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Serum Endocan as a Novel Prognostic Biomarker in Patients with Hepatocellular Carcinoma

Endocan is a vascular endothelium-derived factor regulated by angiogenic factors. The aim of this study was to determine whether serum endocan levels are prognostic for survival in patients with hepatocellular carcinoma (HCC). Serum endocan levels were measured in 64 HCC patients who were naïve to t...

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Autores principales: Ozaki, Kazuaki, Toshikuni, Nobuyuki, George, Joseph, Minato, Takahiro, Matsue, Yasuhiro, Arisawa, Tomiyasu, Tsutsumi, Mikihiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3963079/
https://www.ncbi.nlm.nih.gov/pubmed/24665346
http://dx.doi.org/10.7150/jca.7691
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author Ozaki, Kazuaki
Toshikuni, Nobuyuki
George, Joseph
Minato, Takahiro
Matsue, Yasuhiro
Arisawa, Tomiyasu
Tsutsumi, Mikihiro
author_facet Ozaki, Kazuaki
Toshikuni, Nobuyuki
George, Joseph
Minato, Takahiro
Matsue, Yasuhiro
Arisawa, Tomiyasu
Tsutsumi, Mikihiro
author_sort Ozaki, Kazuaki
collection PubMed
description Endocan is a vascular endothelium-derived factor regulated by angiogenic factors. The aim of this study was to determine whether serum endocan levels are prognostic for survival in patients with hepatocellular carcinoma (HCC). Serum endocan levels were measured in 64 HCC patients who were naïve to treatment, eight apparently healthy subjects, and 68 patients with liver cirrhosis; the latter two groups served as controls. Prognostic factors for the survival of HCC patients were examined using a Cox proportional hazards model. The median serum endocan levels were 1.145 ng/mL (range, 0.93-1.68 ng/mL) in healthy subjects, 1.93 ng/mL (range, 0.45-8.47 ng/mL) in liver cirrhosis patients, and 3.73 ng/mL (range, 0.74-10.95 ng/mL) in HCC patients (P = 0.0001). In HCC patients, elevated serum endocan levels were significantly associated with poor hepatic function (P = 0.015), a greater number of tumors (P = 0.034), and vascular invasion (P = 0.043). The median follow-up period was 23.0 months, and 33 HCC patients died during follow up. Multivariate analysis showed that serum endocan levels ≥ 2.20 ng/mL (hazard ratio 2.36, 95% confidence interval 1.22-5.36, P = 0.008) as well as elevated serum α-fetoprotein and des-γ-carboxy prothrombin levels were independent prognostic biomarkers for poor survival. The combination of serum endocan and these two additional markers was significantly predictive of worse survival (P < 0.0001). Thus, serum endocan may be a prognostic biomarker for survival in HCC patients, and the combination of serum endocan, α-fetoprotein, and des-γ-carboxy prothrombin levels can result in better prognostic stratification of these patients.
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spelling pubmed-39630792014-03-24 Serum Endocan as a Novel Prognostic Biomarker in Patients with Hepatocellular Carcinoma Ozaki, Kazuaki Toshikuni, Nobuyuki George, Joseph Minato, Takahiro Matsue, Yasuhiro Arisawa, Tomiyasu Tsutsumi, Mikihiro J Cancer Research Paper Endocan is a vascular endothelium-derived factor regulated by angiogenic factors. The aim of this study was to determine whether serum endocan levels are prognostic for survival in patients with hepatocellular carcinoma (HCC). Serum endocan levels were measured in 64 HCC patients who were naïve to treatment, eight apparently healthy subjects, and 68 patients with liver cirrhosis; the latter two groups served as controls. Prognostic factors for the survival of HCC patients were examined using a Cox proportional hazards model. The median serum endocan levels were 1.145 ng/mL (range, 0.93-1.68 ng/mL) in healthy subjects, 1.93 ng/mL (range, 0.45-8.47 ng/mL) in liver cirrhosis patients, and 3.73 ng/mL (range, 0.74-10.95 ng/mL) in HCC patients (P = 0.0001). In HCC patients, elevated serum endocan levels were significantly associated with poor hepatic function (P = 0.015), a greater number of tumors (P = 0.034), and vascular invasion (P = 0.043). The median follow-up period was 23.0 months, and 33 HCC patients died during follow up. Multivariate analysis showed that serum endocan levels ≥ 2.20 ng/mL (hazard ratio 2.36, 95% confidence interval 1.22-5.36, P = 0.008) as well as elevated serum α-fetoprotein and des-γ-carboxy prothrombin levels were independent prognostic biomarkers for poor survival. The combination of serum endocan and these two additional markers was significantly predictive of worse survival (P < 0.0001). Thus, serum endocan may be a prognostic biomarker for survival in HCC patients, and the combination of serum endocan, α-fetoprotein, and des-γ-carboxy prothrombin levels can result in better prognostic stratification of these patients. Ivyspring International Publisher 2014-03-04 /pmc/articles/PMC3963079/ /pubmed/24665346 http://dx.doi.org/10.7150/jca.7691 Text en © Ivyspring International Publisher. This is an open-access article distributed under the terms of the Creative Commons License (http://creativecommons.org/licenses/by-nc-nd/3.0/). Reproduction is permitted for personal, noncommercial use, provided that the article is in whole, unmodified, and properly cited.
spellingShingle Research Paper
Ozaki, Kazuaki
Toshikuni, Nobuyuki
George, Joseph
Minato, Takahiro
Matsue, Yasuhiro
Arisawa, Tomiyasu
Tsutsumi, Mikihiro
Serum Endocan as a Novel Prognostic Biomarker in Patients with Hepatocellular Carcinoma
title Serum Endocan as a Novel Prognostic Biomarker in Patients with Hepatocellular Carcinoma
title_full Serum Endocan as a Novel Prognostic Biomarker in Patients with Hepatocellular Carcinoma
title_fullStr Serum Endocan as a Novel Prognostic Biomarker in Patients with Hepatocellular Carcinoma
title_full_unstemmed Serum Endocan as a Novel Prognostic Biomarker in Patients with Hepatocellular Carcinoma
title_short Serum Endocan as a Novel Prognostic Biomarker in Patients with Hepatocellular Carcinoma
title_sort serum endocan as a novel prognostic biomarker in patients with hepatocellular carcinoma
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3963079/
https://www.ncbi.nlm.nih.gov/pubmed/24665346
http://dx.doi.org/10.7150/jca.7691
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