Department of Life Sciences, Birmingham City University, Birmingham, UK.
Division of Cellular and Molecular Pathology, Addenbrooke's Hospital, University of Cambridge, Cambridge, UK.
Open Biol. 2020 Jul;10(7):200121. doi: 10.1098/rsob.200121. Epub 2020 Jul 8.
Gene expression programmes driving cell identity are established by tightly regulated transcription factors that auto- and cross-regulate in a feed-forward manner, forming core regulatory circuitries (CRCs). CRC transcription factors create and engage super-enhancers by recruiting acetylation writers depositing permissive H3K27ac chromatin marks. These super-enhancers are largely associated with BET proteins, including BRD4, that influence higher-order chromatin structure. The orchestration of these events triggers accessibility of RNA polymerase machinery and the imposition of lineage-specific gene expression. In cancers, CRCs drive cell identity by superimposing developmental programmes on a background of genetic alterations. Further, the establishment and maintenance of oncogenic states are reliant on CRCs that drive factors involved in tumour development. Hence, the molecular dissection of CRC components driving cell identity and cancer state can contribute to elucidating mechanisms of diversion from pre-determined developmental programmes and highlight cancer dependencies. These insights can provide valuable opportunities for identifying and re-purposing drug targets. In this article, we review the current understanding of CRCs across solid and liquid malignancies and avenues of investigation for drug development efforts. We also review techniques used to understand CRCs and elaborate the indication of discussed CRC transcription factors in the wider context of cancer CRC models.
驱动细胞身份的基因表达程序是由紧密调控的转录因子建立的,这些转录因子以自反馈和交叉反馈的方式自动调节,形成核心调控回路(CRC)。CRC 转录因子通过招募乙酰化写入器沉积允许的 H3K27ac 染色质标记来创建和参与超级增强子。这些超级增强子主要与 BET 蛋白(包括 BRD4)相关,这些蛋白影响更高阶的染色质结构。这些事件的协调触发了 RNA 聚合酶机制的可及性,并施加了谱系特异性的基因表达。在癌症中,CRC 通过在遗传改变的背景上叠加发育程序来驱动细胞身份。此外,致癌状态的建立和维持依赖于驱动肿瘤发展相关因子的 CRC。因此,对驱动细胞身份和癌症状态的 CRC 成分的分子剖析有助于阐明偏离预定发育程序的机制,并突出癌症的依赖性。这些见解为识别和重新利用药物靶点提供了有价值的机会。在本文中,我们回顾了固体和液体恶性肿瘤中 CRC 的现有认识,以及药物开发工作的研究途径。我们还回顾了用于理解 CRC 的技术,并详细说明了所讨论的 CRC 转录因子在癌症 CRC 模型中的更广泛背景下的适应症。