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Prognostic value of increased expression of RACO-1 in patients with hepatitis B-related hepatocellular carcinoma
RING domain AP-1 coactivator-1 (RACO-1) is a coactivator that links c-Jun to growth factor signaling and is essential for AP-1 function. This study aimed to investigate the expression and clinical significance of RACO-1 protein in hepatitis B virus (HBV)-related hepatocellular carcinoma (HCC) in Chi...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Dove Medical Press
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5317312/ https://www.ncbi.nlm.nih.gov/pubmed/28243109 http://dx.doi.org/10.2147/TCRM.S125331 |
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author | Chen, Jian-yao Liu, Li-ping Xu, Jiang-feng |
author_facet | Chen, Jian-yao Liu, Li-ping Xu, Jiang-feng |
author_sort | Chen, Jian-yao |
collection | PubMed |
description | RING domain AP-1 coactivator-1 (RACO-1) is a coactivator that links c-Jun to growth factor signaling and is essential for AP-1 function. This study aimed to investigate the expression and clinical significance of RACO-1 protein in hepatitis B virus (HBV)-related hepatocellular carcinoma (HCC) in China. A total of 136 tissue samples of HBV-related HCC were detected by immunohistochemistry (including 76 patients in training cohort and 60 patients in validation cohort). Correlation between RACO-1 expression and clinicopathologic features of HBV-related HCC was analyzed in both the cohorts. RACO-1 expression was significantly higher in HBV-related HCC tissues than in adjacent non-tumor liver tissues. All the patients were divided into two groups: the low expression group and the high expression group. RACO-1 expression was significantly related to vascular invasion (P=0.021), tumor numbers (P=0.046), International Union for Cancer Control/American Joint Committee on Cancer stage (P=0.006), cirrhosis (P=0.046), capsular (P=0.039), and Barcelona Clinic Liver Cancer stage (P=0.041) in training cohort. The validation cohort showed the same results. The high RACO-1 expression was the independent prognostic factor for HBV-related HCC patients in both training cohort and validation cohort. Our data implicate RACO-1 as a novel prognostic marker and a potential therapeutic target for HBV-related HCC. |
format | Online Article Text |
id | pubmed-5317312 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-53173122017-02-27 Prognostic value of increased expression of RACO-1 in patients with hepatitis B-related hepatocellular carcinoma Chen, Jian-yao Liu, Li-ping Xu, Jiang-feng Ther Clin Risk Manag Original Research RING domain AP-1 coactivator-1 (RACO-1) is a coactivator that links c-Jun to growth factor signaling and is essential for AP-1 function. This study aimed to investigate the expression and clinical significance of RACO-1 protein in hepatitis B virus (HBV)-related hepatocellular carcinoma (HCC) in China. A total of 136 tissue samples of HBV-related HCC were detected by immunohistochemistry (including 76 patients in training cohort and 60 patients in validation cohort). Correlation between RACO-1 expression and clinicopathologic features of HBV-related HCC was analyzed in both the cohorts. RACO-1 expression was significantly higher in HBV-related HCC tissues than in adjacent non-tumor liver tissues. All the patients were divided into two groups: the low expression group and the high expression group. RACO-1 expression was significantly related to vascular invasion (P=0.021), tumor numbers (P=0.046), International Union for Cancer Control/American Joint Committee on Cancer stage (P=0.006), cirrhosis (P=0.046), capsular (P=0.039), and Barcelona Clinic Liver Cancer stage (P=0.041) in training cohort. The validation cohort showed the same results. The high RACO-1 expression was the independent prognostic factor for HBV-related HCC patients in both training cohort and validation cohort. Our data implicate RACO-1 as a novel prognostic marker and a potential therapeutic target for HBV-related HCC. Dove Medical Press 2017-02-15 /pmc/articles/PMC5317312/ /pubmed/28243109 http://dx.doi.org/10.2147/TCRM.S125331 Text en © 2017 Chen et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Chen, Jian-yao Liu, Li-ping Xu, Jiang-feng Prognostic value of increased expression of RACO-1 in patients with hepatitis B-related hepatocellular carcinoma |
title | Prognostic value of increased expression of RACO-1 in patients with hepatitis B-related hepatocellular carcinoma |
title_full | Prognostic value of increased expression of RACO-1 in patients with hepatitis B-related hepatocellular carcinoma |
title_fullStr | Prognostic value of increased expression of RACO-1 in patients with hepatitis B-related hepatocellular carcinoma |
title_full_unstemmed | Prognostic value of increased expression of RACO-1 in patients with hepatitis B-related hepatocellular carcinoma |
title_short | Prognostic value of increased expression of RACO-1 in patients with hepatitis B-related hepatocellular carcinoma |
title_sort | prognostic value of increased expression of raco-1 in patients with hepatitis b-related hepatocellular carcinoma |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5317312/ https://www.ncbi.nlm.nih.gov/pubmed/28243109 http://dx.doi.org/10.2147/TCRM.S125331 |
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