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EZH2: novel therapeutic target for human cancer

Enhancer of Zeste homlog 2 (EZH2) is a catalytic subunit of epigenetic regulator Polycomb repressive complex 2 (PRC2), which trimethylates Lys 27 of histone H3, leading to silencing of the target genes that are involved in a variety of biological processes including tumor progression and stem cell m...

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Detalles Bibliográficos
Autor principal: Li, Long-Yuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: China Medical University 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4264983/
https://www.ncbi.nlm.nih.gov/pubmed/25520914
http://dx.doi.org/10.7603/s40681-014-0001-6
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author Li, Long-Yuan
author_facet Li, Long-Yuan
author_sort Li, Long-Yuan
collection PubMed
description Enhancer of Zeste homlog 2 (EZH2) is a catalytic subunit of epigenetic regulator Polycomb repressive complex 2 (PRC2), which trimethylates Lys 27 of histone H3, leading to silencing of the target genes that are involved in a variety of biological processes including tumor progression and stem cell maintenance. However, in addition to its canonical PRC2-dependent transcriptional repression function, EZH2 also acts as a gene activator in a noncanonical PRC2-independent manner. Overexpression of EZH2 has been detected in diverse cancers, and is associated with tumor malignancy. Moreover, activating mutations and inactivating mutations of EZH2 are also associated with certain types of cancer. Given EZH2’s multi-faceted function and role in cancer, context-specific strategy for targeting EZH2/EZH2-mediated signaling could serve as future targeted therapy/personalized medicine for human cancer.
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spelling pubmed-42649832014-12-15 EZH2: novel therapeutic target for human cancer Li, Long-Yuan Biomedicine (Taipei) Review Article Enhancer of Zeste homlog 2 (EZH2) is a catalytic subunit of epigenetic regulator Polycomb repressive complex 2 (PRC2), which trimethylates Lys 27 of histone H3, leading to silencing of the target genes that are involved in a variety of biological processes including tumor progression and stem cell maintenance. However, in addition to its canonical PRC2-dependent transcriptional repression function, EZH2 also acts as a gene activator in a noncanonical PRC2-independent manner. Overexpression of EZH2 has been detected in diverse cancers, and is associated with tumor malignancy. Moreover, activating mutations and inactivating mutations of EZH2 are also associated with certain types of cancer. Given EZH2’s multi-faceted function and role in cancer, context-specific strategy for targeting EZH2/EZH2-mediated signaling could serve as future targeted therapy/personalized medicine for human cancer. China Medical University 2014-02-12 /pmc/articles/PMC4264983/ /pubmed/25520914 http://dx.doi.org/10.7603/s40681-014-0001-6 Text en © China Medical University 2014 https://creativecommons.org/licenses/by/4.0/ Open Access. This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Review Article
Li, Long-Yuan
EZH2: novel therapeutic target for human cancer
title EZH2: novel therapeutic target for human cancer
title_full EZH2: novel therapeutic target for human cancer
title_fullStr EZH2: novel therapeutic target for human cancer
title_full_unstemmed EZH2: novel therapeutic target for human cancer
title_short EZH2: novel therapeutic target for human cancer
title_sort ezh2: novel therapeutic target for human cancer
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4264983/
https://www.ncbi.nlm.nih.gov/pubmed/25520914
http://dx.doi.org/10.7603/s40681-014-0001-6
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