Vascular endothelial growth factor A

Vascular endothelial growth factor A (VEGF-A) is a protein that in humans is encoded by the VEGFA gene.[5]

VEGFA
Available structures PDB Ortholog search: PDBe RCSB List of PDB id codes 1BJ1, 1CZ8, 1FLT, 1KAT, 1KMX, 1MJV, 1MKG, 1MKK, 1QTY, 1TZH, 1TZI, 1VGH, 1VPF, 1VPP, 2FJG, 2FJH, 2QR0, 2VGH, 2VPF, 3BDY, 3P9W, 3QTK, 3S1B, 3S1K, 3V2A, 4DEQ, 4GLN, 4GLS, 4KZN, 4QAF, 4WPB, 4ZFF, 5HHC, 5FV1, 5FV2, 5HHD, 5DN2
Identifiers
Aliases	VEGFA, MVCD1, VEGF, VPF, vascular endothelial growth factor A
External IDs	OMIM: 192240 MGI: 103178 HomoloGene: 2534 GeneCards: VEGFA
Gene location (Human) Chr. Chromosome 6 (human)[1] Band 6p21.1 Start 43,770,184 bp[1] End 43,786,487 bp[1]
Gene location (Mouse) Chr. Chromosome 17 (mouse)[2] Band 17 C|17 22.79 cM Start 46,016,993 bp[2] End 46,032,369 bp[2]
RNA expression pattern More reference expression data
Gene ontology Molecular function • heparin binding • extracellular matrix binding • cytokine activity • growth factor activity • neuropilin binding • vascular endothelial growth factor receptor 2 binding • receptor ligand activity • vascular endothelial growth factor receptor 1 binding • protein homodimerization activity • platelet-derived growth factor receptor binding • GO:0001948 protein binding • vascular endothelial growth factor receptor binding • fibronectin binding • chemoattractant activity • identical protein binding • protein heterodimerization activity Cellular component • cytoplasm • membrane • extracellular region • cell surface • secretory granule • platelet alpha granule lumen • extracellular • extracellular matrix Biological process • cardiac vascular smooth muscle cell development • positive regulation of protein phosphorylation • positive regulation of MAP kinase activity • vascular endothelial growth factor signaling pathway • positive regulation of receptor internalization • outflow tract morphogenesis • mammary gland alveolus development • monocyte differentiation • cell migration involved in sprouting angiogenesis • vasculogenesis • positive regulation of retinal ganglion cell axon guidance • vascular endothelial growth factor receptor signaling pathway • positive regulation of vascular permeability • positive regulation of mesenchymal cell proliferation • angiogenesis • positive regulation of blood vessel endothelial cell migration • positive regulation of ERK1 and ERK2 cascade • mesoderm development • positive regulation of positive chemotaxis • positive regulation of p38MAPK cascade • positive regulation of neuroblast proliferation • dopaminergic neuron differentiation • positive regulation of branching involved in ureteric bud morphogenesis • kidney development • lung development • coronary artery morphogenesis • in utero embryonic development • cell maturation • commissural neuron axon guidance • positive regulation of peptidyl-serine phosphorylation • positive regulation of CREB transcription factor activity • basophil chemotaxis • artery morphogenesis • regulation of transcription from RNA polymerase II promoter in response to hypoxia • positive regulation of peptidyl-tyrosine autophosphorylation • positive regulation of peptidyl-tyrosine phosphorylation • branching involved in blood vessel morphogenesis • positive regulation of protein localization to early endosome • primitive erythrocyte differentiation • positive regulation of protein kinase D signaling • lactation • cell differentiation • epithelial cell differentiation • positive regulation of leukocyte migration • positive regulation of epithelial cell proliferation • negative regulation of apoptotic process • negative regulation of transcription from RNA polymerase II promoter • nervous system development • macrophage differentiation • positive regulation of angiogenesis • regulation of retinal ganglion cell axon guidance • lymph vessel morphogenesis • post-embryonic