Protein / target

Vascular endothelial growth factor receptor 2

KDRP35968Homo sapiensSwiss-Prot
Clinically validated
Therapeutic maturity
24
Approved medicines
30
Clinical trials
Small-molecule tractable
Druggability
Approved Drug

Protein at a glance

Biological role

Transmembrane receptor protein tyrosine kinase activity

Primary system

Cardiovascular system

Strongest disease association

neoplasm

Genetic evidence · score 0.28

Therapeutic maturity

Clinically validated target

24 approved medicines against this target

Druggability

Small molecule

Open Targets tractability · Approved Drug

Clinical development

24 approved · 49 in clinical development

30 linked trials

Research activity

Emerging research

5 papers · latest 2024

Derived from structured UniProt, Open Targets and literature data on this page.

Protein profile

UniProt 2026_02

Canonical identity and biological annotation from UniProt.

Function

Tyrosine-protein kinase that acts as a cell-surface receptor for VEGFA, VEGFC and VEGFD. Plays an essential role in the regulation of angiogenesis, vascular development, vascular permeability, and embryonic hematopoiesis. Promotes proliferation, survival, migration and differentiation of endothelial cells. Promotes reorganization of the actin cytoskeleton. Isoforms lacking a transmembrane domain, such as isoform 2 and isoform 3, may function as decoy receptors for VEGFA, VEGFC and/or VEGFD. Isoform 2 plays an important role as negative regulator of VEGFA- and VEGFC-mediated lymphangiogenesis by limiting the amount of free VEGFA and/or VEGFC and preventing their binding to FLT4. Modulates FLT1 and FLT4 signaling by forming heterodimers. Binding of vascular growth factors to isoform 1 leads to the activation of several signaling cascades. Activation of PLCG1 leads to the production of the cellular signaling molecules diacylglycerol and inositol 1,4,5-trisphosphate and the activation of protein kinase C. Mediates activation of MAPK1/ERK2, MAPK3/ERK1 and the MAP kinase signaling pathway, as well as of the AKT1 signaling pathway. Mediates phosphorylation of PIK3R1, the regulatory subunit of phosphatidylinositol 3-kinase, reorganization of the actin cytoskeleton and activation of PTK2/FAK1. Required for VEGFA-mediated induction of NOS2 and NOS3, leading to the production of the signaling molecule nitric oxide (NO) by endothelial cells. Phosphorylates PLCG1. Promotes phosphorylation of FYN, NCK1, NOS3, PIK3R1, PTK2/FAK1 and SRC

Subcellular location

Cell junctionEndoplasmic reticulumCell membraneCytoplasmNucleusCytoplasmic vesicleEarly endosomeSecreted
Domains and Gene Ontology detail (76)

Domains & features

Ig-like C2-type 1Ig-like C2-type 2Ig-like C2-type 3Ig-like C2-type 4Ig-like C2-type 5Ig-like C2-type 6Ig-like C2-type 7Protein kinase

Gene Ontology

  • Canchoring junction
  • Ccell junction
  • Ccytosol
  • Cearly endosome
  • Cendoplasmic reticulum
  • Cendosome
  • Cexternal side of plasma membrane
  • Cextracellular region
  • CGolgi apparatus
  • Cmembrane raft
  • Cnuclear membrane
  • Cplasma membrane

1356 aa · 152 kDa · 3 isoforms

Biological roles

Reactome v97

What this protein does, drawn together from its UniProt function, Gene Ontology terms and Reactome pathways.

Kinase signallingUniProt · GOCell adhesionUniProt · GOApoptosis & cell deathGOTranscriptional regulationGO
View supporting evidence

Kinase signalling

  • ·Tyrosine-protein kinase that acts as a cell-surface receptor for VEGFA, VEGFC and VEGFD.…
  • ·protein tyrosine kinase activity
  • ·transmembrane receptor protein tyrosine kinase activity
  • ·peptidyl-tyrosine phosphorylation

Cell adhesion

  • ·Cell junction
  • ·cell junction

Apoptosis & cell death

  • ·negative regulation of endothelial cell apoptotic process
  • ·negative regulation of neuron apoptotic process

Transcriptional regulation

  • ·negative regulation of gene expression
View underlying pathways (7)

Concepts derived from UniProt GO Reactome — each badge above shows which sources supported that role.

Interaction neighbourhood

STRING v12.0

Proteins with the strongest functional or physical association. Node size and line weight reflect STRING confidence; hover or select a partner to inspect one association.

VEGFBCDH5NRP1VEGFCPGFVEGFDPECAM1FGF2SRCPDGFCKDR

10 strongest partners — larger node and heavier line mean higher confidence

Functional and physical associations from STRING v12.0. Only associations with this protein are drawn — partner-to-partner links are not part of this evidence.

