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Prognostic value of vascular endothelial growth factor (VEGF) in head and neck squamous cell carcinomas

Vascular endothelial growth factor (VEGF) has been identified as the substance that increases the permeability and proliferation of vascular endothelial cells. We examined the clinical significance of VEGF expression in 60 head and neck squamous cell carcinomas using the methods of Western blot, imm...

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Autores principales: Mineta, H, Miura, K, Ogino, T, Takebayashi, S, Misawa, K, Ueda, Y, Suzuki, I, Dictor, M, Borg, Å, Wennerberg, J
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2000
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2363534/
https://www.ncbi.nlm.nih.gov/pubmed/10952783
http://dx.doi.org/10.1054/bjoc.2000.1357
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author Mineta, H
Miura, K
Ogino, T
Takebayashi, S
Misawa, K
Ueda, Y
Suzuki, I
Dictor, M
Borg, Å
Wennerberg, J
author_facet Mineta, H
Miura, K
Ogino, T
Takebayashi, S
Misawa, K
Ueda, Y
Suzuki, I
Dictor, M
Borg, Å
Wennerberg, J
author_sort Mineta, H
collection PubMed
description Vascular endothelial growth factor (VEGF) has been identified as the substance that increases the permeability and proliferation of vascular endothelial cells. We examined the clinical significance of VEGF expression in 60 head and neck squamous cell carcinomas using the methods of Western blot, immunohistochemistry, and reverse transcriptase-polymerase chain reaction (RT-PCR), comparatively, and analysed the relationship between VEGF status in Western blot and tumour size, lymph-node status, histologic grade and disease-free survival (DFS) rate. Western blot analysis revealed high VEGF expressors (tumour/normal tissue density ≥ 3-fold) in 26 patients (43%) and low VEGF expressors (< 3-fold) in 34 patients (57%). The results of the Western blot analysis correlated significantly with those of the RT-PCR (P= 0.00007) or immunohistochemistry (P= 0.00006). High VEGF expressors are associated with the progression of lymph-node spread (P= 0.0009), which are correlated with poor DFS. The 2-year DFS rate of high VEGF expressors (30%) was significantly lower than that of low VEGF expressors (78%) (P= 0.0008). Multivariate analysis showed VEGF expression and stage were independent predictors for the DFS (P= 0.045 and 0.041, respectively). VEGF expression may play an important role in progression of HNSCC. © 2000 Cancer Research Campaign
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spelling pubmed-23635342009-09-10 Prognostic value of vascular endothelial growth factor (VEGF) in head and neck squamous cell carcinomas Mineta, H Miura, K Ogino, T Takebayashi, S Misawa, K Ueda, Y Suzuki, I Dictor, M Borg, Å Wennerberg, J Br J Cancer Regular Article Vascular endothelial growth factor (VEGF) has been identified as the substance that increases the permeability and proliferation of vascular endothelial cells. We examined the clinical significance of VEGF expression in 60 head and neck squamous cell carcinomas using the methods of Western blot, immunohistochemistry, and reverse transcriptase-polymerase chain reaction (RT-PCR), comparatively, and analysed the relationship between VEGF status in Western blot and tumour size, lymph-node status, histologic grade and disease-free survival (DFS) rate. Western blot analysis revealed high VEGF expressors (tumour/normal tissue density ≥ 3-fold) in 26 patients (43%) and low VEGF expressors (< 3-fold) in 34 patients (57%). The results of the Western blot analysis correlated significantly with those of the RT-PCR (P= 0.00007) or immunohistochemistry (P= 0.00006). High VEGF expressors are associated with the progression of lymph-node spread (P= 0.0009), which are correlated with poor DFS. The 2-year DFS rate of high VEGF expressors (30%) was significantly lower than that of low VEGF expressors (78%) (P= 0.0008). Multivariate analysis showed VEGF expression and stage were independent predictors for the DFS (P= 0.045 and 0.041, respectively). VEGF expression may play an important role in progression of HNSCC. © 2000 Cancer Research Campaign Nature Publishing Group 2000-09 2000-08-17 /pmc/articles/PMC2363534/ /pubmed/10952783 http://dx.doi.org/10.1054/bjoc.2000.1357 Text en Copyright © 2000 Cancer Research Campaign https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Regular Article
Mineta, H
Miura, K
Ogino, T
Takebayashi, S
Misawa, K
Ueda, Y
Suzuki, I
Dictor, M
Borg, Å
Wennerberg, J
Prognostic value of vascular endothelial growth factor (VEGF) in head and neck squamous cell carcinomas
title Prognostic value of vascular endothelial growth factor (VEGF) in head and neck squamous cell carcinomas
title_full Prognostic value of vascular endothelial growth factor (VEGF) in head and neck squamous cell carcinomas
title_fullStr Prognostic value of vascular endothelial growth factor (VEGF) in head and neck squamous cell carcinomas
title_full_unstemmed Prognostic value of vascular endothelial growth factor (VEGF) in head and neck squamous cell carcinomas
title_short Prognostic value of vascular endothelial growth factor (VEGF) in head and neck squamous cell carcinomas
title_sort prognostic value of vascular endothelial growth factor (vegf) in head and neck squamous cell carcinomas
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2363534/
https://www.ncbi.nlm.nih.gov/pubmed/10952783
http://dx.doi.org/10.1054/bjoc.2000.1357
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