camera-type eye development • regulation of cell shape • ovarian follicle development • positive regulation of cellular component movement • branching morphogenesis of an epithelial tube • coronary vein morphogenesis • surfactant homeostasis • positive regulation of vascular endothelial growth factor receptor signaling pathway • negative regulation of cysteine-type endopeptidase activity involved in apoptotic process • response to hypoxia • positive regulation of endothelial cell proliferation • positive regulation of protein complex assembly • positive regulation of protein kinase C signaling • positive regulation of cell migration • heart morphogenesis • platelet degranulation • positive regulation of axon extension involved in axon guidance • cardiac muscle fiber development • positive regulation of endothelial cell migration • multicellular organism development • positive regulation of histone deacetylase activity • tube formation • positive regulation of gene expression • positive regulation of protein autophosphorylation • endothelial cell chemotaxis • positive regulation of cell proliferation by VEGF-activated platelet derived growth factor receptor signaling pathway • positive regulation of endothelial cell chemotaxis by VEGF-activated vascular endothelial growth factor receptor signaling pathway • eye photoreceptor cell development • positive regulation of transcription from RNA polymerase II promoter in response to hypoxia • positive regulation of focal adhesion assembly • cellular response to vascular endothelial growth factor stimulus • activation of protein kinase activity • positive regulation of cell division • camera-type eye morphogenesis • positive regulation of transcription from RNA polymerase II promoter • positive regulation of cell adhesion • cellular response to hypoxia • positive chemotaxis • regulation of transcription from RNA polymerase II promoter • positive regulation of cell proliferation • induction of positive chemotaxis • positive regulation of mast cell chemotaxis • motor neuron migration • positive regulation of tyrosine phosphorylation of STAT protein • growth • VEGF-activated neuropilin signaling pathway • positive regulation of phosphorylation • regulation of receptor activity • negative regulation of gene expression • cytokine-mediated signaling pathway • positive regulation of cell migration involved in sprouting angiogenesis • cellular stress response to acid chemical • positive regulation of blood vessel endothelial cell proliferation involved in sprouting angiogenesis • positive regulation of sprouting angiogenesis • positive regulation of DNA biosynthetic process • sprouting angiogenesis • regulation of nitric oxide mediated signal transduction • positive regulation of cold-induced thermogenesis • signal transduction Sources:Amigo / QuickGO
Orthologs
Species	Human	Mouse
Entrez	7422	22339
Ensembl	ENSG00000112715	ENSMUSG00000023951
UniProt	P15692	Q00731
RefSeq (mRNA)	NM_003376 NM_001025366 NM_001025367 NM_001025368 NM_001025369 NM_001025370 NM_001033756 NM_001171622 NM_001171623 NM_001171624 NM_001171625 NM_001171626 NM_001171627 NM_001171628 NM_001171629 NM_001171630 NM_001204384 NM_001204385 NM_001287044 NM_001317010	NM_001025250 NM_001025257 NM_001110266 NM_001110267 NM_001110268 NM_001287056 NM_001287057 NM_001287058 NM_009505 NM_001317041
RefSeq (protein)	NP_001020537 NP_001020538 NP_001020539 NP_001020540 NP_001020541 NP_001028928 NP_001165093 NP_001165094 NP_001165095 NP_001165096 NP_001165097 NP_001165098 NP_001165099 NP_001165100 NP_001165101 NP_001191313 NP_001191314 NP_001273973 NP_001303939 NP_003367	NP_001020421 NP_001020428 NP_001103736 NP_001103737 NP_001103738 NP_001273985 NP_001273986 NP_001273987 NP_001303970 NP_033531
Location (UCSC)	Chr 6: 43.77 – 43.79 Mb	Chr 17: 46.02 – 46.03 Mb
PubMed search	[3]	[4]
Wikidata
View/Edit Human View/Edit Mouse

