CDB25:0003096 ANGPT2 — ITGB1

Experimentally validated in Human; Orthology-inferred in Mouse, Rat, Frog, Zebrafish, Chicken, Macaque, Pig, Dog, Cow, Chimp, Horse, Marmoset, Sheep

Title

Journal:; Year Published:

Abstract

Angiopoietin 2 induces glioma cell invasion by stimulating matrix metalloprotease 2 expression through the alphavbeta1 integrin and focal adhesion kinase signaling pathway.

Cancer research, 2006; PubMed, Homo sapiens ANGPT2 — Homo sapiens ITGB1
ABSTRACT: Accumulating evidence reveals a significant correlation between angiopoietin 2 (Ang2) expression and tumor invasion and metastasis in various human cancers, but the major focus of recent studies has been on the angiogenic effects of Ang2. We recently reported that Ang2-stimulated glioma cell invasion results from the up-regulation and activation of matrix metalloprotease 2 (MMP-2) in tumor cells. In this study, we identify a novel mechanism by which Ang2 stimulates MMP-2 expression leading to glioma cell invasion. We show that Ang2 interacts with alpha(v)beta(1) integrin in Tie2-deficient human glioma cells, activating focal adhesion kinase (FAK), p130(Cas), extracellular signal-regulated protein kinase (ERK) 1/2, and c-jun NH(2)-terminal kinase (JNK) and substantially enhancing MMP-2 expression and secretion. The Ang2/alpha(v)beta(1) integrin signaling pathway was attenuated by functional inhibition of beta(1) and alpha(v) integrins, FAK, p130(Cas), ERK1/2, and JNK. Furthermore, expression of a negative regulator of FAK, FAK-related nonkinase, by U87MG/Ang2-expressing glioma xenografts suppressed Ang2-induced MMP-2 expression and glioma cell infiltration in the murine brain. These data establish a functional link between Ang2 interaction with alpha(v)beta(1) integrin and glioma cell invasion through the FAK/p130(Cas)/ERK1/2 and JNK-mediated signaling pathway.

Endothelial destabilization by angiopoietin-2 via integrin β1 activation.

Nature communications, 2015; PubMed, Homo sapiens ANGPT2 — Homo sapiens ITGB1
ABSTRACT: Angiopoietins regulate vascular homeostasis via the endothelial Tie receptor tyrosine kinases. Angiopoietin-1 (Ang1) supports endothelial stabilization via Tie2 activation. Angiopoietin-2 (Ang2) functions as a context-dependent Tie2 agonist/antagonist promoting pathological angiogenesis, vascular permeability and inflammation. Elucidating Ang2-dependent mechanisms of vascular destablization is critical for rational design of angiopoietin antagonists that have demonstrated therapeutic efficacy in cancer trials. Here, we report that Ang2, but not Ang1, activates β1-integrin, leading to endothelial destablization. Autocrine Ang2 signalling upon Tie2 silencing, or in Ang2 transgenic mice, promotes β1-integrin-positive elongated matrix adhesions and actin stress fibres, regulating vascular endothelial-cadherin-containing cell-cell junctions. The Tie2-silenced monolayer integrity is rescued by β1-integrin, phosphoinositide-3 kinase or Rho kinase inhibition, and by re-expression of a membrane-bound Tie2 ectodomain. Furthermore, Tie2 silencing increases, whereas Ang2 blocking inhibits transendothelial tumour cell migration in vitro. These results establish Ang2-mediated β1-integrin activation as a promoter of endothelial destablization, explaining the controversial vascular functions of Ang1 and Ang2.
Basic Information on ANGPT2
Ligand Name: angiopoietin 2
Other Symbols: Ang2
Ligand Location: secreted based on perplexity, uniprot
HGNC Gene Symbol Report: ANGPT2
GeneCards: ANGPT2
Interactions with other Receptors for ANGPT2
Basic Information on ITGB1
Receptor Name: integrin subunit beta 1
Other Symbols: FNRB, MSK12, MDF2, CD29, GPIIA
Receptor Location: cell membrane based on hpa, perplexity, uniprot
HGNC Gene Symbol Report: ITGB1
GeneCards: ITGB1
HGNC Gene Group: CD molecules, Integrins
Interactions with other Ligands for ITGB1
ADAM12 — ITGB1ADAM15 — ITGB1ADAM17 — ITGB1ADAM2 — ITGB1ADAM9 — ITGB1ANGPT1 — ITGB1CD14 — ITGB1CHAD — ITGB1COL11A1 — ITGB1COL18A1 — ITGB1COL1A1 — ITGB1COL1A2 — ITGB1COL2A1 — ITGB1COL3A1 — ITGB1COL4A1 — ITGB1COL4A3 — ITGB1COL4A4 — ITGB1COL4A5 — ITGB1COL4A6 — ITGB1COL5A1 — ITGB1CXCL12 — ITGB1F13A1 — ITGB1FBLN1 — ITGB1FBN1 — ITGB1FGA — ITGB1VEGFD — ITGB1FN1 — ITGB1HSPG2 — ITGB1ICAM4 — ITGB1LAMA1 — ITGB1LAMA2 — ITGB1LAMA4 — ITGB1LAMA5 — ITGB1LAMB1 — ITGB1LAMB3 — ITGB1LAMC1 — ITGB1LAMC2 — ITGB1LGALS3BP — ITGB1MATN1 — ITGB1MDK — ITGB1NID1 — ITGB1NPNT — ITGB1PLG — ITGB1RELN — ITGB1SEMA7A — ITGB1SPP1 — ITGB1TGM2 — ITGB1THBS1 — ITGB1THBS2 — ITGB1TIMP2 — ITGB1TNC — ITGB1VCAM1 — ITGB1VCAN — ITGB1VEGFA — ITGB1VEGFC — ITGB1VTN — ITGB1ANGPTL2 — ITGB1CCN4 — ITGB1CLEC11A — ITGB1LGALS1 — ITGB1PLA2G2A — ITGB1SPON2 — ITGB1ADAM28 — ITGB1AGGF1 — ITGB1AGRN — ITGB1ANGPTL4 — ITGB1CCN2 — ITGB1CCN3 — ITGB1CD40LG — ITGB1CDH1 — ITGB1COL10A1 — ITGB1COL11A2 — ITGB1COL13A1 — ITGB1COL4A2 — ITGB1COL8A1 — ITGB1COL8A2 — ITGB1CSPG4 — ITGB1CX3CL1 — ITGB1ICAM5 — ITGB1IL1B — ITGB1JAM2 — ITGB1L1CAM — ITGB1LAMA3 — ITGB1LAMB2 — ITGB1LGALS3 — ITGB1LGALS8 — ITGB1MFGE8 — ITGB1MIA — ITGB1NTN4 — ITGB1PLAUR — ITGB1SVEP1 — ITGB1TGFB1 — ITGB1TGFB3 — ITGB1THBS4 — ITGB1THY1 — ITGB1TIMP1 — ITGB1VWF — ITGB1