Shames David S, Minna John D, Gazdar Adi F
Hamon Center for Therapeutic Oncology Research NB8.206, The University of Texas Southwestern Medical Center at Dallas, 6000 Harry Hines Blvd., Dallas, TX 75390-8593, USA.
Curr Mol Med. 2007 Feb;7(1):85-102. doi: 10.2174/156652407779940413.
The spatial arrangement and three-dimensional structure of DNA in the nucleus is controlled through the interdigitation of DNA binding proteins such as histones and their modifiers, the Polycomb-Trithorax proteins, and the DNA methyltransferase enzymes. DNA methylation forms the foundation of chromatin and is crucial to epigenetic gene regulation in mammals. Disease pathogenesis mediated through infectious agents, inflammation, aging, or genetic damage often involves changes in gene expression. In particular, cellular transformation coincides with multiple changes in chromatin architecture, many of which appear to affect genome integrity and gene expression. Infectious agents, such as viruses directly affect genome structure and induce methylation of particular sequences to suppress host immune responses. Hyperproliferative tissues such as those in the gastrointestinal tract and colon have been shown to gradually acquire aberrant promoter hypermethylation. Here we review recent findings on altered DNA methylation in human disease, with particular focus on cancer and the increasingly large number of genes subject to tumor-specific promoter hypermethylation and the possible role of aberrant methylation in tumor development.
细胞核中DNA的空间排列和三维结构是通过DNA结合蛋白(如组蛋白及其修饰因子、多梳-三胸蛋白)以及DNA甲基转移酶的相互作用来控制的。DNA甲基化构成了染色质的基础,对哺乳动物的表观遗传基因调控至关重要。由感染因子、炎症、衰老或遗传损伤介导的疾病发病机制通常涉及基因表达的变化。特别是,细胞转化与染色质结构的多种变化同时发生,其中许多变化似乎会影响基因组完整性和基因表达。感染因子,如病毒,直接影响基因组结构并诱导特定序列的甲基化以抑制宿主免疫反应。已表明胃肠道和结肠等过度增殖组织会逐渐出现异常的启动子高甲基化。在这里,我们综述了人类疾病中DNA甲基化改变的最新研究发现,特别关注癌症以及越来越多的基因发生肿瘤特异性启动子高甲基化,以及异常甲基化在肿瘤发展中的可能作用。