4. External factors controlling division and behaviour of normal and cancerous cells Flashcards

1
Q

Recall the 3 broad categories of external factors influencing cell division

A
  1. Growth factors
  2. Cell-EM adhesion
  3. Cell-cell adhesion
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2
Q

Describe the theory of “density-dependent cell division”

A

At high density, ells compete for growth factors - supercedes theory of contact inhibition somewhat

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3
Q

By what mechanism do growth factors trigger cell division

A

Trigger ERK cascade

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4
Q

How is a strong and sustained stimulus for the ERK cascade maintained?

A

GFs and cell-ECM adhesion will both trigger it, so they work synergistically

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5
Q

Why are signalling pathways involving GFs often implicated in cancer?

A

Cancerous cells lose:

  1. density-dependency
  2. Contact-inhibition
  3. Anchorage-dependency
  4. Cell-cell contacts
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6
Q

Describe the concept of anchorage-dependency

A

Cells cannot respond to GFs unless they are both adhered and spread on a surface

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7
Q

Summarise cell-anchorage

A
Settles on surface
Spreads across
Acquires polarity
Becomes motile
All has ATP requirement
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8
Q

What characteristic is essential for cells to spread on? What molecule most frequently performs this function?

A

Must be adhesive

Fibronectin will stick to most cells

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9
Q

What is the key characteristic of a cell-ECM adhesion molecule

A

Mechanically continuous with cytoplasm so an intracellular signalling pathway can be initiated by association with cytoskeleton

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10
Q

What is the key adhesion molecule in cell-signalling?

A

Integrins

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11
Q

Describe the structure of the integrin family

A

Heterodimers
alpha and beta subunits
20 known combos

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12
Q

How do integrins usually interact in their extracellular domain?

A

Recognise short, specific peptide sequences eg RGD

RGD is found in many molecules including fibrinogen and fibronectin

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13
Q

Summarise the interaction of integrins in their intracellular domain

A

With just one exception, interact with actin cytoskeleton via ABPs
Binding causes integrin complex to cluster and form focal adhesions

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14
Q

Which integrin does NOT interact with the actin cytoskeleton?

A

Cytokeratin-binding integrin (epithelial hemidesmosomes)

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15
Q

In inflammation, what may integrins bind to extracellularly?

A

ICAM-1

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16
Q

Summarise outside-in signalling

A

ECM:integrin complex triggers signal inside cell triggering conformational change
May influence phenotype and differentiation of the cell

17
Q

Describe an experiment that can show the effect of outside-in signalling

A

When mammary epithelium is cultured on T1 collagen it does not become secretory, but on BM matrix the cells organise into “organoids” and produce milk

18
Q

Summarise !inside-out” signalling

A

Signal produced inside cell affects affinity of integrin for ECM binding

19
Q

Give an example of inside-out signalling

A

Hormone acting on an intracellular receptor

20
Q

Removal of what factor is most likely to lead to cell-cell junction breakdown?

A

Ca++

21
Q

What is the result of sustained interactions between cells?

A

Cell-cell junction formed

22
Q

Describe the relationship between proliferation rate and cell-cell junctions

A

Junctions:
Present = low proliferation (MAPK inactive)
Absent = high proliferation (MAPK activated)

23
Q

In what sort of cells is contact-inhibition demonstrated?

A

Non-epithelial

24
Q

What is the function of adherens junctions?

A

Master junctions - control formation of other junctions

25
Q

What are adherens junctions composed of?

A

Cadherin and catenins

26
Q

What is cadherin?

A

Ca++-dependent cell-adhesion molecule

27
Q

Recall the pathway that leads to a signal being generated by a master junction being formed

A

Cadherin binds intracellularly to beta-catenin, which in turn binds alpha-catenin and links the actin cytoskeleton to generate a signal

28
Q

What is the function of beta-catenin?

A

Intracellular 2nd messenger for adherens junctions

29
Q

Describe the metabolism of beta-catenin

A

Rapidly degraded in cytoplasm

30
Q

What is the consequence of beta-catenin buildup?

A

When bound to cadherin it is unavailable for LEF-1 binding
However
When it builds up in the cytoplasm, it can bind to LEF-1 –> TF production and subsequent proliferation

31
Q

Describe the 2 mechanisms of contact-inhibition

A
  1. Beta-catenin bound to cadherin so unavailable for LEF-1 binding, cell not stimulated to proliferate
  2. Cadherin clustering activates Ras superfamily, which influence proliferation - cell-cell contacts can inhibit activation