Wan Yuehan, Hoyle Rosalie G, Xie Nan, Wang Wenjin, Cai Hongshi, Zhang Ming, Ma Zhikun, Xiong Gan, Xu Xiuyun, Huang Zhengxian, Liu Xiqiang, Li Jiong, Wang Cheng
Department of Oral and Maxillofacial Surgery, Hospital of Stomatology, Guanghua School of Stomatology, Sun Yat-Sen University, Guangzhou, China.
Guangdong Provincial Key Laboratory of Stomatology, Sun Yat-Sen University, Guangzhou, China.
Front Oncol. 2021 Apr 16;11:656628. doi: 10.3389/fonc.2021.656628. eCollection 2021.
MiR-21-5p is one of the most common oncogenic miRNAs that is upregulated in many solid cancers by inhibiting its target genes at the posttranscriptional level. However, the upstream regulatory mechanisms of miR-21-5p are still not well documented in cancers. Here, we identify a super-enhancer associated with the gene (MIR21-SE) by analyzing the genomic regulatory landscape in head and neck squamous cell carcinoma (HNSCC). We show that the MIR21-SE regulates miR-21-5p expression in different HNSCC cell lines and disruption of MIR21-SE inhibits miR-21-5p expression. We also identified that a key transcription factor, FOSL1 directly controls miR-21-5p expression by interacting with the MIR21-SE in HNSCC. Moreover, functional studies indicate that restoration of miR-21-5p partially abrogates FOSL1 depletion-mediated inhibition of cell proliferation and invasion. Clinical studies confirmed that miR-21-5p expression is positively correlated with FOSL1 expression. These findings suggest that FOSL1-SE drives miR-21-5p expression to promote malignant progression of HNSCC.
MiR-21-5p是最常见的致癌性微小RNA之一,在许多实体癌中通过在转录后水平抑制其靶基因而上调。然而,miR-21-5p的上游调控机制在癌症中仍未得到充分记录。在这里,我们通过分析头颈部鳞状细胞癌(HNSCC)的基因组调控格局,鉴定出一个与该基因相关的超级增强子(MIR21-SE)。我们表明,MIR21-SE在不同的HNSCC细胞系中调节miR-21-5p的表达,而MIR21-SE的破坏会抑制miR-21-5p的表达。我们还确定,一个关键转录因子FOSL1通过与HNSCC中的MIR21-SE相互作用直接控制miR-21-5p的表达。此外,功能研究表明,miR-21-5p的恢复部分消除了FOSL1缺失介导的对细胞增殖和侵袭的抑制。临床研究证实,miR-21-5p的表达与FOSL1的表达呈正相关。这些发现表明,FOSL1-SE驱动miR-21-5p的表达,以促进HNSCC的恶性进展。