miR-142-3p inhibits LIPS-induced activation of NF-κB it by targeting IRAK1 in colorectal cancer

被引:0
|
作者
Xu Zhiying [1 ]
Zhou, Peng [1 ]
Zhou, Ping Zhen [1 ]
Zhang, Jie [1 ]
Cao, Le Bo [1 ]
Liu, Xia Cui [1 ]
Li, Jie [1 ]
机构
[1] Peoples Hosp Taizhou, Dept Gastroenterol, Taizhou 225300, Jiangsu, Peoples R China
关键词
colorectal cancer; non-coding RNA; inflammatory factors; EPIGENETIC CHANGES; CELLS; MICRORNA; EXPRESSION; CARCINOMA; RISK;
D O I
10.5114/ceji.2013.39755
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Inflammatory signals originating from colorectal cancer cells have a vital role in the development of colorectal cancer (CRC). microRNAs (miRNAs) have been demonstrated to be involved in the development and progression of CRC. miRNA-142-3p (miR-142-3p) has been reported to be a modulator of inflammatory signals. It has also been shown that miR-142-3p is downregulated in CRC and it acts to be a tumor suppressor. In the present study, interleukin-1 receptor-associated kinase 1 (IRAK1), a key mediator of NF-kappa B pathway, was identified as a direct target of miR-142-3p. It was also found that miR-142-3p repressed the activation of NF-kappa B signal induced by LPS in colorectal cancer cells, therefore reducing the expression of inflammatory cytokines, such as IL-6, IL-8, MCP-1, CCL5 and CSF-1. Thus, it is believed that miR-142-3p is a key component in the regulation of NF-kappa B activity and its anti-inflammatory role may contribute to its suppression of carcinogenesis of CRC.
引用
收藏
页码:416 / 420
页数:5
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