Baylin S B, Chen W Y
The Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins, Baltimore, Maryland 21231, USA.
Cold Spring Harb Symp Quant Biol. 2005;70:427-33. doi: 10.1101/sqb.2005.70.010.
Although it is clear that genetic alterations are critical for the initiation and maintenance of human cancer, it is also becoming evident that epigenetic changes may be essential for the development of these diseases as well. The best studied of these latter processes is heritable transcriptional repression of genes associated with aberrant DNA hypermethylation of their promoters. Herein we review how very early occurrence of these gene silencing events may contribute to loss of key gene functions which result in disruption of cell regulatory pathways that may contribute to abnormal cell population expansion. These altered regulatory events may then provide a setting where mutations in the same disrupted pathways may be readily selected and serve to lock tumor progression into place. This hypothesis has potential impact on means to prevent and control cancer and for the use of epigenetic markers for cancer risk assessment and early diagnosis.
虽然基因改变对于人类癌症的起始和维持至关重要这一点很明确,但表观遗传变化对于这些疾病的发展可能同样必不可少这一点也日益明显。这些后期过程中研究得最透彻的是与基因启动子异常DNA高甲基化相关的基因的可遗传转录抑制。在此我们综述这些基因沉默事件的极早期发生如何可能导致关键基因功能丧失,进而导致细胞调节通路中断,这可能促使异常细胞群体扩张。这些改变的调节事件随后可能提供一种环境,在此环境中同一受干扰通路中的突变可能很容易被选择,并有助于锁定肿瘤进展。这一假说对癌症预防和控制手段以及将表观遗传标记用于癌症风险评估和早期诊断具有潜在影响。