Tumour Suppressor Genes (FS Week 8) Flashcards

1
Q

What is the difference between targeted therapies and chemotherapy

A

targeted therapy cancer drugs block the growth and spread of cancer by interfering with specific molecules that are involved in growth, progression and spread of cancer

Chemotherapy is a range of anti-cancer drugs that are used to prolong life and reduce symptoms

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2
Q

What is a tumour suppressor gene

A

they encode proteins that maintain the checkpoints in the cell cycle and control genome stability

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3
Q

How do TSGs inhibit proliferation and replication of damaged cells

A
  • repair damaged DNA (MLH1, BRCA1,2)
  • apoptosis (TP53)
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4
Q

What is the knudson two-hit hypothesis

A

that most TSGs need both alleles to be inactivated either through mutations or epigenetic silencing to cause a phenotypic change

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5
Q

Why do heritable cancers develop

A

they develop after there is an additional loss of a normal functioning allele there is a loss of heterozygosity (one allele was already mutated for which they inherited)

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6
Q

Name the 3 tumour suppressor genes

A
  1. BRCA1,2
  2. TP53
  3. RB1
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7
Q

What is the function of a TSG

A

they are oncogene antagonists

they block the proliferation and cell cycle

DNA repair

induce apoptosis

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8
Q

What are the pathways of BRCA1,2

A
  • removal of DNA lesions
  • tolerance to DNA damage
  • protection from errors of incorporation made during DNA replication
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9
Q

What cancers are associated with BRCA mutations

A
  • breast
  • ovarian
  • male breast cancer
  • prostate
  • pancreatic
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10
Q

What is meant by ‘synthetic leathality’

A

a type of genetic interaction where the combination of two genetic events result in cell death/death of an organism

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11
Q

What is a PARP enzyme

A

a critical enzyme involved in DNA repair

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12
Q

Describe an example of synthetic leathility

A

PARP inhibitors prevent PARP function of repairing single strand DNA. Cells that have a mutated BRCA1,2 gene as well means that double strands of DNA is not repaired - this can lead to cell death

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13
Q

What is TP53

A

is a gene that instructs cells to produce tumour protein P53 which acts as a tumour suppressor so cells don’t divide in an uncontrolled manner

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14
Q

What regulates P53 in a negative feedback loop

A

MDM2 regulates P53 levels which induces MDM2 levels (negative feedback)

by inhibiting transcriptional activity and trigger degradation

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15
Q

What is Li-Fraumani syndrome

A

it is a hereditary genetic condition caused by a mutation in TP53 which is a genetic blueprint for p53

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16
Q

What small molecules can restore wild-type p53

A
  • MIRA-1
  • PRIMA-1
17
Q

What is retinoblastoma

A

it is cancer of the retina

18
Q

How does the Rb gene cause retinoblastoma

A

mutations in the RB1 germline

it happens due to a second hit (somatic mutation) in the RB1 gene