Neoplasms (new) Flashcards

1
Q

suggest different intrinsic and extrinsic risk factors for carcinogenesis - which group is more important?

A

Intrinsic:

  • old age
  • gender (hormones)
  • genetics

Extrinsic (85%):

  • lifestyle (30%): high BMI, low fruit/veg, smoking, alcohol
  • environment: chemicals, radiation, infection
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2
Q

describe the 3 steps of carginogenesis

A

i. initiation: INITIATOR causes mutation
ii. promotion: chronic exposure to PROMOTERS causes cell proliferation and expansion of a monoclonal pop. of mutant cells
iii. progression: step-wise ACCUMULATION of mutations to become malignant neoplasm

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3
Q

describe 3 different types of initiator - how do they cause mutation?

A
  1. chemicals (long delay between exposure and onset, risk depends on dosage, some organ specificity)
  2. radiation, e.g. UV rays or ionising radiation (inc. X-rays). Mutagenic via:
    - direct DNA damage (to DNA bases or single- and double-strand breaks)
    - indirect damage by generating free radicals
  3. infection:
    - direct carcinogens (e.g. HPV and cervical cancer)
    - indirect carcinogens via chronic tissue injury and resulting regeneration… DNA replication errors (e.g. HepB/C and liver cancer, H. pylori and gastric carcinoma)
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4
Q

name a chemical that can cause bladder cancer

A

2-napthylamine

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5
Q

how does HPV cause cancer

A

HPV expresses E6 and E7 proteins that inhibit p53 and pRB… cervical carcinoma

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6
Q

what are pro-carcinogens and complete carcinogens

A

Pro-carcinogens = chemicals that are only converted to carcinogens by CYP450s in liver

Complete carcinogens = both initiators and promoters (e.g. cigarette smoke)

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7
Q

which 3 types of genes must be affected by mutation for cancer to occur - what is their function and how many alleles must be affected

A
  1. tumour suppressor genes
    - act like break on tumour growth
    - both alleles must be inactivated (2 hits)
  2. proto-oncogenes
    - enhance neoplastic growth
    - 1 allele must be activated
  3. care-taker genes
    - type of TS gene that maintains genetic stability
    - e.g. DNA repair genes
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8
Q

describe an example of a tumour suppressor gene

A

pRB: restrains cell proliferation by inhibiting passage through restriction point

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9
Q

describe an example of a proto-oncogene

A

RAS: small G protein that relays signals into cell, eventually pushing cell past cell cycle restriction point… activation of cyclin D… activation of CDK… entry into cell cycle

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10
Q

what is genetic instability

A

accelerated mutation rate caused by germline mutations affecting DNA repair (seen in some inherited cancers)

can involve:

  • nucleotide, microsatellite or chromosomal instability
  • abnormal chromo. segregation during mitosis
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11
Q

suggest why inherited malignancies are more likely to occur than spontaneous malignancies

A

KNUDSON’S 2 HIT HYPOTHESIS:

  • Inherited - 1st hit: germline mutation (affects all cells); 2nd hit = somatic mutation
  • Spontaneous - both hits = somatic mutation in same cell (less likely)
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12
Q

what is the adenoma-carcinoma seqeuence

A

Accumulation of mutations, typically over decades, causing a colonic adenoma to become a colonic carcinoma:

i. normal epithelium…
ii. early adenoma/dysplastic crypt…
iii. intermediate adenoma…
iv. TGF-beta response inactivation… late adenoma…
vi. loss of p53 function… carcinoma…
vi. metastasis

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13
Q

name the 6 hallmarks of a fully evolved malignant neoplasm

what is the enabling characteristic?

A
  1. self-sufficiency in growth signals
  2. resistance to growth-stop signals
  3. cell immortalisation (no division limit), e.g. telomerase gene activation
  4. sustained angiogenesis ability, e.g. VEGF expression
  5. apoptosis resistance
  6. ability to invade and metastasise

enabling characteristic = genetic instability

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14
Q

which cellular changes must occur for a cancerous cell to be become invasive

A

Epithelial-to-mesenchymal transition

  1. altered adhesion: reduced E-cadherin expression (decreased cell-cell adhesion), changed integrin expression (decreased cell-stromal protein adhesion)
  2. altered stromal proteolysis: increased protease expression, esp. MMPs (basement membrane and stroma degradation)
  3. altered motility: changed actin expression via Rho G proteins (cytoskeleton changes)
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15
Q

describe the 3 stages of metastasis

A

i. growth and invasion at primary site
ii. enter transport system and lodge at secondary site
iii. growth at secondary site to form new tumour - colonisation

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16
Q

how can cancer cells disseminate across the body - which method is used by carcinomas and sarcomas

A
  • blood
  • lymph
  • transcoelomic

carcinomas: first lymph then blood
sarcomas: straight to blood

17
Q

name the cancers that most frequently spread to bone

A

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  • prostate
  • breast
  • lung
  • renal
  • thyroid
18
Q

which 2 factors determine location of colonisation

A
  1. regional drainage of blood (next capillary bed: often lungs, liver, bone or brain), lymph (draining lymph nodes) or coelomic fluid (other areas in coelomic space, adjacent organs)
  2. seed and soil phenomenon: requires adequate “cancer niche” - provides growth factors and proteases
19
Q

what is tumour dormancy

A

when metastatic cells fail to grow, instead forming micrometastases which can reactivate later