Repression of Na,K-ATPase β1-subunit by the transcription factor snail in carcinoma

被引:85
作者
Espineda, CE
Chang, JH
Twiss, J
Rajasekaran, SA
Rajasekaran, AK [1 ]
机构
[1] Univ Calif Los Angeles, Dept Pathol & Lab Med, David Geffen Sch Med, Los Angeles, CA 90095 USA
[2] Alfred I duPont Hosp Children, Nemours Biomed Res, Wilmington, DE 19803 USA
关键词
D O I
10.1091/mbc.E03-09-0646
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The Na,K-ATPase consists of two essential alpha- and beta-subunits and regulates the intracellular Na+ and K+ homeostasis. Although the a-subunit contains the catalytic activity, it is not active without functional beta-subunit. Here, we report that poorly differentiated carcinoma cell lines derived from colon, breast, kidney, and pancreas show reduced expression of the Na,K-ATPase beta(1)-subunit. Decreased expression of beta(1)-subunit in poorly differentiated carcinoma cell lines correlated with increased expression of the transcription factor Snail known to down-regulate E-cadherin. Ectopic expression of Snail in well-differentiated epithelial cell lines reduced the protein levels of E-cadherin and beta(1)-subunit and induced a mesenchymal phenotype. Reduction of Snail expression in a poorly differentiated carcinoma cell line by RNA interference increased the levels of Na,K-ATPase beta(1)-subunit. Furthermore, Snail binds to a noncanonical E-box in the Na,K-ATPase beta(1)-subunit promoter and suppresses its promoter activity. These results suggest that down-regulation of Na,K-ATPase beta(1)-subunit and E-cadherin by Snail are associated with events leading to epithelial to mesenchymal transition.
引用
收藏
页码:1364 / 1373
页数:10
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