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High focal adhesion kinase expression in breast carcinoma is associated with lymphovascular invasion and triple-negative phenotype

BACKGROUND: Focal adhesion Kinase (FAK) is a nonreceptor protein tyrosine kinase that is overexpressed in tumors and plays a significant role in tumor survival and metastasis. The purpose of the study is to perform correlation of FAK expression with patient prognostic factors using tissue microarray...

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Autores principales: Golubovskaya, Vita M, Ylagan, Lourdes, Miller, Austin, Hughes, Melissa, Wilson, Jason, Wang, David, Brese, Elizabeth, Bshara, Wiam, Edge, Stephen, Morrison, Carl, Cance, William G
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4213510/
https://www.ncbi.nlm.nih.gov/pubmed/25326692
http://dx.doi.org/10.1186/1471-2407-14-769
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author Golubovskaya, Vita M
Ylagan, Lourdes
Miller, Austin
Hughes, Melissa
Wilson, Jason
Wang, David
Brese, Elizabeth
Bshara, Wiam
Edge, Stephen
Morrison, Carl
Cance, William G
author_facet Golubovskaya, Vita M
Ylagan, Lourdes
Miller, Austin
Hughes, Melissa
Wilson, Jason
Wang, David
Brese, Elizabeth
Bshara, Wiam
Edge, Stephen
Morrison, Carl
Cance, William G
author_sort Golubovskaya, Vita M
collection PubMed
description BACKGROUND: Focal adhesion Kinase (FAK) is a nonreceptor protein tyrosine kinase that is overexpressed in tumors and plays a significant role in tumor survival and metastasis. The purpose of the study is to perform correlation of FAK expression with patient prognostic factors using tissue microarrays (TMA) samples. METHODS: We analyzed FAK expression by immunohistochemical staining in 196 breast primary tumor samples from stage II-IV patients and in 117 metastatic tissues matched to the primary tumors using TMA that were stained with FAK monoclonal antibody. RESULTS: High FAK expression in primary tumors was associated with a younger age of patients (p = 0.033), lymphovascular invasion (p = 0.001) and with the triple-negative phenotype (p = 0.033). FAK expression in 117 metastatic tissues positively correlated with FAK expression in matched primary tumors by Spearman correlation analysis. In addition, a strong positive correlation was observed between high FAK expression and shorter overall survival and progression free survival in patients with metastatic tumors. CONCLUSIONS: The data demonstrate a high potential for FAK as a therapeutic target, especially in triple-negative breast cancer patients with high FAK expression.
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spelling pubmed-42135102014-10-31 High focal adhesion kinase expression in breast carcinoma is associated with lymphovascular invasion and triple-negative phenotype Golubovskaya, Vita M Ylagan, Lourdes Miller, Austin Hughes, Melissa Wilson, Jason Wang, David Brese, Elizabeth Bshara, Wiam Edge, Stephen Morrison, Carl Cance, William G BMC Cancer Research Article BACKGROUND: Focal adhesion Kinase (FAK) is a nonreceptor protein tyrosine kinase that is overexpressed in tumors and plays a significant role in tumor survival and metastasis. The purpose of the study is to perform correlation of FAK expression with patient prognostic factors using tissue microarrays (TMA) samples. METHODS: We analyzed FAK expression by immunohistochemical staining in 196 breast primary tumor samples from stage II-IV patients and in 117 metastatic tissues matched to the primary tumors using TMA that were stained with FAK monoclonal antibody. RESULTS: High FAK expression in primary tumors was associated with a younger age of patients (p = 0.033), lymphovascular invasion (p = 0.001) and with the triple-negative phenotype (p = 0.033). FAK expression in 117 metastatic tissues positively correlated with FAK expression in matched primary tumors by Spearman correlation analysis. In addition, a strong positive correlation was observed between high FAK expression and shorter overall survival and progression free survival in patients with metastatic tumors. CONCLUSIONS: The data demonstrate a high potential for FAK as a therapeutic target, especially in triple-negative breast cancer patients with high FAK expression. BioMed Central 2014-10-17 /pmc/articles/PMC4213510/ /pubmed/25326692 http://dx.doi.org/10.1186/1471-2407-14-769 Text en © Golubovskaya et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Golubovskaya, Vita M
Ylagan, Lourdes
Miller, Austin
Hughes, Melissa
Wilson, Jason
Wang, David
Brese, Elizabeth
Bshara, Wiam
Edge, Stephen
Morrison, Carl
Cance, William G
High focal adhesion kinase expression in breast carcinoma is associated with lymphovascular invasion and triple-negative phenotype
title High focal adhesion kinase expression in breast carcinoma is associated with lymphovascular invasion and triple-negative phenotype
title_full High focal adhesion kinase expression in breast carcinoma is associated with lymphovascular invasion and triple-negative phenotype
title_fullStr High focal adhesion kinase expression in breast carcinoma is associated with lymphovascular invasion and triple-negative phenotype
title_full_unstemmed High focal adhesion kinase expression in breast carcinoma is associated with lymphovascular invasion and triple-negative phenotype
title_short High focal adhesion kinase expression in breast carcinoma is associated with lymphovascular invasion and triple-negative phenotype
title_sort high focal adhesion kinase expression in breast carcinoma is associated with lymphovascular invasion and triple-negative phenotype
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4213510/
https://www.ncbi.nlm.nih.gov/pubmed/25326692
http://dx.doi.org/10.1186/1471-2407-14-769
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