miR-486 通过破坏多个 NF-κB 负反馈环来维持 NF-κB 的活性。

miR-486 sustains NF-κB activity by disrupting multiple NF-κB-negative feedback loops.

机构信息

State Key Laboratory of Oncology in Southern China, Department of Experimental Research, Cancer Center, Sun Yat-sen University, Guangzhou, Guangdong 510060, China.

出版信息

Cell Res. 2013 Feb;23(2):274-89. doi: 10.1038/cr.2012.174. Epub 2012 Dec 18.

Abstract

Deubiquitinases, such as CYLD, A20 and Cezanne, have emerged as important negative regulators that balance the strength and the duration of NF-κB signaling through feedback mechanisms. However, how these serial feedback loops are simultaneously disrupted in cancers, which commonly exhibit constitutively activated NF-κB, remains puzzling. Herein, we report that miR-486 directly suppresses NF-κB-negative regulators, CYLD and Cezanne, as well as multiple A20 activity regulators, including ITCH, TNIP-1, TNIP-2 and TNIP-3, resulting in promotion of ubiquitin conjugations in NF-κB signaling and sustained NF-κB activity. Furthermore, we demonstrate that upregulation of miR-486 promotes glioma aggressiveness both in vitro and in vivo through activation of NF-κB signaling pathway. Importantly, miR-486 levels in primary gliomas significantly correlate with NF-κB activation status. These findings uncover a novel mechanism for constitutive NF-κB activation in gliomas and support a functionally and clinically relevant epigenetic mechanism in cancer progression.

摘要

去泛素化酶,如 CYLD、A20 和 Cezanne,作为重要的负调控因子而出现,通过反馈机制平衡 NF-κB 信号的强度和持续时间。然而,这些串联的反馈环如何在癌症中同时被破坏,这在癌症中通常表现为 NF-κB 的持续激活,仍然令人费解。在这里,我们报告 miR-486 直接抑制 NF-κB 的负调控因子 CYLD 和 Cezanne,以及多个 A20 活性调节剂,包括 ITCH、TNIP-1、TNIP-2 和 TNIP-3,导致 NF-κB 信号中的泛素缀合物的促进和持续的 NF-κB 活性。此外,我们证明 miR-486 的上调通过 NF-κB 信号通路的激活,在体外和体内促进神经胶质瘤的侵袭性。重要的是,原发性神经胶质瘤中的 miR-486 水平与 NF-κB 的激活状态显著相关。这些发现揭示了神经胶质瘤中 NF-κB 持续激活的新机制,并支持癌症进展中具有功能和临床相关性的表观遗传机制。

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