Phenotype ANGIOGENESIS
ANGIOGENESIS@default
References
PMID:18633355
Hypoxic macrophages are known to respond to hypoxia by upregulating hypoxia-inducible transcription factors (mainly hypoxia-inducible factors HIF1 and HIF2)38, 39, the activation of which leads to increased transcription of many genes that regulate cell proliferation, metabolism and angiogenesis40.
Hypoxia induces a distinct pro-angiogenic phenotype in human macrophages in vitro42, 43 including the upregulation of VEGF, bFGF, CXCL8, COX2, hepatocyte growth factor (HGF), VEGFR1, tissue factor (F3) and MMP12.
Modifications:
In compartment: default
- ANGIOGENESIS@default
Participates in complexes:
Participates in reactions:
As Reactant or Product:- VEGFA@default
→
ANGIOGENESIS@default
- IL1A@default
→
ANGIOGENESIS@default
- trILB1@INNATE_IMMUNE_CELL_Cytosol
→
ANGIOGENESIS@default
- IL8*@default
→
ANGIOGENESIS@default
- TYMP@INNATE_IMMUNE_CELL_Cytosol
→
ANGIOGENESIS@default
- FGF2@INNATE_IMMUNE_CELL_Cytosol
→
ANGIOGENESIS@default
- HGF@INNATE_IMMUNE_CELL_Cytosol
→
ANGIOGENESIS@default
- MMP12@INNATE_IMMUNE_CELL_Cytosol
→
ANGIOGENESIS@default
- CXCL1@default
→
ANGIOGENESIS@default
- OSM@INNATE_IMMUNE_CELL_Cytosol
→
ANGIOGENESIS@default
- ADM@INNATE_IMMUNE_CELL_Cytosol
→
ANGIOGENESIS@default
- WNT7B@INNATE_IMMUNE_CELL_Cytosol
→
ANGIOGENESIS@default
- PLAU@INNATE_IMMUNE_CELL_Cytosol
→
ANGIOGENESIS@default
- PDGFB@INNATE_IMMUNE_CELL_Cytosol
→
ANGIOGENESIS@default
- Heparin@INNATE_IMMUNE_CELL_Cytosol
→
ANGIOGENESIS@default
- NGF@INNATE_IMMUNE_CELL_Cytosol
→
ANGIOGENESIS@default
- MMP9@INNATE_IMMUNE_CELL_Cytosol
→
ANGIOGENESIS@default
- Histamine@INNATE_IMMUNE_CELL_Cytosol
→
ANGIOGENESIS@default
- ANGIOGENESIS@default
→
TUMOR_GROWTH@TUMOR_CELL_AS_EFFECTOR
- Hypoxia@TUMOR_CELL_AS_INDUCTOR
→
ANGIOGENESIS@default
- TNF@INNATE_IMMUNE_CELL_Cytosol
→
ANGIOGENESIS@default
As Catalyser: