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Relationships between expression of glucose transporter protein-1 and hypoxia inducible factor-1α, prognosis and (18)F-FDG uptake in laryngeal and hypopharyngeal carcinomas
BACKGROUND: We investigated the relationships between glucose transporter protein-1 (GLUT-1) and hypoxia inducible factor-1α (HIF-1α) expression, 2-deoxy-2-[(18)F]-fluoro-D-glucose ((18)F-FDG) uptake and prognosis in laryngeal and hypopharyngeal carcinomas patients. METHODS: Levels of GLUT-1 and HIF...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AME Publishing Company
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8797923/ https://www.ncbi.nlm.nih.gov/pubmed/35117639 http://dx.doi.org/10.21037/tcr.2020.02.50 |
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author | Shen, Li-Fang Zhou, Shui-Hong Yu, Qi |
author_facet | Shen, Li-Fang Zhou, Shui-Hong Yu, Qi |
author_sort | Shen, Li-Fang |
collection | PubMed |
description | BACKGROUND: We investigated the relationships between glucose transporter protein-1 (GLUT-1) and hypoxia inducible factor-1α (HIF-1α) expression, 2-deoxy-2-[(18)F]-fluoro-D-glucose ((18)F-FDG) uptake and prognosis in laryngeal and hypopharyngeal carcinomas patients. METHODS: Levels of GLUT-1 and HIF-1α proteins were examined by immunohistochemistry in 55 patients with laryngeal and hypopharyngeal carcinomas. All patients underwent (18)F-FDG positron emission tomography-computed tomography (PET/CT) before surgery. RESULTS: Levels of GLUT-1 and HIF-1α in laryngeal and hypopharyngeal carcinomas were significantly higher than in vocal cord polyps. GLUT-1 expression was correlated with HIF-1α expression (r=0.571, P<0.001) and SUV(max) (r=0.495, P<0.001). HIF-1α expression was not correlated with SUV(max) (P=0.199). HIF-1α expression was correlated with tumor size (r=0.351, P=0.009). Multivariate analysis demonstrated that treatment method (P=0.025), tumor size (P=0.008), GLUT-1 expression (P=0.032), and HIF-1α expression (P=0.032) were correlated with overall survival (OS). CONCLUSIONS: Treatment method, tumor size, GLUT-1 and HIF-1α levels were correlated with prognosis in laryngeal and hypopharyngeal carcinomas patients. |
format | Online Article Text |
id | pubmed-8797923 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | AME Publishing Company |
record_format | MEDLINE/PubMed |
spelling | pubmed-87979232022-02-02 Relationships between expression of glucose transporter protein-1 and hypoxia inducible factor-1α, prognosis and (18)F-FDG uptake in laryngeal and hypopharyngeal carcinomas Shen, Li-Fang Zhou, Shui-Hong Yu, Qi Transl Cancer Res Original Article BACKGROUND: We investigated the relationships between glucose transporter protein-1 (GLUT-1) and hypoxia inducible factor-1α (HIF-1α) expression, 2-deoxy-2-[(18)F]-fluoro-D-glucose ((18)F-FDG) uptake and prognosis in laryngeal and hypopharyngeal carcinomas patients. METHODS: Levels of GLUT-1 and HIF-1α proteins were examined by immunohistochemistry in 55 patients with laryngeal and hypopharyngeal carcinomas. All patients underwent (18)F-FDG positron emission tomography-computed tomography (PET/CT) before surgery. RESULTS: Levels of GLUT-1 and HIF-1α in laryngeal and hypopharyngeal carcinomas were significantly higher than in vocal cord polyps. GLUT-1 expression was correlated with HIF-1α expression (r=0.571, P<0.001) and SUV(max) (r=0.495, P<0.001). HIF-1α expression was not correlated with SUV(max) (P=0.199). HIF-1α expression was correlated with tumor size (r=0.351, P=0.009). Multivariate analysis demonstrated that treatment method (P=0.025), tumor size (P=0.008), GLUT-1 expression (P=0.032), and HIF-1α expression (P=0.032) were correlated with overall survival (OS). CONCLUSIONS: Treatment method, tumor size, GLUT-1 and HIF-1α levels were correlated with prognosis in laryngeal and hypopharyngeal carcinomas patients. AME Publishing Company 2020-04 /pmc/articles/PMC8797923/ /pubmed/35117639 http://dx.doi.org/10.21037/tcr.2020.02.50 Text en 2020 Translational Cancer Research. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/. |
spellingShingle | Original Article Shen, Li-Fang Zhou, Shui-Hong Yu, Qi Relationships between expression of glucose transporter protein-1 and hypoxia inducible factor-1α, prognosis and (18)F-FDG uptake in laryngeal and hypopharyngeal carcinomas |
title | Relationships between expression of glucose transporter protein-1 and hypoxia inducible factor-1α, prognosis and (18)F-FDG uptake in laryngeal and hypopharyngeal carcinomas |
title_full | Relationships between expression of glucose transporter protein-1 and hypoxia inducible factor-1α, prognosis and (18)F-FDG uptake in laryngeal and hypopharyngeal carcinomas |
title_fullStr | Relationships between expression of glucose transporter protein-1 and hypoxia inducible factor-1α, prognosis and (18)F-FDG uptake in laryngeal and hypopharyngeal carcinomas |
title_full_unstemmed | Relationships between expression of glucose transporter protein-1 and hypoxia inducible factor-1α, prognosis and (18)F-FDG uptake in laryngeal and hypopharyngeal carcinomas |
title_short | Relationships between expression of glucose transporter protein-1 and hypoxia inducible factor-1α, prognosis and (18)F-FDG uptake in laryngeal and hypopharyngeal carcinomas |
title_sort | relationships between expression of glucose transporter protein-1 and hypoxia inducible factor-1α, prognosis and (18)f-fdg uptake in laryngeal and hypopharyngeal carcinomas |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8797923/ https://www.ncbi.nlm.nih.gov/pubmed/35117639 http://dx.doi.org/10.21037/tcr.2020.02.50 |
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