Table 1 |
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PTKs and their role in lymphatic biology |
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Gene |
Role in lymphatic vessels |
Inhibitors available* |
Effect of pathway inhibition |
References |
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VEGFR-2 |
Receptor for the VEGF family of ligands. Can also heterodimerize with VEGFR-3. |
Yes |
Secreted VEGFR-2 is a naturally occurring inhibitor of lymphatic vessel growth. However, Sorafenib† did not block VEGF-C/D induced tumor lymphangiogenesis. |
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|
VEGFR-3 |
Predominant receptor for the lymphangiogenic growth factors VEGF-C and VEGF-D, transduces survival, proliferation and migration signals. |
Yes |
Cediranib‡ blocks VEGFR-3 activity and inhibits lymphangiogenesis. Anti-VEGFR-3 antibody prevented tumor lymphangiogenesis with no effect on preexisting vessels. |
|
|
Tie1 |
Not critical for lymphatic cell commitment during development, and no ligand has been shown. |
None reported |
Tie1 knockout mouse has lymphatic vascular abnormalities that precede the blood vessel phenotype. |
[55] |
|
Tie2 |
Receptor for Ang-1 and Ang-2, appears to control vessel maturation. |
Yes |
Tie2-/- mice are embryonic lethal due to vascular defects. Inhibition of Ang-2 leads to tumor blood vessel normalization. |
|
|
EphB4 |
Expressed on lymphatic capillary vessels, involved in vascular patterning, binds to the ephrinB2 ligand. |
Yes |
Mice expressing a mutant form of ephrinB2 lacking the PDZ binding domain show major lymphatic defects in capillary vessels and collecting vessel valve formation. |
[60] |
|
SRC |
Signal transduction downstream from receptors. |
Yes |
Src inhibitor AZM475271 was effective at blocking VEGF-C driven lymphangiogenesis in vivo. |
[103] |
|
FGFR3 |
The ligands FGF-1 and FGF-2 promote proliferation, migration, and survival of cultured LECs. FGFR3 is direct transcriptional target of Prox1. |
Yes |
Knockdown of FGFR3 reduced LEC proliferation. |
[47] |
|
IGF1R |
Both of the IGF1R ligands, IGF-1 and IGF-2, significantly stimulated proliferation and migration of primary lymphatic endothelial cells. |
Yes |
None reported. |
[48] |
|
PDGFRβ |
The ligand PDGF-BB stimulated MAP kinase activity and cell motility of isolated lymphatic endothelial cells. |
Yes |
None reported. |
[138] |
|
MET |
The ligand for c-Met, hepatocyte growth factor has lymphangiogenic effect, but it is unclear if c-Met is expressed on LECs. |
Yes |
May be indirect effect. |
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*For reviews detailing available inhibitors see [71,139]. †Sorafenib inhibits B-Raf, PDGFRβ, VEGFR-2 and c-Kit. ‡Cediranib inhibits VEGFR-1, -2, -3, PDGFRβ and c-Kit. |
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Williams et al. Journal of Angiogenesis Research 2010 2:13 doi:10.1186/2040-2384-2-13 |
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