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Laminin activates the p185HER2 oncoprotein and mediates growth inhibition of breast carcinoma cells.
The interaction between laminin and the oncoprotein encoded by the c-erbB-2 oncogene was studied in vitro and in vivo in human breast carcinomas. In vitro analysis of breast carcinoma cell lines overexpressing p185HER2 revealed that laminin, but not fibronectin, induced tyrosine phosphorylation and...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
1996
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2074760/ https://www.ncbi.nlm.nih.gov/pubmed/8912540 |
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author | Tagliabue, E. Ardini, E. Pellegrini, R. Campiglio, M. Bufalino, R. Jeschke, M. Groner, B. Colnaghi, M. I. Ménard, S. |
author_facet | Tagliabue, E. Ardini, E. Pellegrini, R. Campiglio, M. Bufalino, R. Jeschke, M. Groner, B. Colnaghi, M. I. Ménard, S. |
author_sort | Tagliabue, E. |
collection | PubMed |
description | The interaction between laminin and the oncoprotein encoded by the c-erbB-2 oncogene was studied in vitro and in vivo in human breast carcinomas. In vitro analysis of breast carcinoma cell lines overexpressing p185HER2 revealed that laminin, but not fibronectin, induced tyrosine phosphorylation and down-modulation of oncoprotein membrane expression. Laminin also specifically inhibited growth of p185HER2-positive cell lines. No direct binding between the recombinant extracellular domain of p185HER2 and laminin was found. Induction of oncoprotein down-modulation by anti-integrin antibodies and coprecipitation of the oncoprotein with the beta 4 integrin subunit indicate that the interaction between p185HER2 and laminin occurs through integrin molecules. The relevance of this in vitro observation was verified in vivo by analysing the prognostic value of p185HER2 overexpression as a function of laminin production on archival paraffin-embedded sections of 887 primary breast tumours. The results revealed an association between p185HER2 overexpression and unfavourable prognosis in tumours negative for laminin production, whereas in laminin-producing tumours, the oncoprotein overexpression was not associated with tumour aggressiveness. IMAGES: |
format | Text |
id | pubmed-2074760 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1996 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-20747602009-09-10 Laminin activates the p185HER2 oncoprotein and mediates growth inhibition of breast carcinoma cells. Tagliabue, E. Ardini, E. Pellegrini, R. Campiglio, M. Bufalino, R. Jeschke, M. Groner, B. Colnaghi, M. I. Ménard, S. Br J Cancer Research Article The interaction between laminin and the oncoprotein encoded by the c-erbB-2 oncogene was studied in vitro and in vivo in human breast carcinomas. In vitro analysis of breast carcinoma cell lines overexpressing p185HER2 revealed that laminin, but not fibronectin, induced tyrosine phosphorylation and down-modulation of oncoprotein membrane expression. Laminin also specifically inhibited growth of p185HER2-positive cell lines. No direct binding between the recombinant extracellular domain of p185HER2 and laminin was found. Induction of oncoprotein down-modulation by anti-integrin antibodies and coprecipitation of the oncoprotein with the beta 4 integrin subunit indicate that the interaction between p185HER2 and laminin occurs through integrin molecules. The relevance of this in vitro observation was verified in vivo by analysing the prognostic value of p185HER2 overexpression as a function of laminin production on archival paraffin-embedded sections of 887 primary breast tumours. The results revealed an association between p185HER2 overexpression and unfavourable prognosis in tumours negative for laminin production, whereas in laminin-producing tumours, the oncoprotein overexpression was not associated with tumour aggressiveness. IMAGES: Nature Publishing Group 1996-11 /pmc/articles/PMC2074760/ /pubmed/8912540 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 Tagliabue, E. Ardini, E. Pellegrini, R. Campiglio, M. Bufalino, R. Jeschke, M. Groner, B. Colnaghi, M. I. Ménard, S. Laminin activates the p185HER2 oncoprotein and mediates growth inhibition of breast carcinoma cells. |
title | Laminin activates the p185HER2 oncoprotein and mediates growth inhibition of breast carcinoma cells. |
title_full | Laminin activates the p185HER2 oncoprotein and mediates growth inhibition of breast carcinoma cells. |
title_fullStr | Laminin activates the p185HER2 oncoprotein and mediates growth inhibition of breast carcinoma cells. |
title_full_unstemmed | Laminin activates the p185HER2 oncoprotein and mediates growth inhibition of breast carcinoma cells. |
title_short | Laminin activates the p185HER2 oncoprotein and mediates growth inhibition of breast carcinoma cells. |
title_sort | laminin activates the p185her2 oncoprotein and mediates growth inhibition of breast carcinoma cells. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2074760/ https://www.ncbi.nlm.nih.gov/pubmed/8912540 |
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