Loss of ATRX, associated with DNA methylation pattern of chromosome end, impacted biological behaviors of astrocytic tumors

被引:48
作者
Cai, Jinquan [1 ,6 ]
Chen, Jing [2 ,6 ]
Zhang, Wei [2 ,4 ,6 ]
Yang, Pei [2 ,4 ,6 ]
Zhang, Chuanbao [2 ,4 ,6 ]
Li, Mingyang [2 ,4 ,6 ]
Yao, Kun [6 ,7 ]
Wang, Hongjun [1 ,6 ]
Li, Qingbin [1 ,6 ]
Jiang, Chuanlu [1 ,6 ]
Jiang, Tao [2 ,3 ,4 ,5 ,6 ]
机构
[1] Harbin Med Univ, Affiliated Hosp 2, Dept Neurosurg, Harbin, Peoples R China
[2] Capital Med Univ, Beijing Neurosurg Inst, Beijing, Peoples R China
[3] Brain Tumor Ctr, Beijing Inst Brain Disorders, Beijing, Peoples R China
[4] Capital Med Univ, Beijing Tiantan Hosp, Dept Neurosurg, Beijing, Peoples R China
[5] China Natl Clin Res Ctr Neurol Dis, Beijing, Peoples R China
[6] CGCG, Beijing, Peoples R China
[7] Capital Med Univ, Beijing Sanbo Brain Hosp, Dept Pathol, Beijing, Peoples R China
基金
中国国家自然科学基金;
关键词
ATRX; DNA methylation; chromosome end; MGMT; biological behaviors; ENRICHMENT ANALYSIS; CLASSIFICATION; MUTATIONS; GENES; REPLICATION; GENECODIS; INTEGRITY; PROTEIN; GLIOMAS; H3.3;
D O I
10.18632/oncotarget.3906
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Loss of ATRX leads to epigenetic alterations, including abnormal levels of DNA methylation at repetitive elements such as telomeres in murine cells. We conducted an extensive DNA methylation and mRNA expression profile study on a cohort of 82 patients with astrocytic tumors to study whether ATRX expression was associated with DNA methylation level in astrocytic tumors and in which cellular functions it participated. We observed that astrocytic tumors with lower ATRX expression harbored higher DNA methylation level at chromatin end and astrocytic tumors with ATRX-low had distinct gene expression profile and DNA methylation profile compared with ATRX-igh tumors. Then, we uncovered that several ATRX associated biological functions in the DNA methylation and mRNA expression profile (GEP), including apoptotic process, DNA-dependent positive regulation of transcription, chromatin modification, and observed that ATRX expression was companied by MGMT methylation and expression. We also found that loss of ATRX caused by siRNA induced apoptotic cells increasing, reduced tumor cell proliferation and repressed the cell migration in glioma cells. Our results showed ATRX-related regulatory functions of the combined profiles from DNA methylation and mRNA expression in astrocytic tumors, and delineated that loss of ATRX impacted biological behaviors of astrocytic tumor cells, providing important resources for future dissection of ATRX role in glioma.
引用
收藏
页码:18105 / 18115
页数:11
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