Drugs targeting this protein

3

Whether each drug engages this protein directly or through a complex, and how many other targets are recorded for it. Direct binders with few recorded targets are listed first.

sunitinib
ApprovedInhibitor

Vascular endothelial growth factor receptor 2 inhibitor

Appears in clinical studies involving gastrointestinal stromal tumor, renal cell carcinoma, gastrointestinal stromal tumor, neuroendocrine neoplasm

Direct interaction with this protein · 1 of 9 recorded protein targets — broad pharmacology

axitinib
ApprovedInhibitor

Vascular endothelial growth factor receptor inhibitor

Appears in clinical studies involving renal cell carcinoma, renal cell carcinoma, neoplasm, pancreatic adenocarcinoma

Acts on a complex — shared with FLT1, FLT4 · 1 of 3 recorded protein targets — narrow recorded profile

regorafenib
ApprovedInhibitor

Vascular endothelial growth factor receptor inhibitor

Appears in clinical studies involving colorectal cancer, metastatic colorectal cancer, colorectal neoplasm, neoplasm

Acts on a complex — shared with FLT1, FLT4 · 1 of 18 recorded protein targets — broad pharmacology

ChEMBL mechanism, action type and target identity. Open Targets clinical status and indications.

Translational evidence

Open Targets 26

Why this target matters therapeutically — disease associations, drugs in development, tractability and safety, from Open Targets.

Strongest genetic associations

Human genetic evidence — the most direct causal link between this target and a disease.

neoplasm0.28

Genetic · overall 0.68

Highest-confidence therapeutic associations

Diseases where a drug acting on this target has already reached clinical development.

renal cell carcinoma0.99

Clinical · overall 0.66

hepatocellular carcinoma0.98

Clinical · overall 0.68

colorectal cancer0.97

Clinical · overall 0.60

gastrointestinal stromal tumor0.96

Clinical · overall 0.66

gastric adenocarcinoma0.93

Clinical · overall 0.64

Highest overall evidence

Remaining associations by Open Targets' aggregated evidence score.

non-small cell lung carcinoma0.65

Literature

cancer0.64

Literature

acute myeloid leukemia0.63

Clinical

thyroid gland carcinoma0.63

Clinical

Show all associations
neoplasm0.68
hepatocellular carcinoma0.68
gastrointestinal stromal tumor0.66
renal cell carcinoma0.66
non-small cell lung carcinoma0.65
gastric adenocarcinoma0.64
cancer0.64
acute myeloid leukemia0.63
thyroid gland carcinoma0.63
colorectal cancer0.60

Open Targets ranks 1,602 associations for this target and we store the top 10 by aggregated score. The long tail is largely literature co-mention and RNA-expression evidence, not evidence that this target drives those diseases.

Known drugs · 75 total

XL-820Phase 2

gastrointestinal stromal tumor

VATALANIBPhase 3

colorectal cancer · colorectal adenocarcinoma · von Hippel-Lindau disease

RIVOCERANIB MESYLATEApproval

breast cancer · small cell lung carcinoma · gastric cancer

4SC-203Phase 1
LINIFANIBPhase 3

hepatocellular carcinoma · renal cell carcinoma · non-small cell lung carcinoma

OLINVACIMABPhase 2

glioblastoma · breast cancer · colorectal carcinoma

XL-999Phase 2

ovarian cancer · colorectal cancer · renal cell carcinoma

LENVATINIBApproval

thyroid cancer · thyroid tumor · renal cell carcinoma

TELBERMINPhase 2

diabetic foot · lateral sclerosis · amyotrophic lateral sclerosis

FAMITINIBPhase 3

colorectal adenocarcinoma · non-small cell lung carcinoma · gastrointestinal stromal tumor

Tractability

SM · Approved DrugSM · Structure with LigandSM · High-Quality LigandSM · High-Quality PocketSM · Druggable FamilyAB · Approved DrugAB · UniProt loc high confAB · GO CC high confAB · UniProt loc med confAB · UniProt SigP or TMHMMPR · UniProt UbiquitinationPR · Database Ubiquitination

Safety liabilities

Increased, Developmental Defectsdrug toxicityheart diseaserashHypertension and hand-foot skin reactionsaneurysmhaemorrhagemyocardial hypoperfusionnauseavomitingdecreased appetiteregulation of catalytic activity

Clinical trials

30

Trials of drugs that target this protein — reached indirectly through those drugs, so a trial listed here studies the drug, not the protein.

Show remaining trials (24)

COMPLETED · via sunitinib · NCT00357318

ClinicalTrials.gov via the drug-target graph.

Research activity

5 papers · to 2024

Papers linked directly to this protein. This is the protein's own literature — descriptor-derived papers are kept separate below.

