VEGF and Delta-Notch: interacting signalling pathways in tumour angiogenesis

被引:144
作者
Thurston, G. [1 ]
Kitajewski, J. [2 ]
机构
[1] Regeneron Pharmaceut Inc, New York, NY 10591 USA
[2] Columbia Univ, Herbert Irving Comprehens Canc Ctr, New York, NY 10032 USA
关键词
D114; endothelial; Notch1; Kdr; anti-angiogenesis;
D O I
10.1038/sj.bjc.6604484
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Tumour angiogenesis has become an important target for antitumour therapy, with most current therapies aimed at blocking the VEGF pathway. However, not all tumours are responsive to VEGF blockers, and some tumours that are responsive initially may become resistant during the course of treatment, thus there is a need to explore other angiogenesis signalling pathways. Recently, the Delta-Notch pathway, and particularly the ligand Delta-like 4 (D114), was identified as a new target in tumour angiogenesis. An important feature in angiogenesis is the manifold ways in which the VEGF and Delta-Notch pathways interact. The emerging picture is that the VEGF pathway acts as a potent upstream activating stimulus for angiogenesis, whereas Delta-Notch helps to guide cell fate decisions that appropriately shape the activation. Here we review the two signalling pathways and what is currently known about the ways in which they interact during tumour angiogenesis.
引用
收藏
页码:1204 / 1209
页数:6
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