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Prognostic significance of NANOG expression in solid tumors: a meta-analysis

PURPOSE: NANOG is a tumor marker and indicates poor prognosis in various neoplasms; however, the evidence is controversial. This meta-analysis investigated the association of NANOG expression and clinicopathological features, and it impact on survival of patients with malignant tumors. METHODS: Stud...

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Autores principales: Zhao, Lingqiong, Liu, Jie, Chen, Shu, Fang, Chun, Zhang, Xianquan, Luo, Zhibin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6134963/
https://www.ncbi.nlm.nih.gov/pubmed/30233213
http://dx.doi.org/10.2147/OTT.S169593
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author Zhao, Lingqiong
Liu, Jie
Chen, Shu
Fang, Chun
Zhang, Xianquan
Luo, Zhibin
author_facet Zhao, Lingqiong
Liu, Jie
Chen, Shu
Fang, Chun
Zhang, Xianquan
Luo, Zhibin
author_sort Zhao, Lingqiong
collection PubMed
description PURPOSE: NANOG is a tumor marker and indicates poor prognosis in various neoplasms; however, the evidence is controversial. This meta-analysis investigated the association of NANOG expression and clinicopathological features, and it impact on survival of patients with malignant tumors. METHODS: Studies published through May 31, 2018 were retrieved from PubMed, Web of Science, Embase, and the China National Knowledge Infrastructure. Two researchers independently screened the content and quality of studies and extracted data. Correlations of NANOG expression, clinicopathological variables, and survival were analyzed and the combined odds ratios (ORs) and hazard ratios (HRs) with 95% confidence intervals (95% CIs) were calculated. RESULTS: Thirty-three articles including 35 data sets of 3,959 patients were analyzed. Overall, elevated NANOG expression was associated with poor overall survival (HR = 2.19; 95% CI: 1.87–2.58, P<0.001) and poor disease-free survival (HR = 2.21, 95% CI: 1.54–3.18, P<0.001). Subgroup analysis found that NANOG expression was associated with worse overall survival in non–small cell lung (HR = 1.87; 95% CI: 1.26–2.76, P = 0.002), head and neck (HR = 2.29; 95% CI: 1.75–3.02, P<0.001), and digestive system (HR = 2.38; 95% CI: 1.95–2.91, P<0.001) cancers. Moreover, we found that high NANOG expression was associated with poor tumor differentiation (OR = 2.63; 95% CI: 1.59–4.55, P = 0.001), lymph node metastasis (OR = 2.59; 95% CI: 1.50–4.47, P = 0.001), advanced TNM stage (OR = 2.22; 95% CI: 1.42–3.45, P<0.001), and T stage (OR = 0.44; 95% CI: 0.20–0.93, P = 0.031). CONCLUSION: The evidence supports NANOG as a tumor biomarker to guide clinical management and indicate prognosis. Additional studies are needed to further validate these results.
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spelling pubmed-61349632018-09-19 Prognostic significance of NANOG expression in solid tumors: a meta-analysis Zhao, Lingqiong Liu, Jie Chen, Shu Fang, Chun Zhang, Xianquan Luo, Zhibin Onco Targets Ther Review PURPOSE: NANOG is a tumor marker and indicates poor prognosis in various neoplasms; however, the evidence is controversial. This meta-analysis investigated the association of NANOG expression and clinicopathological features, and it impact on survival of patients with malignant tumors. METHODS: Studies published through May 31, 2018 were retrieved from PubMed, Web of Science, Embase, and the China National Knowledge Infrastructure. Two researchers independently screened the content and quality of studies and extracted data. Correlations of NANOG expression, clinicopathological variables, and survival were analyzed and the combined odds ratios (ORs) and hazard ratios (HRs) with 95% confidence intervals (95% CIs) were calculated. RESULTS: Thirty-three articles including 35 data sets of 3,959 patients were analyzed. Overall, elevated NANOG expression was associated with poor overall survival (HR = 2.19; 95% CI: 1.87–2.58, P<0.001) and poor disease-free survival (HR = 2.21, 95% CI: 1.54–3.18, P<0.001). Subgroup analysis found that NANOG expression was associated with worse overall survival in non–small cell lung (HR = 1.87; 95% CI: 1.26–2.76, P = 0.002), head and neck (HR = 2.29; 95% CI: 1.75–3.02, P<0.001), and digestive system (HR = 2.38; 95% CI: 1.95–2.91, P<0.001) cancers. Moreover, we found that high NANOG expression was associated with poor tumor differentiation (OR = 2.63; 95% CI: 1.59–4.55, P = 0.001), lymph node metastasis (OR = 2.59; 95% CI: 1.50–4.47, P = 0.001), advanced TNM stage (OR = 2.22; 95% CI: 1.42–3.45, P<0.001), and T stage (OR = 0.44; 95% CI: 0.20–0.93, P = 0.031). CONCLUSION: The evidence supports NANOG as a tumor biomarker to guide clinical management and indicate prognosis. Additional studies are needed to further validate these results. Dove Medical Press 2018-09-06 /pmc/articles/PMC6134963/ /pubmed/30233213 http://dx.doi.org/10.2147/OTT.S169593 Text en © 2018 Zhao et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Review
Zhao, Lingqiong
Liu, Jie
Chen, Shu
Fang, Chun
Zhang, Xianquan
Luo, Zhibin
Prognostic significance of NANOG expression in solid tumors: a meta-analysis
title Prognostic significance of NANOG expression in solid tumors: a meta-analysis
title_full Prognostic significance of NANOG expression in solid tumors: a meta-analysis
title_fullStr Prognostic significance of NANOG expression in solid tumors: a meta-analysis
title_full_unstemmed Prognostic significance of NANOG expression in solid tumors: a meta-analysis
title_short Prognostic significance of NANOG expression in solid tumors: a meta-analysis
title_sort prognostic significance of nanog expression in solid tumors: a meta-analysis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6134963/
https://www.ncbi.nlm.nih.gov/pubmed/30233213
http://dx.doi.org/10.2147/OTT.S169593
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