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EphA5 protein, a potential marker for distinguishing histological grade and prognosis in ovarian serous carcinoma

BACKGROUND: Ovarian serous carcinoma (OSC) is the most common ovarian epithelial malignancy. Disregulation of Eph/ephrin signaling has been implicated in oncogenesis and tumor progression. EphA5 receptor is one of large families of Eph tyrosine kinase receptor and is documented in the development of...

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Autores principales: Chen, Xiao, Wang, Xuan, Wei, Xue, Wang, Jiandong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5123222/
https://www.ncbi.nlm.nih.gov/pubmed/27887627
http://dx.doi.org/10.1186/s13048-016-0292-1
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author Chen, Xiao
Wang, Xuan
Wei, Xue
Wang, Jiandong
author_facet Chen, Xiao
Wang, Xuan
Wei, Xue
Wang, Jiandong
author_sort Chen, Xiao
collection PubMed
description BACKGROUND: Ovarian serous carcinoma (OSC) is the most common ovarian epithelial malignancy. Disregulation of Eph/ephrin signaling has been implicated in oncogenesis and tumor progression. EphA5 receptor is one of large families of Eph tyrosine kinase receptor and is documented in the development of nervous system. Till now, there is no published data about the role of EphA5 in ovarian epithelial neoplasmas. METHODS: This study aims to investigate the expression of EphA5 protein in ovarian serous carcinoma, and its relationship to clinical pathological characteristics. Sixty-one cases of ovarian serous carcinoma, 24 cases of benign ovarian serous tumors, 42 cases of serous borderline tumors and 20 cases of normal fallopian tubes were examined using immunohistochemical staining. The relationship between EphA5 expression and pathological parameters was analyzed. Kaplan-Meier survival function was used to analyze prognosis of patients. RESULTS: Immunostaining analysis demonstrated that the EphA5 protein was highly expressed in 100% (20/20) of normal fallopian tube samples, 100% (24/24) of benign epithelial ovarian tumors, 76% (32/42) of ovarian serous borderline tumors, and 31% (19/61) of ovarian serous carcinomas. Loss of EphA5expression was associated with tumor grade (P < 0.001) and FIGO stage (P = 0.005). The survival analysis showed that patients with negative or weak expression of EphA5 protein had a poor outcome than those with positive expression (P = 0.004). CONCLUSIONS: Our results show that EphA5 may be a potential biomarker for distinguishing high-and low-grade ovarian serous carcinoma and a potential prognostic marker.
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spelling pubmed-51232222016-12-06 EphA5 protein, a potential marker for distinguishing histological grade and prognosis in ovarian serous carcinoma Chen, Xiao Wang, Xuan Wei, Xue Wang, Jiandong J Ovarian Res Research BACKGROUND: Ovarian serous carcinoma (OSC) is the most common ovarian epithelial malignancy. Disregulation of Eph/ephrin signaling has been implicated in oncogenesis and tumor progression. EphA5 receptor is one of large families of Eph tyrosine kinase receptor and is documented in the development of nervous system. Till now, there is no published data about the role of EphA5 in ovarian epithelial neoplasmas. METHODS: This study aims to investigate the expression of EphA5 protein in ovarian serous carcinoma, and its relationship to clinical pathological characteristics. Sixty-one cases of ovarian serous carcinoma, 24 cases of benign ovarian serous tumors, 42 cases of serous borderline tumors and 20 cases of normal fallopian tubes were examined using immunohistochemical staining. The relationship between EphA5 expression and pathological parameters was analyzed. Kaplan-Meier survival function was used to analyze prognosis of patients. RESULTS: Immunostaining analysis demonstrated that the EphA5 protein was highly expressed in 100% (20/20) of normal fallopian tube samples, 100% (24/24) of benign epithelial ovarian tumors, 76% (32/42) of ovarian serous borderline tumors, and 31% (19/61) of ovarian serous carcinomas. Loss of EphA5expression was associated with tumor grade (P < 0.001) and FIGO stage (P = 0.005). The survival analysis showed that patients with negative or weak expression of EphA5 protein had a poor outcome than those with positive expression (P = 0.004). CONCLUSIONS: Our results show that EphA5 may be a potential biomarker for distinguishing high-and low-grade ovarian serous carcinoma and a potential prognostic marker. BioMed Central 2016-11-25 /pmc/articles/PMC5123222/ /pubmed/27887627 http://dx.doi.org/10.1186/s13048-016-0292-1 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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
Chen, Xiao
Wang, Xuan
Wei, Xue
Wang, Jiandong
EphA5 protein, a potential marker for distinguishing histological grade and prognosis in ovarian serous carcinoma
title EphA5 protein, a potential marker for distinguishing histological grade and prognosis in ovarian serous carcinoma
title_full EphA5 protein, a potential marker for distinguishing histological grade and prognosis in ovarian serous carcinoma
title_fullStr EphA5 protein, a potential marker for distinguishing histological grade and prognosis in ovarian serous carcinoma
title_full_unstemmed EphA5 protein, a potential marker for distinguishing histological grade and prognosis in ovarian serous carcinoma
title_short EphA5 protein, a potential marker for distinguishing histological grade and prognosis in ovarian serous carcinoma
title_sort epha5 protein, a potential marker for distinguishing histological grade and prognosis in ovarian serous carcinoma
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5123222/
https://www.ncbi.nlm.nih.gov/pubmed/27887627
http://dx.doi.org/10.1186/s13048-016-0292-1
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