Function

This gene is a member of the platelet-derived growth factor (PDGF)/vascular endothelial growth factor (VEGF) family and encodes a protein that is often found as a disulfide linked homodimer. This protein is a glycosylated mitogen that specifically acts on endothelial cells and has various effects, including mediating increased vascular permeability, inducing angiogenesis, vasculogenesis and endothelial cell growth, promoting cell migration, and inhibiting apoptosis. Alternatively spliced transcript variants, encoding either freely secreted or cell-associated isoforms, have been characterized.[6]

VEGF-A shows prominent activity with vascular endothelial cells, primarily through its interactions with the VEGFR1 and -R2 receptors found in prominently on the endothelial cell membrane. Although, it does have effects on a number of other cell types (e.g., stimulation monocyte/macrophage migration, neurons, cancer cells, kidney epithelial cells ). In vitro, VEGF-A has been shown to stimulate endothelial cell mitogenesis and cell migration. VEGF-A is also a vasodilator and increases microvascular permeability and was originally referred to as vascular permeability factor.

During embryonic development angiogenesis is initiated as mesoderm mesenchyme cells are specified to differentiate into angioblasts, expressing the Vascular Endothelial Growth Factor Receptor (VEGFR-2). As embryonic tissue utilizes more oxygen than it receives from diffusion, it becomes hypoxic. These cells will secrete the signaling molecule vascular endothelial factor A (VEGFA) which will recruit the angioblasts expressing it's partnering receptor to the site of future angiogenesis. The angioblasts will create scaffolding structures which form the primary capillary plexus from where the local vasculature system will develop. Disruption of this gene in mice resulted in abnormal embryonic blood vessel formation, resulting in underdeveloped vascular structures. This gene is also upregulated in many tumors and its expression is correlated with tumor development and is a target in many developing cancer therapeutics. Elevated levels of this protein are found in patients with POEMS syndrome, also known as Crow-Fukase syndrome which is a hemangioblastic proliferative disorder. Allelic variants of this gene have been associated with microvascular complications of diabetes 1 and atherosclerosis.

VEGF-A Overview

Vascular endothelial growth factor A (VEGF-A) is a dimeric glycoprotein that plays a significant role in neurons and is considered to be the main, dominant inducer to the growth of blood vessels. VEGFA is essential for adults during organ remodeling and diseases that involve blood vessels, for example, in wound healing, tumor angiogenesis, diabetic retinopathy, and age-related macular degeneration. During early vertebrate development, vasculogenesis occurs which means that the endothelial condense into the blood vessels. The differentiation of endothelial cells is dependent upon the expression of VEGFA and if the expression is abolished then it can result in the death of the embryo. VEGFA is produced by a group of three major isoforms as a result of alternative splicing and if any three isoforms are produced (VEGFA120, VEGFA164, and VEGFA188) then this will not result in vessel defects and death of the full VEGFA knockout in mice. VEGFA is essential in the role of neurons because they too need vascular supply and abolishing the expression of VEGFA from neural progenitors will result in defects of the brain vascularization and neuronal apoptosis. Anti-VEGFA therapy can be used to treat patients with undesirable angiogenesis and vascular leakage in cancer and eye diseases but also could result in the inhibition of neurogenesis and neuroprotection. VEGFA could be used to treat patients with neurodegenerative and neuropathic conditions and also increase vascular permeability which will stop the blood-brain barrier and increase inflammatory cell infiltration. References [7] [8][9]

Usage

• Angiogenesis
  • ↑ Migration of endothelial cells
  • ↑ mitosis of endothelial cells
  • ↑ Matrix metalloproteinase activity
  • ↑ αvβ3 activity
  • creation of blood vessel lumen
  • creates lumen
  • creates fenestrations
• Chemotactic for macrophages and granulocytes
• Vasodilation (indirectly by NO release)

Also tumour suppression.[10]

Clinical significance

Elevated levels of this protein is linked to POEMS syndrome, also known as Crow-Fukase syndrome.[11] Mutations in this gene have been associated with proliferative and nonproliferative diabetic retinopathy.[12]

Treatment of ischemic heart disease

In ischemic cardiomyopathy, blood flow to the muscle cells of the heart is either partially or completely reduced, leading to cell death and scar tissue formation. Because the muscle cells are replaced with fibrous tissue, the heart loses its ability to contract, compromising heart function.[13] Normally, if blood flow to the heart is compromised, over time, new blood vessels will develop, providing alternative circulation to the affected cells. The viability of the heart following severely restricted blood flow is dependent on the ability of the heart to provide this collateral circulation.[14] Expression of VEGF-A has been found to be induced by myocardial ischemia and a higher level of expression of VEGF-A has been associated with better collateral circulation development during ischemia.[15][16]

