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NHERF1 together with PARP1 and BRCA1 expression as a new potential biomarker to stratify breast cancer patients

It has been recognized that Na(+)/H(+) Exchanger Regulatory Factor 1 (NHERF1) in breast cancer (BC) acts as a tumor suppressor or as an oncogenic protein, depending on its subcellular localization. This study aims to correlate NHERF1 expression to BRCA1 and PARP1 proteins, to investigate their relat...

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Autores principales: Mangia, Anita, Scarpi, Emanuela, Partipilo, Giulia, Schirosi, Laura, Opinto, Giuseppina, Giotta, Francesco, Simone, Giovanni
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5630367/
https://www.ncbi.nlm.nih.gov/pubmed/29029467
http://dx.doi.org/10.18632/oncotarget.19444
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author Mangia, Anita
Scarpi, Emanuela
Partipilo, Giulia
Schirosi, Laura
Opinto, Giuseppina
Giotta, Francesco
Simone, Giovanni
author_facet Mangia, Anita
Scarpi, Emanuela
Partipilo, Giulia
Schirosi, Laura
Opinto, Giuseppina
Giotta, Francesco
Simone, Giovanni
author_sort Mangia, Anita
collection PubMed
description It has been recognized that Na(+)/H(+) Exchanger Regulatory Factor 1 (NHERF1) in breast cancer (BC) acts as a tumor suppressor or as an oncogenic protein, depending on its subcellular localization. This study aims to correlate NHERF1 expression to BRCA1 and PARP1 proteins, to investigate their relationship, and their biological and clinical significance. Using immunohistochemistry on tissue microarrays, we evaluated subcellular NHERF1, BRCA1 and PARP1 expression in 308 BCs including a subgroup (n=80) of triple negative BCs (TNBCs). Herein, we show that nuclear NHERF1 (nNHERF1) expression was significantly associated with nuclear BRCA1 (nBRCA1) expression (p=0.0008), and an association was also found between nuclear PARP1 (nPARP1) and nBRCA1 (p<0.0001). Cytoplasmic NHERF1 (cNHERF1) was correlated to nPARP1 (p<0.0001). Survival analyses showed that the patients with positive nPARP1 and nNHERF1 tended toward a shorter 5-year overall survival (OS) (p=0.057). In TNBCs, the association between nBRCA1 and nPARP1 was maintained (p<0.0001), and an association between nNHERF1 and nPARP1 was observed (p=0.010). Univariate analysis revealed that TNBCs with positive cNHERF1 and nPARP1 had a shorter 5-year OS (p=0.048). Our data suggest that NHERF1 could be a new potential biomarker in combination with PARP1 and BRCA1 expression to stratify BC patients. In particular, in TNBCs, cNHERF1 associated with nPARP1 expression identified a patient subgroup with a shorter survival, for whom it may be useful to develop novel therapeutic strategies.
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spelling pubmed-56303672017-10-12 NHERF1 together with PARP1 and BRCA1 expression as a new potential biomarker to stratify breast cancer patients Mangia, Anita Scarpi, Emanuela Partipilo, Giulia Schirosi, Laura Opinto, Giuseppina Giotta, Francesco Simone, Giovanni Oncotarget Research Paper It has been recognized that Na(+)/H(+) Exchanger Regulatory Factor 1 (NHERF1) in breast cancer (BC) acts as a tumor suppressor or as an oncogenic protein, depending on its subcellular localization. This study aims to correlate NHERF1 expression to BRCA1 and PARP1 proteins, to investigate their relationship, and their biological and clinical significance. Using immunohistochemistry on tissue microarrays, we evaluated subcellular NHERF1, BRCA1 and PARP1 expression in 308 BCs including a subgroup (n=80) of triple negative BCs (TNBCs). Herein, we show that nuclear NHERF1 (nNHERF1) expression was significantly associated with nuclear BRCA1 (nBRCA1) expression (p=0.0008), and an association was also found between nuclear PARP1 (nPARP1) and nBRCA1 (p<0.0001). Cytoplasmic NHERF1 (cNHERF1) was correlated to nPARP1 (p<0.0001). Survival analyses showed that the patients with positive nPARP1 and nNHERF1 tended toward a shorter 5-year overall survival (OS) (p=0.057). In TNBCs, the association between nBRCA1 and nPARP1 was maintained (p<0.0001), and an association between nNHERF1 and nPARP1 was observed (p=0.010). Univariate analysis revealed that TNBCs with positive cNHERF1 and nPARP1 had a shorter 5-year OS (p=0.048). Our data suggest that NHERF1 could be a new potential biomarker in combination with PARP1 and BRCA1 expression to stratify BC patients. In particular, in TNBCs, cNHERF1 associated with nPARP1 expression identified a patient subgroup with a shorter survival, for whom it may be useful to develop novel therapeutic strategies. Impact Journals LLC 2017-07-22 /pmc/articles/PMC5630367/ /pubmed/29029467 http://dx.doi.org/10.18632/oncotarget.19444 Text en Copyright: © 2017 Mangia et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Mangia, Anita
Scarpi, Emanuela
Partipilo, Giulia
Schirosi, Laura
Opinto, Giuseppina
Giotta, Francesco
Simone, Giovanni
NHERF1 together with PARP1 and BRCA1 expression as a new potential biomarker to stratify breast cancer patients
title NHERF1 together with PARP1 and BRCA1 expression as a new potential biomarker to stratify breast cancer patients
title_full NHERF1 together with PARP1 and BRCA1 expression as a new potential biomarker to stratify breast cancer patients
title_fullStr NHERF1 together with PARP1 and BRCA1 expression as a new potential biomarker to stratify breast cancer patients
title_full_unstemmed NHERF1 together with PARP1 and BRCA1 expression as a new potential biomarker to stratify breast cancer patients
title_short NHERF1 together with PARP1 and BRCA1 expression as a new potential biomarker to stratify breast cancer patients
title_sort nherf1 together with parp1 and brca1 expression as a new potential biomarker to stratify breast cancer patients
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5630367/
https://www.ncbi.nlm.nih.gov/pubmed/29029467
http://dx.doi.org/10.18632/oncotarget.19444
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