Genetic Predisposition to Cancer Flashcards

1
Q

What causes cancer?

A
  • chance
  • environmental factors
  • inherited predisposition
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Somatic vs Germline mutations

A
  • Somatic mutations occur in non-germline tissues and are nonheritable.
  • Germline mutations are present in egg or sperm and are heritable. They cause cancer family syndromes.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What is a proto-oncogene?

A

Normal genes that code for proteins to regulate cell growth and differentiation

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

How does a proto-oncogene become an oncogene?

A

by mutation

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

What do oncogenes do?

A
  • accelerate cell division

- can cause cancer if stuck in ‘on’ mode

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What are tumour suppressor genes?

A

Genes that inhibit the cell cycle or promote apoptosis. They act as the cell’s brakes for cell growth.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

What are DNA damage-response genes?

A

the repair mechanics for DNA

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

How does cancer arise from DNA damage-response genes?

A

Cancer arises when both genes fail, speeding the accumulation of mutations in other critical genes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What does HNPCC result from?

A

Failure of mismatch repair (MMR) genes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

What does failure of MMR lead to?

A

Microsatellite Instability (MSI)=addition of nucleotide repeats

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What does MMR do?

A

MMR corrects errors that spontaneously occur during DNA replication like single base mismatches or short insertions and deletions.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

What evidence is there that MMR is not functioning normally?

A

MSI is the phenotypic evidence

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What happens to cells with abnormally function MMR?

A

Thy tend to accumulate errors as novel microsatellite fragments (simple sequence repeats, SSR) are created

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

What is an example of an autosomal recessive syndrome?

A

MYH polyposis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

What are other causes of cancer?

A
  • autosomal recessive disorders

- multiple modifier genes of lower genetic risk

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What is a De Novo mutation?

A

A new mutation which occurs in the germ cell of a parent. There is no family history of hereditary cancer syndrome.

17
Q

What are 3 conditions in which de novo mutations are common in?

A
  • Familial adenomatous polyposis
  • Multiple endocrine neoplasia 2B
  • Hereditary retinoblastoma
18
Q

What is retinoblastoma?

A

The most common eye tumour in children which occurs in heritable and nonheritable forms

19
Q

What are the risk factors involved in breast cancer? (8)

A
  • ageing
  • family history
  • early menarche
  • late menopause
  • nulliparity
  • estrogen use
  • dietary factors
  • lack of exercise
20
Q

What genes can cause hereditary susceptibility to breast cancer?

A
  • BRCA1
  • BRCA2
  • TP53
  • PTEN
  • Undiscovered genes
21
Q

What are the functions of the BRCA1 gene?

A
  • checkpoint mediator
  • DNA damage signalling and repair
  • chromatin remodelling (inactive X chromosome)
  • transcription (not essential for this)
22
Q

What is the function of the BRCA2 gene?

A

DNA repair by homologous recombination

23
Q

What are the associated cancers of BRCA1?

A
  • breast cancer
  • secondary breast cancer
  • ovarian cancer
  • possible increased risk of other cancers
24
Q

What are the associated cancers of BRCA2?

A
  • breast cancer
  • male breast cancer
  • ovarian cancer
  • increased risk of prostate, laryngeal and pancreatic cancers
25
What are the risk factors associated with colorectal cancer?
- ageing - personal history of CRC or adenomas - high fat, low fibre diet - inflammatory bowel disease - family history of CRC
26
What syndromes are associated with CRC?
- non-polyposis (few to no adenomas) | - polyposis (multiple adenomas)
27
Give an example of a non-polyposis syndrome.
Hereditary non-polyposis colon cancer aka Lynch syndrome- CRC &/or endometrial cancer
28
Give 3 example of polyposis syndromes.
- Familial adenomatous polyposis- severe colonic polyposis - attenuated FAP- less severe colonic polyposis - MYH associated polyposis- varying degrees of colonic polyposis
29
What are the clinical features of HNPCC?
- early but variable age at CRC diagnosis - tumour site throughout colon - extra colonic cancers: endometrium, ovary, stomach, urinary tract, small bowel, bile ducts, sebaceous skin tumours
30
What are the clinical features of FAP?
- estimated penetrance for adenomas >90% - risk of extra colonic tumours (upper GI, desmoid, osteoma, thyroid, brain, othere) - CHRPE may be present (congenital hypertrophy of retinal pigment epithelium) - 100% risk of cancer if untreated
31
What are the clinical features of AFAP?
- later onset - few colonic adenomas - not associated with CHRPE - upper GI lesions - associated with mutations at 5' and 3' ends of APC gene
32
What are the clinical features of MYH polyposis?
- similar clinical GI features to AFAP - common mutations in mut-MYH gene - recessive inheritance
33
What may multiple modifier genes of lower genetic risk explain?
- families with history of cancer and no identified mutation | - differences in cancer penetrance in families with same mutation
34
How can cancer risk in adenomatous polyposis syndromes be managed?
- surveillance - surgery - chemoprevention