Lecture 3: Oncogenes Flashcards

1
Q

What is a proto-oncogene?

A

The wild type allele (normal gene) of an oncogene. Mutation of this can create the oncogene.

USUALLY DOMINANT

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2
Q

What is some early evidence of oncogenes and proto-oncogenes?

A

1911: Rous (RSV)
1914: Theodore Boveri

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3
Q

When were oncogenes discovered?

A

1960: Nowell & Hungerford, evidence for casual role in genomic rearrangement

1969: Huebner & Todaro, proposed viral genes, integrated into genome, causing malignancy

1976: Stehelin et al, Showed RSV contained seq. not found in related, but non-transforming retrovirus

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4
Q

How can retroviruses transform?

A
  1. Integrated provirus activates adjacent cellular proto-oncogene (MMTV)
  2. Provirus carries a ‘captured’ cellular oncogene (RSV)
  3. Provirus-coded protein activates cellular genes (HTLV1)
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5
Q

What are ‘viral oncogenes’?

A
  1. DNA Tumour Viruses
  2. SV40: Large T antigen binds and inactivates p53 and pRb - growing evidence for SV40 in brain cancers, NHL, lymphoma, and mesothelioma
  3. Adenovirus:
    E1A - binds pRb and immortalises cells
    E1B(55K) - inactivates p53
  4. HPV:
    E6 - interacts with p53 and activates telomerase
    E7 - interacts with pRb
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6
Q

What sort of genes have oncogenic potential?

A

GF’s, GF-receptors, G-proteins, cytoplasmic tyrosine kinases, serine-threonine kinases, nuclear proteins, miRNAs

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7
Q

How are proto-oncogenes activated?

A
  1. Deletion or point mutation in coding seq.
  2. Gene amplification
  3. Chromosome rearrangement/ translocation
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8
Q

What oncogene is activated by a point mutation?

A

RAS

  1. Family of small GTP binding proteins
  2. Involved in communicating between protein tyrosine kinases receptors and the Raf-MAP kinase pathway
  3. This pathway activates TFs involved in cell cycle control
  4. mutated in high % of human tumours
  5. Correlates with poor prognosis
  6. In cancers, the GTPase activity is lost, meaning RAS remain active for longer
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9
Q

How can increased cell proliferation via RAS mutation be treated therapeutically?

A

MEK inhibitors such as selumetinib (AZD6244) can be used as a targeted therapy.

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10
Q

What oncogene is activated by amplification?

A

Myc: seq specific DNA-binding protein

Myc has two roles: cell proliferation and cell death, depending on its interaction with other factors.

Interaction with MAX via bHLH-zip domains activates/represses target genes

In cancers, myc has deregulated expression

Neuroblastoma: N-myc amplification suppresses on the protein kinase C isoforms, altering transduction pathways

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11
Q

What oncogene is activated by chromosomal translocation?

A

abl = tyrosine kinase

bcr-abl in chronic myeloid leukaemia (CML)

bcr = serine/threonine kinase activity essential for oncogene function

uncontrolled multiplication of myeloid stem cells

reciprocal translocation between chromosomes 9 and 22. 5kb portion of of 22 called ‘bcr’ join seq of abl exon 2 onwards from chr 9. Promoter and control regions of bcr (not abl) now regulate expression of chimeric protein.

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12
Q

What are BRCA 1&2 genes

A

tumour suppressor genes - DNA repair

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13
Q

Are oncogenes dominant or recessive?

A

Dominant

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