Signaling by VEGF (Homo sapiens)
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Description
In normal development vascular endothelial growth factors (VEGFs) are crucial regulators of vascular development during embryogenesis (vasculogenesis) and blood-vessel formation in the adult (angiogenesis). In tumor progression, activation of VEGF pathways promotes tumor vascularization, facilitating tumor growth and metastasis. Abnormal VEGF function is also associated with inflammatory diseases including atherosclerosis, and hyperthyroidism. The members of the VEGF and VEGF-receptor protein families have distinct but overlapping ligand-receptor specificities, cell-type expression, and function. VEGF-receptor activation in turn regulates a network of signaling processes in the body that promote endothelial cell growth, migration and survival (Hicklin and Ellis, 2005; Shibuya and Claesson-Welsh, 2006).
Molecular features of the VGF signaling cascades are outlined in the figure below (from Olsson et al. 2006; Nature Publishing Group). Tyrosine residues in the intracellular domains of VEGF receptors 1, 2,and 3 are indicated by dark blue boxes; residues susceptible to phosphorylation are numbered. A circled R indicates that phosphorylation is regulated by cell state (VEGFR2), by ligand binding (VEGFR1), or by heterodimerization (VEGFR3). Specific phosphorylation sites (boxed numbers) bind signaling molecules (dark blue ovals), whose interaction with other cytosolic signaling molecules (light blue ovals) leads to specific cellular (pale blue boxes) and tissue-level (pink boxes) responses in vivo. Signaling cascades whose molecular details are unclear are indicated by dashed arrows. DAG, diacylglycerol; EC, endothelial cell; eNOS, endothelial nitric oxide synthase; FAK, focal adhesion kinase; HPC, hematopoietic progenitor cell; HSP27, heat-shock protein-27; MAPK, mitogen-activated protein kinase; MEK, MAPK and ERK kinase; PI3K, phosphatidylinositol 3' kinase; PKC, protein kinase C; PLCgamma, phospholipase C-gamma; Shb, SH2 and beta-cells; TSAd, T-cell-specific adaptor.
In the current release, the first events in these cascades - the interactions between VEGF proteins and their receptors - are annotated. Details of signaling events and their biological outcome, concisely illustrated in the image below, will be available in future versions of this pathway.
Molecular features of the VGF signaling cascades are outlined in the figure below (from Olsson et al. 2006; Nature Publishing Group). Tyrosine residues in the intracellular domains of VEGF receptors 1, 2,and 3 are indicated by dark blue boxes; residues susceptible to phosphorylation are numbered. A circled R indicates that phosphorylation is regulated by cell state (VEGFR2), by ligand binding (VEGFR1), or by heterodimerization (VEGFR3). Specific phosphorylation sites (boxed numbers) bind signaling molecules (dark blue ovals), whose interaction with other cytosolic signaling molecules (light blue ovals) leads to specific cellular (pale blue boxes) and tissue-level (pink boxes) responses in vivo. Signaling cascades whose molecular details are unclear are indicated by dashed arrows. DAG, diacylglycerol; EC, endothelial cell; eNOS, endothelial nitric oxide synthase; FAK, focal adhesion kinase; HPC, hematopoietic progenitor cell; HSP27, heat-shock protein-27; MAPK, mitogen-activated protein kinase; MEK, MAPK and ERK kinase; PI3K, phosphatidylinositol 3' kinase; PKC, protein kinase C; PLCgamma, phospholipase C-gamma; Shb, SH2 and beta-cells; TSAd, T-cell-specific adaptor.
In the current release, the first events in these cascades - the interactions between VEGF proteins and their receptors - are annotated. Details of signaling events and their biological outcome, concisely illustrated in the image below, will be available in future versions of this pathway.
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- Cantwell-Dorris ER, O'Leary JJ, Sheils OM.; ''BRAFV600E: implications for carcinogenesis and molecular therapy.''; PubMed Europe PMC Scholia
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- Woo SY, Kim DH, Jun CB, Kim YM, Haar EV, Lee SI, Hegg JW, Bandhakavi S, Griffin TJ, Kim DH.; ''PRR5, a novel component of mTOR complex 2, regulates platelet-derived growth factor receptor beta expression and signaling.''; PubMed Europe PMC Scholia
- Somanath PR, Malinin NL, Byzova TV.; ''Cooperation between integrin alphavbeta3 and VEGFR2 in angiogenesis.''; PubMed Europe PMC Scholia
- Tu D, Li Y, Song HK, Toms AV, Gould CJ, Ficarro SB, Marto JA, Goode BL, Eck MJ.; ''Crystal structure of a coiled-coil domain from human ROCK I.''; PubMed Europe PMC Scholia
- Franca-Koh J, Kamimura Y, Devreotes PN.; ''Leading-edge research: PtdIns(3,4,5)P3 and directed migration.''; PubMed Europe PMC Scholia
- Tsai YJ, Lee RK, Lin SP, Chen YH.; ''Identification of a novel platelet-derived growth factor-like gene, fallotein, in the human reproductive tract.''; PubMed Europe PMC Scholia
- Koyasu S.; ''The role of PI3K in immune cells.''; PubMed Europe PMC Scholia
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- Kyriakis JM, Avruch J.; ''Mammalian MAPK signal transduction pathways activated by stress and inflammation: a 10-year update.''; PubMed Europe PMC Scholia
- Gresset A, Hicks SN, Harden TK, Sondek J.; ''Mechanism of phosphorylation-induced activation of phospholipase C-gamma isozymes.''; PubMed Europe PMC Scholia
- Bedard K, Krause KH.; ''The NOX family of ROS-generating NADPH oxidases: physiology and pathophysiology.''; PubMed Europe PMC Scholia
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History
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External references
DataNodes
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Name | Type | Database reference | Comment |
---|---|---|---|
NRP-1 | Protein | REACT_12698 (Reactome) | |
NRP-2 | Protein | REACT_13365 (Reactome) | |
NRP-2:VEGFR1 | Complex | REACT_13266 (Reactome) | |
NRP1:VERGF165:
VERGFR2 | Complex | REACT_12681 (Reactome) | |
VEGF | Protein | REACT_12955 (Reactome) | |
VEGF homodimer | Complex | REACT_12721 (Reactome) | |
VEGF-A
variant4/VEGF165 | Protein | P15692-4 (UniProt) | |
VEGF-C,D | Complex | REACT_12875 (Reactome) | |
VEGFA,B,PLGF | Complex | REACT_12921 (Reactome) | |
VEGFA,C,D,E | Complex | REACT_12894 (Reactome) | |
VEGFR1 | Protein | REACT_12746 (Reactome) | |
VEGFR1:VEGFA,B,
PGLF | Complex | REACT_12847 (Reactome) | |
VEGFR2 | Protein | P35968 (UniProt) | |
VEGFR2:VEGFA,C,D,
E | Complex | REACT_13060 (Reactome) | |
VEGFR3 | Protein | P35916 (UniProt) | |
VEGFR3:VEGF-C,
and D | Complex | REACT_12751 (Reactome) |
Annotated Interactions
No annotated interactions