VEGF-A activation

When cells are deprived of oxygen, they increase their production of VEGF-A. VEGF-A mediates the growth of new blood vessels from pre-existing vessels (angiogenesis) by binding to the cell surface receptors VEGFR1 and VEGFR2, two tyrosine kinases located in endothelial cells of the cardiovascular system. These two receptors act through different pathways to contribute to endothelial cell proliferation and migration, and formation of tubular structures.[17]

VEGFR2

The binding of VEGF-A to VEGFR2 causes two VEGFR2 molecules to combine to form a dimer. Following this dimerization, through the action of the receptor itself, a phosphate group is added to certain tyrosines within the molecule in a process called auto-phosphorylation.[18] The autophosphorylation of these amino acids allows for signalling molecules within to the cell to bind to the receptor and become activated. These signalling molecules include VEGF-receptor activated protein (VRAP), PLC- γ and Nck.[19][20][21]

Each of these is important in the signalling required for angiogenesis. VRAP (also known as T-cell specific adaptor) and Nck signalling are important in reorganization of the structural components of the cell, allowing for cells to move around to areas where they are needed.[21][22] PLC- γ is vital to the proliferative effects of VEGF-A signalling. Activation of the phospholipase PLC- γ results in an increase in calcium levels in the cell, leading to the activation of protein kinase C (PKC).[23] PKC phosphorylates the mitogen-activated protein kinase (MAPK) ERK which then moves to the nucleus of the cell and takes part in nuclear signalling.[24] Once in the nucleus, ERK activates various transcription factors which initiate expression of genes involved in cellular proliferation.[25] Activation of a different MAPK (p38 MAPK) by VEGFR2 is important in the transcription of genes associated with cellular migration.[26]

VEGFR1

The tyrosine kinase activity of VEGFR1 is less efficient than that of VEGFR2 and its activation alone is insufficient to bring about the proliferative effects of VEGF-A.[27] The major role of VEGFR1 is to recruit the cells responsible in blood cell development.[28]

Current research

It has been shown that injection of VEGF-A in dogs following severely restricted blood flow to the heart caused an increase in collateral blood vessel formation compared to the dogs who did not receive the VEGF-A treatment.[16] It was also shown in dogs that delivery of VEGF-A to areas of the heart with little or no blood flow enhanced collateral blood vessel formation and increased the viability of the cells in that area.[29] In gene therapy, DNA which encodes the gene of interest is integrated into a vector along with elements that are able to promote the gene's expression. The vector is then injected either into muscle cells of the heart or the blood vessels supplying the heart. The natural machinery of the cell is then used to express these genes.[30] Currently, human clinical trials are being conducted to study the effectiveness of gene therapy with VEGF-A in restoring blood flow and function to areas of the heart that have severely restricted blood flow.[31][32][33] So far, this type of therapy has proven both safe and beneficial.[33][34]

Interactions

Vascular endothelial growth factor A has been shown to interact with:

• ADAMTS1,[35]
• CTGF,[36] and
• NRP1,[37][38]

See also

• Vascular endothelial growth factor
• Bevacizumab (or Avastin) anti VEGF-A human antibody drug.

