Molecular biology of cancer Flashcards

(26 cards)

1
Q

Name the three competing models of cancer origins.

A
  • Differentiation model
  • Viral model
  • Mutagenesis model
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2
Q

What is the Differentiation model ?

A

It is a model of cancer origins:
- Cancer is a misregulated developmental process
- Phenotypic changes are based on an epigenetic process

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3
Q

What is the Viral model ?

A

It is a model of cancer origins:
- Cancer is caused by infections with tumor viruses
- Several tumor-causing viruses were identified in animals and some in humans

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4
Q

What is the Mutagenesis model ?

A

It is a model of cancer origins:
- Cancer arises from DNA mutations in somatic cells
- Radiation and chemicals are linked to tumor formation

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5
Q

Name two genetic abnormalities which are common in cancer cells.

A
  • Point mutations
  • Chromosomal abnormalities
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6
Q

Name the two types of mutations in tumors depending on their functional relevance.

A
  • Driver mutations: Causally linked to tumor behaviour
  • Passenger mutations: Incedental or redundant
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7
Q

Not all changes in cancer cells are genetic. Name another reason for cancer development.

A

Epigenetic changes like methylation or histone modification

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8
Q

Name three types of single-gene alteration.

A
  • Point mutation
  • Insertion
  • Deletion
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9
Q

How are fusion genes usually created ?

A

By chromosomal rearrangements

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10
Q

In point mutations exist two types of base exchanges. Name both and explain them shortly.

A
  • Transitions: A purine is replaced by a purine or a pyrimidine is replaced by a pyrimidine
  • Transversions: A purine is replaced by a pyrimidine or the other way around
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11
Q

What are silent mutations, missense mutations and nonsense mutations ?

A
  • Silent: Codon change without amino acid change
  • Missense: Amino acid change with a neutral, activating or inactivating effect
  • Nonsense: Leads to a premature stop codon
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12
Q

What can be the consequences of mutations in the splice site ?

A
  • Exon skipping
  • Exon elongation
  • Reading frame alteration
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13
Q

How can a chromosomal translocation effect the activation of genes ?

A
  • By disrupting coding regions
  • By altering regulatory regions
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14
Q

What are chromosomal inversions ?

A
  • Intrachromosomal rearrangements
  • Have the same functional effects as translocations
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15
Q

Name three consequences of chromosomal inversions.

A
  • Gene disruptions
  • Misregulation
  • Formation of fusion genes
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16
Q

What is a mitotic nondisjunction ?

A
  • Incorrect chromosome separation during anaphase of mitosis
  • Leading to daughter cells with an abnormal number of chromosomes
17
Q

What is a chromothripsis ?

A

A destructive and random reassembly of a single chromosome

18
Q

What is a chromoplexy ?

A

A series of independent translocations involving multiple chromosomes

19
Q

What is the main difference between chromothripsis and chromoplexy ?

A
  • Chromothripsis: Intrachromosomal rearrangements
  • Chromoplexy: Interchromosomal rearrangements
20
Q

What does the abbreviation LOH mean?

A
  • Loss of heterozygosity
  • Only one allele remains
21
Q

Name three mechanisms which can lead to a loss of heterozygosity (LOH).

A
  • Whole chromosome loss
  • Partial arm deletion
  • Mitotic recombination
22
Q

Name one example how a loss of heterozygosity (LOH) can lead to cancer development.

A

Silencing of tumor suppressor genes

23
Q

What are the two major classes of cancer-related genes ?

A
  • Oncogenes
  • Tumor suppressor genes
24
Q

What are oncogenes ?

A

Genes which promote cancer through increased or misdirected activity

25
What are tumor suppressor genes ?
Genes which promote cancer if their function is lost or reduced
26
Many cancers are influenced by dysregulated noncoding RNAs. Which RNAs are these ?
- MicroRNAs (miRNAs) - Long noncoding RNAs (lncRNAs)