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Angiogenesis. Key features of angiogenesis 1)Tumour growth is angiogenesis-dependent 2)Microvascular endothelial cells (ECs) are genetically-stable 3)ECs.

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Presentation on theme: "Angiogenesis. Key features of angiogenesis 1)Tumour growth is angiogenesis-dependent 2)Microvascular endothelial cells (ECs) are genetically-stable 3)ECs."— Presentation transcript:

1 Angiogenesis

2 Key features of angiogenesis 1)Tumour growth is angiogenesis-dependent 2)Microvascular endothelial cells (ECs) are genetically-stable 3)ECs release angiogenic factors that stimulate proliferation

3 (a)Nascent vessels consist of a tube of ECs, which mature into specialized capillaries, arteries and veins. (b) Capillaries consist of ECs surrounded by basement membrane and a sparse layer of pericytes embedded within the EC basement membrane. Capillary endothelial layer can be continuous (muscle), fenestrated (kidney/ endocrine glands) or discontinuous (liver sinusoids). The endothelia of the blood-brain barrier or blood-retina barrier are further specialized to include tight junctions, and are thus impermeable to various molecules. (c) Arterioles and venules have an increased coverage of mural cells compared with capillaries. Composition of nascent and mature blood vessel walls

4 Steps in network formation and maturation during embryonic (physiological) angiogenesis

5 Key differences in tumour vasculature Different flow characteristics or blood volume Microvasculature permeability Increased fractional volume of extravascular, extracellular space

6 Steps in network formation and maturation during tumour angiogenesis

7 Cellular mechanisms of tumour angiogenesis (1) host vascular network expands by budding of endothelial sprouts or formation of bridges (angiogenesis); (2) tumour vessels remodel and expand by the insertion of interstitial tissue columns into the lumen of pre-existing vessels (intussusception); and (3) endothelial cell precursors (angioblasts) home from the bone marrow or peripheral blood into tumours and contribute to the endothelial lining of tumour vessels (vasculogenesis) (4) Lymphatic vessels around tumours drain the interstitial fluid and provide a gateway for metastasizing tumour cells. 1 2 3 4 1 2 3 4

8 Cellular angiogenesis-overview Nature Reviews Drug Discovery 1, 415-426 (2002)

9 Balance between inhibitory factors and angiogenic factors Inhibitory – endostatin, angiostatin, thrombospondin Angiogenic - VEGF, bFGF, PDGF Tumour cells release pro-angiogenic factors which activate receptors (VEGFR) also stimulates secretion and activation of MMPs which degrade the basement membrane This allows activated endothelial cells (ECs) to migrate towards tumour, helped by integrins ECs deposit a new basement membrane and secrete growth factors such as platelet-derived growth factor (PDGF), which attract supporting cells to stabilize the new vessel. VEGF – Vascular Endothelial Growth Factor bFGF - basic Fibroblast Growth Factor MMPs – Matrix MetalloProteinases PDGF – Platelet-Derived Growth Factor Cellular angiogenesis-overview

10 Metastasis

11 Invasion & Metastasis 1 4 3 2 5 6 Red: E-CadherinsGreen: Integrins

12 Integrins – the velcro of the cell The cell moves by "ruffling" it's membrane. This is done by a series of actin fibers, whose function is controlled by the integrins. These fibers cause the cell membrane to move in certain directions, and the integrins attach to the matrix as this happens, pulling the cell along a micrometer at a time The cell moves by "ruffling" it's membrane. This is done by a series of actin fibers, whose function is controlled by the integrins. These fibers cause the cell membrane to move in certain directions, and the integrins attach to the matrix as this happens, pulling the cell along a micrometer at a time

13 Invasion & Metastasis Red: E-CadherinsGreen: Integrins

14 Epithelial-mesenchymal transition (EMT) necessary for invasiveness

15 Then why do secondary tumours histopathologically resemble primary tumours? EMT induced by stromal signals EMT may be reversible depending on the stromal signals e.g. TGF- TNF-, EGF, HGF, IGF-1.

16 Stromal signals that trigger EMT

17 Cell invasiveness controlled by Matrix Metalloproteinases (MMPs) MMPs secreted by stromal cells MMPs secreted by stromal cells Can be PM-bound or soluble enzymes Can be PM-bound or soluble enzymes MMP activation can be indirect E.g. via urokinase plasminogen activator (uPA) MMP activation can be indirect E.g. via urokinase plasminogen activator (uPA)

18 Cell motility regulated by RhoGTPases Binary switches like Ras Binary switches like Ras 3 sub families; Rho, Rac and cdc42 3 sub families; Rho, Rac and cdc42 Serum- starved Lysophosphatidic acid Overexpressing Rac GEF

19 Metastatic cells travel via lymphatic systems

20 Colonisation depends on a variety of factors metastatic tropisms (Pagets seed & soiltheory)

21 Colonisation depends on complex interactions between metastasising cells and their microenvironments E.g Osteolytic metastasis initiated by breast cancer

22 Breast cancer initiated osteolytic metastasis Bone growth versus loss

23 Reading Chapter 13 and 14 : Biology of Cancer by R Weinberg AND /OR Chapter 12: Cancer Biology by RJB King Angiogenesis in cancer and other diseases by P Carmeliet & RK. Jain Angiogenesis in cancer and other diseases by P Carmeliet & RK. Jain Nature vol 407 14 september 2000 pp 249


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