kinases and cancer Flashcards

1
Q

what are the 6 hallmarks of cancer?

A
  • self-sufficiency in growth signals
  • insensitivity to antigrowth signals
  • sustained angiogenesis
  • tissue invasion and metastasis
  • limitless replicative potential
  • evasion of apoptosis
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2
Q

what do conventional cancer therapies aim to do?

A

target generic properties of cancer cells such as rapid proliferation
- cytotoxic agents, radiotherapy
- surgery

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3
Q

what do ‘modern’ cancer therapies aim to do?

A

tagret properties of cancer such as specific receptors or key proteins that are dysregulated
- monoclonal antibodies
- kinase inhibitors

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4
Q

what are seven potential ways of interefering with cancer cells?

A
  • signalling molecules
  • signal receptors and intracellular receptors
  • intracellular transducers
  • transcription factors
  • apoptotic proteins
  • cell cycle control proteins
  • DNA repair proteins
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5
Q

what are the two genetic basis’s of cancer?

A

1) Gain of function mutations convert proto-oncogenes into oncogenes
2) tumour supressor genes

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6
Q

name the three possible GOF mutations of cancer that convert proto-oncogenes to oncogenes?

A
  • point mutation
  • chromosomal translocation
  • amplification
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7
Q

what is a point mutation?

A

single base pair change leaving protein constitutively active

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8
Q

what is chromosomal translocation?

A
  • results on hybrid gene with uncontrolled activity
  • growth regulatory protein under control of different promoter causing inappropriate expression of the gene
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9
Q

what is amplification ?

A

multiple DNA copies causing overproduction of respective protein

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10
Q

what kinases are prominent members on the mutated list?

A
  • receptor tyrosine kinases (RTK) eg. EGF/ ERB
  • cytosolic kinases eg. src
  • nuclear kinases eg. Jun Fos
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11
Q

What is a parakine ErbB stimulation

A

ERB ligand released from stromal cells

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12
Q

what is autokrine ErbB stimulation

A

ER, GPCR or FZD stimulation activates metalloproteinase cleaving Pro-ERBB liganda

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13
Q

What are the two interventions ideas?

A

1) Inhibit dimerisation of EGF/ ErbB receptors to suppress proliferation signal
2) Inhibit kinase activity using small molecule tyrosine kinase domain inhibitors

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