Bar-Sela Gil, Jacobs Kristi Muldoon, Gius David
Radiation Oncology Branch, Radiation Oncology Sciences Program, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Cancer J. 2007 Jan-Feb;13(1):65-9. doi: 10.1097/PPO.0b013e31803c7565.
It now appears that epigenetics plays a central role in transformation, both in vitro and in vivo. The expression and regulation of DNA methylation and the subsequent chromatin structure are significantly altered in tumor cells, suggesting a direct role in the process of in vivo cellular transformation. If epigenetics and posttranslational modifications of histones play a role in transformation, then it seems logical that the genes regulating chromatin compaction may also be molecular targets and markers in profiling tumor cell resistance. Local remodeling of chromatin is a key step in the regulation of gene expression, and altering the expression of these genes might also favorably alter how tumor cells respond to anticancer agents. Several new agents that alter chromatin compaction, either methyltransferase or histone deacetylases inhibitors, are progressing through clinical trials and have shown promising preclinical interactions when combined with radiation. In this review, we discuss the potential for histone deacetylases inhibitors as radiosensitizing agents.
现在看来,表观遗传学在体外和体内的细胞转化过程中都起着核心作用。肿瘤细胞中DNA甲基化的表达和调控以及随后的染色质结构发生了显著改变,这表明其在体内细胞转化过程中发挥着直接作用。如果表观遗传学和组蛋白的翻译后修饰在细胞转化中起作用,那么调控染色质压缩的基因似乎也可能是肿瘤细胞耐药性分析中的分子靶点和标志物。染色质的局部重塑是基因表达调控的关键步骤,改变这些基因的表达可能也会有利地改变肿瘤细胞对抗癌药物的反应。几种改变染色质压缩的新型药物,即甲基转移酶或组蛋白脱乙酰酶抑制剂,正在进行临床试验,并且在与放疗联合使用时已显示出有前景的临床前相互作用。在这篇综述中,我们讨论了组蛋白脱乙酰酶抑制剂作为放射增敏剂的潜力。