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Prognostic significance of XRCC4 expression in hepatocellular carcinoma
BACKGROUND: Our previous investigations have shown that the variants of X-ray repair complementing 4 (XRCC4) may be involved in hepatocellular carcinoma (hepatocarcinoma) tumorigenesis. This study aimed to investigate the possible prognostic significance of XRCC4 expression for hepatocarcinoma patie...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5675685/ https://www.ncbi.nlm.nih.gov/pubmed/29152133 http://dx.doi.org/10.18632/oncotarget.21360 |
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author | Lu, Jun Wang, Xing-Zhizi Zhang, Tian-Qi Huang, Xiao-Ying Yao, Jin-Guang Wang, Chao Wei, Zhong-Hong Ma, Yun Wu, Xue-Min Luo, Chun-Ying Xia, Qiang Long, Xi-Dai |
author_facet | Lu, Jun Wang, Xing-Zhizi Zhang, Tian-Qi Huang, Xiao-Ying Yao, Jin-Guang Wang, Chao Wei, Zhong-Hong Ma, Yun Wu, Xue-Min Luo, Chun-Ying Xia, Qiang Long, Xi-Dai |
author_sort | Lu, Jun |
collection | PubMed |
description | BACKGROUND: Our previous investigations have shown that the variants of X-ray repair complementing 4 (XRCC4) may be involved in hepatocellular carcinoma (hepatocarcinoma) tumorigenesis. This study aimed to investigate the possible prognostic significance of XRCC4 expression for hepatocarcinoma patients and possible value for the selection of transarterial chemoembolization (TACE) treatment. MATERIALS AND METHODS: We conducted a hospital-based retrospective analysis (including 421 hepatocarcinoma cases) to analyze the effects of XRCC4 on hepatocarcinoma prognosis and TACE. The levels of XRCC4 expression were tested using immunohistochemistry. The sensitivity of cancer cells to anti-cancer drug doxorubicin was evaluated using the half-maximal inhibitory concentration (IC50). RESULTS: XRCC4 expression was significantly correlated with pathological features including tumor stage, liver cirrhosis, and micro-vessel density. XRCC4 expression was an independent prognostic factor of hepatocarcinoma, and TACE treatments had no effects on prognosis of hepatocarcinoma patients with high XRCC4 expression. More intriguingly, TACE improved the prognosis of hepatocarcinoma patients with low XRCC4 expression. Functionally, XRCC4 overexpression increased while XRCC4 knockdown reduced the IC50 of cancer cells to doxorubicin. CONCLUSIONS: These results suggest that XRCC4 may be an independent prognostic factor for hepatocarcinoma patients, and that decreasing XRCC4 expression may be beneficial for post-operative adjuvant TACE treatment in hepatocarcinoma. |
format | Online Article Text |
id | pubmed-5675685 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-56756852017-11-18 Prognostic significance of XRCC4 expression in hepatocellular carcinoma Lu, Jun Wang, Xing-Zhizi Zhang, Tian-Qi Huang, Xiao-Ying Yao, Jin-Guang Wang, Chao Wei, Zhong-Hong Ma, Yun Wu, Xue-Min Luo, Chun-Ying Xia, Qiang Long, Xi-Dai Oncotarget Research Paper BACKGROUND: Our previous investigations have shown that the variants of X-ray repair complementing 4 (XRCC4) may be involved in hepatocellular carcinoma (hepatocarcinoma) tumorigenesis. This study aimed to investigate the possible prognostic significance of XRCC4 expression for hepatocarcinoma patients and possible value for the selection of transarterial chemoembolization (TACE) treatment. MATERIALS AND METHODS: We conducted a hospital-based retrospective analysis (including 421 hepatocarcinoma cases) to analyze the effects of XRCC4 on hepatocarcinoma prognosis and TACE. The levels of XRCC4 expression were tested using immunohistochemistry. The sensitivity of cancer cells to anti-cancer drug doxorubicin was evaluated using the half-maximal inhibitory concentration (IC50). RESULTS: XRCC4 expression was significantly correlated with pathological features including tumor stage, liver cirrhosis, and micro-vessel density. XRCC4 expression was an independent prognostic factor of hepatocarcinoma, and TACE treatments had no effects on prognosis of hepatocarcinoma patients with high XRCC4 expression. More intriguingly, TACE improved the prognosis of hepatocarcinoma patients with low XRCC4 expression. Functionally, XRCC4 overexpression increased while XRCC4 knockdown reduced the IC50 of cancer cells to doxorubicin. CONCLUSIONS: These results suggest that XRCC4 may be an independent prognostic factor for hepatocarcinoma patients, and that decreasing XRCC4 expression may be beneficial for post-operative adjuvant TACE treatment in hepatocarcinoma. Impact Journals LLC 2017-09-28 /pmc/articles/PMC5675685/ /pubmed/29152133 http://dx.doi.org/10.18632/oncotarget.21360 Text en Copyright: © 2017 Lu et al. http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Research Paper Lu, Jun Wang, Xing-Zhizi Zhang, Tian-Qi Huang, Xiao-Ying Yao, Jin-Guang Wang, Chao Wei, Zhong-Hong Ma, Yun Wu, Xue-Min Luo, Chun-Ying Xia, Qiang Long, Xi-Dai Prognostic significance of XRCC4 expression in hepatocellular carcinoma |
title | Prognostic significance of XRCC4 expression in hepatocellular carcinoma |
title_full | Prognostic significance of XRCC4 expression in hepatocellular carcinoma |
title_fullStr | Prognostic significance of XRCC4 expression in hepatocellular carcinoma |
title_full_unstemmed | Prognostic significance of XRCC4 expression in hepatocellular carcinoma |
title_short | Prognostic significance of XRCC4 expression in hepatocellular carcinoma |
title_sort | prognostic significance of xrcc4 expression in hepatocellular carcinoma |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5675685/ https://www.ncbi.nlm.nih.gov/pubmed/29152133 http://dx.doi.org/10.18632/oncotarget.21360 |
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