Cargando…
Zinc finger protein ZBTB20 is an independent prognostic marker and promotes tumor growth of human hepatocellular carcinoma by repressing FoxO1
Zinc finger and BTB domain-containing 20 (ZBTB20) is a new BTB/POZ-domain gene and a member of the POK family of transcriptional repressors. Notably, the role of ZBTB20 and its underlying mechanisms involved in hepatocarcinogenesis are poorly investigated. In this study, the expression of ZBTB20 was...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4924719/ https://www.ncbi.nlm.nih.gov/pubmed/26893361 http://dx.doi.org/10.18632/oncotarget.7425 |
_version_ | 1782439909618876416 |
---|---|
author | Kan, Heping Huang, Yuqi Li, Xianghong Liu, Dingli Chen, Jianjia Shu, Miaojiang |
author_facet | Kan, Heping Huang, Yuqi Li, Xianghong Liu, Dingli Chen, Jianjia Shu, Miaojiang |
author_sort | Kan, Heping |
collection | PubMed |
description | Zinc finger and BTB domain-containing 20 (ZBTB20) is a new BTB/POZ-domain gene and a member of the POK family of transcriptional repressors. Notably, the role of ZBTB20 and its underlying mechanisms involved in hepatocarcinogenesis are poorly investigated. In this study, the expression of ZBTB20 was significantly overexpressed in hepatocellular carcinoma (HCC) tissues. The positive expression of ZBTB20 was associated with large tumor size, high Edmondson-Steiner grading and advanced tumor-node-metastasis (TNM) tumor stage. Additionally, HCC patients with positive expression of ZBTB20 had a poorer 5-year survival. Multivariate analyses revealed that ZBTB20 overexpression was an independent prognostic factor for HCC. Gain- and loss-of-function experiments demonstrated that ZBTB20 promoted HCC cell viability, proliferation, tumorigenicity, and cell cycle progression. Mechanistically, Cyclin D1 and Cyclin E were increased, while p21 and p27 were decreased by ZBTB20 in HCC cells. FoxO1 was inversely correlated with ZBTB20 protein expression in the same cohort of HCC specimens. We further revealed that FoxO1 was transcriptionally repressed by ZBTB20 in HCC. Moreover, restoration of FoxO1 expression partially abrogated ZBTB20-induced HCC cell proliferation and growth entry in vitro and in vivo. Collectively, these results indicate that ZBTB20 may serve as a prognostic marker and promotes tumor growth of HCC via transcriptionally repressing FoxO1. |
format | Online Article Text |
id | pubmed-4924719 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-49247192016-07-13 Zinc finger protein ZBTB20 is an independent prognostic marker and promotes tumor growth of human hepatocellular carcinoma by repressing FoxO1 Kan, Heping Huang, Yuqi Li, Xianghong Liu, Dingli Chen, Jianjia Shu, Miaojiang Oncotarget Research Paper Zinc finger and BTB domain-containing 20 (ZBTB20) is a new BTB/POZ-domain gene and a member of the POK family of transcriptional repressors. Notably, the role of ZBTB20 and its underlying mechanisms involved in hepatocarcinogenesis are poorly investigated. In this study, the expression of ZBTB20 was significantly overexpressed in hepatocellular carcinoma (HCC) tissues. The positive expression of ZBTB20 was associated with large tumor size, high Edmondson-Steiner grading and advanced tumor-node-metastasis (TNM) tumor stage. Additionally, HCC patients with positive expression of ZBTB20 had a poorer 5-year survival. Multivariate analyses revealed that ZBTB20 overexpression was an independent prognostic factor for HCC. Gain- and loss-of-function experiments demonstrated that ZBTB20 promoted HCC cell viability, proliferation, tumorigenicity, and cell cycle progression. Mechanistically, Cyclin D1 and Cyclin E were increased, while p21 and p27 were decreased by ZBTB20 in HCC cells. FoxO1 was inversely correlated with ZBTB20 protein expression in the same cohort of HCC specimens. We further revealed that FoxO1 was transcriptionally repressed by ZBTB20 in HCC. Moreover, restoration of FoxO1 expression partially abrogated ZBTB20-induced HCC cell proliferation and growth entry in vitro and in vivo. Collectively, these results indicate that ZBTB20 may serve as a prognostic marker and promotes tumor growth of HCC via transcriptionally repressing FoxO1. Impact Journals LLC 2016-02-16 /pmc/articles/PMC4924719/ /pubmed/26893361 http://dx.doi.org/10.18632/oncotarget.7425 Text en Copyright: © 2016 Kan et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Kan, Heping Huang, Yuqi Li, Xianghong Liu, Dingli Chen, Jianjia Shu, Miaojiang Zinc finger protein ZBTB20 is an independent prognostic marker and promotes tumor growth of human hepatocellular carcinoma by repressing FoxO1 |
title | Zinc finger protein ZBTB20 is an independent prognostic marker and promotes tumor growth of human hepatocellular carcinoma by repressing FoxO1 |
title_full | Zinc finger protein ZBTB20 is an independent prognostic marker and promotes tumor growth of human hepatocellular carcinoma by repressing FoxO1 |
title_fullStr | Zinc finger protein ZBTB20 is an independent prognostic marker and promotes tumor growth of human hepatocellular carcinoma by repressing FoxO1 |
title_full_unstemmed | Zinc finger protein ZBTB20 is an independent prognostic marker and promotes tumor growth of human hepatocellular carcinoma by repressing FoxO1 |
title_short | Zinc finger protein ZBTB20 is an independent prognostic marker and promotes tumor growth of human hepatocellular carcinoma by repressing FoxO1 |
title_sort | zinc finger protein zbtb20 is an independent prognostic marker and promotes tumor growth of human hepatocellular carcinoma by repressing foxo1 |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4924719/ https://www.ncbi.nlm.nih.gov/pubmed/26893361 http://dx.doi.org/10.18632/oncotarget.7425 |
work_keys_str_mv | AT kanheping zincfingerproteinzbtb20isanindependentprognosticmarkerandpromotestumorgrowthofhumanhepatocellularcarcinomabyrepressingfoxo1 AT huangyuqi zincfingerproteinzbtb20isanindependentprognosticmarkerandpromotestumorgrowthofhumanhepatocellularcarcinomabyrepressingfoxo1 AT lixianghong zincfingerproteinzbtb20isanindependentprognosticmarkerandpromotestumorgrowthofhumanhepatocellularcarcinomabyrepressingfoxo1 AT liudingli zincfingerproteinzbtb20isanindependentprognosticmarkerandpromotestumorgrowthofhumanhepatocellularcarcinomabyrepressingfoxo1 AT chenjianjia zincfingerproteinzbtb20isanindependentprognosticmarkerandpromotestumorgrowthofhumanhepatocellularcarcinomabyrepressingfoxo1 AT shumiaojiang zincfingerproteinzbtb20isanindependentprognosticmarkerandpromotestumorgrowthofhumanhepatocellularcarcinomabyrepressingfoxo1 |