Voutsadakis Ioannis A
Algoma District Cancer Program, Sault Area Hospital Sault Ste. Marie, ON, Canada.
Division of Clinical Sciences, Section of Internal Medicine, Northern Ontario School of Medicine Sudbury, ON, Canada.
Am J Transl Res. 2024 Mar 15;16(3):700-719. doi: 10.62347/QKHB5897. eCollection 2024.
In addition to genetic variants and copy number alterations, epigenetic deregulation of oncogenes and tumor suppressors is a major contributor in cancer development and propagation. Regulatory elements for gene transcription regulation can be found in promoters which are located in the vicinity of transcription start sites but also at a distance, in enhancer sites, brought to interact with proximal sites when occupied by enhancer protein complexes. These sites provide most of the specific regulatory sequences recognized by transcription factors. A sub-set of enhancers characterized by a longer structure and stronger activity, called super-enhancers, are critical for the expression of specific genes, usually associated with individual cell type identity and function. Super-enhancers show deregulation in cancer, which may have profound repercussions for cancer cell survival and response to therapy. Dysfunction of super-enhancers may result from multiple mechanisms that include changes in their sequence, alterations in the topological neighborhoods where they belong, and alterations in the proteins that mediate their function, such as transcription factors and epigenetic modifiers. These can become potential targets for therapeutic interventions. Genes that are targets of super-enhancers are cell and cancer type specific and could also be of interest for therapeutic targeting. In colorectal cancer, a super-enhancer regulated and over-expressed oncogene is MYC, under the influence of the WNT/β-catenin pathway. Identification and targeting of additional oncogenes regulated by super-enhancers in colorectal cancer may pave the way for combination therapies targeting the super-enhancer machinery and signal transduction pathways that regulate the specific transcription factors operative on them.
除了基因变异和拷贝数改变外,癌基因和肿瘤抑制因子的表观遗传失调是癌症发生和发展的主要因素。基因转录调控元件不仅存在于转录起始位点附近的启动子中,还存在于远距离的增强子位点,当被增强子蛋白复合物占据时,这些位点会与近端位点相互作用。这些位点提供了转录因子识别的大部分特异性调控序列。一类结构更长、活性更强的增强子亚群,称为超级增强子,对于特定基因的表达至关重要,这些基因通常与个体细胞类型的特性和功能相关。超级增强子在癌症中表现出失调,这可能对癌细胞的存活和对治疗的反应产生深远影响。超级增强子功能障碍可能由多种机制导致,包括其序列改变、所属拓扑邻域的改变以及介导其功能的蛋白质(如转录因子和表观遗传修饰因子)的改变。这些可能成为治疗干预的潜在靶点。作为超级增强子靶点的基因具有细胞和癌症类型特异性,也可能成为治疗靶向的研究对象。在结直肠癌中,一种受超级增强子调控并过度表达的癌基因是MYC,它受WNT/β-连环蛋白信号通路的影响。识别和靶向结直肠癌中受超级增强子调控的其他癌基因,可能为针对超级增强子机制和调节作用于其上的特定转录因子的信号转导通路的联合治疗铺平道路。