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Flashcards in Causes of cancer Deck (53)
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1
Q

What are the 5 ways of identifying human carcinogens?

A

1) Geographical variation in risk - studies in migrant populations
2) Occupational exposure
3) Accidental exposure
4) Big epidemiological surveys
5) Laboratory experiments

2
Q

What are the categories of carcinogens? 6

A

1) Chemicals eg. PAHs, nitrosamines
2) Infectious agents eg. HPV, H pylori
3) Radiation eg. UV light, radon
4) Minerals eg. asbestos, heavy metals
5) Physiological eg. oestrogen, androgens
6) Chronic inflammation - free radicals and growth factors

3
Q

Aflatoxin targets what tissue?

A

Liver

4
Q

Alcohol targets what 4 tissues?

A

Pharynx, larynx, oesophagus, liver

5
Q

Asbestos targets what tissue?

A

Lung pleura

6
Q

X-rays target what tissue?

A

Bone marrow (leukaemia)

7
Q

UV light targets what tissue?

A

Skin

8
Q

Oestrogen targets what tissue?

A

Breast

9
Q

Tobacco smoke targets what 6 tissues?

A

Mouth, lung, oesophagus, pancreas, kidney, bladder etc.

10
Q

HBV targets what tissue?

A

liver

11
Q

HPV targets which tissue?

A

Cervix

12
Q

What is meant by the term carcinogen?

A

Any agent that significantly increases the risk of developing cancer

13
Q

What is the difference between initiator, promotor and complete carcinogens?

A

Initiators are genotoxic i.e. can chemical modify or damage DNA
Promotors are non genetic and induce proliferation and DNA replication
Complete carcinogens can do both

14
Q

Name a complete carcinogen?

A

UV light

15
Q

What 2 things does mutation indiction (initiation) require?

A

Chemical modification of DNA
Replication of modified DNA and mis-incorporation by DNA polymerase - requires 2 rounds of replication for a mutations to be fixed

16
Q

The presence of what in the DNA exacerbates the tendency of polymerase to make mistakes?

A

Chemical modifications - miscoding or non-coding adducts or lesions

17
Q

In which 2 ways do promotor carcinogens contribute to carcinogenesis?

A

1) They can stimulate the 2 rounds of DNA replication required for mutation fixation
2) Secondly they can stimulate clonal expansion of mutated cells, which enables the accumulation of further mutations

18
Q

Why is clonal expansion of a cell with 1 mutation so important in carcinogenesis?

A

To form a malignant cell need 2-8 specific mutations, very hard for a cell to acquire these without significant clonal expansion

19
Q

Give 2 examples of endogenous mutagens?

A

1) Oxygen radicals

2) Lipid metabolism byproducts

20
Q

Describe the process of initiation, promotion and progression using a mouse model skin tumour?

A

1) Genotoxic initiating agent damages DNA
2) Promoting agent fixes the damage as a mutation and converts normal calls into mutant initiated cell
3) Promoting agent stimulates clonal expansion of initiated cells to produce papillomas
4) Further rounds of mutations and clonal expansion allows papilloma to progress to carcinoma

21
Q

Give the 7 common genetic abnormalities?

A

1) Base pair substitution
2) Frameshift
3) Deletion
4) Gene amplification (having up to a hundred copies of a gene it would normally only have 2 copies of)
5) Chromosomal translocation
6) Chromosomal inversion
7) Aneuploidy

22
Q

What is meant by a TSG?

A

Tumour suppressor gene

23
Q

What is the most common TSG inactivation event?

A

Abberant methylation of gene promotor

24
Q

What is meant by CpG islands and what role do they have in TSG inactivation?

A

Approximately 70% of genes have CpG islands associated with their promoter sequence, CpG methylation is only effective in shutting down the expression of a gene if it occurs within the promotor sequence of the gene - this is how TSGs are inactivated

25
Q

Give 4 mutations that occur in oncogenes?

A

1) Base pair substitutions
2) Amplification
3) Translocation eg. proto-oncogene moved to an area where the genes are more frequently expressed thus ends up expressed more frequently to
4) Inversions

26
Q

What do mutations in oncogenes lead to?

A

A gain of function

27
Q

What do mutations in TSGs lead to?

A

Loss of function

28
Q

Give 7 types of mutation which can occur in TSGs?

A

1) Base pair substitutions
2) Frameshifts
3) Deletions
4) Insertions
5) Chromosomal rearrangements
6) Chromosome loss
7) Promoter methylation

29
Q

What is meant by a direct activating carcinogen? Give 4 examples.

