Ligation of EphA2 by Ephrin A1-Fc inhibits pancreatic adenocarcinoma cellular invasiveness

被引:105
作者
Duxbury, MS [1 ]
Ito, H [1 ]
Zinner, MJ [1 ]
Ashley, SW [1 ]
Whang, EE [1 ]
机构
[1] Harvard Univ, Sch Med, Brigham & Womens Hosp, Dept Surg, Boston, MA 02115 USA
关键词
pancreatic; cancer adenocarcinoma; EphA2; tyrosine kinase; ephrin A1; invasion; focal adhesion kinase;
D O I
10.1016/j.bbrc.2004.06.054
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
The Eph tyrosine kinases interact with ligands of the Ephrin family and have diverse cellular functions. EphA2 has been recognized to be an oncoprotein of importance in a range of cancers. Here, we examine the effect of EphA2 overexpression and ligation by chimeric Ephrin A1-Fc on the invasive phenotype of pancreatic adenocarcinoma cells. We show that EphA2 overexpression induces a FAK-dependent increase in MMP-2 expression and invasiveness. EphA2 ligation induces proteosomal degradation of EphA2, attenuates the invasive phenotype, and decreases both FAK phosphorylation and MMP-2 expression. EphA2 appears to represent a rational therapeutic target and ligation by Ephrin A1-Fc is one strategy to modulate levels of this oncoprotein. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:1096 / 1102
页数:7
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