F. Yr 13 cancer Flashcards

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1
Q

What is a malignant tumour

A

A cancerous tumour

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2
Q

What is a benign tumour

A

A non-cancerous tumour

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3
Q

Name some characteristics of benign tumours

A
  • can grow to large size
  • grow slowly
  • must less likely to be life threatening but can disrupt organ function
  • have localised effect on the body
  • cells are often well differentiated
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4
Q

Name some characteristics of malignant tumours

A
  • can grow to large size
  • grow rapidly
  • more likely to be life threatening as abnormal tissue replaces normal
  • have a systemic (whole body) effect such as weight loss and fatigue
  • cells become de-differentiated
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5
Q

What happens during the development of cancer

A
  • cancer cells are derived from a single mutant cell
  • the initial mutation causes uncontrolled mitosis
  • later a further mutation in one of the descendant cells leads to other changes that cause subsequent cells to be different from normal in growth and appearance
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6
Q

Name the two main types of genes that play a role in cancer

A
  • tumour suppressor genes

- oncogenes

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7
Q

What are proto-oncogenes

A
  • genes that stimulate a cell to divide
  • when growth factors attach to a complementary protein receptor on its cell surface membrane
  • this activates the genes causing DNA to replicate and the cell to divide
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8
Q

How do proto-oncogenes cause the cell to divide

A
  • when growth factors attach to a complementary protein receptor on its cell surface membrane
  • it activates the genes causing DNA to replicate and the cell to divide
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9
Q

What happens when a proto-oncogene mutates into an oncogene

A

It becomes permanently switched on

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10
Q

Why does a proto-oncogene become permanently switched on

A
  • the receptor protein on the cell-surface membrane can be permanently activated so that cell division is switched on even in the absence of growth factors
  • the oncogene may code for a growth factor that is then produced in excessive amounts again, stimulating excessive cell division
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11
Q

Name two ways cancer can occur

A
  • mutation of proto-oncogenes

- mutation of tumour suppressor genes

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12
Q

What do tumour suppressor genes do

A
  • slow down cell division
  • repair mistakes in DNA
  • and ‘tell’ cells when to die (undergo apoptosis)
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13
Q

What is apoptosis

A

Cell programmed death

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14
Q

How do tumour suppressor genes prevent the formation of tumours

A

They maintain normal rates of cell division

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15
Q

How can the mutation of tumour suppressor genes cause cancer

A
  • mutation of tumour suppressor gene causes it to become inactive
  • as a result it stops inhibiting cell division
  • cells growth becomes out of control
  • therefore cancer
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16
Q

How does the hypermethylation of tumour suppressor genes cause the formation of a tumour

A
  • hypermethylation in a specific region of tumour suppressor genes (promotor region)
  • this leads to inactivation of the gene
  • transcription of the promotor regions of the tumour suppressor genes is inhibited
  • inactivation means cell growth rate cannot be controlled
  • leading to the formation of the tumour
17
Q

What is hypermethylation

A

Increased methylation

18
Q

Why does the hypermethylation of the on the tumour suppressor cause it to be inactivated

A
  • preventing the binding of transcriptional factors to the gene
  • attracting proteins that condense the DNA-histone complex (by inducing deacetylation of the histones) making the DNA inaccessible to transcription factors
19
Q

What other type of abnormal methylation can occur that leads to tumours

A
  • hypomethylation of oncogenes
  • therefore activating these oncogenes
  • therefore causing the formation of tumours
20
Q

What happens during menopause

A

Increased production of oestrogen in fat cells of breasts

21
Q

How does oestrogen cause a tumour to develop

A
  • oestrogen activates a gene by binding to a transcription factor which stimulates transcription of a gene
  • if oestrogen acts on a gene that controls cell division and growth it will be activated
22
Q

What can oestrogen cause

A

Breast cancer

23
Q

Define genome

A

The complete set of genes in a cell including those in mitochondria and or chloroplasts

24
Q

What does WGS sequencing stand for

A

Whole genome shotgun sequencing

25
Q

What is WGS sequencing

A

Researches cut the DNA into many small pieces, easily sequenced sections and then using computer algorithms to align overlapping segments to assemble the entire genome

26
Q

What is WGS sequencing used for

A

Determining the complete DNA base sequence of an organism (its genome)

27
Q

Give an example of medical advancements that have been made as a result of the human genome project

A

Over 1 million SNP’s have been found in the human genome which has advanced our understanding of diseases and disorders

28
Q

What is an SNP

A
  • single nucleotide polymorphism

- single base variations associated with disease and disorders

29
Q

What is a proteome

A

All the proteins that can be coded for by the genome

30
Q

What uses could the information gained from the human microbe project have

A

Provide knowledge if genes that can be exploited for example from organisms that can withstand extreme or toxic environments

31
Q

Why is determining the proteome of prokaryotic organisms like bacteria relatively easy

A
  • most prokaryotes have just one circular piece of DNA which is not associated with histones
  • there are no introns (non coding parts of DNA)
32
Q

What application does knowledge of the proteome project have

A
  • identification of the proteins that act as antigens on the surface of human pathogens
  • which can then be used in the production of vaccines
33
Q

Why is determining the proteome of complex organisms difficult

A

the genome contains many non-coding parts

  • genome cannot directly be translated into proteome
  • also everyone has different base sequences in their DNA, making it far more difficult