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GLUT-1 overexpression as an unfavorable prognostic biomarker in patients with colorectal cancer

BACKGROUND: Glucose transporter-1 (GLUT-1) exhibits altered expression in colorectal cancer (CRC). The aim of this study was to explore the association between GLUT-1 and survival conditions, as well as clinical features in CRC by meta-analysis. MATERIALS AND METHODS: Relevant studies were searched...

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Autores principales: Yang, Jing, Wen, Jing, Tian, Tian, Lu, Zhongsheng, Wang, Yao, Wang, Zikai, Wang, Xiangdong, Yang, Yunsheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5355304/
https://www.ncbi.nlm.nih.gov/pubmed/28052033
http://dx.doi.org/10.18632/oncotarget.14352
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author Yang, Jing
Wen, Jing
Tian, Tian
Lu, Zhongsheng
Wang, Yao
Wang, Zikai
Wang, Xiangdong
Yang, Yunsheng
author_facet Yang, Jing
Wen, Jing
Tian, Tian
Lu, Zhongsheng
Wang, Yao
Wang, Zikai
Wang, Xiangdong
Yang, Yunsheng
author_sort Yang, Jing
collection PubMed
description BACKGROUND: Glucose transporter-1 (GLUT-1) exhibits altered expression in colorectal cancer (CRC). The aim of this study was to explore the association between GLUT-1 and survival conditions, as well as clinical features in CRC by meta-analysis. MATERIALS AND METHODS: Relevant studies were searched through predefined strategies, hazard ratios (HRs), odds ratios (ORs), and their 95% confidence intervals (CIs) were used as effective measures. RESULTS: A total of 14 studies with 2,077 patients were included in this meta-analysis. The results showed that GLUT-1 was not significantly associated with overall survival (OS) (HR=1.28, 95% CI=0.86–1.91, p=0.22) or disease-free survival (DFS) (HR=1.71, 95% CI=0.78–3.72, p=0.179). However, subgroup analysis indicated that GLUT-1 was a significant biomarker for poor DFS in rectal cancer (HR=2.47, 95% CI=1.21–5.05, p=0.013). GLUT-1 expression was also found to be significantly correlated with the presence of lymph node metastasis (n=8, OR=2.14, 95% CI=1.66–2.75, p<0.001), T stage (n=6, OR=1.73, 95% CI=1.17–2.58, p=0.007), higher Dukes stage (n=5, OR=2.92, 95% CI=2.16–3.95, p<0.001), female sex (n=4, OR=2.92, 95% CI=2.16–3.95, p<0.001), and presence of liver metastasis (n=3, OR=1.82, 95% CI=1.06–3.12, p=0.03). CONCLUSION: In conclusion, this meta-analysis showed that GLUT-1 was associated with poor DFS in rectal cancer (RC). Furthermore, GLUT-1 was also an indicator of aggressive clinical features in CRC.
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spelling pubmed-53553042017-04-26 GLUT-1 overexpression as an unfavorable prognostic biomarker in patients with colorectal cancer Yang, Jing Wen, Jing Tian, Tian Lu, Zhongsheng Wang, Yao Wang, Zikai Wang, Xiangdong Yang, Yunsheng Oncotarget Research Paper BACKGROUND: Glucose transporter-1 (GLUT-1) exhibits altered expression in colorectal cancer (CRC). The aim of this study was to explore the association between GLUT-1 and survival conditions, as well as clinical features in CRC by meta-analysis. MATERIALS AND METHODS: Relevant studies were searched through predefined strategies, hazard ratios (HRs), odds ratios (ORs), and their 95% confidence intervals (CIs) were used as effective measures. RESULTS: A total of 14 studies with 2,077 patients were included in this meta-analysis. The results showed that GLUT-1 was not significantly associated with overall survival (OS) (HR=1.28, 95% CI=0.86–1.91, p=0.22) or disease-free survival (DFS) (HR=1.71, 95% CI=0.78–3.72, p=0.179). However, subgroup analysis indicated that GLUT-1 was a significant biomarker for poor DFS in rectal cancer (HR=2.47, 95% CI=1.21–5.05, p=0.013). GLUT-1 expression was also found to be significantly correlated with the presence of lymph node metastasis (n=8, OR=2.14, 95% CI=1.66–2.75, p<0.001), T stage (n=6, OR=1.73, 95% CI=1.17–2.58, p=0.007), higher Dukes stage (n=5, OR=2.92, 95% CI=2.16–3.95, p<0.001), female sex (n=4, OR=2.92, 95% CI=2.16–3.95, p<0.001), and presence of liver metastasis (n=3, OR=1.82, 95% CI=1.06–3.12, p=0.03). CONCLUSION: In conclusion, this meta-analysis showed that GLUT-1 was associated with poor DFS in rectal cancer (RC). Furthermore, GLUT-1 was also an indicator of aggressive clinical features in CRC. Impact Journals LLC 2016-12-29 /pmc/articles/PMC5355304/ /pubmed/28052033 http://dx.doi.org/10.18632/oncotarget.14352 Text en Copyright: © 2017 Yang et al. http://creativecommons.org/licenses/by/3.0/ 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
Yang, Jing
Wen, Jing
Tian, Tian
Lu, Zhongsheng
Wang, Yao
Wang, Zikai
Wang, Xiangdong
Yang, Yunsheng
GLUT-1 overexpression as an unfavorable prognostic biomarker in patients with colorectal cancer
title GLUT-1 overexpression as an unfavorable prognostic biomarker in patients with colorectal cancer
title_full GLUT-1 overexpression as an unfavorable prognostic biomarker in patients with colorectal cancer
title_fullStr GLUT-1 overexpression as an unfavorable prognostic biomarker in patients with colorectal cancer
title_full_unstemmed GLUT-1 overexpression as an unfavorable prognostic biomarker in patients with colorectal cancer
title_short GLUT-1 overexpression as an unfavorable prognostic biomarker in patients with colorectal cancer
title_sort glut-1 overexpression as an unfavorable prognostic biomarker in patients with colorectal cancer
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5355304/
https://www.ncbi.nlm.nih.gov/pubmed/28052033
http://dx.doi.org/10.18632/oncotarget.14352
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