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Caveolin 1 and Caveolin 2 are associated with breast cancer basal-like and triple-negative immunophenotype

Caveolin-1 (CAV1) and caveolin 2 (CAV2) are the principal structural proteins of caveolae, sphingolipid and cholesterol-rich invaginations of the plasma membrane involved in vesicular trafficking and signal transduction. Over the recent years there has been controversy about their role in breast can...

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Autores principales: Elsheikh, S E, Green, A R, Rakha, E A, Samaka, R M, Ammar, A A, Powe, D, Reis-Filho, J S, Ellis, I O
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2480981/
https://www.ncbi.nlm.nih.gov/pubmed/18612310
http://dx.doi.org/10.1038/sj.bjc.6604463
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author Elsheikh, S E
Green, A R
Rakha, E A
Samaka, R M
Ammar, A A
Powe, D
Reis-Filho, J S
Ellis, I O
author_facet Elsheikh, S E
Green, A R
Rakha, E A
Samaka, R M
Ammar, A A
Powe, D
Reis-Filho, J S
Ellis, I O
author_sort Elsheikh, S E
collection PubMed
description Caveolin-1 (CAV1) and caveolin 2 (CAV2) are the principal structural proteins of caveolae, sphingolipid and cholesterol-rich invaginations of the plasma membrane involved in vesicular trafficking and signal transduction. Over the recent years there has been controversy about their role in breast cancer and their suitability as markers of basal-like phenotype. Caveolin-1 and CAV2 protein expression was assessed on a tissue microarray containing 880 unselected invasive breast cancer cases, by means of immunohistochemistry. Caveolin-1 and CAV2 expression was observed in 13.4 and 5.9% of all breast cancer, respectively. Their expression was strongly associated with high histological grade, lack of steroid hormone receptor positivity (ER and PR), and expression of basal markers (basal cytokeratins, P63, P-cadherin). Furthermore, there was a significant association between CAV1 and CAV2 expression and basal-like phenotype. On univariate analysis only CAV2 had a prognostic impact on breast cancer-specific survival; however, this was not independent from other traditional markers on multivariate analysis. Our results demonstrate that both CAV1 and CAV2 are associated with basal-like phenotype. Further studies are warranted to determine whether they play an oncogenic role in basal-like/triple-negative breast cancer development or are just surrogate markers for this subgroup.
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spelling pubmed-24809812009-09-11 Caveolin 1 and Caveolin 2 are associated with breast cancer basal-like and triple-negative immunophenotype Elsheikh, S E Green, A R Rakha, E A Samaka, R M Ammar, A A Powe, D Reis-Filho, J S Ellis, I O Br J Cancer Molecular Diagnostics Caveolin-1 (CAV1) and caveolin 2 (CAV2) are the principal structural proteins of caveolae, sphingolipid and cholesterol-rich invaginations of the plasma membrane involved in vesicular trafficking and signal transduction. Over the recent years there has been controversy about their role in breast cancer and their suitability as markers of basal-like phenotype. Caveolin-1 and CAV2 protein expression was assessed on a tissue microarray containing 880 unselected invasive breast cancer cases, by means of immunohistochemistry. Caveolin-1 and CAV2 expression was observed in 13.4 and 5.9% of all breast cancer, respectively. Their expression was strongly associated with high histological grade, lack of steroid hormone receptor positivity (ER and PR), and expression of basal markers (basal cytokeratins, P63, P-cadherin). Furthermore, there was a significant association between CAV1 and CAV2 expression and basal-like phenotype. On univariate analysis only CAV2 had a prognostic impact on breast cancer-specific survival; however, this was not independent from other traditional markers on multivariate analysis. Our results demonstrate that both CAV1 and CAV2 are associated with basal-like phenotype. Further studies are warranted to determine whether they play an oncogenic role in basal-like/triple-negative breast cancer development or are just surrogate markers for this subgroup. Nature Publishing Group 2008-07-22 2008-07-08 /pmc/articles/PMC2480981/ /pubmed/18612310 http://dx.doi.org/10.1038/sj.bjc.6604463 Text en Copyright © 2008 Cancer Research UK 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 Molecular Diagnostics
Elsheikh, S E
Green, A R
Rakha, E A
Samaka, R M
Ammar, A A
Powe, D
Reis-Filho, J S
Ellis, I O
Caveolin 1 and Caveolin 2 are associated with breast cancer basal-like and triple-negative immunophenotype
title Caveolin 1 and Caveolin 2 are associated with breast cancer basal-like and triple-negative immunophenotype
title_full Caveolin 1 and Caveolin 2 are associated with breast cancer basal-like and triple-negative immunophenotype
title_fullStr Caveolin 1 and Caveolin 2 are associated with breast cancer basal-like and triple-negative immunophenotype
title_full_unstemmed Caveolin 1 and Caveolin 2 are associated with breast cancer basal-like and triple-negative immunophenotype
title_short Caveolin 1 and Caveolin 2 are associated with breast cancer basal-like and triple-negative immunophenotype
title_sort caveolin 1 and caveolin 2 are associated with breast cancer basal-like and triple-negative immunophenotype
topic Molecular Diagnostics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2480981/
https://www.ncbi.nlm.nih.gov/pubmed/18612310
http://dx.doi.org/10.1038/sj.bjc.6604463
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