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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2016
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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. |
format | Online Article Text |
id | pubmed-5355304 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
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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