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VLA2 integrin expression in breast carcinomas evaluated by automated and quantitative immunohistochemistry.

VLA2 is thought to be involved in the metastatic process in malignant tumours, in particular in carcinomatous cell adhesion to vessel basement membrane. VLA2 expression was immunohistochemically investigated in 204 breast carcinomas. Frozen tissue sections were probed with monoclonal anti-VLA2 using...

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Autores principales: Charpin, C., Garcia, S., Bergeret, D., Andrac, L., Horschowski, N., Choux, R., Lavaut, M. N.
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1998
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2150386/
https://www.ncbi.nlm.nih.gov/pubmed/9649145
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author Charpin, C.
Garcia, S.
Bergeret, D.
Andrac, L.
Horschowski, N.
Choux, R.
Lavaut, M. N.
author_facet Charpin, C.
Garcia, S.
Bergeret, D.
Andrac, L.
Horschowski, N.
Choux, R.
Lavaut, M. N.
author_sort Charpin, C.
collection PubMed
description VLA2 is thought to be involved in the metastatic process in malignant tumours, in particular in carcinomatous cell adhesion to vessel basement membrane. VLA2 expression was immunohistochemically investigated in 204 breast carcinomas. Frozen tissue sections were probed with monoclonal anti-VLA2 using automated (Ventana ES 320 System) and quantitative (SAMBA 2005 image processor) immunoperoxidase. A positive anti-VLA2 immunoreaction was observed in 48 tumours (23.5%), within epithelial carcinomatous cells. The VLA2-positive surface in tumours varied from 3% to 20% (mean 8.75, S.D. 7.17) and was correlated with histoprognostic indicators and tumour expression of various antigens detected using the same method as that for VLA2. The results show that VLA2 immunoexpression was independent of the tumour size, grade, type and aneuploidy, and of the nodal status. VLA2 significantly correlated with ELAM, VCAM, VLA3 and P-glycoprotein (P-gp) (P < 0.01) and inversely correlated with cathepsin D (P < 0.001), but was independent of Ki67/MIB1, p53, bcl-2, c-erbB-2, E cadherin, CD44v, CD31, oestrogen and progesterone receptors' (ER, PR) antigenic sites and pS2. The exact role, if any, of VLA2 in tumour cell dissemination remains to be elucidated and the clinical relevance of VLA2 immunodetection in breast carcinomas requires further investigation of the correlation between VLA2 immunocytochemical expression and patients' outcome and response to chemotherapy. IMAGES:
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spelling pubmed-21503862009-09-10 VLA2 integrin expression in breast carcinomas evaluated by automated and quantitative immunohistochemistry. Charpin, C. Garcia, S. Bergeret, D. Andrac, L. Horschowski, N. Choux, R. Lavaut, M. N. Br J Cancer Research Article VLA2 is thought to be involved in the metastatic process in malignant tumours, in particular in carcinomatous cell adhesion to vessel basement membrane. VLA2 expression was immunohistochemically investigated in 204 breast carcinomas. Frozen tissue sections were probed with monoclonal anti-VLA2 using automated (Ventana ES 320 System) and quantitative (SAMBA 2005 image processor) immunoperoxidase. A positive anti-VLA2 immunoreaction was observed in 48 tumours (23.5%), within epithelial carcinomatous cells. The VLA2-positive surface in tumours varied from 3% to 20% (mean 8.75, S.D. 7.17) and was correlated with histoprognostic indicators and tumour expression of various antigens detected using the same method as that for VLA2. The results show that VLA2 immunoexpression was independent of the tumour size, grade, type and aneuploidy, and of the nodal status. VLA2 significantly correlated with ELAM, VCAM, VLA3 and P-glycoprotein (P-gp) (P < 0.01) and inversely correlated with cathepsin D (P < 0.001), but was independent of Ki67/MIB1, p53, bcl-2, c-erbB-2, E cadherin, CD44v, CD31, oestrogen and progesterone receptors' (ER, PR) antigenic sites and pS2. The exact role, if any, of VLA2 in tumour cell dissemination remains to be elucidated and the clinical relevance of VLA2 immunodetection in breast carcinomas requires further investigation of the correlation between VLA2 immunocytochemical expression and patients' outcome and response to chemotherapy. IMAGES: Nature Publishing Group 1998-06 /pmc/articles/PMC2150386/ /pubmed/9649145 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
Charpin, C.
Garcia, S.
Bergeret, D.
Andrac, L.
Horschowski, N.
Choux, R.
Lavaut, M. N.
VLA2 integrin expression in breast carcinomas evaluated by automated and quantitative immunohistochemistry.
title VLA2 integrin expression in breast carcinomas evaluated by automated and quantitative immunohistochemistry.
title_full VLA2 integrin expression in breast carcinomas evaluated by automated and quantitative immunohistochemistry.
title_fullStr VLA2 integrin expression in breast carcinomas evaluated by automated and quantitative immunohistochemistry.
title_full_unstemmed VLA2 integrin expression in breast carcinomas evaluated by automated and quantitative immunohistochemistry.
title_short VLA2 integrin expression in breast carcinomas evaluated by automated and quantitative immunohistochemistry.
title_sort vla2 integrin expression in breast carcinomas evaluated by automated and quantitative immunohistochemistry.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2150386/
https://www.ncbi.nlm.nih.gov/pubmed/9649145
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