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Epidermal growth factor receptor in ovarian tumours: correlation of immunohistochemistry with ligand binding assay.

Epidermal growth factor receptor (EGFR) was studied in ovarian tumours with immunohistochemical (IH) and ligand-binding assay (LBA). Two different monoclonal antibodies (MoAbs: 2E9, EGFR1) with respect to detecting EGFR with different ligand-binding affinities (low, high and low) were used. When com...

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Autores principales: Henzen-Logmans, S. C., Berns, E. M., Klijn, J. G., van der Burg, M. E., Foekens, J. A.
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1992
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1978035/
https://www.ncbi.nlm.nih.gov/pubmed/1457340
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author Henzen-Logmans, S. C.
Berns, E. M.
Klijn, J. G.
van der Burg, M. E.
Foekens, J. A.
author_facet Henzen-Logmans, S. C.
Berns, E. M.
Klijn, J. G.
van der Burg, M. E.
Foekens, J. A.
author_sort Henzen-Logmans, S. C.
collection PubMed
description Epidermal growth factor receptor (EGFR) was studied in ovarian tumours with immunohistochemical (IH) and ligand-binding assay (LBA). Two different monoclonal antibodies (MoAbs: 2E9, EGFR1) with respect to detecting EGFR with different ligand-binding affinities (low, high and low) were used. When comparing the IH data of MoAbs, 2E9 and EGFR1 a significant correlation was found (2P < 0.0001). Both antibodies stained 77% of the adenocarcinoma samples. The incidence of positivity as well as the mean percentage of stained cells was increased in metastases when compared with primary lesions. In 12.5% overexpression of EGFR (score 3) was noticed in some of the tumour cells. This was not due to amplification of the EGFR gene in any of the 25 ovarian tumours studied (including 6 which showed high expression of EGFR in IH). EGFR was detected in 66% of the adenocarcinomas analysed with LBA. A statistically significant correlation was found between the maximum binding capacities of EGFR obtained from Scatchard plots and the percentage of positive tumour cells determined by MoAb EGFR1 (2P < 0.0001). A weaker correlation was found between the reactivity of MoAb 2E9 and LBA (2P < 0.1). Clinical studies are necessary to determine the possible prognostic impact of EGFR determined with either method, or whether a combination of both will give a better discrimination between high- and low-risk patients. IMAGES:
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spelling pubmed-19780352009-09-10 Epidermal growth factor receptor in ovarian tumours: correlation of immunohistochemistry with ligand binding assay. Henzen-Logmans, S. C. Berns, E. M. Klijn, J. G. van der Burg, M. E. Foekens, J. A. Br J Cancer Research Article Epidermal growth factor receptor (EGFR) was studied in ovarian tumours with immunohistochemical (IH) and ligand-binding assay (LBA). Two different monoclonal antibodies (MoAbs: 2E9, EGFR1) with respect to detecting EGFR with different ligand-binding affinities (low, high and low) were used. When comparing the IH data of MoAbs, 2E9 and EGFR1 a significant correlation was found (2P < 0.0001). Both antibodies stained 77% of the adenocarcinoma samples. The incidence of positivity as well as the mean percentage of stained cells was increased in metastases when compared with primary lesions. In 12.5% overexpression of EGFR (score 3) was noticed in some of the tumour cells. This was not due to amplification of the EGFR gene in any of the 25 ovarian tumours studied (including 6 which showed high expression of EGFR in IH). EGFR was detected in 66% of the adenocarcinomas analysed with LBA. A statistically significant correlation was found between the maximum binding capacities of EGFR obtained from Scatchard plots and the percentage of positive tumour cells determined by MoAb EGFR1 (2P < 0.0001). A weaker correlation was found between the reactivity of MoAb 2E9 and LBA (2P < 0.1). Clinical studies are necessary to determine the possible prognostic impact of EGFR determined with either method, or whether a combination of both will give a better discrimination between high- and low-risk patients. IMAGES: Nature Publishing Group 1992-12 /pmc/articles/PMC1978035/ /pubmed/1457340 Text en https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Research Article
Henzen-Logmans, S. C.
Berns, E. M.
Klijn, J. G.
van der Burg, M. E.
Foekens, J. A.
Epidermal growth factor receptor in ovarian tumours: correlation of immunohistochemistry with ligand binding assay.
title Epidermal growth factor receptor in ovarian tumours: correlation of immunohistochemistry with ligand binding assay.
title_full Epidermal growth factor receptor in ovarian tumours: correlation of immunohistochemistry with ligand binding assay.
title_fullStr Epidermal growth factor receptor in ovarian tumours: correlation of immunohistochemistry with ligand binding assay.
title_full_unstemmed Epidermal growth factor receptor in ovarian tumours: correlation of immunohistochemistry with ligand binding assay.
title_short Epidermal growth factor receptor in ovarian tumours: correlation of immunohistochemistry with ligand binding assay.
title_sort epidermal growth factor receptor in ovarian tumours: correlation of immunohistochemistry with ligand binding assay.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1978035/
https://www.ncbi.nlm.nih.gov/pubmed/1457340
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