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环状RNA通过与RNA结合蛋白ALKBH5相互作用来调节肝癌细胞中的铁死亡。

Circular RNA regulates ferroptosis in HCC cells through interacting with RNA binding protein ALKBH5.

作者信息

Liu Zhiqian, Wang Qi, Wang Xin, Xu Zongzhen, Wei Xiaoqing, Li Jie

机构信息

Department of Hepatobiliary Surgery, The First Affiliated Hospital of Shandong First Medical University, 250014 Jinan, Shandong China.

Department of Hepatobiliary Surgery, Shandong Provincial Qianfoshan Hospital, Shandong University, 250014 Jinan, Shandong China.

出版信息

Cell Death Discov. 2020 Aug 7;6:72. doi: 10.1038/s41420-020-00306-x. eCollection 2020.

Abstract

Circular RNAs (circRNAs) are a novel and unique class of noncoding RNAs that are back-spliced from pre-mRNAs. It has been confirmed that circRNAs are involved in various malignant behaviors of hepatocellular carcinoma (HCC). However, the role of circRNA in the regulation of ferroptosis and the underlying mechanism remain unknown. Here, (hsa_circ_0008367) was found to be the most highly expressed circRNA after sorafenib (SF) treatment in HCC cells. Small interfering RNA against (si-) significantly suppressed the cellular sensitivity to SF or Erastin through inactivating ferroptosis, which may be partially attributed to the inhibition of autophagy and ferritinophagy. Prediction analysis and mechanistic identification revealed that physically interacted with RNA binding protein (RBP) ALKBH5, which was a negative regulator of autophagic flux in HCC. The dissociation of BCL-2/BECN1 complex, mediated by ALKBH5 silencing was effectively blocked by si-. Furthermore, the inhibition of ferroptotic events, autophagic flux and ferritinophagy resulted from si-, were significantly rescued by ALKBH5 downregulation. Overall, may be an important circRNA, positively regulating SF-induced ferroptosis through suppressing the ALKBH5-mediated autophagy inhibition.

摘要

环状RNA(circRNAs)是一类新型且独特的非编码RNA,由前体信使核糖核酸(pre-mRNAs)反向剪接而成。已证实circRNAs参与肝细胞癌(HCC)的多种恶性行为。然而,circRNA在铁死亡调控中的作用及其潜在机制仍不清楚。在此,发现(hsa_circ_0008367)是索拉非尼(SF)处理肝癌细胞后表达最高的circRNA。针对(si-)的小干扰RNA通过使铁死亡失活显著抑制细胞对SF或埃拉斯汀的敏感性,这可能部分归因于自噬和铁自噬的抑制。预测分析和机制鉴定表明,与RNA结合蛋白(RBP)ALKBH5发生物理相互作用,ALKBH5是HCC自噬通量的负调节因子。由ALKBH5沉默介导的BCL-2/BECN1复合物解离被si-有效阻断。此外,ALKBH5下调显著挽救了由si-导致的铁死亡事件、自噬通量和铁自噬的抑制。总体而言,可能是一种重要的circRNA,通过抑制ALKBH5介导的自噬抑制来正向调节SF诱导的铁死亡。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a85b/7414223/3393b2f1c7dc/41420_2020_306_Fig1_HTML.jpg

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