Regulation of Snail transcription during epithelial to mesenchymal transition of tumor cells

被引:296
作者
Barberà, MJ
Puig, I
Domínguez, D
Julien-Grille, S
Guaita-Esteruelas, S
Peiró, S
Baulida, J
Francí, C
Dedhar, S
Larue, L
de Herreros, AG
机构
[1] Univ Pompeu Fabra, Unitat Bio Celluar & Mol, Inst Municipal Invest Med, Barcelona 08003, Spain
[2] Inst Curie, CNRS, UMR 146, F-91405 Orsay, France
[3] Univ British Columbia, Dept Biochem & Mol Biol, Vancouver, BC V6H 3Z6, Canada
关键词
snail; promoter; transcription; EMT; MEK; NF-kappa B;
D O I
10.1038/sj.onc.1207990
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Expression of Snail transcriptional factor is a determinant in the acquisition of a mesenchymal phenotype by epithelial tumor cells. However, the regulation of the transcription of this gene is still unknown. We describe here the characterization of a human SNAIL promoter that contains the initiation of transcription and regulates the expression of this gene in tumor cells. This promoter was activated in cell lines in response to agents that induce Snail transcription and the mesenchymal phenotype, as addition of the phorbol ester PMA or overexpression of integrin-linked kinase (ILK) or oncogenes such as Ha-ras or v-Akt. Although other regions of the promoter were required for a complete stimulation by Akt or ILK, a minimal fragment ( - 78/ +59) was sufficient to maintain the mesenchymal specificity. Activity of this minimal promoter and SNAIL RNA levels were dependent on ERK signaling pathway. NFkappaB/p65 also stimulated SNAIL transcription through a region located immediately upstream the minimal promoter, between - 194 and - 78. These results indicate that Snail transcription is driven by signaling pathways known to induce epithelial to mesenchymal transition, reinforcing the role of Snail in this process.
引用
收藏
页码:7345 / 7354
页数:10
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