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B7-H7 is a prognostic biomarker in epithelial ovarian cancer
BACKGROUND: B7-H7 is a newly identified member of the B7 immune checkpoint family, but has not been investigated in epithelial ovarian cancer (EOC). This study aimed to determine the B7-H7 expression profile and its potential clinical significance in EOC. METHODS: A tissue microarray (TMA) containin...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AME Publishing Company
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8798714/ https://www.ncbi.nlm.nih.gov/pubmed/35117901 http://dx.doi.org/10.21037/tcr-20-697 |
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author | Fu, Yuanyuan Ding, Yun Liu, Juan Zheng, Xiao Wei, Wei Ying, Yaoyu Wu, Changping Jiang, Jingting Ju, Jingfang |
author_facet | Fu, Yuanyuan Ding, Yun Liu, Juan Zheng, Xiao Wei, Wei Ying, Yaoyu Wu, Changping Jiang, Jingting Ju, Jingfang |
author_sort | Fu, Yuanyuan |
collection | PubMed |
description | BACKGROUND: B7-H7 is a newly identified member of the B7 immune checkpoint family, but has not been investigated in epithelial ovarian cancer (EOC). This study aimed to determine the B7-H7 expression profile and its potential clinical significance in EOC. METHODS: A tissue microarray (TMA) containing 160 ovarian cancer tissues was used in this study and 119 EOC cases were valid for analysis. B7-H7 expression was analyzed separately by multiplex immunohistochemistry (mIHC) staining in different compartment according to tissue segmentation. Correlations of B7-H7 expression and pathological characteristics, including overall survival (OS) and disease-free survival (DFS), were explored. RESULTS: Multiplex immunohistochemistry staining showed that B7-H7 was broadly expressed in EOC. B7-H7 expression was significantly higher in the tumor compartment than in stromal compartment of EOC. In EOC tissues, B7-H7 expression in tumor compartment was significantly associated with age (P<0.05); B7-H7 expression in stromal compartment was significantly associated with Federation of Obstetrics and Gynecology (FIGO) stage, lymph nodes metastasis, distant metastasis, and OS (all, P<0.05). The Kaplan-Meier survival analysis revealed that high B7-H7 expression in stromal compartment was significantly correlated with the poor OS of EOC patients (P<0.05), but B7-H7 expression in tumor compartment was not. CONCLUSIONS: Stromal B7-H7 expression is significantly associated with tumor progression and prognosis in EOC patients, which might be a prognostic predictor and a potential therapeutic target. |
format | Online Article Text |
id | pubmed-8798714 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | AME Publishing Company |
record_format | MEDLINE/PubMed |
spelling | pubmed-87987142022-02-02 B7-H7 is a prognostic biomarker in epithelial ovarian cancer Fu, Yuanyuan Ding, Yun Liu, Juan Zheng, Xiao Wei, Wei Ying, Yaoyu Wu, Changping Jiang, Jingting Ju, Jingfang Transl Cancer Res Original Article BACKGROUND: B7-H7 is a newly identified member of the B7 immune checkpoint family, but has not been investigated in epithelial ovarian cancer (EOC). This study aimed to determine the B7-H7 expression profile and its potential clinical significance in EOC. METHODS: A tissue microarray (TMA) containing 160 ovarian cancer tissues was used in this study and 119 EOC cases were valid for analysis. B7-H7 expression was analyzed separately by multiplex immunohistochemistry (mIHC) staining in different compartment according to tissue segmentation. Correlations of B7-H7 expression and pathological characteristics, including overall survival (OS) and disease-free survival (DFS), were explored. RESULTS: Multiplex immunohistochemistry staining showed that B7-H7 was broadly expressed in EOC. B7-H7 expression was significantly higher in the tumor compartment than in stromal compartment of EOC. In EOC tissues, B7-H7 expression in tumor compartment was significantly associated with age (P<0.05); B7-H7 expression in stromal compartment was significantly associated with Federation of Obstetrics and Gynecology (FIGO) stage, lymph nodes metastasis, distant metastasis, and OS (all, P<0.05). The Kaplan-Meier survival analysis revealed that high B7-H7 expression in stromal compartment was significantly correlated with the poor OS of EOC patients (P<0.05), but B7-H7 expression in tumor compartment was not. CONCLUSIONS: Stromal B7-H7 expression is significantly associated with tumor progression and prognosis in EOC patients, which might be a prognostic predictor and a potential therapeutic target. AME Publishing Company 2020-09 /pmc/articles/PMC8798714/ /pubmed/35117901 http://dx.doi.org/10.21037/tcr-20-697 Text en 2020 Translational Cancer Research. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/. |
spellingShingle | Original Article Fu, Yuanyuan Ding, Yun Liu, Juan Zheng, Xiao Wei, Wei Ying, Yaoyu Wu, Changping Jiang, Jingting Ju, Jingfang B7-H7 is a prognostic biomarker in epithelial ovarian cancer |
title | B7-H7 is a prognostic biomarker in epithelial ovarian cancer |
title_full | B7-H7 is a prognostic biomarker in epithelial ovarian cancer |
title_fullStr | B7-H7 is a prognostic biomarker in epithelial ovarian cancer |
title_full_unstemmed | B7-H7 is a prognostic biomarker in epithelial ovarian cancer |
title_short | B7-H7 is a prognostic biomarker in epithelial ovarian cancer |
title_sort | b7-h7 is a prognostic biomarker in epithelial ovarian cancer |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8798714/ https://www.ncbi.nlm.nih.gov/pubmed/35117901 http://dx.doi.org/10.21037/tcr-20-697 |
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