3.8.2.3 gene expression and cancer and 3.8.3 genome project Flashcards

(17 cards)

1
Q

how do cancers and tumours form

A

mutations in DNA/genes controlling mitosis can lead to uncontrolled cell division, forming a mass of abnormal cells
malignant tumours - cancerous and spread by metastasis
benign tumours - non cancerous

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

compare the main characteristics of benign and malignant tumours

A

benign:
grow slow, cells are specialised, have well defined boarders and do not spread by metastasis
malignant:
grow fast, cells are poorly specialised, poorly defined boarders and spread by metastasis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

describe the function of tumour suppressor genes

A

they code proteins that inhibit the cell cycle or cause apoptosis of potential tumour cells.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

how are tumour suppressor genes involved in the development of tumours

A

mutation in the base sequence ->produce a non-functional protein

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

describe the function of proto-oncogenes

A

code for proteins that stimulate cell division

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

how are oncogenes involved in the development of tumours

A

mutation in the DNA base sequence -> over production of proteins

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

what is an oncogene

A

a mutated form of a proto-oncogene

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

why do both alleles of a tumour suppressor gene need to be mutated compared to one mutation of an oncogene allel

A

1 functional allele of the tumour suppressor gene can still produce enough protein to slow the cell cycle or trigger apoptosis
but 1 mutated oncogene will produce enough proteins which lead to uncontrolled cell division

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

explain the link between epigenetics and cancer treatment

A

increasing DNA methylation/ decreasing histone acetylation will inhibit expression of cancer
decreasing DNA methylation/ increasing histone acetylation will stimulate expression of cancer

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

how does increased oestrogen concentration lead to the development of oestrogen positive breast cancer

A

increase of oestrogen will cause more oestrogen to bind to oestrogen receptors forming more oestrogen receptor complexes which act as transcription factors. increasing the number of transcription factors will increase binding to promoter region of genes that code for proteins which stimulate cell division.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

why do drugs with a similar shape to oestrogen work as treatment to cancer

A

the drug will bind to the oestrogen receptor, preventing oestrogen from binding.
fewer transcription factors bind to promoter regions of genes that stimulate the cell cycle.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

what is the genome

A

the complete set of genes in a cell

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

what is the proteome

A

the full set of proteins that a cell can produce

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

what is genome sequencing and why is it important

A

identifying DNA base sequences of an organism genome
this allows the amino acid sequence of proteins to be determined

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

how does genome sequencing allow for development of vaccines

A

identification of the pathogens proteome, therefore identifying potential antigens to use in the vaccine

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

what are applications of the genome sequencing project

A

identification of genes associated with genetic diseases, allowing for new targeted drugs to be developed and allow early prevention.

17
Q

why cant the genome be translated into the proteome in complex organisms

A

presence of introns