Stabilization of Snail by NF-κB Is Required for Inflammation-Induced Cell Migration and Invasion

被引:735
作者
Wu, Yadi [1 ]
Deng, Jiong [5 ]
Rychahou, Piotr G. [2 ]
Qiu, Suimin [3 ,4 ]
Evers, B. Mark [2 ,4 ]
Zhou, Binhua P. [1 ,4 ]
机构
[1] Univ Texas Med Branch, Dept Pharmacol & Toxicol, Galveston, TX 77555 USA
[2] Univ Texas Med Branch, Dept Surg, Galveston, TX 77555 USA
[3] Univ Texas Med Branch, Dept Pathol, Galveston, TX 77555 USA
[4] Univ Texas Med Branch, Sealy Ctr Canc Cell Biol, Galveston, TX 77555 USA
[5] Univ Texas MD Anderson Canc Ctr, Dept Thorac Head & Neck Med Oncol, Houston, TX 77030 USA
关键词
TRANSCRIPTION FACTOR SNAIL; COP9; SIGNALOSOME; E-CADHERIN; GENE-EXPRESSION; MESENCHYMAL TRANSITION; CANCER DEVELOPMENT; TUMOR-GROWTH; TNF-ALPHA; MACROPHAGES; PROGRESSION;
D O I
10.1016/j.ccr.2009.03.016
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The increased motility and invasiveness of tumor cells are reminiscent of epithelial-mesenchymal transition (EMT), which occurs during embryonic development, wound healing, and metastasis. In this study, we found that Snail is stabilized by the inflammatory cytokine TNF alpha through the activation of the NF-kappa B pathway. We demonstrated that NF-kappa B is required for the induction of COP9 signalosome 2 (CSN2), which, in turn, blocks the ubiquitination and degradation of Snail. Furthermore, we showed that the expression of Snail correlated with the activation of NF-kappa B in cancer cell lines and metastatic tumor samples. Knockdown of Snail expression inhibited cell migration and invasion induced by inflammatory cytokines and suppressed inflammation-mediated breast cancer metastasis. Our study provides a plausible mechanism for inflammation-induced metastasis.
引用
收藏
页码:416 / 428
页数:13
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