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Inducing Angiogenesis
Oct 31, 2017
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Hallmarks of Cancer, 2011
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Angiogenesis -the process of forming new blood vessels from pre-existing ones by growth and migration of epithelial cells -Common during embryogenesis but not in adults (wound healing) -diffusion limit of oxygen ( um)
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Necrosis Cells within the core of the tumor that do not receive oxygen or nutrients undergo cell death or necrosis
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Blood Vessel Structure
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Cancer vs. Wound Healing
Cancer Wound Healing Neovasculature Leaky allowing cells Not leaky to enter Molecular markers Integrins are Normal level of upregulated Integrins Extracellular matrix Angiogenic markers Different markers
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Angiogenic Switch Angiogenic Inhibitors Angiogenic Inducers
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Angiogenic Switch Result: Angiogenesis Angiogenic Inhibitors
Angiogenic Inducers Result: Angiogenesis
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Angiogenic Inducers and Inhibitors
Inhibitors Inducers Angiostatin VEGF Endostatin FGF Prolactin HGF p53 EGF Thrombospondins PDGF
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Angiogenic Inducers VEGF and VEGF Receptor -Initiation of Angiogenesis
Angiopoietins and Tie Receptor -Vessel Maturation Ephrins and Ephrin Receptor
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VEGF Family -5 members -VEGF-A to D -PlGF (Placental Growth Factor)
-3 Receptors -VEGFR-1, 2 and 3 -VEGF-A and VEGFR-2 are major players -VEGFR-1 acts as a decoy competing with VEGF-R2 -weak kinase activity -VEGFR-3 and VEGF-C are involved with development of the lymphatic system
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VEGF-A -Secreted by tumor cells
-Secretion by neighboring non-transformed cells -Induced by the tumor cells -Stores of VEGF-A in the Extracellular matrix released by metalloproteinases (MMP) -proteases whose catalysis involves a metal ion Functions of VEGF-A Promote endothelial cell proliferation Induce permeability and leakage in existing blood vessels -important for new blood vessel formation
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VEGF-A Signaling Pathway
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EGF Signaling Pathway
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VEGF-A Responsive Genes
EGFR ligand Epiregulin (EGF family member) COX2, a cyclooxygenase involved with prostaglandin formation MMP1 and MMP2
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Metalloproteinases
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Metalloproteinases
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Angiogenic Inhibitors
1. Angiostatin 2. Endostatin 3. Thrombospondin-1
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Angiostatin Stored as an inactive molecule within another molecule, Plaminogen Angiostatin binds to Annexin II to cause inhbition Cleavage
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Angiostatin Stored as an inactive molecule within another molecule, Plaminogen Angiostatin binds to Annexin II to cause inhbition
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Endostatin -Fragment of Collagen XVIII
-Endostatin will block MMPs and MAPK
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Concomitant Resistance
A tumor is removed and dominant metastases are often activated Inhibition of micrometastases by Angiogenesis inhibitors from the tumor Once the tumor is removed the inhibitory signal is lost and there is also an increase in growth factors Angiostatin Endostatin
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Angiogenic Switch Oxygen Sensor
-HIFα and HIFβ are constitutively expressed -HIFα and HIFβ ativity is regulated by oxygen concentration -von Hippel-Lindau (VHL) tumor suppressor protein, a ubiquitin ligase Hypoxia Response Element
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Oncogenic Proteins ~30 oncoproteins promote angiogenesis
Growth factors -Stimulate growth of tumor cells, autocrine -Stimulate growth of endothelial cells, paracrine Receptor Tyrosine kinases (EGFR) Intracellular tyrosine kinases (Src) Intracellular transducers (Ras) Transcripition factors (Fos and Jun)
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Tumor Suppressor Proteins
Thrombospondin-1 prevents VEGFR Activation
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Angiogenic Sprouting -Filopodia extend from endothelial cells towards the VEGF signal -VEGF-A/VEGFR-2 becomes activated -Signal is enhanced by Nrp1, a co-receptor
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Angiogenic Sprouting -Filopodia extend from endothelial cells towards the VEGF signal -VEGF-A/VEGFR-2 becomes activated -Signal is enhanced by Nrp1, a co-receptor
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Angiogenic Sprouting -Tip cells induce expression of Notch (DLL-4) and its release -Notch binds to its receptor on neighboring cells -Notch Receptor Intracellular domain (NICD) is released and is transported to the nucleus to repress VEGFR-2 and turns on VEGFR-1
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Angiogenic Sprouting -Notch Receptor Intracellular domain (NICD) is released and is transported to the nucleus to repress VEGFR-2 and turns on VEGFR-1 -VEGFR-1 acts as a VEGF trap, reducing VEGF concentration and reducing VEGFR-2 activation -The growing sprout moves along the VEGF gradient
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Angiogenic Sprouting
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Angiogenic Sprouting -When 2 tips meet, they fuse, connecting the lumen and allowing blood flow
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