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EPHA2, EPHA4, and EPHA7 Expression in Triple-Negative Breast Cancer

Ongoing research continues to elucidate the complex role of ephrin receptors (EPHs) and their ligands (ephrins) in breast cancer pathogenesis, with their varying expression patterns implied to have an important impact on patients’ outcome. The current study aims to investigate the clinical significa...

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Autores principales: Nikas, Ilias, Giaginis, Constantinos, Petrouska, Kalliopi, Alexandrou, Paraskevi, Michail, Artemis, Sarantis, Panagiotis, Tsourouflis, Gerasimos, Danas, Eugene, Pergaris, Alexandros, Politis, Panagiotis K., Nakopoulou, Lydia, Theocharis, Stamatios
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8871500/
https://www.ncbi.nlm.nih.gov/pubmed/35204461
http://dx.doi.org/10.3390/diagnostics12020366
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author Nikas, Ilias
Giaginis, Constantinos
Petrouska, Kalliopi
Alexandrou, Paraskevi
Michail, Artemis
Sarantis, Panagiotis
Tsourouflis, Gerasimos
Danas, Eugene
Pergaris, Alexandros
Politis, Panagiotis K.
Nakopoulou, Lydia
Theocharis, Stamatios
author_facet Nikas, Ilias
Giaginis, Constantinos
Petrouska, Kalliopi
Alexandrou, Paraskevi
Michail, Artemis
Sarantis, Panagiotis
Tsourouflis, Gerasimos
Danas, Eugene
Pergaris, Alexandros
Politis, Panagiotis K.
Nakopoulou, Lydia
Theocharis, Stamatios
author_sort Nikas, Ilias
collection PubMed
description Ongoing research continues to elucidate the complex role of ephrin receptors (EPHs) and their ligands (ephrins) in breast cancer pathogenesis, with their varying expression patterns implied to have an important impact on patients’ outcome. The current study aims to investigate the clinical significance of EPHA2, EPHA4, and EPHA7 expression in triple-negative breast cancer (TNBC) cases. EPHA2, EPHA4, and EPHA7 protein expression was assessed immunohistochemically on formalin-fixed and paraffin-embedded (FFPE) TNBC tissue sections from 52 TNBC patients and correlated with key clinicopathologic parameters and patients’ survival data (overall survival (OS); disease-free survival (DFS)). EPHA2, EPHA4, and EPHA7 expression was further examined in TNBC cell lines. EPHA2 overexpression was observed in 26 (50%) of the TNBC cases, who exhibited a shorter OS and DFS than their low-expression counterparts, with EPHA2 representing an independent prognostic factor for OS and DFS (p = 0.0041 and p = 0.0232, respectively). EPHA4 overexpression was associated with lymph node metastasis in TNBC patients (p = 0.0546). Alterations in EPHA2, EPHA4, and EPHA7 expression levels were also noted in the examined TNBC cell lines. Our study stresses that EPHA2 expression constitutes a potential prognostic factor for TNBC patients. Given the limited treatment options and poorer outcome that accompany the TNBC subtype, EPHA2 could also pose as a target for novel, more personalized, and effective therapeutic approaches for those patients.
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spelling pubmed-88715002022-02-25 EPHA2, EPHA4, and EPHA7 Expression in Triple-Negative Breast Cancer Nikas, Ilias Giaginis, Constantinos Petrouska, Kalliopi Alexandrou, Paraskevi Michail, Artemis Sarantis, Panagiotis Tsourouflis, Gerasimos Danas, Eugene Pergaris, Alexandros Politis, Panagiotis K. Nakopoulou, Lydia Theocharis, Stamatios Diagnostics (Basel) Article Ongoing research continues to elucidate the complex role of ephrin receptors (EPHs) and their ligands (ephrins) in breast cancer pathogenesis, with their varying expression patterns implied to have an important impact on patients’ outcome. The current study aims to investigate the clinical significance of EPHA2, EPHA4, and EPHA7 expression in triple-negative breast cancer (TNBC) cases. EPHA2, EPHA4, and EPHA7 protein expression was assessed immunohistochemically on formalin-fixed and paraffin-embedded (FFPE) TNBC tissue sections from 52 TNBC patients and correlated with key clinicopathologic parameters and patients’ survival data (overall survival (OS); disease-free survival (DFS)). EPHA2, EPHA4, and EPHA7 expression was further examined in TNBC cell lines. EPHA2 overexpression was observed in 26 (50%) of the TNBC cases, who exhibited a shorter OS and DFS than their low-expression counterparts, with EPHA2 representing an independent prognostic factor for OS and DFS (p = 0.0041 and p = 0.0232, respectively). EPHA4 overexpression was associated with lymph node metastasis in TNBC patients (p = 0.0546). Alterations in EPHA2, EPHA4, and EPHA7 expression levels were also noted in the examined TNBC cell lines. Our study stresses that EPHA2 expression constitutes a potential prognostic factor for TNBC patients. Given the limited treatment options and poorer outcome that accompany the TNBC subtype, EPHA2 could also pose as a target for novel, more personalized, and effective therapeutic approaches for those patients. MDPI 2022-02-01 /pmc/articles/PMC8871500/ /pubmed/35204461 http://dx.doi.org/10.3390/diagnostics12020366 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Nikas, Ilias
Giaginis, Constantinos
Petrouska, Kalliopi
Alexandrou, Paraskevi
Michail, Artemis
Sarantis, Panagiotis
Tsourouflis, Gerasimos
Danas, Eugene
Pergaris, Alexandros
Politis, Panagiotis K.
Nakopoulou, Lydia
Theocharis, Stamatios
EPHA2, EPHA4, and EPHA7 Expression in Triple-Negative Breast Cancer
title EPHA2, EPHA4, and EPHA7 Expression in Triple-Negative Breast Cancer
title_full EPHA2, EPHA4, and EPHA7 Expression in Triple-Negative Breast Cancer
title_fullStr EPHA2, EPHA4, and EPHA7 Expression in Triple-Negative Breast Cancer
title_full_unstemmed EPHA2, EPHA4, and EPHA7 Expression in Triple-Negative Breast Cancer
title_short EPHA2, EPHA4, and EPHA7 Expression in Triple-Negative Breast Cancer
title_sort epha2, epha4, and epha7 expression in triple-negative breast cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8871500/
https://www.ncbi.nlm.nih.gov/pubmed/35204461
http://dx.doi.org/10.3390/diagnostics12020366
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