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Clinical relevance of expression of B7-H1 and B7-H4 in ovarian cancer
The aim of the present study was to investigate the expression of B7-H1 and B7-H4 in ovarian neoplasm tissues and to examine their clinical relevance. A total of 112 ovarian biopsies were collected from patients with epithelial ovarian cancer (EOC) and 10 were taken from ovarian benign neoplasms. Th...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4812522/ https://www.ncbi.nlm.nih.gov/pubmed/27073557 http://dx.doi.org/10.3892/ol.2016.4301 |
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author | XU, MEI ZHANG, BEI ZHANG, MENG LIU, YANG YIN, FENG-LING LIU, XIA ZHUO, SHI-CHAO |
author_facet | XU, MEI ZHANG, BEI ZHANG, MENG LIU, YANG YIN, FENG-LING LIU, XIA ZHUO, SHI-CHAO |
author_sort | XU, MEI |
collection | PubMed |
description | The aim of the present study was to investigate the expression of B7-H1 and B7-H4 in ovarian neoplasm tissues and to examine their clinical relevance. A total of 112 ovarian biopsies were collected from patients with epithelial ovarian cancer (EOC) and 10 were taken from ovarian benign neoplasms. The samples were processed in paraffin tissue chips, and subjected to immunohistochemical staining and analysis. Associations of B7-H1 and B7-H4 expression with patients' clinical parameters, such as histological typing, cell grading, International Federation of Gynecology and Obstetrics staging, tumor size, and metastatic status, were examined by statistical analysis. Survival curves were constructed using the Kaplan-Meier method and the log-rank test. Independent prognostic factors were evaluated using the Cox regression model. The results showed an extremely low or negative expression of B7-H1 and B7-H4 in the 10 benign ovarian neoplasm tissues (control): By contrast, a positive expression of B7-H1 and B7-H4 was observed in 55.4% (62/112) and 37.5% (42/112) of the EOC tissues, respectively. The differences between the two groups were significant. In addition, the co-expression of B7-H1 and B7-H4 was found in 31.3% (35/112) of the EOC cases. Furthermore, the progression-free survival and overall survival were significantly lower in EOC patients with a high expression of B7-H1 and B7-H4 (χ(2)=45.60 and 37.99, respectively). These results demonstrated that the expression of B7-H1 and B7-H4 in EOC tissues was significantly associated with poor prognosis and high relapse rate of EOC. The findings suggest that B7-H1 and B7-H4 is a negative prognostic marker for EOC and a potential immunotherapeutic target for patients with EOC. |
format | Online Article Text |
id | pubmed-4812522 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-48125222016-04-12 Clinical relevance of expression of B7-H1 and B7-H4 in ovarian cancer XU, MEI ZHANG, BEI ZHANG, MENG LIU, YANG YIN, FENG-LING LIU, XIA ZHUO, SHI-CHAO Oncol Lett Articles The aim of the present study was to investigate the expression of B7-H1 and B7-H4 in ovarian neoplasm tissues and to examine their clinical relevance. A total of 112 ovarian biopsies were collected from patients with epithelial ovarian cancer (EOC) and 10 were taken from ovarian benign neoplasms. The samples were processed in paraffin tissue chips, and subjected to immunohistochemical staining and analysis. Associations of B7-H1 and B7-H4 expression with patients' clinical parameters, such as histological typing, cell grading, International Federation of Gynecology and Obstetrics staging, tumor size, and metastatic status, were examined by statistical analysis. Survival curves were constructed using the Kaplan-Meier method and the log-rank test. Independent prognostic factors were evaluated using the Cox regression model. The results showed an extremely low or negative expression of B7-H1 and B7-H4 in the 10 benign ovarian neoplasm tissues (control): By contrast, a positive expression of B7-H1 and B7-H4 was observed in 55.4% (62/112) and 37.5% (42/112) of the EOC tissues, respectively. The differences between the two groups were significant. In addition, the co-expression of B7-H1 and B7-H4 was found in 31.3% (35/112) of the EOC cases. Furthermore, the progression-free survival and overall survival were significantly lower in EOC patients with a high expression of B7-H1 and B7-H4 (χ(2)=45.60 and 37.99, respectively). These results demonstrated that the expression of B7-H1 and B7-H4 in EOC tissues was significantly associated with poor prognosis and high relapse rate of EOC. The findings suggest that B7-H1 and B7-H4 is a negative prognostic marker for EOC and a potential immunotherapeutic target for patients with EOC. D.A. Spandidos 2016-04 2016-03-02 /pmc/articles/PMC4812522/ /pubmed/27073557 http://dx.doi.org/10.3892/ol.2016.4301 Text en Copyright: © Xu et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Articles XU, MEI ZHANG, BEI ZHANG, MENG LIU, YANG YIN, FENG-LING LIU, XIA ZHUO, SHI-CHAO Clinical relevance of expression of B7-H1 and B7-H4 in ovarian cancer |
title | Clinical relevance of expression of B7-H1 and B7-H4 in ovarian cancer |
title_full | Clinical relevance of expression of B7-H1 and B7-H4 in ovarian cancer |
title_fullStr | Clinical relevance of expression of B7-H1 and B7-H4 in ovarian cancer |
title_full_unstemmed | Clinical relevance of expression of B7-H1 and B7-H4 in ovarian cancer |
title_short | Clinical relevance of expression of B7-H1 and B7-H4 in ovarian cancer |
title_sort | clinical relevance of expression of b7-h1 and b7-h4 in ovarian cancer |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4812522/ https://www.ncbi.nlm.nih.gov/pubmed/27073557 http://dx.doi.org/10.3892/ol.2016.4301 |
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