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The prognostic value of AGR2 expression in solid tumours: a systematic review and meta-analysis

The prognostic value of anterior gradient-2 (AGR2) in tumours remains inconclusive. Here, we systematically reviewed the literature evidence and assessed the association between AGR2 expression and prognosis in solid tumours. The primary outcomes were overall survival (OS), disease-specific survival...

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Autores principales: Tian, Shao-bo, Tao, Kai-xiong, Hu, Jia, Liu, Zhi-bo, Ding, Xue-liang, Chu, Ya-nan, Cui, Jin-yuan, Shuai, Xiao-ming, Gao, Jin-bo, Cai, Kai-lin, Wang, Ji-liang, Wang, Guo-bin, Wang, Lin, Wang, Zheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5686151/
https://www.ncbi.nlm.nih.gov/pubmed/29138453
http://dx.doi.org/10.1038/s41598-017-15757-z
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author Tian, Shao-bo
Tao, Kai-xiong
Hu, Jia
Liu, Zhi-bo
Ding, Xue-liang
Chu, Ya-nan
Cui, Jin-yuan
Shuai, Xiao-ming
Gao, Jin-bo
Cai, Kai-lin
Wang, Ji-liang
Wang, Guo-bin
Wang, Lin
Wang, Zheng
author_facet Tian, Shao-bo
Tao, Kai-xiong
Hu, Jia
Liu, Zhi-bo
Ding, Xue-liang
Chu, Ya-nan
Cui, Jin-yuan
Shuai, Xiao-ming
Gao, Jin-bo
Cai, Kai-lin
Wang, Ji-liang
Wang, Guo-bin
Wang, Lin
Wang, Zheng
author_sort Tian, Shao-bo
collection PubMed
description The prognostic value of anterior gradient-2 (AGR2) in tumours remains inconclusive. Here, we systematically reviewed the literature evidence and assessed the association between AGR2 expression and prognosis in solid tumours. The primary outcomes were overall survival (OS), disease-specific survival (DSS), and disease-free survival (DFS)/recurrence-free survival (RFS)/progression-free survival (PFS). All analyses were performed by STATA 12.0, with the hazard ratio (HR) or odds ratios (OR), and 95% confidence interval (CI) as the effect size estimate. A total of 20 studies containing 3285 cases were included. Pooled analyses revealed that AGR2 overexpression had an unfavourable impact on OS (HR 1.93, 95% CI 1.32–2.81) and time to tumour progression (TTP) (DFS/RFS/PFS) (HR 1.60 95% CI 1.06–2.40) in solid tumour patients. Subgroup analyses indicated that AGR2 overexpression in breast cancer patients was significantly associated with poor OS (HR 3.02, 95% CI 1.03–8.81) and TTP (HR 1.93, 95% CI 1.17–3.20). Excluding breast cancer, AGR2 overexpression was also found to have a significant correlation with poor OS in the remaining solid tumour patients (HR 1.51, 95% CI 1.04–2.19). Overall, AGR2 might be a potential biomarker to predict prognosis in solid tumour patients.
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spelling pubmed-56861512017-11-29 The prognostic value of AGR2 expression in solid tumours: a systematic review and meta-analysis Tian, Shao-bo Tao, Kai-xiong Hu, Jia Liu, Zhi-bo Ding, Xue-liang Chu, Ya-nan Cui, Jin-yuan Shuai, Xiao-ming Gao, Jin-bo Cai, Kai-lin Wang, Ji-liang Wang, Guo-bin Wang, Lin Wang, Zheng Sci Rep Article The prognostic value of anterior gradient-2 (AGR2) in tumours remains inconclusive. Here, we systematically reviewed the literature evidence and assessed the association between AGR2 expression and prognosis in solid tumours. The primary outcomes were overall survival (OS), disease-specific survival (DSS), and disease-free survival (DFS)/recurrence-free survival (RFS)/progression-free survival (PFS). All analyses were performed by STATA 12.0, with the hazard ratio (HR) or odds ratios (OR), and 95% confidence interval (CI) as the effect size estimate. A total of 20 studies containing 3285 cases were included. Pooled analyses revealed that AGR2 overexpression had an unfavourable impact on OS (HR 1.93, 95% CI 1.32–2.81) and time to tumour progression (TTP) (DFS/RFS/PFS) (HR 1.60 95% CI 1.06–2.40) in solid tumour patients. Subgroup analyses indicated that AGR2 overexpression in breast cancer patients was significantly associated with poor OS (HR 3.02, 95% CI 1.03–8.81) and TTP (HR 1.93, 95% CI 1.17–3.20). Excluding breast cancer, AGR2 overexpression was also found to have a significant correlation with poor OS in the remaining solid tumour patients (HR 1.51, 95% CI 1.04–2.19). Overall, AGR2 might be a potential biomarker to predict prognosis in solid tumour patients. Nature Publishing Group UK 2017-11-14 /pmc/articles/PMC5686151/ /pubmed/29138453 http://dx.doi.org/10.1038/s41598-017-15757-z Text en © The Author(s) 2017 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
Tian, Shao-bo
Tao, Kai-xiong
Hu, Jia
Liu, Zhi-bo
Ding, Xue-liang
Chu, Ya-nan
Cui, Jin-yuan
Shuai, Xiao-ming
Gao, Jin-bo
Cai, Kai-lin
Wang, Ji-liang
Wang, Guo-bin
Wang, Lin
Wang, Zheng
The prognostic value of AGR2 expression in solid tumours: a systematic review and meta-analysis
title The prognostic value of AGR2 expression in solid tumours: a systematic review and meta-analysis
title_full The prognostic value of AGR2 expression in solid tumours: a systematic review and meta-analysis
title_fullStr The prognostic value of AGR2 expression in solid tumours: a systematic review and meta-analysis
title_full_unstemmed The prognostic value of AGR2 expression in solid tumours: a systematic review and meta-analysis
title_short The prognostic value of AGR2 expression in solid tumours: a systematic review and meta-analysis
title_sort prognostic value of agr2 expression in solid tumours: a systematic review and meta-analysis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5686151/
https://www.ncbi.nlm.nih.gov/pubmed/29138453
http://dx.doi.org/10.1038/s41598-017-15757-z
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