References

1. GRCh38: Ensembl release 89: ENSG00000112715 - Ensembl, May 2017
2. GRCm38: Ensembl release 89: ENSMUSG00000023951 - Ensembl, May 2017
3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
5. Mattei MG, Borg JP, Rosnet O, Marmé D, Birnbaum D (February 1996). "Assignment of vascular endothelial growth factor (VEGF) and placenta growth factor (PLGF) genes to human chromosome 6p12-p21 and 14q24-q31 regions, respectively". Genomics. 32 (1): 168–169. doi:10.1006/geno.1996.0098. PMID 8786112.
6. "Entrez Gene: Vascular endothelial growth factor A".
7. Mackenzie, Francesca, and Christiana Ruhrberg. "Diverse Roles for VEGF-A in the Nervous System." Development (n.d.): 1371-380. http://dev.biologist.org/. 15 Apr. 2012. Web. 19 Mar. 2013.
8. Creuzet, Sophie, Gérard Couly, Christine Vincent, and Nicole M. Douarin. "Negative Effect of Hox Gene Expression on the Development of the Neural." Development (n.d.): 4301-313. http://dev.biologists.org/. 15 Sept. 2002. Web. 19 Mar. 2013.
9. United States of America. Johns Hopkins University. http://omim.org. By Victor A. McKusick. Johns Hopkins University, 26 Feb. 2013. Web. 19 Mar. 2013.
10. Stockmann C, Doedens A, Weidemann A, Zhang N, Takeda N, Greenberg JI, Cheresh DA, Johnson RS (November 2008). "Deletion of vascular endothelial growth factor in myeloid cells accelerates tumorigenesis". Nature. 456 (7223): 814–818. doi:10.1038/nature07445. PMC 3103772. PMID 18997773.
11. Dispenzieri A (November 2007). "POEMS syndrome". Blood Rev. 21 (6): 285–299. doi:10.1016/j.blre.2007.07.004. PMID 17850941.
12. Watanabe D, Suzuma K, Suzuma I, Ohashi H, Ojima T, Kurimoto M, Murakami T, Kimura T, Takagi H (March 2005). "Vitreous levels of angiopoietin 2 and vascular endothelial growth factor in patients with proliferative diabetic retinopathy". Am. J. Ophthalmol. 139 (3): 476–481. doi:10.1016/j.ajo.2004.10.004. PMID 15767056.
13. Beltrami CA, Finato N, Rocco M, Feruglio GA, Puricelli C, Cigola E, Quaini F, Sonnenblick EH, Olivetti G, Anversa P (January 1994). "Structural basis of end-stage failure in ischemic cardiomyopathy in humans". Circulation. 89 (1): 151–63. doi:10.1161/01.cir.89.1.151. PMID 8281642.
14. Sabia PJ, Powers ER, Ragosta M, Sarembock IJ, Burwell LR, Kaul S (December 1992). "An association between collateral blood flow and myocardial viability in patients with recent myocardial infarction". N. Engl. J. Med. 327 (26): 1825–1831. doi:10.1056/NEJM199212243272601. PMID 1448120.
15. Banai S, Shweiki D, Pinson A, Chandra M, Lazarovici G, Keshet E (August 1994). "Upregulation of vascular endothelial growth factor expression induced by myocardial ischaemia: implications for coronary angiogenesis". Cardiovasc. Res. 28 (8): 1176–9. doi:10.1093/cvr/28.8.1176. PMID 7525061.
16. Chalothorn D, Clayton JA, Zhang H, Pomp D, Faber JE (July 2007). "Collateral density, remodeling, and VEGF-A expression differ widely between mouse strains". Physiol. Genomics. 30 (2): 179–191. CiteSeerX 10.1.1.325.6534. doi:10.1152/physiolgenomics.00047.2007. PMID 17426116.
17. Huusko J, Merentie M, Dijkstra MH, Ryhänen MM, Karvinen H, Rissanen TT, Vanwildemeersch M, Hedman M, Lipponen J, Heinonen SE, Eriksson U, Shibuya M, Ylä-Herttuala S (April 2010). "The effects of VEGF-R1 and VEGF-R2 ligands on angiogenic responses and left ventricular function in mice". Cardiovasc. Res. 86 (1): 122–30. doi:10.1093/cvr/cvp382. PMID 19955220.
