CPT: General principles of Cancer Flashcards

1
Q

What is cancer?

A

“Cancer is the rapid and uncontrolled proliferation of cells in the body”

Cancer occurs when existing body cells become abnormal and duplicate out of control

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What do the following terms mean?

  • Tumour
  • Neoplasm
  • Oncology
A
  • Tumour - swelling
  • Neoplasm - “new growth”
  • Oncology - the study of tumours
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What can cancer be divided into?

A

Cancer is not one disease can be classified into 2 broad types

haematological or solid tumours

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

The following are classifications of tumours. What do each mean?

  • Sarcoma
  • Lymphoma
  • Leukaemia
  • Myelomas
  • Gliomas

Which do each belong to: solid or haematological tumours?

A
  • Carcinoma - cancer of the covering tissues (skin, lining of the mouth and intestine) (ST)
  • Sarcoma - cancer of the supporting tissues (bone, fat, muscle and connective tissue) (ST)
  • Lymphoma - cancer of the lymph nodes and other lymphatic tissue (HT)
  • Leukaemia - haematological cancers (HT)
  • Myelomas- cancer involving the white blood cells responsible for the production of antibodies (B lymphocytes or B-cells) (HT)
  • Gliomas- cancer of the brain and spinal cord that begins in glial cells (cells that surround and support nerve cells) (ST)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Describe the difference in properties between benign and malignant diseases

A

Benign:

  • remain confined to original location
  • doesn’t invade surrounding tissue or metastasize
  • e.g. skin wart
  • can be removed by surgery
  • generally not life threatening
  • except those in inoperable location eg. brain tumors

Malignant:

  • referred to as “cancer”
  • can invade adjacent tissue and metastasize
  • often life threatening
  • metastases treat with chemotherapy
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What are the common characteisitics of a normal cells?

A

Common characteristics of cells:

  • •Need nourishment
  • •Require oxygen
  • •Most cells reproduce.
  • •Regulated cell death (Apoptosis)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Describe how carcinogenesis occurs (Knudson two – hit hypothesis)

A

At least two independent events must occur in a cell for it to undergo malignant transformation

Usually separate in time but they can occur simultaneously

A normal cell goes through a series of steps before it becomes a cancer cell. These steps usually include:

  • An initiating agent (carcinogen)
    • e.g. smoking
  • A promoting agent (co-carcinogen)
    • e.g. alcohol
  • Tumour progression
    • Usually occurs over a period of time
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Describe the epidimology of cancer

A
  • Cancer was the leading cause of death in the UK
    • (2nd to CV-disease).
  • 1 in 3 people affected
  • men = women
  • Every two minutes someone in the UK is diagnosed with cancer.
  • Breast, prostate, lung and bowel cancers most common
  • Incidence rates in the UK are highest in people aged 85 to 89
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What are ateiologies of cancer?

A

Environmental factors

  • Inhaled carcinogens - cigarette smoke
  • Ionising radiation - UV radiation-skin cancer; X-rays-acute Leukaemia and Skin carcinoma; Nuclear accidents-acute Leukaemia and Breast Cancer.
  • Life-style and diet - processed foods and fats

Genetic factors

  • Genetic predisposition has been found to be important for the development and survival rate of some tumours e.g. breast cancer, colon cancer, eye cancer i.e. retinoblastoma
    • E.g. mutations in BRCA 1 or 2

Problems with the immune system

  • Less able to combat infections by viruses that are linked to the disease.
  • Rare genetic diseases that affect the immune system – e.g ataxia telangiectasia or A-T - at higher risk of developing cancer
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Describe the steps of the cell cycle

A

Starting with Go Clinical Pharmacology and Therapeutics 2 Handout Oncology General Principle of Cancer Dr Morag McFadyen e.mail m.mcfadyen@rgu.ac.uk PD3 a quiescent or resting stage eventually progressing to the M phase, the mitotic phase where cell division takes place. The stages of the cell cycle are known as Go, G1, G2, S, G2 and M. In addition there is what is known as the restriction point, R in the G1 phase, this restriction point determines whether a cell progresses through the cell cycle or remains in the Go or early G1 phase. Specialised proteins act as gatekeepers of the restriction point, these proteins allow passage into the S phase where DNA replication occurs leading inexorably to the M stage or mitotic stage where cell division occurs, if and only if they are heavily phosphorylated at serine and threonine hydroxyls

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

How does a tumour grow?

