Epigenetics in human gliomas

被引:48
作者
Kreth, Simone [1 ]
Thon, Niklas [2 ]
Kreth, Friedrich W. [2 ]
机构
[1] Univ Munich LMU, Dept Anesthesiol, Res Grp Mol Med, Munich, Germany
[2] Univ Munich LMU, Dept Neurosurg, Munich, Germany
关键词
Glioblastoma; Epigenetic networks; MicroRNAs; Stereotactic biopsy; SUBEROYLANILIDE HYDROXAMIC ACID; HISTONE DEACETYLASE INHIBITOR; CPG ISLAND HYPERMETHYLATION; INTEGRATED GENOMIC ANALYSIS; PROGRESSION-FREE SURVIVAL; DNA METHYLATION; PHASE-III; DOWN-REGULATION; ADJUVANT TEMOZOLOMIDE; MICRORNA EXPRESSION;
D O I
10.1016/j.canlet.2012.04.008
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Aberrant epigenetic landscapes and their involvement in genesis and progression of tumors, as well as in treatment responses and prognosis, indicate one of the most emerging fields in cancer research. In gliomas, the most common human primary brain tumors, and in particular in glioblastoma, the most malignant and devastating brain tumor entity in adults, the elucidation of distinct patterns of aberrant DNA methylation, histone modification, and miRNA expression and their interrelationship has fundamentally changed our point of view on these highly heterogeneous tumors. In the current review article, we address the basic principles of epigenetic control in gliomas, their current and putative future role in prognostic and predictive models and possible interactions within the epigenetic network. We discuss diagnostic and therapeutic opportunities appearing at horizon of epigenetic research. Moreover, we present current and propose future clinical workflow models for molecular characterization of malignant gliomas. (C) 2012 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:185 / 192
页数:8
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