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High expression of EZR (ezrin) gene is correlated with the poor overall survival of breast cancer patients
BACKGROUND: To evaluate the EZR (ezrin) gene expression in breast cancer and correlation with the prognosis through bioinformatics analysis and immunohistochemistry assay. METHODS: EZR gene expression in breast cancer and corresponding normal breast tissue was compared in the TCGA database. Protein‐...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons Australia, Ltd
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6775014/ https://www.ncbi.nlm.nih.gov/pubmed/31452341 http://dx.doi.org/10.1111/1759-7714.13174 |
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author | Zhang, Rongju Zhang, Shaohui Xing, Rongge Zhang, Qin |
author_facet | Zhang, Rongju Zhang, Shaohui Xing, Rongge Zhang, Qin |
author_sort | Zhang, Rongju |
collection | PubMed |
description | BACKGROUND: To evaluate the EZR (ezrin) gene expression in breast cancer and correlation with the prognosis through bioinformatics analysis and immunohistochemistry assay. METHODS: EZR gene expression in breast cancer and corresponding normal breast tissue was compared in the TCGA database. Protein‐protein interaction (PPI) network relevant EZR was established through the STRING database. The correlation between EZR expression and prognosis of breast cancer was analyzed by the log‐rank analysis from the TCGA. Ezrin protein (coded by EZR) expression was also examined by immunohistochemistry assay in 120 breast cancer patients. RESULTS: EZR expression level in tumor tissue was significantly upregulated compared to that of normal breast tissue of breast cancer patients (P < 0.05). In the PPI analysis, there were 51 nodes and 455 edges in the network. The top 10 hub genes of the network were identified. High expression of EZR mRNA was correlated with poor overall survival (OS) of the breast cancer patients (HR = 1.40, P = 0.038). However, the disease‐free survival (DFS) of breast cancer patients did not correlate with the EZR mRNA level (HR = 0.86, P = 0.44). The ezrin protein expression was positive with uniform brown‐yellow granules in the cell membrane, cavity surface and cytoplasm of the breast cancer cells. Of the included 120 cancer samples, 98 cases were positive for ezrin expression and 22 were negative. No correlation was found between ezrin expression site and patients’ clinicopathological features. CONCLUSION: EZR is upregulated in breast cancer and can be used as potential biomarker for overall survival. |
format | Online Article Text |
id | pubmed-6775014 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley & Sons Australia, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-67750142019-10-07 High expression of EZR (ezrin) gene is correlated with the poor overall survival of breast cancer patients Zhang, Rongju Zhang, Shaohui Xing, Rongge Zhang, Qin Thorac Cancer Original Articles BACKGROUND: To evaluate the EZR (ezrin) gene expression in breast cancer and correlation with the prognosis through bioinformatics analysis and immunohistochemistry assay. METHODS: EZR gene expression in breast cancer and corresponding normal breast tissue was compared in the TCGA database. Protein‐protein interaction (PPI) network relevant EZR was established through the STRING database. The correlation between EZR expression and prognosis of breast cancer was analyzed by the log‐rank analysis from the TCGA. Ezrin protein (coded by EZR) expression was also examined by immunohistochemistry assay in 120 breast cancer patients. RESULTS: EZR expression level in tumor tissue was significantly upregulated compared to that of normal breast tissue of breast cancer patients (P < 0.05). In the PPI analysis, there were 51 nodes and 455 edges in the network. The top 10 hub genes of the network were identified. High expression of EZR mRNA was correlated with poor overall survival (OS) of the breast cancer patients (HR = 1.40, P = 0.038). However, the disease‐free survival (DFS) of breast cancer patients did not correlate with the EZR mRNA level (HR = 0.86, P = 0.44). The ezrin protein expression was positive with uniform brown‐yellow granules in the cell membrane, cavity surface and cytoplasm of the breast cancer cells. Of the included 120 cancer samples, 98 cases were positive for ezrin expression and 22 were negative. No correlation was found between ezrin expression site and patients’ clinicopathological features. CONCLUSION: EZR is upregulated in breast cancer and can be used as potential biomarker for overall survival. John Wiley & Sons Australia, Ltd 2019-08-26 2019-10 /pmc/articles/PMC6775014/ /pubmed/31452341 http://dx.doi.org/10.1111/1759-7714.13174 Text en © 2019 The Authors. Thoracic Cancer published by China Lung Oncology Group and John Wiley & Sons Australia, Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Zhang, Rongju Zhang, Shaohui Xing, Rongge Zhang, Qin High expression of EZR (ezrin) gene is correlated with the poor overall survival of breast cancer patients |
title | High expression of EZR (ezrin) gene is correlated with the poor overall survival of breast cancer patients |
title_full | High expression of EZR (ezrin) gene is correlated with the poor overall survival of breast cancer patients |
title_fullStr | High expression of EZR (ezrin) gene is correlated with the poor overall survival of breast cancer patients |
title_full_unstemmed | High expression of EZR (ezrin) gene is correlated with the poor overall survival of breast cancer patients |
title_short | High expression of EZR (ezrin) gene is correlated with the poor overall survival of breast cancer patients |
title_sort | high expression of ezr (ezrin) gene is correlated with the poor overall survival of breast cancer patients |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6775014/ https://www.ncbi.nlm.nih.gov/pubmed/31452341 http://dx.doi.org/10.1111/1759-7714.13174 |
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