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Changes in expression of alpha 6/beta 4 integrin heterodimer in primary and metastatic breast cancer.

The alpha 6/beta 4 integrin complex has been shown to be expressed in murine tissues at the basolateral aspect of most epithelial cells including the mammary epithelium, thus suggesting that this heterodimer may interact with components of the basement membrane. Because transformation of mammary epi...

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Autores principales: Natali, P. G., Nicotra, M. R., Botti, C., Mottolese, M., Bigotti, A., Segatto, O.
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1992
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1977802/
https://www.ncbi.nlm.nih.gov/pubmed/1503905
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author Natali, P. G.
Nicotra, M. R.
Botti, C.
Mottolese, M.
Bigotti, A.
Segatto, O.
author_facet Natali, P. G.
Nicotra, M. R.
Botti, C.
Mottolese, M.
Bigotti, A.
Segatto, O.
author_sort Natali, P. G.
collection PubMed
description The alpha 6/beta 4 integrin complex has been shown to be expressed in murine tissues at the basolateral aspect of most epithelial cells including the mammary epithelium, thus suggesting that this heterodimer may interact with components of the basement membrane. Because transformation of mammary epithelium frequently results in disappearance of basement membranes and loss of cell polarisation we have analysed in the present study whether expression of the alpha 6/beta 4 complex is altered in human breast tumours. The results of the present study confirm that in human mammary gland alpha 6 and beta 4 subunits colocalise at the basolateral aspect of the epithelium. While in benign breast lesions this distribution pattern remains mostly unchanged, in primary carcinomas the expression of both chains is either redistributed over the cells surface or significantly reduced. This altered pattern of expression is paralleled by the lack of detection of basement membrane laminin and collagen type IV. In metastatic lesions the expression of the heterodimer is maintained in most of the lymphnodal foci, but less frequently detected in metastasis localised in the pleural cavity and in parenchymal tissues. These findings indicate that in breast epithelium expression of the alpha 6/beta 4 heterodimer is modulated by the presence of basement membrane and is possibly influenced by microenvironmental factors as suggested by the different pattern of alpha 6/beta 4 expression in nodal and extranodal metastatic foci. IMAGES:
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spelling pubmed-19778022009-09-10 Changes in expression of alpha 6/beta 4 integrin heterodimer in primary and metastatic breast cancer. Natali, P. G. Nicotra, M. R. Botti, C. Mottolese, M. Bigotti, A. Segatto, O. Br J Cancer Research Article The alpha 6/beta 4 integrin complex has been shown to be expressed in murine tissues at the basolateral aspect of most epithelial cells including the mammary epithelium, thus suggesting that this heterodimer may interact with components of the basement membrane. Because transformation of mammary epithelium frequently results in disappearance of basement membranes and loss of cell polarisation we have analysed in the present study whether expression of the alpha 6/beta 4 complex is altered in human breast tumours. The results of the present study confirm that in human mammary gland alpha 6 and beta 4 subunits colocalise at the basolateral aspect of the epithelium. While in benign breast lesions this distribution pattern remains mostly unchanged, in primary carcinomas the expression of both chains is either redistributed over the cells surface or significantly reduced. This altered pattern of expression is paralleled by the lack of detection of basement membrane laminin and collagen type IV. In metastatic lesions the expression of the heterodimer is maintained in most of the lymphnodal foci, but less frequently detected in metastasis localised in the pleural cavity and in parenchymal tissues. These findings indicate that in breast epithelium expression of the alpha 6/beta 4 heterodimer is modulated by the presence of basement membrane and is possibly influenced by microenvironmental factors as suggested by the different pattern of alpha 6/beta 4 expression in nodal and extranodal metastatic foci. IMAGES: Nature Publishing Group 1992-08 /pmc/articles/PMC1977802/ /pubmed/1503905 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
Natali, P. G.
Nicotra, M. R.
Botti, C.
Mottolese, M.
Bigotti, A.
Segatto, O.
Changes in expression of alpha 6/beta 4 integrin heterodimer in primary and metastatic breast cancer.
title Changes in expression of alpha 6/beta 4 integrin heterodimer in primary and metastatic breast cancer.
title_full Changes in expression of alpha 6/beta 4 integrin heterodimer in primary and metastatic breast cancer.
title_fullStr Changes in expression of alpha 6/beta 4 integrin heterodimer in primary and metastatic breast cancer.
title_full_unstemmed Changes in expression of alpha 6/beta 4 integrin heterodimer in primary and metastatic breast cancer.
title_short Changes in expression of alpha 6/beta 4 integrin heterodimer in primary and metastatic breast cancer.
title_sort changes in expression of alpha 6/beta 4 integrin heterodimer in primary and metastatic breast cancer.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1977802/
https://www.ncbi.nlm.nih.gov/pubmed/1503905
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