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Evaluation of C-ErbB-2 Overexpression and Her-2/neu Gene Copy Number Heterogeneity in Barrett’s Adenocarcinoma

Amplifiction of the Her-2/neu gene is accompanied by overexpression of its cell surface receptor product, c‐erbB‐2 protein. To investigate the degree of intratumoural heterogeneity we applied immunohistochemistry in primary Barrett’s adenocarcinoma (BCA) (n = 6) and dysplasia adjacent to the carcino...

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Autores principales: Walch, Axel, Bink, Karin, Gais, Peter, Stangl, Stefan, Hutzler, Peter, Aubele, Michaela, Mueller, James, Höfler, Heinz, Werner, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: IOS Press 2000
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4615972/
https://www.ncbi.nlm.nih.gov/pubmed/11007435
http://dx.doi.org/10.1155/2000/947249
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author Walch, Axel
Bink, Karin
Gais, Peter
Stangl, Stefan
Hutzler, Peter
Aubele, Michaela
Mueller, James
Höfler, Heinz
Werner, Martin
author_facet Walch, Axel
Bink, Karin
Gais, Peter
Stangl, Stefan
Hutzler, Peter
Aubele, Michaela
Mueller, James
Höfler, Heinz
Werner, Martin
author_sort Walch, Axel
collection PubMed
description Amplifiction of the Her-2/neu gene is accompanied by overexpression of its cell surface receptor product, c‐erbB‐2 protein. To investigate the degree of intratumoural heterogeneity we applied immunohistochemistry in primary Barrett’s adenocarcinoma (BCA) (n = 6) and dysplasia adjacent to the carcinoma (n = 4). In addition, fluorescence in situ hybridisation (FISH) was performed in primary BCA (n=5) and dysplastic areas (n=4). For an objective evaluation digital image analysis and laser scanning microscopy were used. Five of six BCA showed a marked intratumoural heterogeneous staining pattern ranging from areas in which the tumour cells were negative or faintly positive to tumour areas with a strong staining of the entire membrane. Among the two dysplastic areas also a heterogenous staining pattern was observed. FISH analysis revealed marked heterogeneity of intratumoural gene copy number changes in all BCA showing populations with different fractions of cells with polysomy, low level amplification and high level amplification. One dysplasia showed a minor population with Her‐2/neu signal clusters. In conclusion, we observed marked intratumoural heterogeneity of c‐erbB‐2 protein overexpression and Her‐2/neu gene copy number in the majority of the primary BCA analyzed. Digital image analysis and laser scanning microscopy were helpful in quantifying the variations in protein expression and DNA copy number in individual tumour cells. The observed heterogeneity could hamper the exact diagnostic determination of the c‐erbB‐2 status in small biopsies and possibly influence the effectiveness of a potential c‐erbB‐2 targeting therapy. Figures on http://www.esacp.org/acp/2000/20‐1/walch.htm.
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spelling pubmed-46159722016-01-12 Evaluation of C-ErbB-2 Overexpression and Her-2/neu Gene Copy Number Heterogeneity in Barrett’s Adenocarcinoma Walch, Axel Bink, Karin Gais, Peter Stangl, Stefan Hutzler, Peter Aubele, Michaela Mueller, James Höfler, Heinz Werner, Martin Anal Cell Pathol Other Amplifiction of the Her-2/neu gene is accompanied by overexpression of its cell surface receptor product, c‐erbB‐2 protein. To investigate the degree of intratumoural heterogeneity we applied immunohistochemistry in primary Barrett’s adenocarcinoma (BCA) (n = 6) and dysplasia adjacent to the carcinoma (n = 4). In addition, fluorescence in situ hybridisation (FISH) was performed in primary BCA (n=5) and dysplastic areas (n=4). For an objective evaluation digital image analysis and laser scanning microscopy were used. Five of six BCA showed a marked intratumoural heterogeneous staining pattern ranging from areas in which the tumour cells were negative or faintly positive to tumour areas with a strong staining of the entire membrane. Among the two dysplastic areas also a heterogenous staining pattern was observed. FISH analysis revealed marked heterogeneity of intratumoural gene copy number changes in all BCA showing populations with different fractions of cells with polysomy, low level amplification and high level amplification. One dysplasia showed a minor population with Her‐2/neu signal clusters. In conclusion, we observed marked intratumoural heterogeneity of c‐erbB‐2 protein overexpression and Her‐2/neu gene copy number in the majority of the primary BCA analyzed. Digital image analysis and laser scanning microscopy were helpful in quantifying the variations in protein expression and DNA copy number in individual tumour cells. The observed heterogeneity could hamper the exact diagnostic determination of the c‐erbB‐2 status in small biopsies and possibly influence the effectiveness of a potential c‐erbB‐2 targeting therapy. Figures on http://www.esacp.org/acp/2000/20‐1/walch.htm. IOS Press 2000 2000-01-01 /pmc/articles/PMC4615972/ /pubmed/11007435 http://dx.doi.org/10.1155/2000/947249 Text en Copyright © 2000 Hindawi Publishing Corporation.
spellingShingle Other
Walch, Axel
Bink, Karin
Gais, Peter
Stangl, Stefan
Hutzler, Peter
Aubele, Michaela
Mueller, James
Höfler, Heinz
Werner, Martin
Evaluation of C-ErbB-2 Overexpression and Her-2/neu Gene Copy Number Heterogeneity in Barrett’s Adenocarcinoma
title Evaluation of C-ErbB-2 Overexpression and Her-2/neu Gene Copy Number Heterogeneity in Barrett’s Adenocarcinoma
title_full Evaluation of C-ErbB-2 Overexpression and Her-2/neu Gene Copy Number Heterogeneity in Barrett’s Adenocarcinoma
title_fullStr Evaluation of C-ErbB-2 Overexpression and Her-2/neu Gene Copy Number Heterogeneity in Barrett’s Adenocarcinoma
title_full_unstemmed Evaluation of C-ErbB-2 Overexpression and Her-2/neu Gene Copy Number Heterogeneity in Barrett’s Adenocarcinoma
title_short Evaluation of C-ErbB-2 Overexpression and Her-2/neu Gene Copy Number Heterogeneity in Barrett’s Adenocarcinoma
title_sort evaluation of c-erbb-2 overexpression and her-2/neu gene copy number heterogeneity in barrett’s adenocarcinoma
topic Other
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4615972/
https://www.ncbi.nlm.nih.gov/pubmed/11007435
http://dx.doi.org/10.1155/2000/947249
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