Literature DB >> 24003209

Receptor tyrosine kinase-mediated angiogenesis.

Michael Jeltsch1, Veli-Matti Leppänen, Pipsa Saharinen, Kari Alitalo.   

Abstract

The endothelial cell is the essential cell type forming the inner layer of the vasculature. Two families of receptor tyrosine kinases (RTKs) are almost completely endothelial cell specific: the vascular endothelial growth factor (VEGF) receptors (VEGFR1-3) and the Tie receptors (Tie1 and Tie2). Both are key players governing the generation of blood and lymphatic vessels during embryonic development. Because the growth of new blood and lymphatic vessels (or the lack thereof) is a central element in many diseases, the VEGF and the Tie receptors provide attractive therapeutic targets in various diseases. Indeed, several drugs directed to these RTK signaling pathways are already on the market, whereas many are in clinical trials. Here we review the VEGFR and Tie families, their involvement in developmental and pathological angiogenesis, and the different possibilities for targeting them to either block or enhance angiogenesis and lymphangiogenesis.

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Year:  2013        PMID: 24003209      PMCID: PMC3753715          DOI: 10.1101/cshperspect.a009183

Source DB:  PubMed          Journal:  Cold Spring Harb Perspect Biol        ISSN: 1943-0264            Impact factor:   10.005


  204 in total

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Journal:  Cancer Cell       Date:  2010-08-09       Impact factor: 31.743

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9.  Accelerated metastasis after short-term treatment with a potent inhibitor of tumor angiogenesis.

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2.  The angiopoietin-Tie2 signaling axis in the vascular leakage of systemic inflammation.

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Review 5.  Lymphatic vessels and tertiary lymphoid organs.

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9.  Loss of Estrogen-Related Receptor Alpha Facilitates Angiogenesis in Endothelial Cells.

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Review 10.  New radiotracers for imaging of vascular targets in angiogenesis-related diseases.

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