Cargando…

Characterization of global 5-hydroxymethylcytosine in pediatric posterior fossa ependymoma

BACKGROUND: 5-Hydroxymethylcytosine (5hmC) is a novel epigenetic mark and may be involved in the mechanisms of tumorigenesis and malignant transformation. However, the role of 5hmC in ependymoma, the third most common brain tumor in children, remains unclear. The aim of this study sought to identify...

Descripción completa

Detalles Bibliográficos
Autores principales: Wu, Tao, Zhang, Zhi-wei, Li, Shiwei, Wang, Bo, Yang, Zhijun, Li, Peng, Zhang, Jing, Tong, Wei-min, Li, Chunde, Zhao, Fu, Niu, Yamei, Liu, Pinan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6988368/
https://www.ncbi.nlm.nih.gov/pubmed/31992357
http://dx.doi.org/10.1186/s13148-020-0809-8
_version_ 1783492255869304832
author Wu, Tao
Zhang, Zhi-wei
Li, Shiwei
Wang, Bo
Yang, Zhijun
Li, Peng
Zhang, Jing
Tong, Wei-min
Li, Chunde
Zhao, Fu
Niu, Yamei
Liu, Pinan
author_facet Wu, Tao
Zhang, Zhi-wei
Li, Shiwei
Wang, Bo
Yang, Zhijun
Li, Peng
Zhang, Jing
Tong, Wei-min
Li, Chunde
Zhao, Fu
Niu, Yamei
Liu, Pinan
author_sort Wu, Tao
collection PubMed
description BACKGROUND: 5-Hydroxymethylcytosine (5hmC) is a novel epigenetic mark and may be involved in the mechanisms of tumorigenesis and malignant transformation. However, the role of 5hmC in ependymoma, the third most common brain tumor in children, remains unclear. The aim of this study sought to identify the characterization of 5hmC levels in pediatric posterior fossa ependymoma and to evaluate whether 5hmC levels could be a potential factor to predict clinical outcomes. RESULTS: Our results showed that 5hmC levels were globally decreased in posterior fossa ependymoma compared with normal cerebellum tissues (P < 0.001). Group A posterior fossa ependymomas had higher 5hmC levels than group B tumors (P = 0.007). Moreover, 5hmC levels positively correlated with Ki-67 index in posterior fossa ependymoma (r = 0.428, P = 0.003). Multivariate Cox hazards model revealed that patients with high 5hmC levels (> 0.102%) had worse PFS and OS than patients with lower 5hmC levels (< 0.102%) (PFS: HR = 3.014; 95% CI, 1.040–8.738; P = 0.042; OS: HR = 2.788; 95% CI, 0.974–7.982; P = 0.047). CONCLUSIONS: Our findings suggest that loss of 5hmC is an epigenetic hallmark for pediatric posterior fossa ependymoma. 5hmC levels may represent a potential biomarker to predict prognosis in children with posterior fossa ependymoma.
format Online
Article
Text
id pubmed-6988368
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-69883682020-02-03 Characterization of global 5-hydroxymethylcytosine in pediatric posterior fossa ependymoma Wu, Tao Zhang, Zhi-wei Li, Shiwei Wang, Bo Yang, Zhijun Li, Peng Zhang, Jing Tong, Wei-min Li, Chunde Zhao, Fu Niu, Yamei Liu, Pinan Clin Epigenetics Research BACKGROUND: 5-Hydroxymethylcytosine (5hmC) is a novel epigenetic mark and may be involved in the mechanisms of tumorigenesis and malignant transformation. However, the role of 5hmC in ependymoma, the third most common brain tumor in children, remains unclear. The aim of this study sought to identify the characterization of 5hmC levels in pediatric posterior fossa ependymoma and to evaluate whether 5hmC levels could be a potential factor to predict clinical outcomes. RESULTS: Our results showed that 5hmC levels were globally decreased in posterior fossa ependymoma compared with normal cerebellum tissues (P < 0.001). Group A posterior fossa ependymomas had higher 5hmC levels than group B tumors (P = 0.007). Moreover, 5hmC levels positively correlated with Ki-67 index in posterior fossa ependymoma (r = 0.428, P = 0.003). Multivariate Cox hazards model revealed that patients with high 5hmC levels (> 0.102%) had worse PFS and OS than patients with lower 5hmC levels (< 0.102%) (PFS: HR = 3.014; 95% CI, 1.040–8.738; P = 0.042; OS: HR = 2.788; 95% CI, 0.974–7.982; P = 0.047). CONCLUSIONS: Our findings suggest that loss of 5hmC is an epigenetic hallmark for pediatric posterior fossa ependymoma. 5hmC levels may represent a potential biomarker to predict prognosis in children with posterior fossa ependymoma. BioMed Central 2020-01-28 /pmc/articles/PMC6988368/ /pubmed/31992357 http://dx.doi.org/10.1186/s13148-020-0809-8 Text en © The Author(s). 2020 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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
Wu, Tao
Zhang, Zhi-wei
Li, Shiwei
Wang, Bo
Yang, Zhijun
Li, Peng
Zhang, Jing
Tong, Wei-min
Li, Chunde
Zhao, Fu
Niu, Yamei
Liu, Pinan
Characterization of global 5-hydroxymethylcytosine in pediatric posterior fossa ependymoma
title Characterization of global 5-hydroxymethylcytosine in pediatric posterior fossa ependymoma
title_full Characterization of global 5-hydroxymethylcytosine in pediatric posterior fossa ependymoma
title_fullStr Characterization of global 5-hydroxymethylcytosine in pediatric posterior fossa ependymoma
title_full_unstemmed Characterization of global 5-hydroxymethylcytosine in pediatric posterior fossa ependymoma
title_short Characterization of global 5-hydroxymethylcytosine in pediatric posterior fossa ependymoma
title_sort characterization of global 5-hydroxymethylcytosine in pediatric posterior fossa ependymoma
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6988368/
https://www.ncbi.nlm.nih.gov/pubmed/31992357
http://dx.doi.org/10.1186/s13148-020-0809-8
work_keys_str_mv AT wutao characterizationofglobal5hydroxymethylcytosineinpediatricposteriorfossaependymoma
AT zhangzhiwei characterizationofglobal5hydroxymethylcytosineinpediatricposteriorfossaependymoma
AT lishiwei characterizationofglobal5hydroxymethylcytosineinpediatricposteriorfossaependymoma
AT wangbo characterizationofglobal5hydroxymethylcytosineinpediatricposteriorfossaependymoma
AT yangzhijun characterizationofglobal5hydroxymethylcytosineinpediatricposteriorfossaependymoma
AT lipeng characterizationofglobal5hydroxymethylcytosineinpediatricposteriorfossaependymoma
AT zhangjing characterizationofglobal5hydroxymethylcytosineinpediatricposteriorfossaependymoma
AT tongweimin characterizationofglobal5hydroxymethylcytosineinpediatricposteriorfossaependymoma
AT lichunde characterizationofglobal5hydroxymethylcytosineinpediatricposteriorfossaependymoma
AT zhaofu characterizationofglobal5hydroxymethylcytosineinpediatricposteriorfossaependymoma
AT niuyamei characterizationofglobal5hydroxymethylcytosineinpediatricposteriorfossaependymoma
AT liupinan characterizationofglobal5hydroxymethylcytosineinpediatricposteriorfossaependymoma