Chen Sixing, Chen Yu, Wen Yao, Cai Wanwan, Zhu Ping, Yuan Wuzhou, Li Yongqing, Fan Xiongwei, Wan Yongqi, Li Fang, Zhuang Jian, Jiang Zhigang, Wu Xiushan, Wang Yuequn
The Center for Heart Development, State Key Laboratory of Developmental Biology of Freshwater Fish, College of Life Sciences, Hunan Normal University, Changsha, Hunan 410081, P.R. China.
Guangdong Cardiovascular Institute, Guangdong General Hospital, Guangdong Academy of Medical Sciences, Guangzhou, Guangdong 510100, P.R. China.
Oncol Lett. 2021 Jul;22(1):532. doi: 10.3892/ol.2021.12793. Epub 2021 May 17.
Required for meiotic nuclear division 5 homolog A (RMND5A) functions as an E3 ubiquitin ligase. To date, few studies have investigated the role of RMND5A in cancer. In the present study, the expression levels of RMND5A in multiple types of cancer were analyzed using the Gene Expression Profiling Interactive Analysis platform. The results revealed that RMND5A was highly expressed and associated with overall survival in patients with pancreatic adenocarcinoma (PAAD). A wound-healing assay revealed that RMND5A overexpression significantly increased cell migration in the PAAD cell lines AsPC-1 and PANC-1. analysis predicted that RMND5A was a potential target of microRNA(miR)-590-5p. Further experiments demonstrated that overexpression of miR-590-5p downregulated the expression levels of RMND5A and decreased the migratory ability of the AsPC-1 and PANC-1 cell lines. In addition, overexpression of miR-590-5p attenuated the promoting effects of RMND5A on the migration of AsPC-1 and PANC-1 cells. The results of the present study may further elucidate the mechanisms underlying PAAD progression and provide novel targets for the treatment of PAAD.
减数分裂核分裂5同源物A(RMND5A)作为一种E3泛素连接酶发挥作用。迄今为止,很少有研究调查RMND5A在癌症中的作用。在本研究中,使用基因表达谱交互式分析平台分析了RMND5A在多种癌症类型中的表达水平。结果显示,RMND5A在胰腺腺癌(PAAD)患者中高表达且与总生存期相关。伤口愈合试验表明,RMND5A过表达显著增加了PAAD细胞系AsPC-1和PANC-1中的细胞迁移。分析预测RMND5A是微小RNA(miR)-590-5p的潜在靶标。进一步的实验表明,miR-590-5p过表达下调了RMND5A的表达水平,并降低了AsPC-1和PANC-1细胞系的迁移能力。此外,miR-590-5p过表达减弱了RMND5A对AsPC-1和PANC-1细胞迁移的促进作用。本研究结果可能进一步阐明PAAD进展的潜在机制,并为PAAD的治疗提供新的靶点。