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Significance of PRO2000/ANCCA expression, a novel proliferation-associated protein in hepatocellular carcinoma

BACKGROUND: PRO2000/ANCCA may be an important candidate gene which located within a region of chromosome 8q in hepatocellular carcinoma (HCC). However, its significance remains unclear. The aim of this study was to explore the clinical significance of PRO2000/ANCCA expression in HCC. METHODS: The co...

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Autores principales: Yang, Jie, Huang, Jie, Luo, Luqiao, Chen, Zhenzhu, Guo, Ying, Guo, Linlang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3997233/
https://www.ncbi.nlm.nih.gov/pubmed/24708861
http://dx.doi.org/10.1186/1475-2867-14-33
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author Yang, Jie
Huang, Jie
Luo, Luqiao
Chen, Zhenzhu
Guo, Ying
Guo, Linlang
author_facet Yang, Jie
Huang, Jie
Luo, Luqiao
Chen, Zhenzhu
Guo, Ying
Guo, Linlang
author_sort Yang, Jie
collection PubMed
description BACKGROUND: PRO2000/ANCCA may be an important candidate gene which located within a region of chromosome 8q in hepatocellular carcinoma (HCC). However, its significance remains unclear. The aim of this study was to explore the clinical significance of PRO2000/ANCCA expression in HCC. METHODS: The correlations of PRO2000/ANCCA expression with clinicopathological factors and prognosis of HCC patients were analyzed. Expression of PRO2000/ANCCA, ki-67, cyclinD1, p53 and p21 was detected in HCCs from 107 patients along with corresponding non-tumor tissues by immunohistochemistry. RESULTS: PRO2000/ANCCA expression was present in 66 of 107 (64.94%) HCC specimens in which 36 of 76 (47.37%) in well differentiated tumors and 30 of 31 (96.77%) in poorly differentiated tumors respectively, while 8 (7.48%) in adjacent non-tumor tissues with scattered positive cells. PRO2000/ANCCA expression was associated with clinicopathological features such as histological differentiation, number of tumor nodules, TNM stage, tumor microsatellite, portal vein tumor thrombus and recurrence, but not with gender, age, tumor size, cirrhosis, HBV infection and serum fetoprotein (AFP) level. There was a close relationship between PRO2000/ANCCA and ki-67 and cyclinD1 in HCC. PRO2000/ANCCA immunopositivity was independent of p53 and p21(WAF1/Cip1). CONCLUSIONS: Increased expression of PRO2000/ANCCA is associated with adverse outcome in patients with HCC and is a predictor of poor prognosis for HCC. PRO2000/ANCCA may be involved in the development of HCC and might promote cell proliferation through a p53/ P21(WAF1/Cip1)-independent pathway.
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spelling pubmed-39972332014-04-24 Significance of PRO2000/ANCCA expression, a novel proliferation-associated protein in hepatocellular carcinoma Yang, Jie Huang, Jie Luo, Luqiao Chen, Zhenzhu Guo, Ying Guo, Linlang Cancer Cell Int Primary Research BACKGROUND: PRO2000/ANCCA may be an important candidate gene which located within a region of chromosome 8q in hepatocellular carcinoma (HCC). However, its significance remains unclear. The aim of this study was to explore the clinical significance of PRO2000/ANCCA expression in HCC. METHODS: The correlations of PRO2000/ANCCA expression with clinicopathological factors and prognosis of HCC patients were analyzed. Expression of PRO2000/ANCCA, ki-67, cyclinD1, p53 and p21 was detected in HCCs from 107 patients along with corresponding non-tumor tissues by immunohistochemistry. RESULTS: PRO2000/ANCCA expression was present in 66 of 107 (64.94%) HCC specimens in which 36 of 76 (47.37%) in well differentiated tumors and 30 of 31 (96.77%) in poorly differentiated tumors respectively, while 8 (7.48%) in adjacent non-tumor tissues with scattered positive cells. PRO2000/ANCCA expression was associated with clinicopathological features such as histological differentiation, number of tumor nodules, TNM stage, tumor microsatellite, portal vein tumor thrombus and recurrence, but not with gender, age, tumor size, cirrhosis, HBV infection and serum fetoprotein (AFP) level. There was a close relationship between PRO2000/ANCCA and ki-67 and cyclinD1 in HCC. PRO2000/ANCCA immunopositivity was independent of p53 and p21(WAF1/Cip1). CONCLUSIONS: Increased expression of PRO2000/ANCCA is associated with adverse outcome in patients with HCC and is a predictor of poor prognosis for HCC. PRO2000/ANCCA may be involved in the development of HCC and might promote cell proliferation through a p53/ P21(WAF1/Cip1)-independent pathway. BioMed Central 2014-04-04 /pmc/articles/PMC3997233/ /pubmed/24708861 http://dx.doi.org/10.1186/1475-2867-14-33 Text en Copyright © 2014 Yang et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), 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 Primary Research
Yang, Jie
Huang, Jie
Luo, Luqiao
Chen, Zhenzhu
Guo, Ying
Guo, Linlang
Significance of PRO2000/ANCCA expression, a novel proliferation-associated protein in hepatocellular carcinoma
title Significance of PRO2000/ANCCA expression, a novel proliferation-associated protein in hepatocellular carcinoma
title_full Significance of PRO2000/ANCCA expression, a novel proliferation-associated protein in hepatocellular carcinoma
title_fullStr Significance of PRO2000/ANCCA expression, a novel proliferation-associated protein in hepatocellular carcinoma
title_full_unstemmed Significance of PRO2000/ANCCA expression, a novel proliferation-associated protein in hepatocellular carcinoma
title_short Significance of PRO2000/ANCCA expression, a novel proliferation-associated protein in hepatocellular carcinoma
title_sort significance of pro2000/ancca expression, a novel proliferation-associated protein in hepatocellular carcinoma
topic Primary Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3997233/
https://www.ncbi.nlm.nih.gov/pubmed/24708861
http://dx.doi.org/10.1186/1475-2867-14-33
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