Moggs Jonathan G, Goodman Jay I, Trosko James E, Roberts Ruth A
Syngenta CTL, Alderley Park, Cheshire SK10 4TJ, UK.
Toxicol Appl Pharmacol. 2004 May 1;196(3):422-30. doi: 10.1016/j.taap.2004.01.009.
It is necessary to determine whether chemicals or drugs have the potential to pose a threat to human health. Research conducted over the last two decades has led to the paradigm that chemicals can cause cancer either by damaging DNA or by altering cellular growth, probably via receptor-mediated changes in gene expression. However, recent evidence suggests that gene expression can be altered markedly via several diverse epigenetic mechanisms that can lead to permanent or reversible changes in cellular behavior. Key molecular events underlying these mechanisms include the alteration of DNA methylation and chromatin, and changes in the function of cell surface molecules. Thus, for example, DNA methyltransferase enzymes together with chromatin-associated proteins such as histone modifying enzymes and remodelling factors can modify the genetic code and contribute to the establishment and maintenance of altered epigenetic states. This is relevant to many types of toxicity including but not limited to cancer. In this paper, we describe the potential for interplay between genetic alteration and epigenetic changes in cell growth regulation and discuss the implications for drug discovery and safety assessment.
有必要确定化学物质或药物是否有可能对人类健康构成威胁。过去二十年进行的研究形成了一种范式,即化学物质可通过损害DNA或改变细胞生长(可能是通过受体介导的基因表达变化)来导致癌症。然而,最近的证据表明,基因表达可通过多种不同的表观遗传机制发生显著改变,这些机制可导致细胞行为的永久性或可逆性变化。这些机制背后的关键分子事件包括DNA甲基化和染色质的改变,以及细胞表面分子功能的变化。因此,例如,DNA甲基转移酶与染色质相关蛋白(如组蛋白修饰酶和重塑因子)一起可修饰遗传密码,并有助于建立和维持改变的表观遗传状态。这与许多类型的毒性相关,包括但不限于癌症。在本文中,我们描述了细胞生长调节中基因改变和表观遗传变化之间相互作用的可能性,并讨论了其对药物发现和安全性评估的影响。