Most cited

Recent

Europe PMC papers linked directly to this protein.

Forefront confidence

Synthesis

Our own weighting of the evidence behind each disease association. Human genetics and clinical evidence count for most; literature co-mention counts for little, because two entities sharing an abstract is not evidence that one drives the other.

neoplasmWell supported
0.88
agreement 0.790.97
Clinical50%Somatic mutation20%Genetic20%Literature10%

Open Targets aggregate 0.68 · 4 independent evidence families

hepatocellular carcinomaWell supported
0.84
agreement 0.720.96
Clinical63%Somatic mutation25%Literature12%

Open Targets aggregate 0.68 · 3 independent evidence families

gastrointestinal stromal tumorWell supported
0.82
agreement 0.700.94
Clinical64%Somatic mutation27%Literature9%

Open Targets aggregate 0.66 · 3 independent evidence families

non-small cell lung carcinomaWell supported
0.82
agreement 0.710.93
Clinical60%Somatic mutation26%Literature12%RNA expression2%

Open Targets aggregate 0.65 · 4 independent evidence families

renal cell carcinomaWell supported
0.81
agreement 0.690.93
Clinical72%Somatic mutation19%Literature9%

Open Targets aggregate 0.66 · 3 independent evidence families

The evidence agreement range shows how closely the independent evidence families agree — it is not a statistical confidence interval, and nothing here is fitted to outcome data. Derived from Open Targets evidence types under Forefront weighting; the underlying per-type scores are shown above so the calculation can be checked.

What's happening now

34

Recent activity around this target, drawn from one canonical event stream. Every item is reached through 3 drugs that target this protein, so each event is news about that drug rather than about the protein directly.

  1. New publication2026-01-28
    Fecal microbiota transplantation plus pembrolizumab and axitinib in metastatic renal cell carcinoma: the randomized phase 2 TACITO trial.

    Nature medicine · 2026 · 8 citations · Europe PMC · via axitinib

  2. New publication2025-01-06
    Efficacy of pembrolizumab in microsatellite-stable, tumor mutational burden-high metastatic colorectal cancer: genomic signatures and clinical outcomes.

    ESMO open · 2025 · 10 citations · Europe PMC · via regorafenib

  3. Regulatory approval2024-09-19

    Approval: Axitinib Accord (EMA)

    ema · regulatory · ema · via axitinib

  4. New publication2024-06-04
    Lenvatinib Plus Pembrolizumab Versus Standard of Care for Previously Treated Metastatic Colorectal Cancer: Final Analysis of the Randomized, Open-Label, Phase III LEAP-017 Study.

    Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2024 · 69 citations · Europe PMC · via regorafenib

  5. New publication2024-05-03
    Machine-learning and mechanistic modeling of metastatic breast cancer after neoadjuvant treatment.

    PLoS computational biology · 2024 · 10 citations · Europe PMC · via sunitinib

  6. New publication2024-03-15
    The more the merrier? Evidence and efficacy of immune checkpoint- and tyrosine kinase inhibitor combinations in advanced solid cancers.

    Cancer treatment reviews · 2024 · 17 citations · Europe PMC · via axitinib

  7. New publication2024-01-05
    Genomic profiling in GIST: Implications in clinical outcome and future challenges.

    Neoplasia (New York, N.Y.) · 2024 · 20 citations · Europe PMC · via sunitinib

  8. New publication2021-03-01
    Nivolumab plus Cabozantinib versus Sunitinib for Advanced Renal-Cell Carcinoma.

    The New England journal of medicine · 2021 · 1,297 citations · Europe PMC · via sunitinib

  9. Regulatory approval2021-02-11

    Approval: Sunitinib Accord (EMA)

    ema · regulatory · ema · via sunitinib

  10. New publication2020-08-11
    Targeted therapy for hepatocellular carcinoma.

    Signal transduction and targeted therapy · 2020 · 565 citations · Europe PMC · via regorafenib

  11. New publication2020-06-21
    Liver transarterial chemoembolization and sunitinib for unresectable hepatocellular carcinoma: Results of the PRODIGE 16 study.

    Clinics and research in hepatology and gastroenterology · 2021 · 15 citations · Europe PMC · via sunitinib

  12. New publication2020-04-25
    Updated efficacy results from the JAVELIN Renal 101 trial: first-line avelumab plus axitinib versus sunitinib in patients with advanced renal cell carcinoma.

    Annals of oncology : official journal of the European Society for Medical Oncology · 2020 · 319 citations · Europe PMC · via axitinib

Objective event titles are shown unmodified; the event kind and significance line are derived from structured fields. Forefront AttentionEvent stream aggregating Europe PMC Regulatory filings ClinicalTrials.gov.