MicroRNA-7/NF-κB signaling regulatory feedback circuit regulates gastric carcinogenesis

Author:

Zhao Xiao-Di1,Lu Yuan-Yuan1,Guo Hao1,Xie Hua-Hong1,He Li-Jie12,Shen Gao-Fei1,Zhou Jin-Feng1,Li Ting1,Hu Si-Jun1,Zhou Lin1,Han Ya-Nan1,Liang Shu-Li1,Wang Xin1,Wu Kai-Chun1,Shi Yong-Quan1,Nie Yong-Zhan1,Fan Dai-Ming1

Affiliation:

1. State Key Laboratory of Cancer Biology, Xijing Hospital of Digestive Diseases, The Fourth Military Medical University, Xi’an, Shaanxi 710032, China

2. Department of Nephrology, Xijing Hospital, The Fourth Military Medical University, Xi’an, Shaanxi 710032, China

Abstract

MicroRNAs play essential roles in gene expression regulation during carcinogenesis. Here, we investigated the role of miR-7 and the mechanism by which it is dysregulated in gastric cancer (GC). We used genome-wide screenings and identified RELA and FOS as novel targets of miR-7. Overexpression of miR-7 repressed RELA and FOS expression and prevented GC cell proliferation and tumorigenesis. These effects were clinically relevant, as low miR-7 expression was correlated with high RELA and FOS expression and poor survival in GC patients. Intriguingly, we found that miR-7 indirectly regulated RELA activation by targeting the IκB kinase IKKε. Furthermore, IKKε and RELA can repress miR-7 transcription, which forms a feedback circuit between miR-7 and nuclear factor κB (NF-κB) signaling. Additionally, we demonstrate that down-regulation of miR-7 may occur as a result of the aberrant activation of NF-κB signaling by Helicobacter pylori infection. These findings suggest that miR-7 may serve as an important regulator in GC development and progression.

Publisher

Rockefeller University Press

Subject

Cell Biology

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