Oncogenes, Cell Growth, and Cancer (2) Flashcards

1
Q

What are the oncogene transformation mechanisms?

A

Translocation
Amplification
Point mutation in control element
Point mutation in gene

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2
Q

Give an example of a growth factor gene as an oncogene

A

Sis oncogene
From Simian sarcoma virus
Encodes PDGF-like growth factor
Stimulates cell proliferation - causes hyperplasia

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3
Q

Give an example of a deletion in a growth factor receptor gene forming an oncogene

A

v-erbB
Mutant EGF tyrosine kinase receptor without ligand-binding domain or autoinhibitory region
Signals to nucleus without EGF binding - stimulates cell proliferation

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4
Q

What forms the autoinhibitory region of a tyrosine kinase receptor?

A

22AA sequence - at C-terminus

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5
Q

Give an example of a point mutation in a growth factor receptor gene forming an oncogene

A

Mutation in EGF receptor transmembrane domain - changes conformation - dimerisation without ligand - activation

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6
Q

Give an example of overexpression of a growth factor receptor gene forming an oncogene

A

c-erbB2
Overexpressed in some breast cancer cases
Causes tumour growth

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7
Q

Which proteins are activated by EGFR activation?

A

SRC, PI3K, Ras, PLC

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8
Q

Give an example of a DNA re-arrangement in a growth factor receptor gene forming an oncogene

A

HGFR (c-Met)
Causes cluster of cancer cells to scatter
Onc-Met mutation has cytosolic domain fused to another protein - activated - overexpression in tumours

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9
Q

What is HGF usually produced by?

A

Fibroblasts in basal membrane (epithelial monolayer) over vessels

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10
Q

What is the effect of an HGF mutation on epithelial cells?

A

Produce growth factors themselves
Grow on top of each other
Produce proteases - penetrate basal membrane - move into blood - obtain O2 and nutrients - move around body

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11
Q

How does HGF mediate cell motility and cell survival?

A

Via PI3K

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12
Q

How does HGF mediate cell proliferation?

A

Via MAPK

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13
Q

What is the Philadelphia chromosome translocation?

A

From chromosome 9 to 22

Fusion product is oncogene

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14
Q

What type of molecules are Rac1 and RhoA?

A

Small GTPases

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15
Q

What do Rac1 and RhoA control?

A

Tight cell-cell junctions

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16
Q

How are Rac1 and RhoA affected in cancer cells?

A

Constant activation of one
Cell polarity lost - tight cell-cell junctions lost
May also be motility signalling - cells grow on top of each other - chemotaxis of cells towards blood vessels

17
Q

What is required for cancer cells to become malignant?

A

Must become sticky - attach to endothelial cells of blood vessels

18
Q

What is the overall role of GTPases?

A

Cytoskeleton regulation and cell motility

19
Q

What is the role of E-cadherin?

A

In cell-cell junctions - holds cells together
Mediated by GTPases
Decreased expression in malignant growth - cells dissociate