Cancer Biology Flashcards

1
Q

What are characteristics of a Benign tumour?

A
  • Slow growing
  • Well-organized
  • Differentiated (known origin)
  • Generally non-destructive (not harmful)
  • Rarely cause death
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2
Q

What are the characteristics of a Malignant tumour?

A
  • Fast growing
  • Unorganized
  • Loss of differentiation
  • Increased invasiveness
  • Ability to kill host tissue
  • Usually cancerous
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3
Q

Explain the benign and malignant tumour continuum

A

A benign tumour can have characteristics that lead towards malignant and become benign, but malignant tumours cannot become begign

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4
Q

What are Carcinomas?

A

Solid mass/tumours that originate in the epithelial cells (lining of all tissues)
- Most common cancer cases, 85-90% of all cancers are carcinomas

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5
Q

What are Melanomas?

A
  • Originates in melanocytes (can be apparent as a mole or can be found in the eye)
  • Most commonly found on skin
  • Most serious type of cancer
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6
Q

What is the difference between a melanoma skin cancer and a non-melanoma skin cancer?

A

Melanoma - more deadly and have the ability to spread
Non-melanoma - More common but not deadly and cannot spread

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7
Q

What are Sarcomas?

A

Solid tumours found in connective tissues, bones, muscles, cartilage and fat (soft tissue sarcomas or osteosarcomas)
- Account for less than 2% of all cancers

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8
Q

Are sarcomas life threatening?

A

Yes, the survival rate is not great.
- Can lead to amputations due to osteosarcomas (more common in younger ages)

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9
Q

Where are osteosarcomas found?

A

Typically in long bones - Femur, Tibia, etc - but can form on any bone
- Small and hard to detect

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10
Q

What is Leukemia?

A

Non-solid type of cancer that forms in blood organs (Bone marrow, lymphatic system)

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11
Q

What are the two main types of leukemia?

A
  1. Acute - Sudden onset
  2. Chronic - Slow onset, low grade level for a long period of time
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12
Q

How else can leukemia be classified?

A

Based on cell types
- Myeloid (myelogenous leukemia)
- Lymphocytes (lymphocytic leukemia)

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13
Q

What are Lymphomas?

A

Non-solid cancer of the lymphocytes that results in enlargement of lymph nodes
- 5% of cancers are lymphomas

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14
Q

What are the two distinct lymphoma groups?

A
  1. Non-Hodgkin’s Lymphoma (NHL) > throughout the lymphatic system, quick to progress but hard to treat
  2. Hodgkin’s Lymphoma > Progress through lymphatic system one node at a time, easier to treat
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15
Q

What is the origin of cancer?

A

Cancer develops from normal cells

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16
Q

Is cancer an invader?

A

No, cancer does not invade cells it forms within them however invaders like viruses/bacteria may promote cancerous cell growth

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17
Q

Do all cells in tumours have the same characteristics?

A

Cells within a tumour all have the same genetic makeup

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18
Q

How can you determine the origin of cells in a tumour?

A

Because of their genetic makeup, all cells in a tumour are developed in one single cell. Their genetics determine their origin cell

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19
Q

How does a tumour arise?

A

From a series of mutations in the original cell and progeny of the cell

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20
Q

What is a mutation?

A

Permanent changes in DNA

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21
Q

How many mutations in specific genes does it take to produce a tumour?

A

6 independent mutations to a specific gene to produce a tumour (can occur over years of time)

21
Q

What is the mutation rate in Humans?

A

1 in 1 million genes per cell generation (most harmless or cell repairs self)

22
Q

How do mutations occur?

A
  • Inherited (genetics)
  • Arise during DNA replication and recombination
  • Caused by mutagens
23
Q

What are mutagens? Give examples

A

A mutagen is an environmental agent that cause mutations
- UV rays = risk of skin cancer
- Pollutants (air, work place substances)
- Smoking = risk of lung cancer

24
Q

What can genetic mutations result in?

A

Results in the activation of oncogenes

25
Q

What does the activation of oncogenes do?

A

Increases the chance of developing cancer

26
Q

What are oncogenes?

A

Excessively active versions of normal cellular genes called proto-oncogenes

27
Q

What do proto-oncogenes do?

A

Parts of DNA that
- Control cell division
- Cell death
- Other cell functions

28
Q

What happens if proto-oncogenes don’t work properly?

