基因敲除
结直肠癌
癌症研究
转录因子
信号转导
泛素
NF-κB
受体
癌症
生物
化学
细胞凋亡
医学
内科学
细胞生物学
基因
遗传学
作者
Wen Ye,Yachao Cui,Jian Rong,Wenlin Huang,Zhousan Zheng,Anqi Li,Yingchang Li
标识
DOI:10.1038/s41417-022-00528-4
摘要
The abnormal activation of the nuclear factor-kappa B (NF-κB) signaling pathway is an important precipitating factor for the inception and development of colorectal cancer (CRC), one of the most common tumors worldwide. As a pro-apoptotic transcription factor, monocyte chemotactic protein-induced protein 1 (MCPIP1) has been closely associated with many tumor types. In the present study, the expression of MCPIP1 was firstly discovered reduced in CRC tissues and correlated with poor patient prognosis. The decreased expression was caused by promoter hypermethylation. Overexpressed MCPIP1 was found to inhibit the proliferative and migratory abilities of CRC cells, whereas knockdown of MCPIP1 produced the opposite result. The subsequent investigation demonstrated that MCPIP1 exerted its “anti-cancer” effect by suppression of the NF-κB signaling pathway through negative regulation of K63-linked ubiquitylation of TNF receptor associated factor 6 (TRAF6). Therefore, our results indicate a prognostic marker for CRC and a theoretical basis for MCPIP1 as a treatment.
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