Whitehead Institute for Biomedical Research, 9 Cambridge Center, Cambridge, MA 02142, USA.
Cell. 2013 Apr 11;153(2):320-34. doi: 10.1016/j.cell.2013.03.036.
Chromatin regulators have become attractive targets for cancer therapy, but it is unclear why inhibition of these ubiquitous regulators should have gene-specific effects in tumor cells. Here, we investigate how inhibition of the widely expressed transcriptional coactivator BRD4 leads to selective inhibition of the MYC oncogene in multiple myeloma (MM). BRD4 and Mediator were found to co-occupy thousands of enhancers associated with active genes. They also co-occupied a small set of exceptionally large super-enhancers associated with genes that feature prominently in MM biology, including the MYC oncogene. Treatment of MM tumor cells with the BET-bromodomain inhibitor JQ1 led to preferential loss of BRD4 at super-enhancers and consequent transcription elongation defects that preferentially impacted genes with super-enhancers, including MYC. Super-enhancers were found at key oncogenic drivers in many other tumor cells. These observations have implications for the discovery of cancer therapeutics directed at components of super-enhancers in diverse tumor types.
染色质调控因子已成为癌症治疗的热门靶点,但尚不清楚抑制这些普遍存在的调控因子为何会在肿瘤细胞中产生特定于基因的效应。在这里,我们研究了广泛表达的转录共激活因子 BRD4 的抑制如何导致多发性骨髓瘤 (MM) 中 MYC 癌基因的选择性抑制。发现 BRD4 和 Mediator 共同占据了数千个与活性基因相关的增强子。它们还共同占据了一小部分异常大的超级增强子,这些超级增强子与 MM 生物学中突出的基因有关,包括 MYC 癌基因。用 BET 溴结构域抑制剂 JQ1 处理 MM 肿瘤细胞,导致超级增强子上 BRD4 的优先丢失,继而导致转录延伸缺陷,这些缺陷优先影响具有超级增强子的基因,包括 MYC。在许多其他肿瘤细胞中的关键致癌驱动基因中也发现了超级增强子。这些观察结果对于发现针对不同肿瘤类型超级增强子成分的癌症治疗药物具有重要意义。