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The prognostic value of B7-H6 in esophageal squamous cell carcinoma

B7-H6, a member of the B7 family molecules, participates in the clearance of tumor cells by binding to NKp30 on NK cells. B7-H6 expression level in esophageal squamous cell carcinoma (ESCC) and the clinical value remain unknown. The goal of this study was to determine the expression of B7-H6 in ESCC...

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Autores principales: Zhou, Huan, Dong, Jun, Guo, Liyi, Wang, Xicheng, Wang, Kailin, Cai, Xiuyu, Yang, Shu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6889130/
https://www.ncbi.nlm.nih.gov/pubmed/31792298
http://dx.doi.org/10.1038/s41598-019-54731-9
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author Zhou, Huan
Dong, Jun
Guo, Liyi
Wang, Xicheng
Wang, Kailin
Cai, Xiuyu
Yang, Shu
author_facet Zhou, Huan
Dong, Jun
Guo, Liyi
Wang, Xicheng
Wang, Kailin
Cai, Xiuyu
Yang, Shu
author_sort Zhou, Huan
collection PubMed
description B7-H6, a member of the B7 family molecules, participates in the clearance of tumor cells by binding to NKp30 on NK cells. B7-H6 expression level in esophageal squamous cell carcinoma (ESCC) and the clinical value remain unknown. The goal of this study was to determine the expression of B7-H6 in ESCC and further explore its clinical significance. We retrospectively collected the clinical data of 145 patients diagnosed with ESCC between January 2007 and December 2008. The expression of B7-H6 of the pathological tissue samples was detected by immunohistochemistry. The chi-square (χ(2)) test was used to analyse the relationships of B7-H6 and clinicopathological characteristics. Survival and hazard functions were estimated using the Kaplan-Meier method, and survival between groups was compared using the two-sided log-rank test. The Cox proportional hazards regression model was used to adjust for the risk factors related to overall survival (OS). 133/145 (91.72%) of the ESCC tissue samples exhibited B7-H6 expression. The expression level of B7-H6 was correlated with T stage (P = 0.036) and lymphatic metastasis status (P = 0.044). High B7-H6 expression (P = 0.003) was associated with a significantly worse OS than low B7-H6 expression. Multivariate Cox proportional hazards regression analysis demonstrated that tumour size (P = 0.021), B7-H6 expression (P = 0.025) and lymphatic metastasis status (P = 0.049) were independent prognostic factors of OS for ESCC. Collectively, our findings suggest that B7-H6 is widely expressed in ESCC samples. And B7-H6 may represent a predictor of poor prognosis for ESCC.
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spelling pubmed-68891302019-12-10 The prognostic value of B7-H6 in esophageal squamous cell carcinoma Zhou, Huan Dong, Jun Guo, Liyi Wang, Xicheng Wang, Kailin Cai, Xiuyu Yang, Shu Sci Rep Article B7-H6, a member of the B7 family molecules, participates in the clearance of tumor cells by binding to NKp30 on NK cells. B7-H6 expression level in esophageal squamous cell carcinoma (ESCC) and the clinical value remain unknown. The goal of this study was to determine the expression of B7-H6 in ESCC and further explore its clinical significance. We retrospectively collected the clinical data of 145 patients diagnosed with ESCC between January 2007 and December 2008. The expression of B7-H6 of the pathological tissue samples was detected by immunohistochemistry. The chi-square (χ(2)) test was used to analyse the relationships of B7-H6 and clinicopathological characteristics. Survival and hazard functions were estimated using the Kaplan-Meier method, and survival between groups was compared using the two-sided log-rank test. The Cox proportional hazards regression model was used to adjust for the risk factors related to overall survival (OS). 133/145 (91.72%) of the ESCC tissue samples exhibited B7-H6 expression. The expression level of B7-H6 was correlated with T stage (P = 0.036) and lymphatic metastasis status (P = 0.044). High B7-H6 expression (P = 0.003) was associated with a significantly worse OS than low B7-H6 expression. Multivariate Cox proportional hazards regression analysis demonstrated that tumour size (P = 0.021), B7-H6 expression (P = 0.025) and lymphatic metastasis status (P = 0.049) were independent prognostic factors of OS for ESCC. Collectively, our findings suggest that B7-H6 is widely expressed in ESCC samples. And B7-H6 may represent a predictor of poor prognosis for ESCC. Nature Publishing Group UK 2019-12-02 /pmc/articles/PMC6889130/ /pubmed/31792298 http://dx.doi.org/10.1038/s41598-019-54731-9 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Zhou, Huan
Dong, Jun
Guo, Liyi
Wang, Xicheng
Wang, Kailin
Cai, Xiuyu
Yang, Shu
The prognostic value of B7-H6 in esophageal squamous cell carcinoma
title The prognostic value of B7-H6 in esophageal squamous cell carcinoma
title_full The prognostic value of B7-H6 in esophageal squamous cell carcinoma
title_fullStr The prognostic value of B7-H6 in esophageal squamous cell carcinoma
title_full_unstemmed The prognostic value of B7-H6 in esophageal squamous cell carcinoma
title_short The prognostic value of B7-H6 in esophageal squamous cell carcinoma
title_sort prognostic value of b7-h6 in esophageal squamous cell carcinoma
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6889130/
https://www.ncbi.nlm.nih.gov/pubmed/31792298
http://dx.doi.org/10.1038/s41598-019-54731-9
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