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Positive and Negative Modulation of Angiogenesis by VEGFR1 Ligands
被引:225
|作者:
Cao, Yihai
[1
]
机构:
[1] Karolinska Inst, Dept Microbiol Tumor & Cell Biol, S-17177 Stockholm, Sweden
关键词:
ENDOTHELIAL-GROWTH-FACTOR;
FACTOR GENE-EXPRESSION;
INHIBITS TUMOR-GROWTH;
HIGH-AFFINITY BINDING;
TYROSINE-KINASE;
FACTOR-B;
FACTOR RECEPTOR-1;
SIGNAL-TRANSDUCTION;
FACTOR-I;
VASCULAR-PERMEABILITY;
D O I:
10.1126/scisignal.259re1
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:
Vascular endothelial growth factor-A (VEGF-A) is a key target for new antiangiogenic drugs for the treatment of both malignant and nonmalignant human diseases. Vascular effects of VEGF family members are mainly mediated by VEGF receptor 2 (VEGFR2). Conversely, the function and signaling of VEGFR1, which is present on endothelial and nonendothelial cells, are poorly understood. Intriguingly, two of five members in the VEGF family-VEGF-B and placental growth factor (PlGF)-are exclusive ligands for VEGFR1 and do not interact with the other VEGFRs, VEGFR2 and VEGFR3. These VEGFR1-specific ligands may be important therapeutic targets for the treatment of cancer. This Review discusses the distinctive roles of VEGFR1 and its ligands PlGF and VEGF-B in the mediation of angiogenic signaling and considers the therapeutic potential of targeting these particular vascular factors.
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页数:11
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