Inherited Predisposition to Cancer Flashcards

1
Q

What are inherited cancer predispositions?

A

An inherited increase in the risk of developing a disease

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2
Q

Is inherited cancer predisposition common?

A

No it is rare with only approx 4% of cancers associated with genetic predisposition

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3
Q

What are the characteristics of cancers with an inherited predisposition?

A
  • Family history of (same) cancer
  • Early age of onset (especially childhood)
  • Multiple cancers in one individual
  • High occurrence of rare cancer
  • Premalignant conditions (eg polyps)
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4
Q

What is a cancer predisposition gene?

A
  • Genes in which rare mutations confer >2x relative risk of cancer
  • At least 5% of individuals with relevant mutations develop cancer
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5
Q

How many cancer predisposition genes are there?

A

114 across the genome affecting every chromosome apart from chromosome 20

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6
Q

What type of genes are cancer predisposition genes?

A
  • 103 are TSGs
  • 11 are activated by mutations
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7
Q

What are the inheritance patterns of the cancer predisposition genes?

A
  • 65 autosomal dominant
  • 28 autosomal recessive
  • 16 both autosomal dominant and recessive
  • 5 sex linked
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8
Q

What is retinoblastoma?

A
  • Eye cancer in children
  • Affects 1 in 20,000 children
  • 90% cases present in children <5
  • Caused by mutation to TSG RB1
  • Can be sporadic or familial
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9
Q

What is the difference in hits between non-hereditary and hereditary cancers

A

Non-hereditary require 2 hits both by mutation whereas hereditary already contains a hit which has been passed down so it only requires 1 more hit

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10
Q

What type of inheritance is predisposition?

A

It is inherited as dominant so a hit is in one allele but tumour development requires both alleles to be hit

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11
Q

What is Li-Fraumeni syndrome?

A
  • Rare inherited predisposition to a range of cancers
  • Only diagnosed if the patient had sarcoma before 45 yrs old and has a relative with any cancer before 45 yrs old or a sarcoma at any age
  • 50% risk of developing cancer by 40
  • 90% risk of developing cancer by 60
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12
Q

How can patients be clinically managed?

A
  • genetic testing to identify carriers
  • surveillance to detect cancers early
  • MRI, blood tests, ultrasounds etc
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13
Q

Give 2 examples of cancer predispositions cased by mutations to TSGs

A

Retinoblastoma and Li Fraumeni syndrome

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14
Q

How common is breast cancer?

A
  • 20% of all new cancer cases
  • Affects 1 in 10 women, 1 in 100,000 men
  • Average age of onset is approx 60
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15
Q

Is breast cancer sporadic?

A
  • Approx 75-80% of breast cancer is sporadic
  • Somatic mutations are acquired over a lifetime
  • There is no increased risk to family members beyond general population risk
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16
Q

Is breast cancer familial?

A
  • Only approx 10-15% of breast cancer is familial
  • Characterised by an unclear inheritance pattern
  • Generally not eligible for genetic testing
17
Q

What are the characteristics of hereditary breast cancer?

A
  • 5-10% of BRCA mutations are associated with an inherited predisposition
  • younger age of onset (before menopause)
  • higher prevalence of bilateral breast cancer
  • associated tumours in family members
  • dominant inheritance pattern
  • increased risk in BRCA1 compared to BRCA2 mutation
18
Q

What are the cellular functions of BRCA1/2?

A
  • chromosome integrity
  • repair ds breaks in DNA
  • reactivate stalled DNA replication forks
  • resolve R loops during transcription
19
Q

How many other breast cancer predisposition genes are there?

A

Approx 100 other genes that focus mainly on DNA repair and genome integrity