Shang Hao, Liu Yang, Li Zhenzhen, Liu Qianqian, Cui Wenwen, Zhang Liang, Pang Yuwen, Liu Chunxia, Li Feng
Department of Pathology, School of Medicine, Shihezi University and The Key Laboratories for Xinjiang Endemic and Ethnic Diseases, Chinese Ministry of Education Shihezi 832002, Xinjiang, P. R. China.
Department of Pathology and Medical Research Center, Beijing Chaoyang Hospital, Capital Medical University Beijing 100020, P. R. China.
Am J Cancer Res. 2019 Apr 1;9(4):668-681. eCollection 2019.
MicroRNA-874 (miR-874) is downregulated and acts as a tumor suppressor gene in several human cancers. Its biological function and underlying molecular mechanism in rhabdomyosarcoma (RMS), however, remain unclear. In this study, we found that miR-874 expression was downregulated in human RMS tissue samples and cell lines through quantitative real-time polymerase chain reaction (qRT-PCR). Functional studies revealed that miR-874 overexpression in RMS cells remarkably inhibited proliferation, invasion, migration, and induced apoptosis. The results of luciferase activity assay, qRT-PCR and western blot analyses showed that miR-874 inhibited GEFT translation and suppressed GEFT expression by directly targeting the 3'-untranslated region (3'-UTR) of GEFT mRNA. GEFT expression was upregulated in RMS tissue samples and cell lines and was inversely correlated with miR-874 expression. Downregulation of GEFT has similar effects to miR-874 overexpression in RMS cells. Notably, GEFT restoration partially reversed the tumor-suppressive effects of miR-874. Our results indicated that miR-874 functions as a tumor suppressor in RMS and may suppress the growth and metastasis of RMS cells partially by targeting GEFT.
微小RNA - 874(miR - 874)在多种人类癌症中表达下调,并作为一种肿瘤抑制基因发挥作用。然而,其在横纹肌肉瘤(RMS)中的生物学功能及潜在分子机制仍不清楚。在本研究中,我们通过定量实时聚合酶链反应(qRT - PCR)发现,miR - 874在人RMS组织样本和细胞系中表达下调。功能研究表明,RMS细胞中miR - 874过表达显著抑制增殖、侵袭、迁移并诱导凋亡。荧光素酶活性测定、qRT - PCR和蛋白质免疫印迹分析结果显示,miR - 874通过直接靶向GEFT mRNA的3'非翻译区(3'-UTR)抑制GEFT翻译并抑制GEFT表达。GEFT在RMS组织样本和细胞系中表达上调,且与miR - 874表达呈负相关。GEFT下调在RMS细胞中具有与miR - 874过表达类似的作用。值得注意的是,GEFT恢复部分逆转了miR - 874的肿瘤抑制作用。我们的结果表明,miR - 874在RMS中作为肿瘤抑制因子发挥作用,并且可能部分通过靶向GEFT抑制RMS细胞的生长和转移。