Sakatani Takashi, Onyango Patrick
Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
Expert Rev Anticancer Ther. 2003 Dec;3(6):891-901. doi: 10.1586/14737140.3.6.891.
Genomics has generated a wealth of data that is now being used to identify additional molecular alterations associated with cancer development. Mapping these alterations in the cancer genome is a critical first step in dissecting oncological pathways. There are two ways in which cancer research has changed in recent years. The first is the progressive elucidation of the genomic basis of cancer. This has been accomplished by the generation of detailed information using procedures such as global expression profiling. The second is a renewed emphasis on the role of epigenetic modifications in the etiology of cancer. Changes in DNA methylation and chromatin modification patterns are some of the epigenetic factors that cause gene deregulation in cancer. In this article, current and evolving genomic applications and the hypotheses underlying the modality for cancer therapy will be reviewed.
基因组学已产生了大量数据,这些数据目前正被用于识别与癌症发展相关的其他分子改变。在癌症基因组中描绘这些改变是剖析肿瘤发生途径的关键第一步。近年来癌症研究在两个方面发生了变化。第一个方面是对癌症基因组基础的逐步阐明。这是通过使用诸如全基因组表达谱分析等程序生成详细信息来实现的。第二个方面是重新强调表观遗传修饰在癌症病因学中的作用。DNA甲基化和染色质修饰模式的变化是导致癌症中基因失调的一些表观遗传因素。在本文中,将对当前和不断发展的基因组学应用以及癌症治疗方式背后的假设进行综述。