Oncogenes and Tumour Suppressor Genes Flashcards

1
Q

What are the six hallmarks of cancer?

A
Disregard of signals to stop proliferating 
Disregard of signals to differentiate 
Capacity for sustained proliferation  
Evasion of apoptosis 
Ability to invade  
Ability to promote angiogenesis
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2
Q

What is gene amplification?

A

Production of multiple gene copies

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3
Q

What are chimeric genes?

A

Genes that are formed by combinations of portions of one or more coding sequence to produce new genes (e.g. the swapping of tips of chromosomes)

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4
Q

When can the formation of chimeric genes be a problem?

A

If one of the pieces of translocated DNA is a promoter, it could lead to upregulation of the other gene portion (this occurs in Burkitt’s lymphoma)
If the fusion gene codes for an abnormal protein that promotes cancer

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5
Q

What is the Philadelphia Chromosome?

A

Chromosome produced by the translocation of the ABL gene on chromosome 9 to the BCR gene on chromosome 22
The BCR-ABL fusion gene encodes a protein that promotes the development of cancer

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6
Q

State some important oncogenes in human cancers.

A
SRC – tyrosine kinase  
Myc – transcription factor  
JUN – transcription factor 
Ha-Ras – membrane bound GTPase 
Ki-Ras – membrane bound GTPase
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7
Q

What is an example of an inherited cancer?

A

Retinoblastoma – malignant cancer of the developing retinal cells

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8
Q

What mutation causes retinoblastoma?

A

RB1 gene

13q14

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9
Q

What are the functional classes of tumour suppressor genes?

A
Regulate cell proliferation  
Maintain cellular integrity  
Regulate cell growth  
Regulate the cell cycle  
Nuclear transcription factors  
DNA repair proteins  
Cell adhesion molecules  
Cell death regulators
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10
Q

State some important tumour suppressor genes in human cancers

A

P53 – cell cycle regulator
BRCA1 – cell cycle regulator
PTEN – tyrosine and lipid phosphatase
APC – cell signalling

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11
Q

In what form is p53 inactive?

A

When it is bound to MDM2

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12
Q

What is p53 important for?

A

It is important for regulation of p53 target genes (involved in DNA repair, growth arrest, senescence etc.) and protein-protein interactions (e.g. apoptosis)

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13
Q

What is odd about p53 considering it is a tumour suppressor gene?

A

It acts in a DOMINANT manner –mutation of a single copy is sufficient to achieve dysregulation of activity

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14
Q

What deletion causes loss of the APC gene?

A

5q21

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15
Q

What is APC involved in?

A

Cell adhesion

Cell signalling

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16
Q

What is the risk of people with this mutation developing colon cancer?

A

90%

17
Q

What signalling pathway is APC involved in?

A

WNT signalling

18
Q

What is the main role of APC that prevents uncontrolled growth?

A

It breaks down beta-catenin so that it doesn’t bind to LEF1 and promote uncontrolled proliferation

19
Q

Describe the step-by-step development of colorectal cancer.

A

APC mutations –> hyperproliferative epithelium
DNA hypomethylation + K-ras mutation will make the polyps –> adenomas
P53 mutation will result in the development of carcinoma