miR-486 sustains NF-kappa B activity by disrupting multiple NF-kappa B-negative feedback loops

作者：Song Libing; Lin Chuyong; Gong Hui; Wang Chanjuan; Liu Liping; Wu Jueheng; Tao Sha; Hu Bo; Cheng Shi Yuan; Li Mengfeng; Li Jun^*

来源：Cell Research, 2013, 23(2): 274-289.

DOI：10.1038/cr.2012.174

• miR-486
• NF-kappa B
• ubiquitin
• aggressiveness
• gliomas

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

• 单位
  西北大学