The good, the bad and the ugly: Epigenetic mechanisms' in glioblastoma

被引:42
作者
Caren, Helena [1 ]
Pollard, Steven M. [1 ]
Beck, Stephan [1 ]
机构
[1] UCL, UCL Canc Inst, London WC1E 6BT, England
基金
英国惠康基金; 瑞典研究理事会;
关键词
Epigenetics; Glioma; DNA methylation; Central nervous system (CNS); Differentiation; Cancer stem cells; SUBEROYLANILIDE HYDROXAMIC ACID; ISLAND METHYLATOR PHENOTYPE; INTEGRATED GENOMIC ANALYSIS; CANDIDATE TUMOR-SUPPRESSOR; PHASE-II TRIAL; DNA METHYLATION; STEM-CELLS; PROMOTER HYPERMETHYLATION; RECURRENT GLIOBLASTOMA; MULTIPLE GENES;
D O I
10.1016/j.mam.2012.06.007
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Cell type-specific patterns of gene expression reflect epigenetic changes imposed through a particular developmental lineage as well as those triggered by environmental cues within adult tissues. There is great interest in elucidating the molecular basis and functional importance of epigenetic mechanisms in both normal physiology and disease - particularly in cancer, where abnormal '-omic' states are often observed. In this article we review recent progress in studies of epigenetic mechanisms in the most common primary adult brain cancer, glioblastoma multiforme. Three distinct areas are discussed. First, the evidence in support of ongoing 'normal' epigenetic processes associated with differentiation - as predicted by 'cancer stem cell' models of the disease. Second, identification of site-specific and global epigenetic abnormalities. Third, genetic disruptions directly within the core epigenetic machinery, exemplified by the recently identified mutations within isocitrate dehydrogenase genes IDH1/2 and variant histone genes H3.3/H3F3A. These constitute the 'good, the bad and the ugly' of epigenetic mechanisms in cancer. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:849 / 862
页数:14
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