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Post-translational modifications of EZH2 in cancer
Enhancer of zeste homolog 2 (EZH2), as a main component of Polycomb Repressive Complex 2, catalyzes histone H3K27me3 to silence its target gene expression. EZH2 upregulation results in cancer development and poor prognosis of cancer patients. Post-translational modifications (PTMs) are important bio...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7731458/ https://www.ncbi.nlm.nih.gov/pubmed/33308321 http://dx.doi.org/10.1186/s13578-020-00505-0 |
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author | Li, Zhongwei Li, Minle Wang, Diandian Hou, Pingfu Chen, Xintian Chu, Sufang Chai, Dafei Zheng, Junnian Bai, Jin |
author_facet | Li, Zhongwei Li, Minle Wang, Diandian Hou, Pingfu Chen, Xintian Chu, Sufang Chai, Dafei Zheng, Junnian Bai, Jin |
author_sort | Li, Zhongwei |
collection | PubMed |
description | Enhancer of zeste homolog 2 (EZH2), as a main component of Polycomb Repressive Complex 2, catalyzes histone H3K27me3 to silence its target gene expression. EZH2 upregulation results in cancer development and poor prognosis of cancer patients. Post-translational modifications (PTMs) are important biological events in cancer progression. PTMs regulate protein conformation and diversity functions. Recently, mounting studies have demonstrated that EZH2 stability, histone methyltransferase activity, localization, and binding partners can be regulated by PTMs, including phosphorylation, O-GlcNAcylation, acetylation, methylation and ubiquitination. However, the detailed molecular mechanisms of the EZH2-PTMs and whether other types of PTMs occur in EZH2 remain largely unclear. This review presents an overview of different roles of EZH2 modification and EZH2-PTMs crosstalk during tumorigenesis and cancer metastasis. We also discussed the therapeutic potential of targeting EZH2 modifications for cancer therapy. |
format | Online Article Text |
id | pubmed-7731458 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-77314582020-12-11 Post-translational modifications of EZH2 in cancer Li, Zhongwei Li, Minle Wang, Diandian Hou, Pingfu Chen, Xintian Chu, Sufang Chai, Dafei Zheng, Junnian Bai, Jin Cell Biosci Review Enhancer of zeste homolog 2 (EZH2), as a main component of Polycomb Repressive Complex 2, catalyzes histone H3K27me3 to silence its target gene expression. EZH2 upregulation results in cancer development and poor prognosis of cancer patients. Post-translational modifications (PTMs) are important biological events in cancer progression. PTMs regulate protein conformation and diversity functions. Recently, mounting studies have demonstrated that EZH2 stability, histone methyltransferase activity, localization, and binding partners can be regulated by PTMs, including phosphorylation, O-GlcNAcylation, acetylation, methylation and ubiquitination. However, the detailed molecular mechanisms of the EZH2-PTMs and whether other types of PTMs occur in EZH2 remain largely unclear. This review presents an overview of different roles of EZH2 modification and EZH2-PTMs crosstalk during tumorigenesis and cancer metastasis. We also discussed the therapeutic potential of targeting EZH2 modifications for cancer therapy. BioMed Central 2020-12-11 /pmc/articles/PMC7731458/ /pubmed/33308321 http://dx.doi.org/10.1186/s13578-020-00505-0 Text en © The Author(s) 2020 Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data. |
spellingShingle | Review Li, Zhongwei Li, Minle Wang, Diandian Hou, Pingfu Chen, Xintian Chu, Sufang Chai, Dafei Zheng, Junnian Bai, Jin Post-translational modifications of EZH2 in cancer |
title | Post-translational modifications of EZH2 in cancer |
title_full | Post-translational modifications of EZH2 in cancer |
title_fullStr | Post-translational modifications of EZH2 in cancer |
title_full_unstemmed | Post-translational modifications of EZH2 in cancer |
title_short | Post-translational modifications of EZH2 in cancer |
title_sort | post-translational modifications of ezh2 in cancer |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7731458/ https://www.ncbi.nlm.nih.gov/pubmed/33308321 http://dx.doi.org/10.1186/s13578-020-00505-0 |
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