A

Become oncogenes which
- causes increase in uncontrolled cell division
- Potential problems with cell death
- Increases the risk of cancer

29
Q

What do oncogenes do to increase risk of cancer development?

A

Leads to excessive proliferation (cell division) and problems in signalling cell apoptosis (cell death)
- Cancer is rarely caused by one activation of a single oncogene (usually multiple)

30
Q

What does a tumour suppressor do?

A

Normally they suppress oncogenes by controlling excessive cell division

31
Q

What happens when there is a mutation in tumour-suppressor genes?

A

Typically less of function of t-s genes, therefore there is nothing suppressing oncogenes

32
Q

How can a person have inactive tumour suppressor genes?

A
  1. Most commonly inactivation is associated with inherited cancers
  2. Can also be sporadic (by chance) and not inherited
33
Q

What is an example of a sporadic tumour cancer suppressor?

A

Wilm’s tumour

34
Q

What is Wilm’s Tumour (nephorblastoma)?

A
  • It’s a tumour that originates in cells of the kidney
  • Most common Kidney (renal) cancer
35
Q

What is the cause of Wilm’s Tumour?

A

Caused by mutations in kidney cells in utero (embryonic tumour) = Paediatric tumour
- Most are not inherited but rather sporadic

36
Q

What population does Wilm’s Tumour affect?

A
  • Children up to age 10
  • Majority affects age 43 months - 48 months
  • Accounts for 6% of all childhood cancers (1 in 10,000 live births)
  • 90-95% of cases are in a single kidney, can happen in both (commonly inherited)
37
Q

What are the 4 gene types associated (mutated) in Wilm’s Tumour?

A

TP53 - classic tumour suppressor gene
CTNNB1 - classic oncogene
WTX - tumour suppressor gene
WT1 - similar to tumour suppressor gene

38
Q

What are properties of tumour cells?

A
  • Proliferate (divide) indefinitely
  • Less cell adhesion (sticking together)
  • Ability to continue growing despite crowding
  • Reduced apoptosis (cell death)
39
Q

What is Metastasis?

A

Migration of cancer cells from the original tumour site through the blood and lymph to other tissues

40
Q

Why are metastases so crucial in relation to cancer?

A

Without metastasis, cancer would be harmless. Metastasis is a major cause of death

41
Q

Is metastasis growth random?

A

No. Main thing to remember is each different type of cancer has a specific site where metastasis form.
E.G: Liver cancer can form metastasis in the lungs but it’s still considered liver cancer because of it’s origin

42
Q

What must be in place for metastatic cells to be successful?

A
  1. Angiogenesis
  2. Motility
  3. Alterations in cell adhesion
  4. Secretion of proteolytic enzymes
  5. Ability to escape immune surveillance
43
Q

What is Angiogenesis?

A

The development of new blood vessels to supply blood needed for primary tumour growth

44
Q

Why is angiogenesis related to metastatic cells?

A

New blood vessels provide a route for metastatic cells to escape into the blood and travel to another part of the body
- The degree of angiogenesis determines likelihood of metastases, more blood supply = more chance of metastases

45
Q

What is Motility?

A

The ability of a cell to move under its own power

46
Q

Why is motility related to metastases?

A

It’s needed in order for a tumour cell to leave the primary tumour and circulate throughout the blood or lymphatic system

47
Q

What is Cell Adhesion?

A

Allows cancer cells to stick to extracellular matrix and not to other cells allowing metastases to adhere successfully to other structures/organs

48
Q

What do Proteolytic Enzymes do?

A

Secreted by cancer cells to break down barriers such as:
- Basement membrane
- Extracellular matrix
- Endothelial barrier

49
Q

Why are proteolytic enzymes important for metastases?

A

Need to break down barriers to get into circulation and the new tumour bed to settle and continue growing

50
Q

What immune system cells do cancer have to escape from? (cells that kill off disease)

A
  1. Cytotoxic T lymphocytes
  2. Activated macrophages
  3. Natural killer cells
51
Q

What is the Metastatic Cascade?

A

Primary Tumour forms > Angiogenesis and Invasion >
Survival in Circulation > Tumour Cells Arrest in Capillary Bed of Organ > Establishment of Secondary Tumour