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Mutations in EZH2 are associated with poor prognosis for patients with myeloid neoplasms

EZH2 is a component of the polycomb repressive complex 2 (PRC2), which is a highly conserved histone methyltransferase that methylates lysine 27 of histone 3. EZH2 mutations are associated with oncogenesis and progression of cancers. However, the relationship between the clinical outcome of patients...

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Detalles Bibliográficos
Autores principales: Zhang, Qi, Han, Qi, Zi, Jie, Ma, Jinlong, Song, Huihui, Tian, Yulu, McGrath, Mary, Song, Chunhua, Ge, Zheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Chongqing Medical University 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6997607/
https://www.ncbi.nlm.nih.gov/pubmed/32042866
http://dx.doi.org/10.1016/j.gendis.2019.05.001
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author Zhang, Qi
Han, Qi
Zi, Jie
Ma, Jinlong
Song, Huihui
Tian, Yulu
McGrath, Mary
Song, Chunhua
Ge, Zheng
author_facet Zhang, Qi
Han, Qi
Zi, Jie
Ma, Jinlong
Song, Huihui
Tian, Yulu
McGrath, Mary
Song, Chunhua
Ge, Zheng
author_sort Zhang, Qi
collection PubMed
description EZH2 is a component of the polycomb repressive complex 2 (PRC2), which is a highly conserved histone methyltransferase that methylates lysine 27 of histone 3. EZH2 mutations are associated with oncogenesis and progression of cancers. However, the relationship between the clinical outcome of patients with myeloid malignancies and EZH2 mutations is controversial. Therefore, we performed a meta-analysis of 8 studies (n = 2243 patients) that evaluates the correlation between EZH2 mutations and overall survival (OS) in patients with myeloid neoplasms. EZH2 mutations were associated with significantly worse OS (hazard ratio [HR] = 2.37, 95% confidential interval (CI), 1.48–3.79). In a word, EZH2 mutations indicate a poor prognosis for patients with myeloid neoplasms.
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spelling pubmed-69976072020-02-10 Mutations in EZH2 are associated with poor prognosis for patients with myeloid neoplasms Zhang, Qi Han, Qi Zi, Jie Ma, Jinlong Song, Huihui Tian, Yulu McGrath, Mary Song, Chunhua Ge, Zheng Genes Dis Article EZH2 is a component of the polycomb repressive complex 2 (PRC2), which is a highly conserved histone methyltransferase that methylates lysine 27 of histone 3. EZH2 mutations are associated with oncogenesis and progression of cancers. However, the relationship between the clinical outcome of patients with myeloid malignancies and EZH2 mutations is controversial. Therefore, we performed a meta-analysis of 8 studies (n = 2243 patients) that evaluates the correlation between EZH2 mutations and overall survival (OS) in patients with myeloid neoplasms. EZH2 mutations were associated with significantly worse OS (hazard ratio [HR] = 2.37, 95% confidential interval (CI), 1.48–3.79). In a word, EZH2 mutations indicate a poor prognosis for patients with myeloid neoplasms. Chongqing Medical University 2019-05-16 /pmc/articles/PMC6997607/ /pubmed/32042866 http://dx.doi.org/10.1016/j.gendis.2019.05.001 Text en © 2019 Chongqing Medical University. Production and hosting by Elsevier B.V. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Zhang, Qi
Han, Qi
Zi, Jie
Ma, Jinlong
Song, Huihui
Tian, Yulu
McGrath, Mary
Song, Chunhua
Ge, Zheng
Mutations in EZH2 are associated with poor prognosis for patients with myeloid neoplasms
title Mutations in EZH2 are associated with poor prognosis for patients with myeloid neoplasms
title_full Mutations in EZH2 are associated with poor prognosis for patients with myeloid neoplasms
title_fullStr Mutations in EZH2 are associated with poor prognosis for patients with myeloid neoplasms
title_full_unstemmed Mutations in EZH2 are associated with poor prognosis for patients with myeloid neoplasms
title_short Mutations in EZH2 are associated with poor prognosis for patients with myeloid neoplasms
title_sort mutations in ezh2 are associated with poor prognosis for patients with myeloid neoplasms
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6997607/
https://www.ncbi.nlm.nih.gov/pubmed/32042866
http://dx.doi.org/10.1016/j.gendis.2019.05.001
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