Novel insights into cadherin processing by subtilisin-like convertases

被引:26
作者
Posthaus, H
Dubois, CM
Müller, E
机构
[1] Univ Bern, Inst Anim Pathol, CH-3012 Bern, Switzerland
[2] Univ Sherbrooke, Fac Med, Dept Pediat, Div Immunol, Sherbrooke, PQ J1H 5N4, Canada
关键词
desmoglein; E-cadherin; furin; proprotein cleavage; alpha; 1-PDX;
D O I
10.1016/S0014-5793(02)03897-8
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
Proprotein convertases (PCs) are known to activate many important molecules and their overexpression plays a significant role in tumor progression. Only little is known about the involvement of PCs in the processing of cadherin adhesion molecules, which are potent tumor suppressors. Here we show in a baculovirus overexpression system that the desmosomal cadherins Dsg1 and Dsg3 are substrates for the PC furin. Accordingly, inhibition of PCs in differentiating mouse keratinocytes by alpha1-anti-trypsin Portland (alpha1-PDX) negatively interfered with proepithelial (proE)-cadherin processing, but unexpectedly also resulted in a dramatic reduction of E-cadherin, Dsg1 and Dsg3 protein and Dsg1 mRNA. Because loss of intercellular adhesion is a rate-limiting step in the transition from benign to malignant tumors, these results have significant implications for the use of PC inhibitors as possible therapeutic tools. (C) 2003 Published by Elsevier Science B.V. on behalf of the Federation of European Biochemical Societies.
引用
收藏
页码:203 / 208
页数:6
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