Wang Jian, Li Yongli, Jiang Chuanlu
Department of Neurosurgery, the Second Affiliated Hospital of Harbin Medical University, Harbin, 150081, People's Republic of China.
J Mol Neurosci. 2015 Apr;55(4):985-94. doi: 10.1007/s12031-014-0455-8. Epub 2014 Oct 30.
Substantial evidence indicates that the human ether-a-go-go-related gene potassium channel (hERG, Kv11.1, KCNH2) is overexpressed in human glioblastoma multiforme (GBM) specimens and plays an essential role in the malignant proliferation of glioma cells. However, its upstream regulator in glioma cells is not fully elucidated. The present study was designed to determine whether the expression of hERG gene is regulated by miR-133b or miR-34a, thereby contributing to the anti-proliferation effect of arsenic trioxide (ATO) in U251 human glioma cells. Real-time polymerase chain reactions (qRT-PCR) and Western blot results demonstrated that hERG mRNA and protein levels were dramatically upregulated in clinical GBM specimens. Conversely, both miR-133b and miR-34a were markedly downregulated in clinical GBM specimens by qRT-PCR. The hERG gene was a direct target of miR-133b and miR-34a by bioinformatics analyses and luciferase reporter assays. Moreover, ATO, which is an emerging chemotherapy drug for glioma disease, remarkably elevated the level of miR-133b, but not miR-34a in U251 glioma cells. The level of miR-133b upstream transactivator serum response factor (SRF) was also suppressed by ATO. The transfection of anti-miR-133b oligonucleotide (AMO-133b) remarkably prevented the decrease of hERG protein by 5 μM ATO treatment for 24 h in U251 cells, whereas anti-miR-34a oligonucleotide (AMO-34a) did not exhibit recuperated effect. Finally, the transient overexpression by miR-133b mimics and treatment with the hERG channel-specific blocker E4031 markedly facilitated the ATO inhibition of proliferation of and induced apoptosis in U251 cells, whereas AMO-miR-133b attenuated these changes. Our study provided the evidence for the pathological role of miR-133b and miR-34a in the development of GBM and thus expanded our understanding of the hERG gene expression and ATO chemotherapeutic roles of miRNAs. Targeting miR-133b/hERG pathway may be a new strategy for chemotherapy of malignant gliomas.
大量证据表明,人类醚 - 去极化相关基因钾通道(hERG,Kv11.1,KCNH2)在多形性胶质母细胞瘤(GBM)标本中过表达,并在胶质瘤细胞的恶性增殖中起重要作用。然而,其在胶质瘤细胞中的上游调节因子尚未完全阐明。本研究旨在确定hERG基因的表达是否受miR - 133b或miR - 34a调控,从而有助于三氧化二砷(ATO)对U251人胶质瘤细胞的抗增殖作用。实时聚合酶链反应(qRT - PCR)和蛋白质印迹结果表明,临床GBM标本中hERG mRNA和蛋白质水平显著上调。相反,通过qRT - PCR检测发现,临床GBM标本中miR - 133b和miR - 34a均明显下调。通过生物信息学分析和荧光素酶报告基因检测表明,hERG基因是miR - 133b和miR - 34a的直接靶点。此外,ATO作为一种新兴的胶质瘤化疗药物,显著提高了U251胶质瘤细胞中miR - 133b的水平,但未提高miR - 34a的水平。ATO还抑制了miR - 133b上游反式激活因子血清反应因子(SRF)的水平。在U251细胞中,转染抗miR - 133b寡核苷酸(AMO - 133b)可显著阻止5 μM ATO处理24小时导致的hERG蛋白减少,而抗miR - 34a寡核苷酸(AMO - 34a)则未表现出恢复作用。最后,miR - 133b模拟物的瞬时过表达以及使用hERG通道特异性阻滞剂E4031处理显著促进了ATO对U251细胞增殖的抑制并诱导其凋亡,而AMO - miR - 133b则减弱了这些变化。我们的研究为miR - 133b和miR - 34a在GBM发生发展中的病理作用提供了证据,从而扩展了我们对hERG基因表达以及miRNAs的ATO化疗作用的理解。靶向miR - 133b/hERG通路可能是恶性胶质瘤化疗的新策略。