Tumour supressor genes Flashcards

1
Q

how does p53 work

A

when the DNA is damaged it acts as a transcription factor and makes proteins for cell cycle arrest e.g. p21

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2
Q

what is p21 and what does it do?

A

it is a protein that causes cell arrest by inhibiting CDKs and cyclins

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3
Q

what other proteins does p53 make

A

proteins for DNA repair so when the cell is arrested it can repair its DNA, proteins for apoptosis incase cell cannot repair itself

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4
Q

what happens when p53 is inactivated

A

no proteins for cell arrest, repair or apoptosis. cell therefore goes into cell cycle and surpass checkpoints

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5
Q

what do TSGs do

A

act as a brake to stop healthy cells becoming cancerous by inhibiting cell division, repairing DNA or apoptosis

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6
Q

what is p120 (GAP) and what does it do

A

it is a GTPase activating protein that inactivates ras

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7
Q

what is neurofibromin 1 (NF1) and what does it do

A

a mutant form of p120 (GAP) that fails to inactivate ras-GTP signalling

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8
Q

what is the two hit hypothesis

A

both copies of TSGs must be mutated for a cell to be considered cancerous

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9
Q

what is loss of heterozygosity (LOH)

A

loss of one parents contribution to the cell, allowing the expression of the recessive mutation is TSGs

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10
Q

allelic imbalance

A

heterozygous somatic cells become homozygous as an allele is lost

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11
Q

what can allelic imbalance lead to

A

inactivation of the secondary TSG - 2 hit hypothesis

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12
Q

6 stimulators of p53

A
  1. lack of nucleotides
  2. UV
  3. ionising radiation
  4. oncogene signalling
  5. hypoxia
  6. blockage of transcription
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13
Q

what can cell cycle arrest lead to (2)

A

senescence or return to proliferation

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14
Q

4 functions of p53

A
  1. cell cycle arrest
  2. DNA repair
  3. block angiogenesis
  4. apoptosis
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15
Q

why can mice be used for drug discovery

A

they have a similar genome to humans

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16
Q

how many molecules of p53 are needed for it to function

A

4 - tetramer

17
Q

how is p53 protein stability mediated

A

post translational modifications

18
Q

how is p53 degraded

A

by binding mdm2 that targets it for ubiquitylation

19
Q

p53 half life in tumours

A

it is increased by inhibition of mdm2-mediated p53 degradation

20
Q

how is the binding between p53 and mdm2 inhibited

A

phosphorylation

21
Q

what does ARF do

A

prevents nuclear export of mdm2, no p53 degradation

22
Q

how do you inhibit mdm2 mediated degradation of p53 (4)

A
  1. nuclear exclusion
  2. interaction with viral proteins
  3. interaction with overexpressed mdm2 protein
  4. inactivation of ARF, this sequesters mdm2 to the nucleus preventing p53-Ub’n in the cytosol
23
Q

what causes p53 to be upregulated after DNA is damaged

A

DNA damage results in ATM and ATR kinases being activated so p53 is upregulated and there are more p53-mdm2 complexes and therefore more active p53

24
Q

p53 target genes - in cell cycle

A

p21

25
Q

p53 target genes - DNA repair

A

PCNA and XPC

26
Q

p53 target genes - apoptosis

A

Bax, FASR, PUMA

27
Q

targetting p53 in cancer - novel chemo

A

small molecules used to turn mutated into the original protein, downstream genes then activated as normal

28
Q

targetting p53 in cancer - gene therapy

A

research shows that mice that over express p53 are resistant to tumour formation BUT age prematurly

29
Q

4 more ways of targetting p53 in cancer

A
  1. mutant adenovirus
  2. target mutant p53
  3. stimulate immune response to mutant p53
  4. drugs that disrupt the interaction between p53 and mdm2 or E6 proteins
30
Q

why don’t we like p53 degradation

A

no stopping of the cell cycle so therefore uncontrolled cell division

31
Q

what does E6 do to p53

A

forms a complex and degrades it

32
Q

what protein in cells infected by adenoviruses shuts down p53

A

E1b

33
Q

what gives rise to variants of p53

A

splicing

34
Q

what is conserved in p73

A

residues within the central domain that are frequently mutated in p53