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Clinicopathological significance of EZH2 mRNA expression in patients with hepatocellular carcinoma

Enhancer of zeste homologue 2 (EZH2), a member of the polycomb group protein family, plays a crucial role in the regulation of embryonic development and has been associated with the regulation of the cell cycle. Recently, several studies have shown that EZH2 is highly expressed in aggressive tumours...

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Autores principales: Sudo, T, Utsunomiya, T, Mimori, K, Nagahara, H, Ogawa, K, Inoue, H, Wakiyama, S, Fujita, H, Shirouzu, K, Mori, M
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2362028/
https://www.ncbi.nlm.nih.gov/pubmed/15856046
http://dx.doi.org/10.1038/sj.bjc.6602531
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author Sudo, T
Utsunomiya, T
Mimori, K
Nagahara, H
Ogawa, K
Inoue, H
Wakiyama, S
Fujita, H
Shirouzu, K
Mori, M
author_facet Sudo, T
Utsunomiya, T
Mimori, K
Nagahara, H
Ogawa, K
Inoue, H
Wakiyama, S
Fujita, H
Shirouzu, K
Mori, M
author_sort Sudo, T
collection PubMed
description Enhancer of zeste homologue 2 (EZH2), a member of the polycomb group protein family, plays a crucial role in the regulation of embryonic development and has been associated with the regulation of the cell cycle. Recently, several studies have shown that EZH2 is highly expressed in aggressive tumours, including human breast cancer, prostate cancer, and lymphomas. We thus analysed EZH2 expression using real-time reverse transcription–polymerase chain reaction, and correlated its expression status with various clinicopathological parameters in 66 patients with hepatocellular carcinoma (HCC). We found high expression of EZH2 in human liver cancer cell lines. Furthermore, EZH2 gene-expression levels in tumour tissue specimens (0.34±0.52) were significantly higher (P<0.0001) than those in the corresponding nontumour tissue specimens (0.07±0.09). The incidence of cancer cell invasion into the portal vein was significantly higher (P<0.001) in the high EZH2 expression group (26 of the 33, 79%) than in the low expression group (13 of the 33, 39%). However, there was no significant difference in the disease-free survival rate between the two groups. The findings of this study indicate that EZH2 mRNA expression was upregulated in human HCC and may play an important role in tumour progression, especially by facilitating portal vein invasion.
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spelling pubmed-23620282009-09-10 Clinicopathological significance of EZH2 mRNA expression in patients with hepatocellular carcinoma Sudo, T Utsunomiya, T Mimori, K Nagahara, H Ogawa, K Inoue, H Wakiyama, S Fujita, H Shirouzu, K Mori, M Br J Cancer Molecular Diagnostics Enhancer of zeste homologue 2 (EZH2), a member of the polycomb group protein family, plays a crucial role in the regulation of embryonic development and has been associated with the regulation of the cell cycle. Recently, several studies have shown that EZH2 is highly expressed in aggressive tumours, including human breast cancer, prostate cancer, and lymphomas. We thus analysed EZH2 expression using real-time reverse transcription–polymerase chain reaction, and correlated its expression status with various clinicopathological parameters in 66 patients with hepatocellular carcinoma (HCC). We found high expression of EZH2 in human liver cancer cell lines. Furthermore, EZH2 gene-expression levels in tumour tissue specimens (0.34±0.52) were significantly higher (P<0.0001) than those in the corresponding nontumour tissue specimens (0.07±0.09). The incidence of cancer cell invasion into the portal vein was significantly higher (P<0.001) in the high EZH2 expression group (26 of the 33, 79%) than in the low expression group (13 of the 33, 39%). However, there was no significant difference in the disease-free survival rate between the two groups. The findings of this study indicate that EZH2 mRNA expression was upregulated in human HCC and may play an important role in tumour progression, especially by facilitating portal vein invasion. Nature Publishing Group 2005-05-09 2005-04-26 /pmc/articles/PMC2362028/ /pubmed/15856046 http://dx.doi.org/10.1038/sj.bjc.6602531 Text en Copyright © 2005 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Molecular Diagnostics
Sudo, T
Utsunomiya, T
Mimori, K
Nagahara, H
Ogawa, K
Inoue, H
Wakiyama, S
Fujita, H
Shirouzu, K
Mori, M
Clinicopathological significance of EZH2 mRNA expression in patients with hepatocellular carcinoma
title Clinicopathological significance of EZH2 mRNA expression in patients with hepatocellular carcinoma
title_full Clinicopathological significance of EZH2 mRNA expression in patients with hepatocellular carcinoma
title_fullStr Clinicopathological significance of EZH2 mRNA expression in patients with hepatocellular carcinoma
title_full_unstemmed Clinicopathological significance of EZH2 mRNA expression in patients with hepatocellular carcinoma
title_short Clinicopathological significance of EZH2 mRNA expression in patients with hepatocellular carcinoma
title_sort clinicopathological significance of ezh2 mrna expression in patients with hepatocellular carcinoma
topic Molecular Diagnostics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2362028/
https://www.ncbi.nlm.nih.gov/pubmed/15856046
http://dx.doi.org/10.1038/sj.bjc.6602531
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