neck malignancies using FITC-labelled EpCAM- and EGF-R-antibodies in cell lines and tumor biopsies",
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.",
keywords = "Antibodies, Antibody Specificity, Biopsy, Carcinoma, Squamous Cell, Cell Line, Tumor, Epithelial Cell Adhesion Molecule, Fluorescein-5-isothiocyanate, Head and Neck Neoplasms, Humans, Lasers, Microscopy, Confocal, Receptor, Epidermal Growth Factor, Journal Article",
author = "Englhard, {Anna S} and Alexander Palaras and Veronika Volgger and Herbert Stepp and Brigitte Mack and Darko Libl and Olivier Gires and Betz, {Christian S}",
note = "{\textcopyright} 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.",
year = "2017",
month = oct,
doi = "10.1002/jbio.201600238",
language = "English",
volume = "10",
pages = "1365--1376",
journal = "J BIOPHOTONICS",
issn = "1864-063X",
publisher = "Wiley-VCH Verlag GmbH",
number = "10",

}

RIS

TY - JOUR

T1 - Confocal laser endomicroscopy in head and neck malignancies using FITC-labelled EpCAM- and EGF-R-antibodies in cell lines and tumor biopsies

AU - Englhard, Anna S

AU - Palaras, Alexander

AU - Volgger, Veronika

AU - Stepp, Herbert

AU - Mack, Brigitte

AU - Libl, Darko

AU - Gires, Olivier

AU - Betz, Christian S

N1 - © 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

PY - 2017/10

Y1 - 2017/10

N2 - 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.

AB - 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.

KW - Antibodies

KW - Antibody Specificity

KW - Biopsy

KW - Carcinoma, Squamous Cell

KW - Cell Line, Tumor

KW - Epithelial Cell Adhesion Molecule

KW - Fluorescein-5-isothiocyanate

KW - Head and Neck Neoplasms

KW - Humans

KW - Lasers

KW - Microscopy, Confocal

KW - Receptor, Epidermal Growth Factor

KW - Journal Article

U2 - 10.1002/jbio.201600238

DO - 10.1002/jbio.201600238

M3 - SCORING: Journal article

C2 - 28106950

VL - 10

SP - 1365

EP - 1376

JO - J BIOPHOTONICS

JF - J BIOPHOTONICS

SN - 1864-063X

IS - 10

ER -