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Prognostic value of GLUT-1 expression in oral squamous cell carcinoma: A prisma-compliant meta-analysis

BACKGROUND: A variety of studies have evaluated the correlation between glucose transporter-1 (GLUT-1) expression and prognosis of oral squamous cell carcinoma (OSCC); however, the results were inconsistent and inconclusive. A meta-analysis was performed to assess the prognostic significance of GLUT...

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Autores principales: Li, Chen-Xi, Sun, Jia-Lin, Gong, Zhong-Cheng, Lin, Zhao-Quan, Liu, Hui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5106058/
https://www.ncbi.nlm.nih.gov/pubmed/27828852
http://dx.doi.org/10.1097/MD.0000000000005324
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author Li, Chen-Xi
Sun, Jia-Lin
Gong, Zhong-Cheng
Lin, Zhao-Quan
Liu, Hui
author_facet Li, Chen-Xi
Sun, Jia-Lin
Gong, Zhong-Cheng
Lin, Zhao-Quan
Liu, Hui
author_sort Li, Chen-Xi
collection PubMed
description BACKGROUND: A variety of studies have evaluated the correlation between glucose transporter-1 (GLUT-1) expression and prognosis of oral squamous cell carcinoma (OSCC); however, the results were inconsistent and inconclusive. A meta-analysis was performed to assess the prognostic significance of GLUT-1 in OSCC. METHODS: Electronic databases of PubMed, Embase, and Web of Science were searched for relevant studies. The last search was updated on July 2016. Odds ratio (OR) and 95% confidence interval (CI) were pooled to evaluate the relationship between GLUT-1 and clinical features and hazard ratio (HR) and 95% CI were combined to measure the effect of GLUT-1 on overall survival (OS). P value < 0.05 was considered as statistically significant. RESULTS: A total of 13 studies with 1301 subjects were included for meta-analysis. The pooled data showed that high GLUT-1 expression was associated with advanced tumor stages (n = 7, OR = 2.99, 95% CI: 2.01–4.46, P < 0.001), higher tumor grade (n = 5, OR = 3.34, 95%CI: 1.12–9.94, P = 0.031), tumor size (n = 5, OR = 3.36, 95%CI: 2.04–5.51, P < 0.001), lymph node metastasis (n = 5, OR = 3.15, 95%CI: 1.89–5.25, P < 0.001), tobacco use (n = 3, OR = 2.18, 95%CI: 1.18–4.01, P = 0.013), and distant metastasis (n = 2, OR = 3.06, 95%CI: 1.19–7.9, P = 0.02). Furthermore, increased GLUT-1 expression was also correlated with shorter OS (n = 8, HR = 1.88, 95%CI: 1.51–2.33, P < 0.001). No significant publication bias was detected in this meta-analysis. CONCLUSION: GLUT-1 overexpression was in connection with aggressive clinical features and worse OS in OSCC. However, further studies are still needed to verify whether GLUT-1 could serve as a prognostic biomarker for OSCC.
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spelling pubmed-51060582016-11-16 Prognostic value of GLUT-1 expression in oral squamous cell carcinoma: A prisma-compliant meta-analysis Li, Chen-Xi Sun, Jia-Lin Gong, Zhong-Cheng Lin, Zhao-Quan Liu, Hui Medicine (Baltimore) 5900 BACKGROUND: A variety of studies have evaluated the correlation between glucose transporter-1 (GLUT-1) expression and prognosis of oral squamous cell carcinoma (OSCC); however, the results were inconsistent and inconclusive. A meta-analysis was performed to assess the prognostic significance of GLUT-1 in OSCC. METHODS: Electronic databases of PubMed, Embase, and Web of Science were searched for relevant studies. The last search was updated on July 2016. Odds ratio (OR) and 95% confidence interval (CI) were pooled to evaluate the relationship between GLUT-1 and clinical features and hazard ratio (HR) and 95% CI were combined to measure the effect of GLUT-1 on overall survival (OS). P value < 0.05 was considered as statistically significant. RESULTS: A total of 13 studies with 1301 subjects were included for meta-analysis. The pooled data showed that high GLUT-1 expression was associated with advanced tumor stages (n = 7, OR = 2.99, 95% CI: 2.01–4.46, P < 0.001), higher tumor grade (n = 5, OR = 3.34, 95%CI: 1.12–9.94, P = 0.031), tumor size (n = 5, OR = 3.36, 95%CI: 2.04–5.51, P < 0.001), lymph node metastasis (n = 5, OR = 3.15, 95%CI: 1.89–5.25, P < 0.001), tobacco use (n = 3, OR = 2.18, 95%CI: 1.18–4.01, P = 0.013), and distant metastasis (n = 2, OR = 3.06, 95%CI: 1.19–7.9, P = 0.02). Furthermore, increased GLUT-1 expression was also correlated with shorter OS (n = 8, HR = 1.88, 95%CI: 1.51–2.33, P < 0.001). No significant publication bias was detected in this meta-analysis. CONCLUSION: GLUT-1 overexpression was in connection with aggressive clinical features and worse OS in OSCC. However, further studies are still needed to verify whether GLUT-1 could serve as a prognostic biomarker for OSCC. Wolters Kluwer Health 2016-11-11 /pmc/articles/PMC5106058/ /pubmed/27828852 http://dx.doi.org/10.1097/MD.0000000000005324 Text en Copyright © 2016 the Author(s). Published by Wolters Kluwer Health, Inc. All rights reserved. http://creativecommons.org/licenses/by/4.0 This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0
spellingShingle 5900
Li, Chen-Xi
Sun, Jia-Lin
Gong, Zhong-Cheng
Lin, Zhao-Quan
Liu, Hui
Prognostic value of GLUT-1 expression in oral squamous cell carcinoma: A prisma-compliant meta-analysis
title Prognostic value of GLUT-1 expression in oral squamous cell carcinoma: A prisma-compliant meta-analysis
title_full Prognostic value of GLUT-1 expression in oral squamous cell carcinoma: A prisma-compliant meta-analysis
title_fullStr Prognostic value of GLUT-1 expression in oral squamous cell carcinoma: A prisma-compliant meta-analysis
title_full_unstemmed Prognostic value of GLUT-1 expression in oral squamous cell carcinoma: A prisma-compliant meta-analysis
title_short Prognostic value of GLUT-1 expression in oral squamous cell carcinoma: A prisma-compliant meta-analysis
title_sort prognostic value of glut-1 expression in oral squamous cell carcinoma: a prisma-compliant meta-analysis
topic 5900
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5106058/
https://www.ncbi.nlm.nih.gov/pubmed/27828852
http://dx.doi.org/10.1097/MD.0000000000005324
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