Super-enhancers in hepatocellular carcinoma: regulatory mechanism and therapeutic targets

被引:0
|
作者
Lu, Xuejin [1 ]
Zhu, Meizi [1 ]
Pei, Xingyue [1 ]
Ma, Jinhu [1 ,3 ]
Wang, Rui [1 ]
Wang, Yi [1 ]
Chen, Shuwen [1 ]
Yan, Yan [2 ]
Zhu, Yaling [1 ,2 ]
机构
[1] Anhui Med Univ, Coll Basic Med Sci, Dept Pathophysiol, Hefei, Peoples R China
[2] Anhui Med Univ, Coll Basic Med Sci, Lab Anim Res Ctr, Hefei, Peoples R China
[3] Univ Sci & Technol China, Affiliated Hosp USTC 1, Ctr Leading Med & Adv Technol IHM, Dept Hepatobiliary Surg,Div Life Sci & Med, Hefei, Peoples R China
基金
中国国家自然科学基金;
关键词
Hepatocellular carcinoma; Super-enhancer; Therapeutic targets; EPITHELIAL-MESENCHYMAL TRANSITION; RNA-POLYMERASE-II; BETA-GLOBIN GENE; TRANSCRIPTION FACTORS; CELL IDENTITY; P-TEFB; BROMODOMAIN INHIBITOR; SELECTIVE-INHIBITION; EXPRESSION; MEDIATOR;
D O I
10.1186/s12935-024-03599-5
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Super-enhancers (SEs) represent a distinct category of cis-regulatory elements notable for their robust transcriptional activation capabilities. In tumor cells, SEs intricately regulate the expression of oncogenes and pivotal cancer-associated signaling pathways, offering significant potential for cancer treatment. However, few studies have systematically discussed the crucial role of SEs in hepatocellular carcinoma (HCC), which is one of the most common liver cancers with late-stage diagnosis and limited treatment methods for advanced disease. Herein, we first summarize the identification methods and the intricate processes of formation and organization of super-enhancers. Subsequently, we delve into the roles and molecular mechanisms of SEs within the framework of HCC. Finally, we discuss the inhibitors targeting the key SE-components and their potential effects on the treatment of HCC. In conclusion, this review meticulously encapsulates the distinctive characteristics of SEs and underscores their pivotal roles in the context of hepatocellular carcinoma, presenting a novel perspective on the potential of super-enhancers as emerging therapeutic targets for HCC.
引用
收藏
页数:11
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