Ph.D. Program for Cancer Biology and Drug Discovery, College of Medical Science and Technology, Taipei Medical University, Taipei 110, Taiwan.
Research Center of Cancer Translational Medicine, Taipei Medical University, Taipei 110, Taiwan.
Nat Commun. 2017 Jun 22;8:15874. doi: 10.1038/ncomms15874.
Long noncoding RNAs (lncRNAs) have been implicated in hypoxia/HIF-1-associated cancer progression through largely unknown mechanisms. Here we identify MIR31HG as a hypoxia-inducible lncRNA and therefore we name it LncHIFCAR (long noncoding HIF-1α co-activating RNA); we describe its oncogenic role as a HIF-1α co-activator that regulates the HIF-1 transcriptional network, crucial for cancer development. Extensive analyses of clinical data indicate LncHIFCAR level is substantially upregulated in oral carcinoma, significantly associated with poor clinical outcomes and representing an independent prognostic predictor. Overexpression of LncHIFCAR induces pseudo-hypoxic gene signature, whereas knockdown of LncHIFCAR impairs the hypoxia-induced HIF-1α transactivation, sphere-forming ability, metabolic shift and metastatic potential in vitro and in vivo. Mechanistically, LncHIFCAR forms a complex with HIF-1α via direct binding and facilitates the recruitment of HIF-1α and p300 cofactor to the target promoters. Our results uncover an lncRNA-mediated mechanism for HIF-1 activation and establish the clinical values of LncHIFCAR in prognosis and potential therapeutic strategy for oral carcinoma.
长链非编码 RNA(lncRNAs)通过很大程度上未知的机制参与了低氧/HIF-1 相关的癌症进展。在这里,我们鉴定出 MIR31HG 是一种缺氧诱导的 lncRNA,因此我们将其命名为 LncHIFCAR(长非编码 HIF-1α 共激活 RNA);我们描述了其作为 HIF-1α 共激活因子的致癌作用,它调节 HIF-1 转录网络,对癌症发展至关重要。对临床数据的广泛分析表明,LncHIFCAR 在口腔癌中显著上调,与不良的临床结局显著相关,并代表独立的预后预测因子。LncHIFCAR 的过表达诱导了伪低氧基因特征,而 LncHIFCAR 的敲低则损害了体外和体内低氧诱导的 HIF-1α 反式激活、球体形成能力、代谢转变和转移潜能。在机制上,LncHIFCAR 通过直接结合与 HIF-1α 形成复合物,并促进 HIF-1α 和 p300 辅助因子募集到靶启动子。我们的研究结果揭示了一种 lncRNA 介导的 HIF-1 激活机制,并确立了 LncHIFCAR 在口腔癌预后和潜在治疗策略中的临床价值。