McKenna Elizabeth S, Roberts Charles W M
Department of Pediatric Oncology, Dana-Farber Cancer Institute, 44 Binney Street, Boston, MA 02115, USA.
Cell Cycle. 2009 Jan 1;8(1):23-6. doi: 10.4161/cc.8.1.7290. Epub 2009 Jan 30.
Genomic instability is often considered a hallmark of cancer. However, it remains unclear whether chromosomal disorganization is most frequently a cause or a consequence of tumorigenesis. The fact that subsets of many cancers lack chromosomal or microsatellite instability argues against the hypothesis that genomic instability plays an essential role in the initiation and maintenance of oncogenesis. Cancer-specific, epigenetically-based changes in gene expression caused by abnormalities in DNA methylation, in histone modifications, and in nucleosome positioning are gaining recognition as driving events in tumorigenesis. But are these changes merely a small piece of the oncogenesis puzzle or could they be the major component, or even sufficient for cancer? Here we discuss evidence that the progression of aggressive cancers can be driven by epigenetic events without genomic instability.
基因组不稳定通常被认为是癌症的一个标志。然而,染色体紊乱究竟是肿瘤发生最常见的原因还是结果,仍不清楚。许多癌症的亚群缺乏染色体或微卫星不稳定这一事实,与基因组不稳定在肿瘤发生的起始和维持中起关键作用的假说相悖。由DNA甲基化、组蛋白修饰和核小体定位异常引起的癌症特异性、基于表观遗传学的基因表达变化,正日益被视为肿瘤发生中的驱动事件。但这些变化仅仅是肿瘤发生难题中的一小部分,还是可能是主要组成部分,甚至足以引发癌症呢?在这里,我们讨论了相关证据,即侵袭性癌症的进展可能由表观遗传事件驱动,而不存在基因组不稳定。