Revision of Cancer Biology Flashcards

1
Q

What are the most common causes of cancer deaths?

A

Breast
Prostate
Lung
Bowel

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2
Q

What are the hallmarks of cancer cells?

A
  • growth signal not required for cell survival, growth and differentiation
  • unresponsiveness to growth-inhibitory signals
  • evasion of apoptosis
  • defects in DNA repair
  • cells become immortal (limitless reproduction potential)
  • ability to invade and metastasise
  • angiogenesis sustained and increased
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3
Q

What types of mutations involve proto-oncogenes?

A
  • translocation/transposition
  • gene amplification
  • point mutations
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4
Q

What translocations/transpositions involve proto-oncogenes?

A
  • new promotor added to gene switching the gene on = abnormal growth
  • Bcl2 is anti-apoptotic
  • overexpression of t14:18, q32:21
  • leads to follicular lymphoma
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5
Q

What is an example of gene amplification?

A
  • HER2/ErB2
  • overexpression of GF
  • invasive breast carcinoma
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6
Q

What are 2 examples of point mutations?

A

In a gene/coding region (c-H-ras) or non-coding region (c-Fos)

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7
Q

What is point mutation occurring within a coding region?

A
  • occurs within the gene:
  • c-H-ras
  • glycine to valine
  • bladder cancer
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8
Q

What is a point mutation occurring in a non-coding region?

A
  • occurs in non-coding region (promoter/enhancer region)
  • c-Fos (TF)
  • melanoma
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9
Q

How are oncogenes dominantly active?

A
  • GF
  • receptors
  • signal transduction proteins
  • TF
  • pro/anti-apoptotic proteins
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10
Q

What are some examples of GF oncogenes?

A
  • EGF

- HER2

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11
Q

What are some examples of GF receptor oncogenes?

A
  • EGF

- VEGF

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12
Q

What are some examples of signal-transduction proteins?

A
  • KRAS

- B-Raf

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13
Q

What are some examples of TF oncogenes?

A

c-mvc

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14
Q

What are some examples of anti-apoptotic protein oncogenes?

A

Bcl-2

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15
Q

How do tumour suppressor genes work?

A
  • loss of function
  • point mutations
  • divided into gatekeeper genes, caretaker genes and pro-apoptotic genes
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16
Q

How do tumour suppressor genes allow protein mutations?

A
  • within control element (Bax which is an anti-apoptotic protein)
  • within gene (P53 which is genome guardian preventing cells leaving G1)
17
Q

What are examples of gatekeeper tumour suppressor genes?

A

p53

pRb

18
Q

What are examples of caretaker tumour suppressor genes?

A

BRCA

MMR

19
Q

What are examples of pro-apoptotic genes?

A

Bax

20
Q

What are the types of DNA damage?

A
  • oxidation of bases (reactive oxygen species = DNA strand interruptions)
  • alkylation of bases (methylation)
  • hydrolysis of bases (deamination, depurination, depyrimidination)
  • Bulky adduct formation
  • mismatch of bases (DNA replication errors)
21
Q

What are the clinical features of benign tumours?

A
  • slow growing but progressive (rare mitotic figures)
  • non-invasive
  • non-metastasising
  • well differentiated
22
Q

What are the clinical features of malignant tumours?

A
  • fast growing
  • numerous and abnormal
  • ulcerate of surface
  • local invasion
  • may metastasise
  • may see weight loss, anorexia, anaemia