AQA A-Level Biology 7402
Biological Molecules
Cells
Organisms Exchange Substances with Their Environment
Genetic Information, Variation and Relationships Between Organisms
Energy Transfers in and Between Organisms
Organisms Respond to Changes in Their Internal and External Environments
Genetics, Populations, Evolution and Ecosystems
The Control of Gene Expression
The Control of Gene Expression
Abnormal methylation, oestrogen and evidence on causes of cancer
- 3 things to know
- Papers 2 and 3
Overview
Recall questions on hypermethylation of tumour suppressor genes and hypomethylation of oncogenes, oestrogen and breast cancer, and evaluating genetic and environmental evidence from migrant and population studies.
What you need to know
Answer each one before you reveal it.
Describe the mechanism by which oestrogen promotes cell proliferation in breast cells.
Name four factors that increase lifetime oestrogen exposure.
Questions from this subtopic
Each one with the model answer underneath.
- 1
How does hypermethylation of tumour suppressor gene promoters contribute to cancer?
Model answer
It silences their expression, preventing production of proteins that inhibit cell division.
- 2
What effect does hypomethylation of oncogene promoters have on cell division?
Model answer
It increases oncogene expression, leading to excessive stimulation of cell division.
- 3
Why are abnormal methylation patterns described as epigenetic changes?
Model answer
Because they affect gene expression without altering the DNA base sequence.
- 4
How do increased oestrogen concentrations raise the risk of breast cancer?
Model answer
Oestrogen stimulates increased cell division in breast tissue, raising the risk of mutations accumulating.
- 5
Describe the mechanism by which oestrogen promotes cell proliferation in breast cells.
Model answer
Oestrogen binds to oestrogen receptors in breast cells, activating transcription of genes that promote cell proliferation.
- 6
Name four factors that increase lifetime oestrogen exposure.
Model answer
Early menarche, late menopause, hormone replacement therapy, and obesity.
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