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Nuclear Ep-ICD accumulation predicts aggressive clinical course in early stage breast cancer patients
BACKGROUND: Regulated intramembrane proteolysis of Epithelial cell adhesion molecule (EpCAM) results in release of its intracellular domain (Ep-ICD) which triggers oncogenic signalling. The clinical significance of Ep-ICD in breast cancer remains to be determined. Herein, we examined the expression...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4190296/ https://www.ncbi.nlm.nih.gov/pubmed/25265904 http://dx.doi.org/10.1186/1471-2407-14-726 |
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author | Srivastava, Gunjan Assi, Jasmeet Kashat, Lawrence Matta, Ajay Chang, Martin Walfish, Paul G Ralhan, Ranju |
author_facet | Srivastava, Gunjan Assi, Jasmeet Kashat, Lawrence Matta, Ajay Chang, Martin Walfish, Paul G Ralhan, Ranju |
author_sort | Srivastava, Gunjan |
collection | PubMed |
description | BACKGROUND: Regulated intramembrane proteolysis of Epithelial cell adhesion molecule (EpCAM) results in release of its intracellular domain (Ep-ICD) which triggers oncogenic signalling. The clinical significance of Ep-ICD in breast cancer remains to be determined. Herein, we examined the expression of nuclear and cytoplasmic Ep-ICD, and membranous extracellular domain of EpCAM (EpEx) in breast cancer patients, to determine its potential utility in predicting aggressive clinical course of the disease. METHODS: In this retrospective study, 266 breast cancers and 45 normal breast tissues were immunohistochemically analyzed to determine the expression patterns of nuclear and cytoplasmic Ep-ICD and membranous EpEx and correlated with clinicopathological parameters and follow up. Disease-free survival was determined by Kaplan-Meier method and multivariate Cox regression analysis. RESULTS: Nuclear Ep-ICD was more frequently expressed in breast cancers compared to normal tissues. Significant association was observed between increased nuclear Ep-ICD expression and reduced disease-free survival in patients with ductal carcinoma in situ (DCIS) and invasive ductal carcinoma (IDC) (p < 0.001). Nuclear Ep-ICD was positive in all the 13 DCIS and 25 IDC patients who had reduced disease-free survival, while none of the nuclear Ep-ICD negative DCIS or IDC patients had recurrence during the follow up period. Notably, majority of IDC patients who had recurrence had early stage tumors. Multivariate Cox regression analysis identified nuclear Ep-ICD as the most significant predictive factor for reduced disease-free survival in IDC patients (p = 0.011, Hazard ratio = 80.18). CONCLUSION: Patients with nuclear Ep-ICD positive breast cancers had poor prognosis. The high recurrence of disease in nuclear Ep-ICD positive patients, especially those with early tumor stage suggests that nuclear Ep-ICD accumulation holds the promise of identifying early stage patients with aggressive disease who are likely to be in need of more rigorous post-operative surveillance and/or treatment. |
format | Online Article Text |
id | pubmed-4190296 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-41902962014-10-10 Nuclear Ep-ICD accumulation predicts aggressive clinical course in early stage breast cancer patients Srivastava, Gunjan Assi, Jasmeet Kashat, Lawrence Matta, Ajay Chang, Martin Walfish, Paul G Ralhan, Ranju BMC Cancer Research Article BACKGROUND: Regulated intramembrane proteolysis of Epithelial cell adhesion molecule (EpCAM) results in release of its intracellular domain (Ep-ICD) which triggers oncogenic signalling. The clinical significance of Ep-ICD in breast cancer remains to be determined. Herein, we examined the expression of nuclear and cytoplasmic Ep-ICD, and membranous extracellular domain of EpCAM (EpEx) in breast cancer patients, to determine its potential utility in predicting aggressive clinical course of the disease. METHODS: In this retrospective study, 266 breast cancers and 45 normal breast tissues were immunohistochemically analyzed to determine the expression patterns of nuclear and cytoplasmic Ep-ICD and membranous EpEx and correlated with clinicopathological parameters and follow up. Disease-free survival was determined by Kaplan-Meier method and multivariate Cox regression analysis. RESULTS: Nuclear Ep-ICD was more frequently expressed in breast cancers compared to normal tissues. Significant association was observed between increased nuclear Ep-ICD expression and reduced disease-free survival in patients with ductal carcinoma in situ (DCIS) and invasive ductal carcinoma (IDC) (p < 0.001). Nuclear Ep-ICD was positive in all the 13 DCIS and 25 IDC patients who had reduced disease-free survival, while none of the nuclear Ep-ICD negative DCIS or IDC patients had recurrence during the follow up period. Notably, majority of IDC patients who had recurrence had early stage tumors. Multivariate Cox regression analysis identified nuclear Ep-ICD as the most significant predictive factor for reduced disease-free survival in IDC patients (p = 0.011, Hazard ratio = 80.18). CONCLUSION: Patients with nuclear Ep-ICD positive breast cancers had poor prognosis. The high recurrence of disease in nuclear Ep-ICD positive patients, especially those with early tumor stage suggests that nuclear Ep-ICD accumulation holds the promise of identifying early stage patients with aggressive disease who are likely to be in need of more rigorous post-operative surveillance and/or treatment. BioMed Central 2014-09-29 /pmc/articles/PMC4190296/ /pubmed/25265904 http://dx.doi.org/10.1186/1471-2407-14-726 Text en © Srivastava 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 Srivastava, Gunjan Assi, Jasmeet Kashat, Lawrence Matta, Ajay Chang, Martin Walfish, Paul G Ralhan, Ranju Nuclear Ep-ICD accumulation predicts aggressive clinical course in early stage breast cancer patients |
title | Nuclear Ep-ICD accumulation predicts aggressive clinical course in early stage breast cancer patients |
title_full | Nuclear Ep-ICD accumulation predicts aggressive clinical course in early stage breast cancer patients |
title_fullStr | Nuclear Ep-ICD accumulation predicts aggressive clinical course in early stage breast cancer patients |
title_full_unstemmed | Nuclear Ep-ICD accumulation predicts aggressive clinical course in early stage breast cancer patients |
title_short | Nuclear Ep-ICD accumulation predicts aggressive clinical course in early stage breast cancer patients |
title_sort | nuclear ep-icd accumulation predicts aggressive clinical course in early stage breast cancer patients |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4190296/ https://www.ncbi.nlm.nih.gov/pubmed/25265904 http://dx.doi.org/10.1186/1471-2407-14-726 |
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