20.5 & 20.6: Gene expression & cancer & genome projects Flashcards

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1
Q

Types of tumour

2

A

benign

malignant

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2
Q

Benign tumour

A

non - cancerous

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3
Q

Malignant tumour

A

cancerous

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4
Q

Benign tumour

growth rate and size

A

grow very slowly and can grow to a large size

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5
Q

Malignant tumour

growth rate and size

A

grow rapidly and can grow to a large size

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6
Q

Cell nucleus in a benign tumour

A

Relatively normal appearance

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7
Q

Cell nucleus in a malignant tumour

A

Often larger and appear darker due to an abundance of DNA

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8
Q

Benign tumour cells

A

Differentiated and produce adhesion molecules which makes them stick together and remain in the tissues from which they arise.

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9
Q

Malignant tumour cells

A

Become de-differentiated and don’t produce adhesion molecules

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10
Q

Metastasis

A

Forming of secondary tumours

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11
Q

Characteristics of a benign tumour

A

surrounded by a capsule and remain as a compact structure

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12
Q

Characteristics of a malignant tumour

A

not surrounded by a capsule and have finger like projections that can grow into the surrounding tissue

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13
Q

Effects of malignant tumour

A

often systemic effects such as weight loss and disease

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14
Q

Systemic

A

whole body

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15
Q

Treatment of malignant tumours

A

usually involves chemotherapy, radiotherapy and surgery

and more frequently reoccur after treatment

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16
Q

Treatment of benign tumours

A

surgery

17
Q

Oncogenes

A

Mutations of proto-oncogenes

18
Q

Protooncogenes

A

Stimulate a cell to divide when growth factors attach to a protein receptor on its cell-surface membrane. Which activates genes that cause DNA replication an cell division.

19
Q

Reasons why the mutation of a protooncogene into an oncogene can permanently activate an oncogene
2

A
  • Receptor protein on the cell surface membrane can be permanently activated so cell division occurs even without growth factors
  • The oncogene may code for a growth factor that is produced in excessive amounts, again stimulating excessive cell division
20
Q

Tumour suppressor genes

A

Slow down cell division, repair mistakes in DNA and trigger apoptosis.

21
Q

Tumour suppressor genes mutation

A

switches it off/ inactivates it
stops inhibiting cell division
cells can grow out of control

22
Q

Most cancers are

A

acquired not inherited

23
Q

Hypermethylation

A

Increased methylation

24
Q

Hypomethylation

A

Reduced methylation

25
Q

Process by which hypermethylation may lead to cancer

A

Occurs in a specific region of tumour suppressor genes.
Leads to the tumour suppressor gene being inactivated.
Leads to increased cell division and formation of a tumour.

26
Q

Oestrogen concentrations and breast cancer

A

Fat cells in breasts tend to produce more oestrogen after menopause. Oestrogen causes proto-oncogenes in breast tissue to develop into oncogenes which leads to development of a tumour.