Acute, but not constitutive, loss of endothelial β3-integrin inhibits tumour growth and angiogenesis
نویسندگان
چکیده
Background Angiogenesis, the formation of new vessels from pre-existing ones, is essential for tumour growth and metastasis. Endothelial cells play a central role in this process: they drive blood vessel formation in response to signals from the local environment, by a mechanism that is integrindependent. We are particularly interested in understanding what role avb3-integrin plays in governing tumour angiogenesis. avb3-integrin seemingly poses an ideal anti-angiogenic target. Its expression is vastly up-regulated in neo-angiogenic vessels, while its expression in quiescent vasculature is minimal. However, anti-angiogenic therapy targeting avb3-integrin has proven somewhat disappointing. In part this likely relates to the fact that avb3-integrin is not expressed solely by endothelial cells, but across a wide range of cell types that each contribute to angiogenesis. The aim of the research we present here is to elucidate the role of avb3-integrin in tumour growth and angiogenesis as it is expressed specifically by endothelial cells.
منابع مشابه
Acute depletion of endothelial β3-integrin transiently inhibits tumor growth and angiogenesis in mice.
RATIONALE The dramatic upregulation of αvβ3-integrin that occurs in the vasculature during tumor growth has long suggested that the endothelial expression of this molecule is an ideal target for antiangiogenic therapy to treat cancer. This discovery led to the development of small-molecule inhibitors directed against αvβ3-integrin that are currently in clinical trials. In 2002, we reported that...
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عنوان ژورنال:
دوره 7 شماره
صفحات -
تاریخ انتشار 2013