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The Association of HMGB1 Gene with the Prognosis of HCC
High-mobility group box 1 protein (HMGB1) is an evolutionarily ancient and critical regulator of cell death and survival. HMGB1 is a chromatin-associated nuclear protein molecule that triggers extracellular damage. The expression of HMGB1 has been reported in many types of cancers, but the role of H...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3929653/ https://www.ncbi.nlm.nih.gov/pubmed/24586525 http://dx.doi.org/10.1371/journal.pone.0089097 |
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author | Xiao, Jianbiao Ding, Yi Huang, Jing Li, Qisheng Liu, Ying Ni, Wen Zhang, Yuqin Zhu, Yanfei Chen, Longhua Chen, Bin |
author_facet | Xiao, Jianbiao Ding, Yi Huang, Jing Li, Qisheng Liu, Ying Ni, Wen Zhang, Yuqin Zhu, Yanfei Chen, Longhua Chen, Bin |
author_sort | Xiao, Jianbiao |
collection | PubMed |
description | High-mobility group box 1 protein (HMGB1) is an evolutionarily ancient and critical regulator of cell death and survival. HMGB1 is a chromatin-associated nuclear protein molecule that triggers extracellular damage. The expression of HMGB1 has been reported in many types of cancers, but the role of HMGB1 in hepato cellular carcinoma (HCC) is unknown.The aim of this study was to analyze the roles of HMGB1 in HCC progression using HCC clinical samples. We also investigated the clinical outcomes of HCC samples with a special focus on HMBG1 expression. In an immunohistochemical study conducted on 208 cases of HCC, HMGB1 had high expression in 134 cases(64.4%).The HMGB1 expression level did not correlate with any clinicopathological parameters, except alpha fetoprotein (AFP) (p = 0.041) and CLIP stage (p = 0.007). However, survival analysis showed that the group with HMBG1 overexpression had a significantly shorter overall survival time than the group with a down-regulatedexpression of HMBG1 (HR = 0.568, CI (0.398, 0.811), p = 0.002). Multivariate analysis showed that HMGB1 expression was a significant and independent prognostic parameter (HR = 0.562, CI (0.388, 0.815), p = 0.002) for HCC patients. The ability of proliferation, migration and invasion of HCC cells was suppressed with the disruption of endogenous HMGB1 using small interfering RNAs. On the other hand, the ability of proliferation, migration and invasion of HCC cells was strengthened when the expression endogenous HMGB1 was enhanced using HMGB1 DNA. HMGB1 expression may be a novel and independent predictor for the prognosis of HCC patients. The overexpression of HMGB1 in HCC could be a novel, effective, and supplementary biomarker for HCC, since it plays a vital role in the progression of HCC. |
format | Online Article Text |
id | pubmed-3929653 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-39296532014-02-25 The Association of HMGB1 Gene with the Prognosis of HCC Xiao, Jianbiao Ding, Yi Huang, Jing Li, Qisheng Liu, Ying Ni, Wen Zhang, Yuqin Zhu, Yanfei Chen, Longhua Chen, Bin PLoS One Research Article High-mobility group box 1 protein (HMGB1) is an evolutionarily ancient and critical regulator of cell death and survival. HMGB1 is a chromatin-associated nuclear protein molecule that triggers extracellular damage. The expression of HMGB1 has been reported in many types of cancers, but the role of HMGB1 in hepato cellular carcinoma (HCC) is unknown.The aim of this study was to analyze the roles of HMGB1 in HCC progression using HCC clinical samples. We also investigated the clinical outcomes of HCC samples with a special focus on HMBG1 expression. In an immunohistochemical study conducted on 208 cases of HCC, HMGB1 had high expression in 134 cases(64.4%).The HMGB1 expression level did not correlate with any clinicopathological parameters, except alpha fetoprotein (AFP) (p = 0.041) and CLIP stage (p = 0.007). However, survival analysis showed that the group with HMBG1 overexpression had a significantly shorter overall survival time than the group with a down-regulatedexpression of HMBG1 (HR = 0.568, CI (0.398, 0.811), p = 0.002). Multivariate analysis showed that HMGB1 expression was a significant and independent prognostic parameter (HR = 0.562, CI (0.388, 0.815), p = 0.002) for HCC patients. The ability of proliferation, migration and invasion of HCC cells was suppressed with the disruption of endogenous HMGB1 using small interfering RNAs. On the other hand, the ability of proliferation, migration and invasion of HCC cells was strengthened when the expression endogenous HMGB1 was enhanced using HMGB1 DNA. HMGB1 expression may be a novel and independent predictor for the prognosis of HCC patients. The overexpression of HMGB1 in HCC could be a novel, effective, and supplementary biomarker for HCC, since it plays a vital role in the progression of HCC. Public Library of Science 2014-02-19 /pmc/articles/PMC3929653/ /pubmed/24586525 http://dx.doi.org/10.1371/journal.pone.0089097 Text en © 2014 Xiao et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Xiao, Jianbiao Ding, Yi Huang, Jing Li, Qisheng Liu, Ying Ni, Wen Zhang, Yuqin Zhu, Yanfei Chen, Longhua Chen, Bin The Association of HMGB1 Gene with the Prognosis of HCC |
title | The Association of HMGB1 Gene with the Prognosis of HCC |
title_full | The Association of HMGB1 Gene with the Prognosis of HCC |
title_fullStr | The Association of HMGB1 Gene with the Prognosis of HCC |
title_full_unstemmed | The Association of HMGB1 Gene with the Prognosis of HCC |
title_short | The Association of HMGB1 Gene with the Prognosis of HCC |
title_sort | association of hmgb1 gene with the prognosis of hcc |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3929653/ https://www.ncbi.nlm.nih.gov/pubmed/24586525 http://dx.doi.org/10.1371/journal.pone.0089097 |
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