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ITPKA expression is a novel prognostic factor in hepatocellular carcinoma
BACKGROUND: Inositol-1,4,5-trisphosphate-3-kinase-A (ITPKA) has recently been found to be implicated in the tumor progression of various cancers. However, the expression and the prognostic value of ITPKA in hepatocellular carcinoma (HCC) remains unexplored. The aim of this study is to investigate th...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4528344/ https://www.ncbi.nlm.nih.gov/pubmed/26249031 http://dx.doi.org/10.1186/s13000-015-0374-1 |
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author | Li, Jianbiao Zhu, Ying-Hui Huang, Pinzhu Zhang, Baozhu Sun, Jian Guan, Xin-Yuan |
author_facet | Li, Jianbiao Zhu, Ying-Hui Huang, Pinzhu Zhang, Baozhu Sun, Jian Guan, Xin-Yuan |
author_sort | Li, Jianbiao |
collection | PubMed |
description | BACKGROUND: Inositol-1,4,5-trisphosphate-3-kinase-A (ITPKA) has recently been found to be implicated in the tumor progression of various cancers. However, the expression and the prognostic value of ITPKA in hepatocellular carcinoma (HCC) remains unexplored. The aim of this study is to investigate the clinical significance of ITPKA expression in HCC. METHODS: We determined the expression level of ITPKA in 135 cases of HCC tissues and the matched adjacent nontumorous tissues by quantitative real-time RT-PCR. The correlation between ITPKA expression and prognosis of HCC patients was further evaluated by univariate and multivariate analysis. Multivariate analysis of the prognostic factors was performed with Cox proportional hazards model. RESULTS: Up-regulation of ITPKA occurred in 48.9 % of primary HCCs compared with their nontumor counterparts (P < 0.001). In addition, high expression of ITPKA was significantly associated with vascular invasion (P = 0.001) and TNM stage (P = 0.005). Kaplan–Meier analysis showed that the 5-year overall survival (OS) and relapse-free survival (RFS) rate in the group with high expression of ITPKA is poorer than that in low expression group (32.2 and 26.8 % versus 59.2 and 57.7 %). Univariate and multivariate analyses revealed that ITPKA was an independent prognostic factor for OS and RFS. Moreover, Stratified analysis revealed that its prognostic significance still existed within the subgroup of patients with early clinical stage (TNM stage I) or normal serum AFP level (≤25 μg/L). CONCLUSION: Our data indicated that ITPKA expression was significantly up-regulated in HCC and could serve as a potential novel prognostic biomarker for HCC patients after surgery. |
format | Online Article Text |
id | pubmed-4528344 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-45283442015-08-08 ITPKA expression is a novel prognostic factor in hepatocellular carcinoma Li, Jianbiao Zhu, Ying-Hui Huang, Pinzhu Zhang, Baozhu Sun, Jian Guan, Xin-Yuan Diagn Pathol Research BACKGROUND: Inositol-1,4,5-trisphosphate-3-kinase-A (ITPKA) has recently been found to be implicated in the tumor progression of various cancers. However, the expression and the prognostic value of ITPKA in hepatocellular carcinoma (HCC) remains unexplored. The aim of this study is to investigate the clinical significance of ITPKA expression in HCC. METHODS: We determined the expression level of ITPKA in 135 cases of HCC tissues and the matched adjacent nontumorous tissues by quantitative real-time RT-PCR. The correlation between ITPKA expression and prognosis of HCC patients was further evaluated by univariate and multivariate analysis. Multivariate analysis of the prognostic factors was performed with Cox proportional hazards model. RESULTS: Up-regulation of ITPKA occurred in 48.9 % of primary HCCs compared with their nontumor counterparts (P < 0.001). In addition, high expression of ITPKA was significantly associated with vascular invasion (P = 0.001) and TNM stage (P = 0.005). Kaplan–Meier analysis showed that the 5-year overall survival (OS) and relapse-free survival (RFS) rate in the group with high expression of ITPKA is poorer than that in low expression group (32.2 and 26.8 % versus 59.2 and 57.7 %). Univariate and multivariate analyses revealed that ITPKA was an independent prognostic factor for OS and RFS. Moreover, Stratified analysis revealed that its prognostic significance still existed within the subgroup of patients with early clinical stage (TNM stage I) or normal serum AFP level (≤25 μg/L). CONCLUSION: Our data indicated that ITPKA expression was significantly up-regulated in HCC and could serve as a potential novel prognostic biomarker for HCC patients after surgery. BioMed Central 2015-08-07 /pmc/articles/PMC4528344/ /pubmed/26249031 http://dx.doi.org/10.1186/s13000-015-0374-1 Text en © Li et al. 2015 Open Access This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Li, Jianbiao Zhu, Ying-Hui Huang, Pinzhu Zhang, Baozhu Sun, Jian Guan, Xin-Yuan ITPKA expression is a novel prognostic factor in hepatocellular carcinoma |
title | ITPKA expression is a novel prognostic factor in hepatocellular carcinoma |
title_full | ITPKA expression is a novel prognostic factor in hepatocellular carcinoma |
title_fullStr | ITPKA expression is a novel prognostic factor in hepatocellular carcinoma |
title_full_unstemmed | ITPKA expression is a novel prognostic factor in hepatocellular carcinoma |
title_short | ITPKA expression is a novel prognostic factor in hepatocellular carcinoma |
title_sort | itpka expression is a novel prognostic factor in hepatocellular carcinoma |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4528344/ https://www.ncbi.nlm.nih.gov/pubmed/26249031 http://dx.doi.org/10.1186/s13000-015-0374-1 |
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