A
  • Tumour cells do not have a negative feedback mechanism like normal cells that stops cell overgrowth (Apoptosis)
  • Cells in certain tissues will divide slower than others.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

How does a normal cell turn into a cancer cell?

A

. . . because of DNA mutation

  • inactivation of tumour suppressor genes (suppress malignant changes)
  • activation of oncogenes (promote malignancy)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Describe the function of oncogenes and its relation to cancer

A

Oncogenes

  • Genes that normally tell cells to start dividing.
  • When oncogenes are activated, they speed up a cell’s growth rate. When one of them becomes damaged, causing cancer, the cell, and all its daughter cells, are permanently instructed to divide.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Describe tumour suppressor genes function and relation to cancer

A

Tumour suppressor genes

  • Normal function the opposite of oncogenes. They stop a cell from dividing, and must be switched off by other proteins before a cell can grow.
  • P53 is one of the most important tumour suppressor genes .
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Describe suicide genes and their relation to cancer

A
  • Apoptosis - usually occurs when something goes wrong, to prevent damage to neighbouring cell.
  • Different genes involved. If these ‘suicide genes’ become damaged, then a faulty cell can keep dividing and become cancerous
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Describe DNA repair genes and their relation to cancer

A

DNA repair genes

  • DNA is under constant assault from a variety of directions. If DNA damage occurs to a gene that makes a DNA repair protein, a cell’s ability to repair itself will be reduced,
  • Errors accumulate in other genes over time. Result can be cancer, explaining why cancer is mainly a disease of the elderly.
17
Q

Describe the development of pancreatic cancer

A
  • Phosphorylation of retinoblastoma gene product (pRb) controls passage through G1.
  • Control is exerted by the oncogene K-ras and tumor suppressor genes p53 and p16
  • through their actions on the cyclin-dependent kinase/cyclin complexes that regulate phosphorylation.

In cancer their is inhibiton of TGS or activation of OG which affect this process

18
Q

Describe tumour growth in relation to effectivness of chemotherapy treatment

When is growth fastest?

A
  • The knowledge of the tumour growth rate is important to design an appropriate chemotherapy treatment regime. The ability of chemotherapy to produce a maximum effect is greatest during the initial rapid tumour growth phase.
  • Therefore chemotherapy is most effective in small groups of cells that are rapidly dividing.
  • However the earliest at which a tumour is normally detected is at 1g (109 cells) in size. At this stage the tumour growth is already declining. This reduces the effectiveness of the chemotherapy treatment.

The earlier a tumour is detected the better!

19
Q

Look at cell growth graph

A
20
Q

What are the goals of chemotherapy?

A

There are 3 possible goals for chemotherapy

  • Cure: curative intent
  • Control: If cure is not possible
  • Palliation: When the only goal of a certain treatment is to improve the quality of life but not treat the disease itself, it’s called palliative treatment or palliation.
21
Q

Describe dose indivualisation for chemotherapy rugs

A
  • Most chemotherapy agents are still dosed based on a dose per m2 in line with the patients body surface area.
  • Carboplatin differs in that the dose is dependent on the patients glomerular filtration rate (GFR). The formula used is known as the Calvert formula and is calculated as follows:
  • Dose = AUC (regimen dependent but often 5) x (GFR+25)
  • AUC= 4 to 6mg/ml in previously treated patients and 6 to 8mg/ml for previously untreated patients

  • GFR is calculated using the Cockcroft and Gault equation.
  • Estimated creatinine clearance in ml/minute =
  • (140 -Age)*Weight*constant

Serum creatinne

oAge in years

oWeight in Kg

oSerum creatinine in micromole/litre

oConstant =1.23 for men; 1.04 or women

  • For several cytotoxic drugs there are cumulative or maximum ceilings.
  • Most well known of these is vincristine where the intravenous dose should not exceed 2mg in any one administration
  • Cardiotoxic thresholds exist for all the anthracyclines