18. Dougher-Vermazen M, Hulmes JD, Böhlen P, Terman BI (November 1994). "Biological activity and phosphorylation sites of the bacterially expressed cytosolic domain of the KDR VEGF-receptor". Biochem. Biophys. Res. Commun. 205 (1): 728–38. doi:10.1006/bbrc.1994.2726. PMID 7999104.
19. Wu LW, Mayo LD, Dunbar JD, Kessler KM, Ozes ON, Warren RS, Donner DB (March 2000). "VRAP is an adaptor protein that binds KDR, a receptor for vascular endothelial cell growth factor". J. Biol. Chem. 275 (9): 6059–6062. doi:10.1074/jbc.275.9.6059. PMID 10692392.
20. Takahashi T, Yamaguchi S, Chida K, Shibuya M (June 2001). "A single autophosphorylation site on KDR/Flk-1 is essential for VEGF-A-dependent activation of PLC-gamma and DNA synthesis in vascular endothelial cells". EMBO J. 20 (11): 2768–2778. doi:10.1093/emboj/20.11.2768. PMC 125481. PMID 11387210.
21. Lamalice L, Houle F, Huot J (November 2006). "Phosphorylation of Tyr1214 within VEGFR-2 triggers the recruitment of Nck and activation of Fyn leading to SAPK2/p38 activation and endothelial cell migration in response to VEGF". J. Biol. Chem. 281 (45): 34009–34020. doi:10.1074/jbc.M603928200. PMID 16966330.
22. Matsumoto T, Bohman S, Dixelius J, Berge T, Dimberg A, Magnusson P, Wang L, Wikner C, Qi JH, Wernstedt C, Wu J, Bruheim S, Mugishima H, Mukhopadhyay D, Spurkland A, Claesson-Welsh L (July 2005). "VEGF receptor-2 Y951 signaling and a role for the adapter molecule TSAd in tumor angiogenesis". EMBO J. 24 (13): 2342–2353. doi:10.1038/sj.emboj.7600709. PMC 1173150. PMID 15962004.
23. Xia P, Aiello LP, Ishii H, Jiang ZY, Park DJ, Robinson GS, Takagi H, Newsome WP, Jirousek MR, King GL (November 1996). "Characterization of vascular endothelial growth factor's effect on the activation of protein kinase C, its isoforms, and endothelial cell growth". J. Clin. Invest. 98 (9): 2018–2026. doi:10.1172/JCI119006. PMC 507645. PMID 8903320.
24. Khokhlatchev AV, Canagarajah B, Wilsbacher J, Robinson M, Atkinson M, Goldsmith E, Cobb MH (May 1998). "Phosphorylation of the MAP kinase ERK2 promotes its homodimerization and nuclear translocation". Cell. 93 (4): 605–615. doi:10.1016/S0092-8674(00)81189-7. PMID 9604935.
25. Cui TX, Lin G, Lapensee CR, Calinescu AA, Rathore M, Streeter C, Piwien-Pilipuk G, Lanning N, Jin H, Carter-Su C, Qin ZS, Schwartz J (April 2011). "C/EBP{beta} Mediates Growth Hormone-Regulated Expression of Multiple Target Genes". Mol. Endocrinol. 25 (4): 681–93. doi:10.1210/me.2010-0232. PMC 3063086. PMID 21292824.
26. Kobayashi M, Nishita M, Mishima T, Ohashi K, Mizuno K (February 2006). "MAPKAPK-2-mediated LIM-kinase activation is critical for VEGF-induced actin remodeling and cell migration". EMBO J. 25 (4): 713–726. doi:10.1038/sj.emboj.7600973. PMC 1383554. PMID 16456544.
27. Seetharam L, Gotoh N, Maru Y, Neufeld G, Yamaguchi S, Shibuya M (January 1995). "A unique signal transduction from FLT tyrosine kinase, a receptor for vascular endothelial growth factor VEGF". Oncogene. 10 (1): 135–47. PMID 7824266.
28. Luttun A, Tjwa M, Moons L, Wu Y, Angelillo-Scherrer A, Liao F, Nagy JA, Hooper A, Priller J, De Klerck B, Compernolle V, Daci E, Bohlen P, Dewerchin M, Herbert JM, Fava R, Matthys P, Carmeliet G, Collen D, Dvorak HF, Hicklin DJ, Carmeliet P (August 2002). "Revascularization of ischemic tissues by PlGF treatment, and inhibition of tumor angiogenesis, arthritis and atherosclerosis by anti-Flt1". Nat. Med. 8 (8): 831–40. doi:10.1038/nm731. PMID 12091877.
29. Ferrarini M, Arsic N, Recchia FA, Zentilin L, Zacchigna S, Xu X, Linke A, Giacca M, Hintze TH (April 2006). "Adeno-associated virus-mediated transduction of VEGF165 improves cardiac tissue viability and functional recovery after permanent coronary occlusion in conscious dogs". Circ. Res. 98 (7): 954–961. doi:10.1161/01.RES.0000217342.83731.89. PMID 16543500.
