Lin Yao, Zhao Xudong, Du Zhenhua, Jia Zhili, Zhou Siyu, Cao Gengsheng, Wang Hengbin
School of Life Sciences, Henan University, Kaifeng 475004, China.
Department of Obstetrics and Gynecology, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong 999077, China.
Cells. 2025 Jun 19;14(12):928. doi: 10.3390/cells14120928.
Esophageal cancer (ESCA) is the sixth leading cause of cancer-related mortality worldwide. Despite the significant impact, the molecular mechanisms underlying its initiation and progression remain poorly understood. In this study, we identified mircoRNA miR-193b-3p as a critical regulator of ESCA progression and the Remodeling and Spacing Factor 1 (RSF1) as an essential target of miR-193b-3p. Analysis of the TCGA_ESCA dataset and RT-qPCR experiments revealed that RSF1 levels are significantly elevated in ESCA and inversely correlated with miR-193b-3p levels. Using a dual-luciferase reporter assay, as well as transfection of miR-193-3p mimics or inhibitors, we confirmed RSF1 as a direct target of miR-193b-3p in ESCA cells. Transfection of miR-193b-3p suppresses ESCA cell proliferation, migration, and invasion. These effects were partially reversed by exogenous RSF1 expression. Injection of AgomiR-193b-3p into mice bearing ESCA xenografts impeded tumor growth. These findings underscore the critical role of the miR-193b-3p/RSF1 axis in esophageal cancer progression.
食管癌(ESCA)是全球第六大致癌相关死亡原因。尽管其影响重大,但其发生和发展的分子机制仍知之甚少。在本研究中,我们确定微小RNA miR-193b-3p是ESCA进展的关键调节因子,重塑与间隔因子1(RSF1)是miR-193b-3p的重要靶点。对TCGA_ESCA数据集的分析和RT-qPCR实验表明,ESCA中RSF1水平显著升高,且与miR-193b-3p水平呈负相关。使用双荧光素酶报告基因检测以及转染miR-193-3p模拟物或抑制剂,我们证实RSF1是ESCA细胞中miR-193b-3p的直接靶点。转染miR-193b-3p可抑制ESCA细胞的增殖、迁移和侵袭。外源性RSF1表达可部分逆转这些作用。将AgomiR-193b-3p注射到携带ESCA异种移植瘤的小鼠体内可抑制肿瘤生长。这些发现强调了miR-193b-3p/RSF1轴在食管癌进展中的关键作用。