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Potential Role of Glucose Transporter-1 Expression in Gastric Cancer: A Meta-Analysis and Systematic Review

BACKGROUND: Glucose transporter-1 (GLUT-1) has been differentially expressed in various malignancies including gastric cancer (GC). Several previous meta-analyses of GLUT-1 have some significant limitations, such as researching the association between GLUT-1 and various cancer types with no specific...

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Autores principales: TAO, Jianxin, ZHANG, Ye, WANG, Tong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tehran University of Medical Sciences 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7917512/
https://www.ncbi.nlm.nih.gov/pubmed/33708725
http://dx.doi.org/10.18502/ijph.v49i11.4719
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author TAO, Jianxin
ZHANG, Ye
WANG, Tong
author_facet TAO, Jianxin
ZHANG, Ye
WANG, Tong
author_sort TAO, Jianxin
collection PubMed
description BACKGROUND: Glucose transporter-1 (GLUT-1) has been differentially expressed in various malignancies including gastric cancer (GC). Several previous meta-analyses of GLUT-1 have some significant limitations, such as researching the association between GLUT-1 and various cancer types with no specificity, not studying clinicopathological parameters with GLUT-1, existing conspicuous heterogeneity and so forth. Therefore, we performed a meta-analysis to evaluate the association between GLUT-1 expression and survival of gastric cancer patients, as well as clinicopathological characteristics. METHODS: We systematically searched PubMed, Embase, Web of Science and China National Knowledge Infrastructure for relevant studies in accordance with the applicable criteria up to Aug 2017. Hazard ratios (HRs) and odds ratios (ORs) with their 95% confidence intervals (CIs) were used as the effective measures. RESULTS: A total of 13 studies involving 1972 patients were included in this meta-analysis. The results demonstrated that there was a significant association between GLUT-1 expression and overall survival (OS) (HR=1.45, 95% CI=1.13–1.87) or disease-free survival (DFS) (HR=2.18, 95% CI=1.46–3.25). Moreover, GLUT-1 expression was significantly correlated with worse tumor nodes metastases (TNM) stage (OR=0.34, 95% CI=0.28–0.43), presence of lymph node metastasis (OR=2.88, 95% CI=1.34–6.19), intestinal type of Lauren classification (OR=3.84, 95% CI=2.57–5.74) and invasion of serosa (OR=0.25, 95% CI=0.18–0.35). CONCLUSION: Our meta-analysis showed that GLUT-1 was significantly correlated with poor OS and DFS in gastric cancer. Additionally, GLUT-1 was also a potential prognostic indicator of aggressive clinicopathological parameters in gastric cancer.
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spelling pubmed-79175122021-03-10 Potential Role of Glucose Transporter-1 Expression in Gastric Cancer: A Meta-Analysis and Systematic Review TAO, Jianxin ZHANG, Ye WANG, Tong Iran J Public Health Review Article BACKGROUND: Glucose transporter-1 (GLUT-1) has been differentially expressed in various malignancies including gastric cancer (GC). Several previous meta-analyses of GLUT-1 have some significant limitations, such as researching the association between GLUT-1 and various cancer types with no specificity, not studying clinicopathological parameters with GLUT-1, existing conspicuous heterogeneity and so forth. Therefore, we performed a meta-analysis to evaluate the association between GLUT-1 expression and survival of gastric cancer patients, as well as clinicopathological characteristics. METHODS: We systematically searched PubMed, Embase, Web of Science and China National Knowledge Infrastructure for relevant studies in accordance with the applicable criteria up to Aug 2017. Hazard ratios (HRs) and odds ratios (ORs) with their 95% confidence intervals (CIs) were used as the effective measures. RESULTS: A total of 13 studies involving 1972 patients were included in this meta-analysis. The results demonstrated that there was a significant association between GLUT-1 expression and overall survival (OS) (HR=1.45, 95% CI=1.13–1.87) or disease-free survival (DFS) (HR=2.18, 95% CI=1.46–3.25). Moreover, GLUT-1 expression was significantly correlated with worse tumor nodes metastases (TNM) stage (OR=0.34, 95% CI=0.28–0.43), presence of lymph node metastasis (OR=2.88, 95% CI=1.34–6.19), intestinal type of Lauren classification (OR=3.84, 95% CI=2.57–5.74) and invasion of serosa (OR=0.25, 95% CI=0.18–0.35). CONCLUSION: Our meta-analysis showed that GLUT-1 was significantly correlated with poor OS and DFS in gastric cancer. Additionally, GLUT-1 was also a potential prognostic indicator of aggressive clinicopathological parameters in gastric cancer. Tehran University of Medical Sciences 2020-11 /pmc/articles/PMC7917512/ /pubmed/33708725 http://dx.doi.org/10.18502/ijph.v49i11.4719 Text en Copyright © 2020 Tao et al. Published by Tehran University of Medical Sciences https://creativecommons.org/licenses/by-nc/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International license (https://creativecommons.org/licenses/by-nc/4.0/). Non-commercial uses of the work are permitted, provided the original work is properly cited.
spellingShingle Review Article
TAO, Jianxin
ZHANG, Ye
WANG, Tong
Potential Role of Glucose Transporter-1 Expression in Gastric Cancer: A Meta-Analysis and Systematic Review
title Potential Role of Glucose Transporter-1 Expression in Gastric Cancer: A Meta-Analysis and Systematic Review
title_full Potential Role of Glucose Transporter-1 Expression in Gastric Cancer: A Meta-Analysis and Systematic Review
title_fullStr Potential Role of Glucose Transporter-1 Expression in Gastric Cancer: A Meta-Analysis and Systematic Review
title_full_unstemmed Potential Role of Glucose Transporter-1 Expression in Gastric Cancer: A Meta-Analysis and Systematic Review
title_short Potential Role of Glucose Transporter-1 Expression in Gastric Cancer: A Meta-Analysis and Systematic Review
title_sort potential role of glucose transporter-1 expression in gastric cancer: a meta-analysis and systematic review
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7917512/
https://www.ncbi.nlm.nih.gov/pubmed/33708725
http://dx.doi.org/10.18502/ijph.v49i11.4719
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