30. Lavu M, Gundewar S, Lefer DJ (May 2011). "Gene therapy for ischemic heart disease". J. Mol. Cell. Cardiol. 50 (5): 742–750. doi:10.1016/j.yjmcc.2010.06.007. PMC 2995818. PMID 20600100.
31. Rosengart TK, Lee LY, Patel SR, Sanborn TA, Parikh M, Bergman GW, Hachamovitch R, Szulc M, Kligfield PD, Okin PM, Hahn RT, Devereux RB, Post MR, Hackett NR, Foster T, Grasso TM, Lesser ML, Isom OW, Crystal RG (August 1999). "Angiogenesis gene therapy: phase I assessment of direct intramyocardial administration of an adenovirus vector expressing VEGF121 cDNA to individuals with clinically significant severe coronary artery disease". Circulation. 100 (5): 468–74. doi:10.1161/01.cir.100.5.468. PMID 10430759.
32. Ripa RS, Wang Y, Jørgensen E, Johnsen HE, Hesse B, Kastrup J (August 2006). "Intramyocardial injection of vascular endothelial growth factor-A165 plasmid followed by granulocyte-colony stimulating factor to induce angiogenesis in patients with severe chronic ischaemic heart disease". Eur. Heart J. 27 (15): 1785–1792. doi:10.1093/eurheartj/ehl117. PMID 16825290.
33. Hedman M, Hartikainen J, Syvänne M, Stjernvall J, Hedman A, Kivelä A, Vanninen E, Mussalo H, Kauppila E, Simula S, Närvänen O, Rantala A, Peuhkurinen K, Nieminen MS, Laakso M, Ylä-Herttuala S (June 2003). "Safety and feasibility of catheter-based local intracoronary vascular endothelial growth factor gene transfer in the prevention of postangioplasty and in-stent restenosis and in the treatment of chronic myocardial ischemia: phase II results of the Kuopio Angiogenesis Trial (KAT)". Circulation. 107 (21): 2677–2683. doi:10.1161/01.CIR.0000070540.80780.92. PMID 12742981.
34. Hedman M, Muona K, Hedman A, Kivelä A, Syvänne M, Eränen J, Rantala A, Stjernvall J, Nieminen MS, Hartikainen J, Ylä-Herttuala S (May 2009). "Eight-year safety follow-up of coronary artery disease patients after local intracoronary VEGF gene transfer". Gene Ther. 16 (5): 629–634. doi:10.1038/gt.2009.4. PMID 19212427.
35. Luque A, Carpizo DR, Iruela-Arispe ML (June 2003). "ADAMTS1/METH1 inhibits endothelial cell proliferation by direct binding and sequestration of VEGF165". J. Biol. Chem. 278 (26): 23656–23665. doi:10.1074/jbc.M212964200. PMID 12716911.
36. Inoki I, Shiomi T, Hashimoto G, Enomoto H, Nakamura H, Makino K, Ikeda E, Takata S, Kobayashi K, Okada Y (February 2002). "Connective tissue growth factor binds vascular endothelial growth factor (VEGF) and inhibits VEGF-induced angiogenesis". FASEB J. 16 (2): 219–21. doi:10.1096/fj.01-0332fje. PMID 11744618.
37. Mamluk R, Gechtman Z, Kutcher ME, Gasiunas N, Gallagher J, Klagsbrun M (July 2002). "Neuropilin-1 binds vascular endothelial growth factor 165, placenta growth factor-2, and heparin via its b1b2 domain". J. Biol. Chem. 277 (27): 24818–24825. doi:10.1074/jbc.M200730200. PMID 11986311.
38. Soker S, Takashima S, Miao HQ, Neufeld G, Klagsbrun M (March 1998). "Neuropilin-1 is expressed by endothelial and tumor cells as an isoform-specific receptor for vascular endothelial growth factor". Cell. 92 (6): 735–745. doi:10.1016/S0092-8674(00)81402-6. PMID 9529250.

External links

• Overview of all the structural information available in the PDB for UniProt: P15692 (Vascular endothelial growth factor A) at the PDBe-KB.

This article incorporates text from the United States National Library of Medicine, which is in the public domain.