Lecture 9: Tumor Angiogenesis Flashcards

1
Q

Tumor growth beyond _____________ in diameter requires induction and maintenance of a new blood supply (Angiogenesis)

A

1-2 millimeters

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2
Q

In the absence of vascular support, tumors may become __________________. Therefore, angiogenesis is an important factor in cancer progression

A

Necrotic or apoptotic

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3
Q

Thrombosis

A

Formation of a thrombus (Blood clot) inside a blood vessel.

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4
Q

Angiogenic growth factors (Proangiogenic)

A

Class of molecules that stimulate the process of blood vessel formation
-Vascular endothelial growth factor
-Fibroblast growth factor-2
-Platelet derived growth factor
-Angiopoietins

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5
Q

Anti-angiogenic factors

A

Inhibitors of angiogenesis
-Thrombospondins
-Endostatin is a 20 kD C-term fragment of Collagen XVIII
-Angiostatin, fragment of plasminogen

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6
Q

Blood vessels are located around the ________ of cancer epithelial cells in the ________________

A
  1. Island
  2. Tumor Stroma
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7
Q

When injected into ______________ dyes leak out of the capillaries and diffuses into nearby parenchyma yielding diffusely staining of the blood vessels

A

Tumor vasculature

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8
Q

Consequence of the leakiness of tumor-associated vasculature

A

Continuous leaking of thrombin and fibrinogen molecules from the plasma into the parenchyma surrounding blood vessels leading to thrombosis. Resulting in extensive network of fibrin bundles at the border between growing cancer and stroma.

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9
Q

Cancer-associated thrombosis is __________ times more fatal for cancer patients compared to people without cancer

A

Three

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10
Q

If cancer-associated thrombosis is not treated it can break off and travel to lungs causing_______

A

-Deep vein thrombosis
-Pulmonary embolism
-Heart –> Heart attack
-Brain –> Stroke

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11
Q

2 sources of proliferation of vascular endothelial cells

A
  1. Existing vascular endothelial cells, including adjacent normal tissue
  2. Distant sites: VEGF secreted by tumor cells, fibroblasts, immune cells, and local vascular endothelial cells recruit circulating endothelial progenitor cells (EPCs) from bone marrow.
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12
Q

Alternative source for tumor vascularization

A

Transdifferentiating: Endothelial differentiation of glioblastoma stem-like cells. Glioblastoma stem-like cells become endothelial cells

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13
Q

Role of tumor-associated fibroblasts in tumor angiogenesis

A

TAFs recruit vascular endothelial precursor cells and stimulate their differentiation to increase tumor angiogenesis

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14
Q

Myofibroblasts of tumor-associated stroma express _________

A

High levels of VEGF-A, which recruits circulating EC and stimulates EC proliferation at tumor site, in the TME

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15
Q

Vascular endothelial growth factor-A

A

Growth factor expressed both on lymphoma cells and endothelial cells in angioimmunoblastic T-cell lymphoma and related to lymphoma progression

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16
Q

Conclusion of glioblastoma experiment where mice were injected with human glioblastoma cells

A

Human glioblastoma cells have stem-cell plasticity that allows these tumor cells to become endothelial. Tumor vascularization occurred via endothelial differentiation of glioblastoma stem-like cells

17
Q

Threshold of distance a tumor can be away from blood vessels so that oxygen can effectively diffuse in order for tumor growth to occur

A

0.2 mm

18
Q

Cells situated more than 0.2 mm away from blood vessels

A

Non-growing, white, hypozemic, low-pH, and necrotic.

19
Q

ZD6474

A

Inhibitor of VEGF-R2 in mice bearing human adenocarcionma xenographs.

19
Q

The necrotic regions

A

Region as close as 85 micrometers from melanoma capillary

20
Q

Cellular and structural abnormalities of tumor vasculature

A

-Excessive branching
-Leaky vessels
-Fenestrated appearance
-Loose association between pericytes and EC
-Chaotic organizations & blood flow
-Increased diameter of tumor associated capillaries
-Lack of arteriole-venule-capillary hierarchy
-High vascular density
-Lack lymphatic vasculature

21
Q

Effect of vascular density during tumor growth

A

Vascular tendency decreases leading to zones of ischemia and ultimately necrosis as tumors outgrow their blood supply

22
Q

Consequences of VEGF administration

A

Tumor microvessels became increasingly permeable after administration of VEGF

23
Q

Pericytes

A

Perivascular cells surrounding capillaries that help maintain capillary rigidity and intraluminal blood pressure.

24
Q

Pericytes in tumors

A

Endothelial cells forming the vessel lumen are only partially overlayed by pericytes and smooth muscle cells.

25
Q

Consequence of leaky blood vessels

A

Tumor cells can penetrate into circulation and metastasize to other parts of the body

26
Q

Pericytes in normal cells

A

Pericytes and smooth muscle cells cover completely the endothelial cells in normal vasculature

27
Q

Lymphatic vessel characteristics

A

Diameter far larger than capillaries. Lymphatic vessels are also not supported by pericytes and smooth muscle tissue

28
Q

2 potential attributions for lack of lymphatic vessels in tumors

A
  1. Lack of formation of these ducts
  2. Collapse and degeneration of these ducts because of the high hydrostatic pressure of solid tumors
29
Q

Normal instances of angiogenesis

A

-Embryonic development
-Wound healing
-Vascularization of endometrium
-Placental growth

30
Q

Most active form of VEGF

A

VEGF-A165

31
Q

Vascular quiescence

A

A process in normal tissues maintained by the dominant influence of endogenous angiogenesis inhibitors over angiogenic stimuli

32
Q

Clinical outcomes of angiogenesis

A

Patients with high microvessel count has a lower probability of disease-free survival in the 20 years following initial diagnosis

33
Q

Angiogenic switch activators

A

-VEGF-A
-VEGF-B, C
-FGF1
-FGF2

34
Q

Angiogenic switch inhibitors

A

-Thrombospondin-1.-2
-Interferon a/B
-Angiostatin
-Endostatin
-Collagen IV fragments

35
Q

SU6668

A

PDGF receptor inhibitor

36
Q

SU5416

A

VEGF-R inhibitor

37
Q

Avastom/Bevacizumab

A

Monoclonal antibody of VEGF that would extend life <5 months. Eventually withdrew by FDA.

38
Q

DC101

A

Monoclonal antibody against VEGF-R2