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Expression and prognostic value of VEGFR-2, PDGFR-β, and c-Met in advanced hepatocellular carcinoma

BACKGROUND: We explore the clinical and prognostic significance of expression of vascular endothelial growth factor receptor (VEGFR)-2, platelet-derived growth factor receptor (PDGFR)-β, and c-Met in patients with hepatocellular carcinoma (HCC). METHODS: The expression of VEGFR-2, PDGFR-β, and c-Met...

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Autores principales: Chu, Jie Sheng, Ge, Fei Jiao, Zhang, Bo, Wang, Yan, Silvestris, Nicola, Liu, Lie Jun, Zhao, Chuan Hua, Lin, Li, Brunetti, Anna Elisabetta, Fu, Ya Li, Wang, Jun, Paradiso, Angelo, Xu, Jian Ming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3623756/
https://www.ncbi.nlm.nih.gov/pubmed/23552472
http://dx.doi.org/10.1186/1756-9966-32-16
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author Chu, Jie Sheng
Ge, Fei Jiao
Zhang, Bo
Wang, Yan
Silvestris, Nicola
Liu, Lie Jun
Zhao, Chuan Hua
Lin, Li
Brunetti, Anna Elisabetta
Fu, Ya Li
Wang, Jun
Paradiso, Angelo
Xu, Jian Ming
author_facet Chu, Jie Sheng
Ge, Fei Jiao
Zhang, Bo
Wang, Yan
Silvestris, Nicola
Liu, Lie Jun
Zhao, Chuan Hua
Lin, Li
Brunetti, Anna Elisabetta
Fu, Ya Li
Wang, Jun
Paradiso, Angelo
Xu, Jian Ming
author_sort Chu, Jie Sheng
collection PubMed
description BACKGROUND: We explore the clinical and prognostic significance of expression of vascular endothelial growth factor receptor (VEGFR)-2, platelet-derived growth factor receptor (PDGFR)-β, and c-Met in patients with hepatocellular carcinoma (HCC). METHODS: The expression of VEGFR-2, PDGFR-β, and c-Met were determined by immunohistochemical examination of the tissues of 93 HCC patients. The relationships of these markers with clinicopathological factors and prognosis were then analyzed. RESULTS: High expression of VEGFR-2, PDGFR-β, and c-Met was found in 86%, 19.4%, and 80.6% of patients, respectively. Expression of VEGFR-2 correlated with gender (P = 0.044), hepatitis B surface antigen positivity (P = 0.024), degree of tumor differentiation (P = 0.023), and hepatic cirrhosis (P = 0.026). Expression of PDGFR-β correlated with alpha-fetoprotein level (P = 0.029), tumor size (P = 0.033), and hepatic cirrhosis (P = 0.023). No significant correlations were identified between expression of c-Met and clinicopathological factors. Expression of PDGFR-β correlated with overall survival (P = 0.046) and expression of c-Met correlated with progression-free survival (P = 0.01). CONCLUSIONS: We found that in patients with HCC, high expression of VEGFR-2 correlates with chronic hepatitis B virus infection and hepatic cirrhosis. High expression of PDGFR-β is a predictor of poor prognosis. High expression of C-Met may predict therapeutic effectiveness of sorafenib in HCC patients.
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spelling pubmed-36237562013-04-12 Expression and prognostic value of VEGFR-2, PDGFR-β, and c-Met in advanced hepatocellular carcinoma Chu, Jie Sheng Ge, Fei Jiao Zhang, Bo Wang, Yan Silvestris, Nicola Liu, Lie Jun Zhao, Chuan Hua Lin, Li Brunetti, Anna Elisabetta Fu, Ya Li Wang, Jun Paradiso, Angelo Xu, Jian Ming J Exp Clin Cancer Res Research BACKGROUND: We explore the clinical and prognostic significance of expression of vascular endothelial growth factor receptor (VEGFR)-2, platelet-derived growth factor receptor (PDGFR)-β, and c-Met in patients with hepatocellular carcinoma (HCC). METHODS: The expression of VEGFR-2, PDGFR-β, and c-Met were determined by immunohistochemical examination of the tissues of 93 HCC patients. The relationships of these markers with clinicopathological factors and prognosis were then analyzed. RESULTS: High expression of VEGFR-2, PDGFR-β, and c-Met was found in 86%, 19.4%, and 80.6% of patients, respectively. Expression of VEGFR-2 correlated with gender (P = 0.044), hepatitis B surface antigen positivity (P = 0.024), degree of tumor differentiation (P = 0.023), and hepatic cirrhosis (P = 0.026). Expression of PDGFR-β correlated with alpha-fetoprotein level (P = 0.029), tumor size (P = 0.033), and hepatic cirrhosis (P = 0.023). No significant correlations were identified between expression of c-Met and clinicopathological factors. Expression of PDGFR-β correlated with overall survival (P = 0.046) and expression of c-Met correlated with progression-free survival (P = 0.01). CONCLUSIONS: We found that in patients with HCC, high expression of VEGFR-2 correlates with chronic hepatitis B virus infection and hepatic cirrhosis. High expression of PDGFR-β is a predictor of poor prognosis. High expression of C-Met may predict therapeutic effectiveness of sorafenib in HCC patients. BioMed Central 2013-04-03 /pmc/articles/PMC3623756/ /pubmed/23552472 http://dx.doi.org/10.1186/1756-9966-32-16 Text en Copyright © 2013 Chu et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Chu, Jie Sheng
Ge, Fei Jiao
Zhang, Bo
Wang, Yan
Silvestris, Nicola
Liu, Lie Jun
Zhao, Chuan Hua
Lin, Li
Brunetti, Anna Elisabetta
Fu, Ya Li
Wang, Jun
Paradiso, Angelo
Xu, Jian Ming
Expression and prognostic value of VEGFR-2, PDGFR-β, and c-Met in advanced hepatocellular carcinoma
title Expression and prognostic value of VEGFR-2, PDGFR-β, and c-Met in advanced hepatocellular carcinoma
title_full Expression and prognostic value of VEGFR-2, PDGFR-β, and c-Met in advanced hepatocellular carcinoma
title_fullStr Expression and prognostic value of VEGFR-2, PDGFR-β, and c-Met in advanced hepatocellular carcinoma
title_full_unstemmed Expression and prognostic value of VEGFR-2, PDGFR-β, and c-Met in advanced hepatocellular carcinoma
title_short Expression and prognostic value of VEGFR-2, PDGFR-β, and c-Met in advanced hepatocellular carcinoma
title_sort expression and prognostic value of vegfr-2, pdgfr-β, and c-met in advanced hepatocellular carcinoma
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3623756/
https://www.ncbi.nlm.nih.gov/pubmed/23552472
http://dx.doi.org/10.1186/1756-9966-32-16
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