The two-handed E box binding zinc finger protein SIP1 downregulates E-cadherin and induces invasion

被引:1187
作者
Comijn, J
Berx, G
Vermassen, P
Verschueren, K
van Grunsven, L
Bruyneel, E
Mareel, M
Huylebroeck, D
van Roy, F [1 ]
机构
[1] State Univ Ghent VIB, Mol Cell Biol Unit, Dept Biol Mol, B-9000 Ghent, Belgium
[2] VIB, Dept Cell Growth Differentiat & Dev, B-3000 Louvain, Belgium
[3] Katholieke Univ Leuven, Lab Mol Biol Celgen, B-3000 Louvain, Belgium
[4] State Univ Ghent Hosp, Dept Expt Cancerol, B-9000 Ghent, Belgium
关键词
D O I
10.1016/S1097-2765(01)00260-X
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Transcriptional downregulation of E-cadherin appears to be an important event in the progression of various epithelial tumors. SIP1 (ZEB-2) is a Smad-interacting, multi-zinc finger protein that shows specific DNA binding activity. Here, we report that expression of wildtype but not of mutated SIP1 downregulates mammalian E-cadherin transcription via binding to both conserved E2 boxes of the minimal E-cadherin promoter. SIP1 and Snail bind to partly overlapping promoter sequences and showed similar silencing effects. SIP1 can be induced by TGF-P treatment and shows high expression in several E-cadherin-negative human carcinoma cell lines. Conditional expression of SIP1 in E-cadherin-positive MDCK cells abrogates E-cadherin-mediated intercellular adhesion and simultaneously induces invasion. SIP1 therefore appears to be a promoter of invasion in malignant epithelial tumors.
引用
收藏
页码:1267 / 1278
页数:12
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