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Nrf2 is a potential prognostic marker and promotes proliferation and invasion in human hepatocellular carcinoma

BACKGROUND: Nuclear factor E2-related factor 2 (Nrf2 or NFE2L2) is abundantly expressed in cancer cells and relates to proliferation, invasion, and chemoresistance. Our early observations also found that expression of Nrf2 was up-regulated in kinds of cancer including human hepatocellular carcinoma...

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Autores principales: Zhang, Mingxin, Zhang, Chao, Zhang, Lingmin, Yang, Qi, Zhou, Suna, Wen, Qinsheng, Wang, Jingjie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4507320/
https://www.ncbi.nlm.nih.gov/pubmed/26194347
http://dx.doi.org/10.1186/s12885-015-1541-1
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author Zhang, Mingxin
Zhang, Chao
Zhang, Lingmin
Yang, Qi
Zhou, Suna
Wen, Qinsheng
Wang, Jingjie
author_facet Zhang, Mingxin
Zhang, Chao
Zhang, Lingmin
Yang, Qi
Zhou, Suna
Wen, Qinsheng
Wang, Jingjie
author_sort Zhang, Mingxin
collection PubMed
description BACKGROUND: Nuclear factor E2-related factor 2 (Nrf2 or NFE2L2) is abundantly expressed in cancer cells and relates to proliferation, invasion, and chemoresistance. Our early observations also found that expression of Nrf2 was up-regulated in kinds of cancer including human hepatocellular carcinoma (HCC) cells. But there are limited reports about the expression, significance, function of Nrf2 in HCC. METHODS: First, Nrf2 expression was analyzed in HCC cell lines and tumor samples. Then, the relationship of Nrf2 with clinicopathological factors and survival were analyzed. Further, the effect of Nrf2 on cell proliferation, apoptosis, and metastasis was examined in vitro by modulating expression of Nrf2 through specific shRNA or expression plasmid. Last, the potential mechanisms were also investigated. RESULTS: Nrf2 was up-regulated in HCC, and expression of Nrf2 was correlated with tumor differentiation, metastasis, and tumor size. Univariate and multivariate analyses indicated that high Nrf2 expression might be a poor prognostic factor. Further studies demonstrated that inhibition of Nrf2 expression inhibited proliferation by inducing apoptosis and repressed invasion, and up-regulation of Nrf2 expression resulted in opposite phenotypes. Moreover, there are positive correlation between Nrf2 expression and that of Bcl-xL and MMP-9. CONCLUSION: Nrf2 is a potential prognostic marker and promotes proliferation and invasion in human hepatocellular carcinoma partly through regulating expression of Bcl-xL and MMP-9.
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spelling pubmed-45073202015-07-21 Nrf2 is a potential prognostic marker and promotes proliferation and invasion in human hepatocellular carcinoma Zhang, Mingxin Zhang, Chao Zhang, Lingmin Yang, Qi Zhou, Suna Wen, Qinsheng Wang, Jingjie BMC Cancer Research Article BACKGROUND: Nuclear factor E2-related factor 2 (Nrf2 or NFE2L2) is abundantly expressed in cancer cells and relates to proliferation, invasion, and chemoresistance. Our early observations also found that expression of Nrf2 was up-regulated in kinds of cancer including human hepatocellular carcinoma (HCC) cells. But there are limited reports about the expression, significance, function of Nrf2 in HCC. METHODS: First, Nrf2 expression was analyzed in HCC cell lines and tumor samples. Then, the relationship of Nrf2 with clinicopathological factors and survival were analyzed. Further, the effect of Nrf2 on cell proliferation, apoptosis, and metastasis was examined in vitro by modulating expression of Nrf2 through specific shRNA or expression plasmid. Last, the potential mechanisms were also investigated. RESULTS: Nrf2 was up-regulated in HCC, and expression of Nrf2 was correlated with tumor differentiation, metastasis, and tumor size. Univariate and multivariate analyses indicated that high Nrf2 expression might be a poor prognostic factor. Further studies demonstrated that inhibition of Nrf2 expression inhibited proliferation by inducing apoptosis and repressed invasion, and up-regulation of Nrf2 expression resulted in opposite phenotypes. Moreover, there are positive correlation between Nrf2 expression and that of Bcl-xL and MMP-9. CONCLUSION: Nrf2 is a potential prognostic marker and promotes proliferation and invasion in human hepatocellular carcinoma partly through regulating expression of Bcl-xL and MMP-9. BioMed Central 2015-07-21 /pmc/articles/PMC4507320/ /pubmed/26194347 http://dx.doi.org/10.1186/s12885-015-1541-1 Text en © Zhang et al. 2015 This article is published under license to BioMed Central Ltd. This is an Open Access article 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 Article
Zhang, Mingxin
Zhang, Chao
Zhang, Lingmin
Yang, Qi
Zhou, Suna
Wen, Qinsheng
Wang, Jingjie
Nrf2 is a potential prognostic marker and promotes proliferation and invasion in human hepatocellular carcinoma
title Nrf2 is a potential prognostic marker and promotes proliferation and invasion in human hepatocellular carcinoma
title_full Nrf2 is a potential prognostic marker and promotes proliferation and invasion in human hepatocellular carcinoma
title_fullStr Nrf2 is a potential prognostic marker and promotes proliferation and invasion in human hepatocellular carcinoma
title_full_unstemmed Nrf2 is a potential prognostic marker and promotes proliferation and invasion in human hepatocellular carcinoma
title_short Nrf2 is a potential prognostic marker and promotes proliferation and invasion in human hepatocellular carcinoma
title_sort nrf2 is a potential prognostic marker and promotes proliferation and invasion in human hepatocellular carcinoma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4507320/
https://www.ncbi.nlm.nih.gov/pubmed/26194347
http://dx.doi.org/10.1186/s12885-015-1541-1
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