Outline of Disease Processes Flashcards

1
Q

What is cancer

A

A carcinoma or disorderly growth of cells (80% originate from epithelial cells and 20% in connective, musculoskeletal or nervous tissue) which invade adjacent tissue and spread by the lymphatics and blood vessels to other parts of the body

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2
Q

Most cancers are…

A

Monoclonal

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3
Q

How do cancer cells divide

A

Mitosis

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4
Q

State the features of cancer cell growth

A
Loss of contact inhibition
Increase in growth factor secretion
Increase in oncogene expression
Loss of tumour suppressor genes
Frequent mitoses
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5
Q

State the features of normal cell growth

A

Few mitoses
Oncogene expression is rare
Intermittent or coordinated growth factor secretion
Presence of tumour suppressor genes

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6
Q

Why is cancer sometimes diagnosed late

A

It cannot be detected until there is 10^9 cancer cells present

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7
Q

What are the causes that initiate cancer cell growth

A

Chemical
Physical
Viral

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8
Q

What are the causes that promote cancer cell growth

A

Growth factors

Oncogenes

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9
Q

What are the causes of cancer cell progression

A

Metastasis

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10
Q

Give examples of chemical carcinogens

A

Aniline dyes in bladder cancer
Aflatoxin in liver
Nitrogen mustard in leukaemia
Alcohol and smoking in lung, head, neck and gastrointestinal cancers

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11
Q

Give examples of physical carcinogens

A

Ionising radiation

Mecanisms (e.g. chromosome translocation, gene amplification and oncogene activation)

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12
Q

give examples of viral carcinogens

A

Herpes virus - Burkitt’s lymphoma
Papillomavirus - Cervical cancer
Retroviruses - Adult T-cell leukaemia/lymphoma (HTLV1), Hairy cell leukaemia (HTLV2)
Hep B - Liver cancer

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13
Q

What are oncogenes

A

Transforming genes
Positive regulators of growth
Represent a gain in function to transformed cells (e.g. in follicular lymphoma, BCL2 activation prevents apoptosis and p53 a tumour suppressor gene).

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14
Q

What are growth factors

A

Polypeptide molecules which regulate cell growth and function by binding to cell membrane receptors to stimulate the activation of intracellular signal transduction pathways.

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15
Q

How do growth factors and oncogenes work together

A

Growth factor attaches to the growth factor receptor
Triggers a post receptor signal transduction pathway
Activates oncogenes which promote growth factor and receptor synthesis.
Receptors produced will move to the cell membrane and the receptors can either cause autocrine stimulation (self-stimulating) or paracrine stimulation (adjacent cells)

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16
Q

What is autocrine stimulation

A

When the cell carries the receptor and secretes the growth factor to escape the normal control mechanism

17
Q

What is paracrine stimulation

A

When the growth factors acting on a cell are produced locally by the cell or its immediate neighbours

18
Q

What is p53

A

The most commonly altered tumour suppressor gene in human tumours (37% but higher in lung and colon cancers)

19
Q

What is p53’s normal function

A

Act as a transcriptional regulator
Promote DNA repair
Apoptosis
Differentiation

20
Q

How is p53 induced

A

By DNA damage

Hypoxia

21
Q

What checkpoint does p53 control

A

G1/S checkpoint

22
Q

State 4 details of metastasis

A

Its not random
Has a cascade of limited sequential steps
Involves tumour-host interactions
‘Survival of the fittest’ pertains

23
Q

How does a tumour metastasise

A

Tumour invades through basement membrane
Moves into the extracellular matrix/connective tissue/surrounding cells
Invades blood vessels allowing tumour cells to be ‘arrested’ in distant organs

24
Q

Which enzymes in the process are present in the ECM

A

Matrix metalloproteinases (MMPs) which has several subclasses e.g. gelatinases
Plasmin
Cathepsin

25
Q

Which enzymes in the process are present in cell adhesion

A

Cahedrins (loss correlates with tumour invasion and metastasis)
Integrins
CD44

26
Q

What is angiogenesis

A

Formation of new blood vessels

27
Q

Why is angiogenesis important for tumour growth

A

It’s a key factor in the maintenance and progression of malignant tumours
New blood vessels must form in order for a tumour mass to exceed 2 mm in diameter

Clinical correlations can be seen between vessel density, tumour malignancy and metastasis

28
Q

What is necessary for angeogenesis

A

Degradation of the extracellular matrix is necessary for new blood vessel formation to occur

29
Q

How can VEGF releated cancers be treated

A

Using an anti-VEGF antibody avastin, which binds VEGF
It prevents VEGF interacting with receptors and the activation of downstream signalling pathways Therefore it results in vascular regression and the tumour remaining dormant

30
Q

What does VEGF stand for

A

Vascular endothelial growth factor

31
Q

What does the activation of the downstream signalling pathways normally lead to

A
Endothelial cell:
Growth
Proliferation
Migration
Survival
32
Q

How does the anti-VEGF antibody cause vascular regression and the tumour remaining dormant

A

It reduces microvascular growth
inhibits the progression of metastatic disease
Reduces intratumoral pressure which may improve the delivery of cytotoxic agents

33
Q

Why does the immune system not recognise cancer cells as foreign

A

They are able to ‘hide’ from T cells
PD1, a programmed death receptor, presents on T lymphocytes
The ligand, PDL-1, on tumour cells
The interaction between these two suppresses the action of T cells

34
Q

How can the action of PD1 and PDL-1 be used to treat cancer

A

Drugs could be developed to block PD1 or PDL-1
This stops them from inhibiting the immune response and allow immune damage to occur to the cell

Nivolumab was developed to have this action and studies have shown that the overall survival of patients increased