CEA-related cell adhesion molecule 1:: A potent angiogenic factor and a major effector of vascular endothelial growth factor

被引:212
作者
Ergün, S
Kilic, N
Ziegeler, G
Hansen, A
Nollau, P
Götze, J
Wurmbach, JH
Horst, A
Weil, J
Fernando, M
Wagener, C
机构
[1] Univ Hamburg, Hosp Eppendorf, Dept Anat, D-20246 Hamburg, Germany
[2] Univ Hamburg, Hosp Eppendorf, Dept Clin Chem, Med Clin, D-20246 Hamburg, Germany
[3] Univ Hamburg, Hosp Eppendorf, Dept Urol, D-20246 Hamburg, Germany
[4] Univ Hamburg, Hosp Eppendorf, Dept Pharmacol, D-20246 Hamburg, Germany
关键词
D O I
10.1016/S1097-2765(00)80426-8
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
CPA-related cell adhesion molecule 1 (CEACAM1) exhibits angiogenic properties in in vitro and in vivo angiogenesis assays. CEACAM1 purified from granulocytes and endothelial cell media as well as recombinant CEACAM1 expressed in HEK293 cells stimulate proliferation, chemotaxis, and capillary-like tube formation of human microvascular endothelial cells. They increase vascularization of chick chorioallantoic membrane and potentiate the effects of vascular endothelial growth factor (VEGF)(165). VEGF(165) increases CEACAM1 expression both on the mRNA and the protein level. VEGF(165)-induced endothelial tube formation is blocked by a monoclonal CEACAM1 antibody. These data suggest that CEACAM1 is a major effector of VEGF in the early microvessel formation. Since CEACAM1 is expressed in tumor microvessels but not in large blood vessels, CEACAM1 may be a target for the inhibition of tumor angiogenesis.
引用
收藏
页码:311 / 320
页数:10
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