EphB6 promotes anoikis by modulating EphA2 signaling

被引:28
作者
Akada, Mai [1 ]
Harada, Kohei [2 ]
Negishi, Manabu [1 ,2 ]
Katoh, Hironori [1 ,2 ]
机构
[1] Kyoto Univ, Grad Sch Pharmaceut Sci, Mol Neurobiol Lab, Sakyo Ku, Kyoto 6068501, Japan
[2] Kyoto Univ, Grad Sch Biostudies, Mol Neurobiol Lab, Sakyo Ku, Kyoto 6068501, Japan
关键词
EphA2; EphB6; Ephexin4; Anoikis; Heterotypic interaction; RECEPTOR TYROSINE KINASE; BREAST-CARCINOMA CELLS; RHO-GTPASES; ACTIVATION; EXPRESSION; MIGRATION; GROWTH; RAC1; PHOSPHORYLATION; INVASIVENESS;
D O I
10.1016/j.cellsig.2014.08.031
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Anoikis is a specific type of apoptosis induced by detachment of epithelial cells from extracellular matrix, and acquiring resistance to anoikis is an important step that enables cancer cells to metastasize. EphA2, which is overexpressed in a variety of human cancers, is phosphorylated by Akt on serine 897 and mediates ligand ephrin-independent promotion of anoikis resistance through the RhoG activator Ephexin4. EphB6 is frequently silenced in invasive and metastatic cancers; however, its role in cancer progression is poorly understood. Here we show that EphB6 interacts with EphA2 and suppresses EphA2-mediated promotion of anoikis resistance in MCF7 breast cancer cells. On the other hand, knockdown of EphB6 promotes anoikis resistance. We further show that expression of EphB6 decreases serine 897 phosphorylation of EphA2 and suppresses EphA2-Ephexin4 interaction and the RhoG activation. These findings implicate EphB6 as a negative regulator of EphA2 oncogenic signaling. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:2879 / 2884
页数:6
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