metastasis Flashcards

1
Q

metastatis

A

pressure on and destruction of adjacent tissue

obstruction of flow (e.g. malignant tumour of the colon causing intestinal obstruction)

production of hormones (e.g. adrenocorticotropic hormone [ACTH] and vasopressin [ADH] from some lung tumours)

other paraneoplastic effects (eg cachexia)

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2
Q

metastatic cascade

A
  1. reduced cell-cell adhesion
  2. altered cell-substratum adhesion
  3. increased motility
  4. increased proteolytic ability
  5. ability to intravasate and
    extravasate
  6. angiogenic ability
  7. ability to proliferate
    (locally & ectopic sites)

invasion, intravasation, transport, extravasation, colonisation, angiogenesis

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3
Q

tumour cell invasion

A
  1. reduced cell-cell adhesion
  2. altered cell-substratum 3. adhesion
  3. increased motility
    increased proteolytic ability
    ability to intravasate &
    extravasate
    ability to proliferate
    angiogenisis
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4
Q

epithelial cells

A

cohesive interactions among cells, forming continuous cell layers

three membrane domains: apical, lateral and basal

presence of tight junctions between apical and lateral domains

polarised distribution of cell components

lack of mobility with respect to their local environment

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5
Q

mesenchymal cells

A

loose or no interactions between cells

no clear apical/basolateral membranes

no cell-cell junctions

no apicobasal polarised distribution of organelles/cytoskeleton

motile cells that may have invasive properties

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6
Q

epithelial- mesenchyme transition, EMT

A

process in which epithelial cells lose their characteristic polarity, disassemble cell-cell junctions and become more migratory

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7
Q

e- cadherin

A
  • adherent junction
  • ca ++ dependent homotypic binding
  • beta and alpha catenin
  • actin cytoskeleton
  • aberrant e-cadherin expression in human tumours:
    e-cadherin———-> n- cadherin (no cell-cell glue), no junctions keeping cell together
  • most carcinomas have reduced/no e-cadherin
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8
Q

integrins

A
  • cell- ECM junction
    -Component of focal adhesions
    found in basal epithelial cells & in focal adhesions of migrating cells
    -Altered integrin expression
    is frequently detected in tumours
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9
Q

increased proteolytic activity

A

Proteases expressed by both tumour and stroma
Facilitate: a. invasion of ECM at primary & secondary sites
b. digestion of endothelial BM
c. angiogenesis
d. activate proteases

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10
Q

serine proteases

A

Urokinase plasminogen activator (uPA) -> plasmin
Plasmin activates MMPs & degrades ECM

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11
Q

matrix metalloproteinases

A

MMP-2 degrades type IV collagen

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12
Q

cysteine proteases

A

Cathepsin K collagenolytic activity -> matrix degradation

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13
Q

modes of tumour spread- lymphatic spread

A
  • Common mode of spread of carcinomas,
    e.g. breast, colon, lung
    Travel to draining lymph nodes,
    e.g. from breast cancer to axillary LNs
    Thereby to thoracic duct and systemic blood circulation
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14
Q

modes of tumour spread- haematogenous spread

A

Common mode of spread of sarcomas
Also some carcinomas, e.g. kidney, colorectum, prostate

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15
Q

modes of tumour spread- transcoaelomic spread

A
  • across the peritoneal cavity
  • incidence higher with tumours that arise from the peritoneal cavity, e.g., ovarian (up to 70 % of patients at presentation) and colorectal (up to 28 % of patients at presentation)
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16
Q

intravasation

A

Intravasation:
Attachment
Degrade BM
diapedesis
New blood vessels are leaky
Assisted by tumour-associated
macrophages: chemotactic signals

17
Q

transport of tumour cells

A

Most tumour cells do not survive
shear stress of blood flow
immune detection

18
Q

extravasation

A

Attachment
Degrade BM
diapedesis
blood vessels structurally sound
Similar mechanism used by WBCs

19
Q

angiogenesis

A

new vessels are generated from existing vasculature

Tumours (both benign & malignant) need oxygen and nutrients
to survive

A tumour cell >1 mm from a capillary will become hypoxic

20
Q

angiogenesis process

A

low oxygen, HIF transcription factor binds to VEGF
signals production of new blood vessels,
migration- interns
sprout formation- proliferation
invasion- proteases

21
Q

seed and soil hypothesis

A

Metastasis is selective for cells that are capable of invasion, survival, intra/extravasation and proliferation at distant sites.

The success of metastatic colonisation is dependent on the interaction of tumour and the tumour microenvironment

22
Q

cancer- associated fibroblasts

A

secrete MMPs cytokines IL-8 and VEGF

23
Q

pericyte

A

low pericyte coverage -> leaky vessel structure -> facilitating tumour cell invasion/extravasion

24
Q

immune inflammatory cells

A
  • macrophages, neutrophils, mast cells
  • Tumour-associated macrophages produce growth factors and MMPs to promote angiogenesis, cell invasion
    and intravasation