Holloway A F, Oakford P C
Menzies Research Institute, University of Tasmania, Hobart, Tasmania 7001, Australia.
Curr Med Chem. 2007;14(24):2540-7. doi: 10.2174/092986707782023271.
The chromatin structure of a gene plays an important role in regulating its expression. This structure is established through the action of various protein complexes that remodel nucleosomes, catalyse post-translational modifications, deposit histone variants and methylate DNA. Together these complexes establish epigenetic marks that influence expression of the gene. Some of these epigenetic marks are transient while others, such as those involved in silencing genes are more stable and can require several cell divisions to be fully implemented or reversed. Deregulated gene expression programs are a feature of cancer biology and it is now apparent that epigenetic changes, as well as genetic changes, are important in establishing these aberrant expression patterns. However, unlike genetic alterations, epigenetic changes are reversible. The complexes that catalyse these modifications therefore represent valuable targets for therapeutic intervention. Here we will review the most recent literature describing the protein complexes that catalyse epigenetic modifications and the inhibitors of these complexes that are being pursued as cancer drugs. In addition we will highlight those epigenetic modifiers that provide promise as therapeutic targets but for which inhibitors are not currently available.
基因的染色质结构在调控其表达方面起着重要作用。这种结构是通过各种蛋白质复合物的作用建立起来的,这些复合物可重塑核小体、催化翻译后修饰、沉积组蛋白变体以及使DNA甲基化。这些复合物共同建立起影响基因表达的表观遗传标记。其中一些表观遗传标记是短暂的,而其他的,如参与基因沉默的那些标记则更为稳定,可能需要经过几次细胞分裂才能完全实现或逆转。失调的基因表达程序是癌症生物学的一个特征,现在很明显,表观遗传变化以及基因变化在建立这些异常表达模式中都很重要。然而,与基因改变不同,表观遗传变化是可逆的。因此,催化这些修饰的复合物是治疗干预的有价值靶点。在这里,我们将回顾描述催化表观遗传修饰的蛋白质复合物以及作为癌症药物正在研发的这些复合物抑制剂的最新文献。此外,我们将强调那些有望成为治疗靶点但目前尚无抑制剂的表观遗传修饰因子。