Abstract
BackgroundAlthough several anti-angiogenic therapies have been approved in the treatment of cancer, the survival benefits of such therapies are relatively modest. Discovering new molecules and/or better understating signaling pathways of angiogenesis is therefore essential for therapeutic improvements. The objective of the present study was to determine the involvement of nerve growth factor (NGF) in breast cancer angiogenesis and the underlying molecular mechanisms.ResultsWe showed that both recombinant NGF and NGF produced by breast cancer cells stimulated angiogenesis in Matrigel plugs in immunodeficient mice. NGF strongly increased invasion, cord formation and the monolayer permeability of endothelial cells. Moreover, NGF-stimulated invasion was under the control of its tyrosine kinase receptor (TrkA) and downstream signaling pathways such as PI3K and ERK, leading to the activation of matrix metalloprotease 2 and nitric oxide synthase. Interestingly, NGF increased the secretion of VEGF in both endothelial and breast cancer cells. Inhibition of VEGF, with a neutralizing antibody, reduced about half of NGF-induced endothelial cell invasion and angiogenesis in vivo.ConclusionsOur findings provided direct evidence that NGF could be an important stimulator for breast cancer angiogenesis. Thus, NGF, as well as the activated signaling pathways, should be regarded as potential new targets for anti-angiogenic therapy against breast cancer.
Highlights
Several anti-angiogenic therapies have been approved in the treatment of cancer, the survival benefits of such therapies are relatively modest
We have previously shown that nerve growth factor (NGF) and its tyrosine kinase receptor TrkA are overexpressed compared to normal breast tissues [24,25]
We demonstrated the involvement of multiple pathways such as PI3K-Akt, ERK, MMP2, and Nitric oxide (NO) synthase as well as the role of vascular endothelial growth factor (VEGF) in the angiogenic effect of NGF
Summary
Several anti-angiogenic therapies have been approved in the treatment of cancer, the survival benefits of such therapies are relatively modest. It is well established that tumor growth beyond the size of 1-2 mm is dependent upon angiogenesis [1]. This process is regulated by numerous proangiogenic factors which are secreted by tumor or surrounding stromal cells. Among these proangiogenic factors, vascular endothelial growth factor (VEGF) plays a pivotal role in tumor angiogenesis. Inhibition of VEGF reduces angiogenesis and tumor growth in vivo [5]. TrkA overexpression in breast cancer cells leads to a constitutive activation of its tyrosine kinase, resulting in increased tumorigenicity as well as enhanced angiogenesis [25]. Similar link between NGF and angiogenesis has been suggested in ovarian carcinomas [26]
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