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Cancer epigenomics.

机译:癌症表观基因组学。

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摘要

Research in cancer epigenomics is driven by the development of novel technologies and the utilization of model organisms ranging from yeasts to plants to vertebrates. For decades, the search for cancer genes has focused on genetic defects that were used as tags for identification of these genes. With the realization that epigenetic modifications, most importantly DNA methylation events, are frequently involved in transcriptional changes in both tumor suppressor genes and oncogenes, techniques have been developed that support the identification of novel cancer genes altered by DNA methylation alone or in combination with genetic events. Recent data demonstrate that, in addition to DNA methylation, chromatin modifications are also involved in gene regulation. We are now beginning to understand this interesting interplay between chromatin modifications, DNA methylation and gene regulation. This review will summarize our current knowledge of DNA methylation and histone modification in normal cells, introduce emerging concepts that show the intimate link between DNA methylation and chromatin modifications, and highlight recent advancements in our understanding of aberrant DNA methylation, with special emphasis on genome-wide hypermethylation.
机译:癌症表观基因组学的研究是由新技术的发展以及从酵母到植物再到脊椎动物等模型生物的利用而推动的。几十年来,对癌症基因的搜索一直集中在遗传缺陷上,这些缺陷被用作识别这些基因的标签。随着认识到表观遗传修饰(最重要的是DNA甲基化事件)经常参与肿瘤抑制基因和癌基因的转录变化,已开发出技术来支持鉴定仅通过DNA甲基化或与遗传事件结合而改变的新癌症基因。最新数据表明,除DNA甲基化外,染色质修饰也参与基因调控。现在,我们开始了解染色质修饰,DNA甲基化和基因调控之间这种有趣的相互作用。这篇评论将总结我们目前在正常细胞中对DNA甲基化和组蛋白修饰的知识,并介绍一些新兴的概念来显示DNA甲基化和染色质修饰之间的紧密联系,并着重强调我们对异常DNA甲基化的最新进展,特别是对基因组的关注广泛的超甲基化。

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