Magic roundabout, a tumor endothelial marker: Expression and signaling

被引:95
作者
Seth, P
Lin, YF
Hanai, J
Shivalingappa, V
Duyao, MP
Sukhatme, VP [1 ]
机构
[1] Harvard Univ, Sch Med, Div Renal, Boston, MA 02215 USA
[2] Harvard Univ, Sch Med, Beth Israel Deaconess Med Ctr, Dept Med,Ctr Study Tumor Microenvironm, Boston, MA 02215 USA
[3] Ardais Corp, Lexington, MA 02421 USA
关键词
tumor endothelium; magic roundabout; FAK; SLIT2;
D O I
10.1016/j.bbrc.2005.03.250
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
Molecular signals that guide blood vessels to specific paths are not fully deciphered, but are thought to be similar to signals that mediate neuronal guidance. These cues are not only critical for normal blood vessel development, but rnay also play a major role ill tumor angiogenesis. In this Study, we have demonstrated the tumor endothelial specific expression of a Robo family member, magic roundabout (MRB), functionally characterized its role in endothelial cell migration and defined a signaling pathway that might mediate this function. We show that MRB is differentially over-expressed in tumor endothelial cells versus normal adult endothelial cells in numerous solid tumors. Moreover, over-expression of MRB in endothelial cells activates MRB in a ligand-independent fashion, and activation of MRB via Slit2, a Putative ligand, results in inhibition of VEGF and FGF induced migration. We also demonstrate that MRB induced inhibition of endothelial migration is partially mediated by the Ras-Raf-Mek-Erk signaling pathway. We therefore hypothesize that expression of MRB is involved in regulating the migration of endothelial cells during tumor angiogenesis. (C) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:533 / 541
页数:9
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