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High expression of galectin-7 associates with poor overall survival in patients with non-metastatic clear-cell renal cell carcinoma

BACKGROUND: Galectin-7, has a controversial role in tumor progression, can either suppress tumor growth or induce chemoresistance depends on different tumor histology types. The aim was to appraise Galectin-7 expression on the overall survival (OS) of patients with non-metastatic clear cell renal ce...

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Autores principales: Wang, Jieti, Liu, Yidong, Yang, Yuanfeng, Xu, Zhiying, Zhang, Guodong, Liu, Zheng, Fu, Hangcheng, Wang, Zewei, Liu, Haiou, Xu, Jiejie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5173110/
https://www.ncbi.nlm.nih.gov/pubmed/27259255
http://dx.doi.org/10.18632/oncotarget.9749
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author Wang, Jieti
Liu, Yidong
Yang, Yuanfeng
Xu, Zhiying
Zhang, Guodong
Liu, Zheng
Fu, Hangcheng
Wang, Zewei
Liu, Haiou
Xu, Jiejie
author_facet Wang, Jieti
Liu, Yidong
Yang, Yuanfeng
Xu, Zhiying
Zhang, Guodong
Liu, Zheng
Fu, Hangcheng
Wang, Zewei
Liu, Haiou
Xu, Jiejie
author_sort Wang, Jieti
collection PubMed
description BACKGROUND: Galectin-7, has a controversial role in tumor progression, can either suppress tumor growth or induce chemoresistance depends on different tumor histology types. The aim was to appraise Galectin-7 expression on the overall survival (OS) of patients with non-metastatic clear cell renal cell carcinoma (ccRCC) following surgery. RESULTS: High galectin-7 expression was specifically correlated with necrosis (P = 0.015). Multivariate analysis confirmed galectin-7 as an independent prognosticator for OS (P = 0.005). High galectin-7 expression suggested poor OS (P < 0.001), particularly with UISS intermediate and high score groups. Notably, the predictive accuracy of the traditional prognostic scores was improved when combined with galectin-7 expression. MATERIALS AND METHODS: We retrospectively enrolled 416 patients who underwent nephrectomy at a single institute between 2008 and 2009 and detected their intratumor galectin-7 expression by immunohistochemistry. Kaplan-Meier method was conducted to plot survival curves and multivariate cox regression analysis for potential independent prognostic factors on OS. A nomogram was constructed with concordance index (C-index) and Akaike's Information Criteria (AIC) to appraise prognostic accuracy of different models. CONCLUSIONS: High galectin-7 expression is an independent adverse predictor for survival. Evaluation of galectin-7 could help guide postsurgical management for non-metastatic ccRCC patients.
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spelling pubmed-51731102016-12-23 High expression of galectin-7 associates with poor overall survival in patients with non-metastatic clear-cell renal cell carcinoma Wang, Jieti Liu, Yidong Yang, Yuanfeng Xu, Zhiying Zhang, Guodong Liu, Zheng Fu, Hangcheng Wang, Zewei Liu, Haiou Xu, Jiejie Oncotarget Research Paper BACKGROUND: Galectin-7, has a controversial role in tumor progression, can either suppress tumor growth or induce chemoresistance depends on different tumor histology types. The aim was to appraise Galectin-7 expression on the overall survival (OS) of patients with non-metastatic clear cell renal cell carcinoma (ccRCC) following surgery. RESULTS: High galectin-7 expression was specifically correlated with necrosis (P = 0.015). Multivariate analysis confirmed galectin-7 as an independent prognosticator for OS (P = 0.005). High galectin-7 expression suggested poor OS (P < 0.001), particularly with UISS intermediate and high score groups. Notably, the predictive accuracy of the traditional prognostic scores was improved when combined with galectin-7 expression. MATERIALS AND METHODS: We retrospectively enrolled 416 patients who underwent nephrectomy at a single institute between 2008 and 2009 and detected their intratumor galectin-7 expression by immunohistochemistry. Kaplan-Meier method was conducted to plot survival curves and multivariate cox regression analysis for potential independent prognostic factors on OS. A nomogram was constructed with concordance index (C-index) and Akaike's Information Criteria (AIC) to appraise prognostic accuracy of different models. CONCLUSIONS: High galectin-7 expression is an independent adverse predictor for survival. Evaluation of galectin-7 could help guide postsurgical management for non-metastatic ccRCC patients. Impact Journals LLC 2016-05-31 /pmc/articles/PMC5173110/ /pubmed/27259255 http://dx.doi.org/10.18632/oncotarget.9749 Text en Copyright: © 2016 Wang et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Wang, Jieti
Liu, Yidong
Yang, Yuanfeng
Xu, Zhiying
Zhang, Guodong
Liu, Zheng
Fu, Hangcheng
Wang, Zewei
Liu, Haiou
Xu, Jiejie
High expression of galectin-7 associates with poor overall survival in patients with non-metastatic clear-cell renal cell carcinoma
title High expression of galectin-7 associates with poor overall survival in patients with non-metastatic clear-cell renal cell carcinoma
title_full High expression of galectin-7 associates with poor overall survival in patients with non-metastatic clear-cell renal cell carcinoma
title_fullStr High expression of galectin-7 associates with poor overall survival in patients with non-metastatic clear-cell renal cell carcinoma
title_full_unstemmed High expression of galectin-7 associates with poor overall survival in patients with non-metastatic clear-cell renal cell carcinoma
title_short High expression of galectin-7 associates with poor overall survival in patients with non-metastatic clear-cell renal cell carcinoma
title_sort high expression of galectin-7 associates with poor overall survival in patients with non-metastatic clear-cell renal cell carcinoma
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5173110/
https://www.ncbi.nlm.nih.gov/pubmed/27259255
http://dx.doi.org/10.18632/oncotarget.9749
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