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High levels of EGFR expression in tumor stroma are associated with aggressive clinical features in epithelial ovarian cancer

PURPOSE: The aim of this study was to investigate the clinical significance and biological function of epidermal growth factor receptor (EGFR) expressed in tumor stroma of epithelial ovarian cancer. METHODS: Immunohistological staining of EGFR was evaluated in 242 patients with epithelial ovarian ca...

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Autores principales: Wang, Ke, Li, Dan, Sun, Lu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4727521/
https://www.ncbi.nlm.nih.gov/pubmed/26855586
http://dx.doi.org/10.2147/OTT.S96309
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author Wang, Ke
Li, Dan
Sun, Lu
author_facet Wang, Ke
Li, Dan
Sun, Lu
author_sort Wang, Ke
collection PubMed
description PURPOSE: The aim of this study was to investigate the clinical significance and biological function of epidermal growth factor receptor (EGFR) expressed in tumor stroma of epithelial ovarian cancer. METHODS: Immunohistological staining of EGFR was evaluated in 242 patients with epithelial ovarian cancer. The correlations of EGFR expression in tumor stroma with clinicopathological features and with the expression level of Ki-67 were analyzed by SPSS software. Kaplan–Meier analysis and the Cox proportional hazard model were used to analyze the effect of EGFR expression in tumor stroma on the prognosis of patients with epithelial ovarian cancer. Meanwhile, the activities of proliferation and migration of tumor cells were detected when EGFR overexpressed in stroma cells. RESULTS: EGFR expression in tumor stroma correlated significantly with clinical stage (χ(2)=7.002, P=0.008) and distant metastases (χ(2)=16.59, P<0.001). Furthermore, there was a significantly positive correlation between the level of EGFR expressed in tumor stroma and the level of Ki-67 expressed in tumor cells (χ(2)=6.120, P=0.013). Patients with high EGFR expression level in tumor stroma showed poor survival (P=0.002). Multivariate analysis showed that high expression of EGFR in tumor stroma was an independent predictor for epithelial ovarian cancer patients (hazard ratio =1.703; 95% confidence interval 1.125–2.578, P=0.012). Furthermore, stroma cells overexpressing EGFR could promote the proliferation and migration of adjacent tumor cells. CONCLUSION: High expression of EGFR in tumor stroma correlates with aggressive clinical features in epithelial ovarian cancer, and is an independent prognostic factor.
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spelling pubmed-47275212016-02-05 High levels of EGFR expression in tumor stroma are associated with aggressive clinical features in epithelial ovarian cancer Wang, Ke Li, Dan Sun, Lu Onco Targets Ther Original Research PURPOSE: The aim of this study was to investigate the clinical significance and biological function of epidermal growth factor receptor (EGFR) expressed in tumor stroma of epithelial ovarian cancer. METHODS: Immunohistological staining of EGFR was evaluated in 242 patients with epithelial ovarian cancer. The correlations of EGFR expression in tumor stroma with clinicopathological features and with the expression level of Ki-67 were analyzed by SPSS software. Kaplan–Meier analysis and the Cox proportional hazard model were used to analyze the effect of EGFR expression in tumor stroma on the prognosis of patients with epithelial ovarian cancer. Meanwhile, the activities of proliferation and migration of tumor cells were detected when EGFR overexpressed in stroma cells. RESULTS: EGFR expression in tumor stroma correlated significantly with clinical stage (χ(2)=7.002, P=0.008) and distant metastases (χ(2)=16.59, P<0.001). Furthermore, there was a significantly positive correlation between the level of EGFR expressed in tumor stroma and the level of Ki-67 expressed in tumor cells (χ(2)=6.120, P=0.013). Patients with high EGFR expression level in tumor stroma showed poor survival (P=0.002). Multivariate analysis showed that high expression of EGFR in tumor stroma was an independent predictor for epithelial ovarian cancer patients (hazard ratio =1.703; 95% confidence interval 1.125–2.578, P=0.012). Furthermore, stroma cells overexpressing EGFR could promote the proliferation and migration of adjacent tumor cells. CONCLUSION: High expression of EGFR in tumor stroma correlates with aggressive clinical features in epithelial ovarian cancer, and is an independent prognostic factor. Dove Medical Press 2016-01-19 /pmc/articles/PMC4727521/ /pubmed/26855586 http://dx.doi.org/10.2147/OTT.S96309 Text en © 2016 Wang et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Wang, Ke
Li, Dan
Sun, Lu
High levels of EGFR expression in tumor stroma are associated with aggressive clinical features in epithelial ovarian cancer
title High levels of EGFR expression in tumor stroma are associated with aggressive clinical features in epithelial ovarian cancer
title_full High levels of EGFR expression in tumor stroma are associated with aggressive clinical features in epithelial ovarian cancer
title_fullStr High levels of EGFR expression in tumor stroma are associated with aggressive clinical features in epithelial ovarian cancer
title_full_unstemmed High levels of EGFR expression in tumor stroma are associated with aggressive clinical features in epithelial ovarian cancer
title_short High levels of EGFR expression in tumor stroma are associated with aggressive clinical features in epithelial ovarian cancer
title_sort high levels of egfr expression in tumor stroma are associated with aggressive clinical features in epithelial ovarian cancer
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4727521/
https://www.ncbi.nlm.nih.gov/pubmed/26855586
http://dx.doi.org/10.2147/OTT.S96309
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