Department of Urology, Xiangyang Central Hospital, Hospital Affiliated to Hubei University of Arts and Science, 39 Jingzhou Street, Xiangyang, 441021, Hubei, People's Republic of China.
Clin Transl Oncol. 2018 Jun;20(6):761-767. doi: 10.1007/s12094-017-1786-z. Epub 2017 Oct 30.
Although overexpression of the eukaryotic translation initiation factor 4E (eIF4E) is detected in patients with renal cell carcinoma (RCC) and associated with poor prognosis, the possible roles of eIF4E in RCC have not been revealed.
The effects of eIF4E inhibition on cell growth, migration, survival, chemo-/immunotherapy and eIF4E pathways via pharmacological inhibitor and genetic siRNA knockdown were analyzed in RCC cells.
In this work, we demonstrate that eIF4E is critically involved in multiple biological functions of RCC. We firstly inhibited eIF4E activity by ribavirin in two cell lines (Caki-1 and ACHN) representing RCC metastasis models. We demonstrated that ribavirin inhibited proliferation and migration and induced apoptosis in RCC in a dose-dependent manner. We further confirmed that the inhibitory effects of ribavirin were attributed to its ability in inhibiting eIF4E-regulated protein translation and activity. eIF4E inhibition using siRNA knockdown mimicked ribavirin's effector in RCC cells. Importantly, eIF4E inhibition by both ribavirin and siRNA knockdown significantly sensitized RCC response to chemo- and immunotherapeutic agents in vitro as well as in vivo.
Our findings clearly demonstrate the roles of eIF4E in RCC growth, survival, metastasis and resistance. Ribavirin is an antiviral drug, and its clinical efficacy is currently being investigated in the treatment of various cancers. Our findings support and provide a preclinical evidence for clinical trial for the combination of ribavirin with chemo-/immunotherapy in RCC.
尽管真核翻译起始因子 4E(eIF4E)在肾细胞癌(RCC)患者中过表达,并与不良预后相关,但 eIF4E 在 RCC 中的可能作用尚未被揭示。
通过药理学抑制剂和基因 siRNA 敲低,分析 eIF4E 抑制对 RCC 细胞中细胞生长、迁移、存活、化疗/免疫治疗和 eIF4E 通路的影响。
在这项工作中,我们证明了 eIF4E 是 RCC 多种生物学功能的关键调节因子。我们首先使用利巴韦林在两种代表 RCC 转移模型的细胞系(Caki-1 和 ACHN)中抑制 eIF4E 活性。我们证明了利巴韦林以剂量依赖的方式抑制 RCC 的增殖和迁移,并诱导其凋亡。我们进一步证实,利巴韦林的抑制作用归因于其抑制 eIF4E 调节的蛋白翻译和活性的能力。使用 siRNA 敲低抑制 eIF4E 模拟了利巴韦林在 RCC 细胞中的效应。重要的是,eIF4E 抑制无论是通过利巴韦林还是 siRNA 敲低,都显著增强了 RCC 对体外和体内化疗和免疫治疗药物的敏感性。
我们的研究结果清楚地表明了 eIF4E 在 RCC 生长、存活、转移和耐药中的作用。利巴韦林是一种抗病毒药物,其在治疗各种癌症中的临床疗效目前正在研究中。我们的研究结果支持并为临床研究提供了临床前证据,即在 RCC 中联合利巴韦林与化疗/免疫治疗。