A

Interact directly with DNA:

1) Oxygen radicals
2) Nitrosamines
3) UV light
4) Ionising radiation

30
Q

What is meant by a procarcinogen?

A

Carcinogens which require enzymatic (metabolic) activation before they react with DNA, though not yet carcinogenic they are often toxic and its the enzymes that normally function in the detoxification and excretion of toxic chemicals which are normally implicated in their activation

31
Q

How can the process of metabolic activation of procarcinogens present a genetic influence on the formation of a malignant tumour?

A

Enzymes involved in activation of procarcinogens are normally those involved in excretion and detoxification. People who have enzymes which activate a particular chemical more efficiently are more likely to get cancer as are those which excrete the activated chemical less efficiently

32
Q

Name 2 procarcinogens?

A

1) Aromatic amines

2) Polycyclic aromatic hydrocarbons (PAHs)

33
Q

Which enzymes are involved in the conversion of Benzopyrene to BDPE and thus the activation of benzopyrene a procarcinogen?

A

P450 mixed function oxidases and epoxide hydrolase

34
Q

How does BDPE damage DNA and how is Benzopyrene produced?

A

Benzopyrene is generated through the combustion of most organic material such as meat, tobacco and fuel
BDPE forms a DNA adduct

35
Q

Mutational defects in mismatch repair enzymes gives a predisposition to what disease?

A

Hereditary non polyposis colorectal cancer, also known as Lynch syndrome

36
Q

Mutational defects in recombinational repair proteins gives a predisposition to what disease?

A

Ataxia telangiectasia

37
Q

Mutational defects in nucleotide-excision repair proteins gives a pre-disposition to what disease?

A

Xeroderma pigmentosum

38
Q

Genetic polymorphisms in genes encoding which 3 types of enzyme involved in the process from carinogen exposure to cancer may confer greater or lesser susceptibility to the effects of carcinogenic exposure?

A

1) Metabolic activation enzymes
2) Detoxification/ Excretion enzymes
3) DNA repair eznymes

39
Q

Give 5 of the bodies defences against cancer?

A

1) Dietary antioxidants
2) Detoxification mechanisms
3) DNA repair enzymes
4) Apoptotic response to unrepaired genetic damage
5) Immune response to infection and abnormal cells

40
Q

How many carcinogens have been identified in tobacco smoke?

A

19

41
Q

Give 5 carcinogens which have been found in tobacco smoke?

A

1) Polycyclic aromatic hydrocarbons eg. benzopyrene, require metabolic activation
2) Acrolein - acrid smell, potent direct-actin mutagen
3) Nitrosamines - formed during curing of leaves
4) Radioactive lead and polonium
5) Heavy metals - cadmium, chromium

42
Q

In combination with promotion by alcohol tobacco smoke leads to what increased risk for head and neck cancer?

A

100 fold increased risk

43
Q

Alcohol is linked to what 7 cancers?

A

1) Oral
2) Oesophageal
3) Bowel
4) Liver
5) Pharynx
6) Larynx
7) Breast

44
Q

Alcohol is converted into what substance which can cause DNA damage?

A

Acetaldehyde

45
Q

Alcohol increases the levels of which 2 hormones?

A

oestrogen and testosterone

46
Q

How does alcohol affect the cells of the upper GI system?

A

Increases uptake of carcinogenic chemicals into cells within the upper GI system

47
Q

How can alcohol affect surface epithelium what does this lead to?

A

Can kill surface epithelium leading to unscheduled proliferation - increases chance of mutation

48
Q

Alcohol reduces levels of what chemical needed for accurate DNA replication?

A

Reduces levels of folate

49
Q

All of the strongest risk factors for breast cancer are associated with what?

A

Increased exposure to oestrogen which can both stimulate cell division and induce DNA damage

50
Q

Give 7 breast cancer risk factors?

A

1) HRT
2) Oral contraception
3) Alcohol consumption
4) Age of 1st pregnancy >30 years
5) Early menarche
6) Later menopause
7) Post-menopausal obesity

51
Q

Why does chronic inflammation play an important role in cancer?

A

The inflammatory response results in a double hit:

1) DNA damage from release of free radicals by immune cells - initiation
2) Growth factor induced cell division to repair tissue damage - promotion

52
Q

What proportion of cancer deaths are attributable to environmental or behavioural factors ie preventable causes?

A

> 50%

53
Q

What role can diet play in cancer incidence?

A

In some cases diet leads to exposure to carcinogens eg. red meat, burnt food, heavy metals and in some its the absence of protective factors which can lead to the increased cancer incidence eg. fibre and antioxidants.