Department of Pathology, New York University School of Medicine, New York, NY 10016, USA; Laura & Isaac Perlmutter Cancer Center, New York University School of Medicine, New York, NY 10016, USA.
Pharmacol Ther. 2019 Jul;199:129-138. doi: 10.1016/j.pharmthera.2019.02.014. Epub 2019 Mar 16.
Cancer is fueled by the aberrant activity of oncogenic and tumor suppressive pathways. Transcriptional dysregulation of these pathways play a major role both in the genesis and development of cancer. Dysregulation of transcriptional programs can be mediated by genetic and epigenetic alterations targeting both protein coding genes and non-coding regulatory elements like enhancers and super-enhancers. Super-enhancers, characterized as large clusters of enhancers in close proximity, have been identified as essential oncogenic drivers required for the maintenance of cancer cell identity. As a result, cancer cells are often addicted to the super-enhancer driven transcriptional programs. Furthermore, pharmacological inhibitors targeting key components of super-enhancer assembly and activation have shown great promise in reducing tumor growth and proliferation in several pre-clinical tumor models. This article reviews the current understanding of super-enhancer assembly and activation, the different mechanisms by which cancer cells acquire oncogenic super-enhancers and, finally, the potential of targeting super-enhancers as future therapeutics.
癌症是由致癌和肿瘤抑制途径的异常活性所驱动的。这些途径的转录失调在癌症的发生和发展中起着主要作用。转录程序的失调可以通过针对蛋白质编码基因和非编码调节元件(如增强子和超级增强子)的遗传和表观遗传改变来介导。超级增强子被定义为紧密邻近的增强子的大簇,已被确定为维持癌细胞特性所必需的关键致癌驱动因子。因此,癌细胞通常依赖于超级增强子驱动的转录程序。此外,针对超级增强子组装和激活关键成分的药理学抑制剂在几种临床前肿瘤模型中显示出了降低肿瘤生长和增殖的巨大潜力。本文综述了超级增强子组装和激活的最新认识,癌细胞获得致癌超级增强子的不同机制,以及作为未来治疗靶点的超级增强子的潜在应用。