lecture 9 - cancer genetics Flashcards

(19 cards)

1
Q

What is cancer?

A

All cancers derive from single cells that have acquired the characteristics of continually dividing in an unrestrained manner and invading surrounding tissues.

Cancer cells behave abnormally due to changes in the DNA sequence of key genes, known as cancer genes.

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2
Q

What percentage of people in the Western world develop cancer?

A

One in three people

This statistic highlights the prevalence of cancer in the population.

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3
Q

What is the approximate number of cancer types?

A

Approximately 200 types

Each type has different causes, symptoms, and treatments.

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4
Q

What factors influence an individual’s risk of developing cancer?

A

Age, lifestyle, and genetic make-up

These are key elements that can increase or decrease cancer risk.

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5
Q

What is a mutation?

A

A change in the DNA sequence

There are two types: germline mutations and somatic mutations.

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6
Q

What is a germline mutation?

A

A change in the DNA sequence that can be inherited from either parent

This type of mutation can be passed on to offspring.

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7
Q

What is a somatic mutation?

A

A change in the DNA sequence in cells other than sperm or egg

These mutations are not inherited but can lead to cancer.

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8
Q

What are cancer genes?

A

Genes causally implicated in oncogenesis

Mutations in these genes can occur somatically or be inherited.

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9
Q

What are the two types of cancer genes?

A

Tumour suppressor genes and Oncogenes

These play different roles in cell growth and division.

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10
Q

What is the function of tumour suppressor genes?

A

To PREVENT cell growth/division

They act as a check on cell proliferation.

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11
Q

What is the function of oncogenes?

A

To PROMOTE cell growth/division in a controlled manner

When mutated, they can lead to uncontrolled growth.

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12
Q

Give examples of mutation types.

A
  • Substitution
  • Deletion
  • Insertion
  • Inversion
  • Duplication

These mutations can affect the function of genes.

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13
Q

What are the stages of cancer progression?

A
  • Benign Tumour
  • In situ cancer
  • Invasive cancer
  • Metastatic cancer

Understanding these stages is crucial for diagnosis and treatment.

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14
Q

Name external causes of cancer.

A
  • Ultraviolet radiation
  • Tobacco smoke
  • Lifestyle factor: diet
  • Biological factor: virus (HPV and cervical cancer)

These factors can increase the likelihood of developing cancer.

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15
Q

What is the KRAS gene responsible for?

A

It codes for a signalling molecule

Mutations in this gene are found in many cancers, including pancreatic cancer.

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16
Q

What do heterozygous mutations indicate?

A

A double peak indicates a mutation on one chromosome and not the other

This can provide insights into cancer genetics.

17
Q

What are significant KRAS mutations?

A
  • Amino acids 12
  • 13
  • 61
  • 146

These mutations are commonly associated with various cancers.

18
Q

What is the role of KRAS in cellular signaling?

A

Helps transmit external growth signals to the cell nucleus

It is activated by GTP and inactivated when GTP is hydrolyzed to GDP.

19
Q

What is the hereditary component percentage in cancer cases?

A

Only 5–10% of cancer cases have a clear hereditary component

Examples include BRCA1 and BRCA2 in breast cancer.