Invisible radiation that is produced by radioactive materials
The body's natural defence mechanism against infectious diseases.
Any substance that causes cancer.
The basic building blocks of proteins. There are twenty amino acids used, in different combinations, to make every protein required by the human body.
Phagocytes are the white blood cells that protect the body by ingesting harmful foreign particles, bacteria, and dead or dying cells
The process by which cells from a primary tumour (cancer) break off, are carried around the body in the blood or lymph until they lodge in another organ, where they grow and invade healthy tissues forming secondary cancers.
The emission of heat, light or other electromagnetic waves.
Programmed cell death that may be triggered when a cell is old, damaged, infected or abnormal in any way.
A malignant tumour has the capacity to destroy surrounding tissues and can spread to other areas of the body as cells detach and are transported away in the blood or lymphatic system.
A swelling made up of a mass of abnormal cells which keep multiplying in an uncontrolled way.
Bases, sometimes called nitrogenous bases, are the parts of the DNA molecule that join the two helix strands. They are like rungs on a ladder. There are four bases: adenine (A), thymine (T), guanine (G) and cytosine (C). Each base can only join with one other base; i.e. they join together in pairs: A with T and G with C.
A structure with a particular function which is made up of different tissues.
A short piece of DNA which is responsible for the inheritance of a particular characteristic. It codes for the production of a specific protein. Genes occupy a fixed position, called a locus, on a particular DNA molecule.
Mutations are changes in the genetic material. It is normal for random breaks to occur in DNA during mitosis and meiosis. They are usually repaired by maintenance enzymes. But sometimes the change is missed. Mutations may involve anything from a single base to a whole chromosome. Mutations can occur in the somatic (body) cells during mitosis or during meiosis when the gametes are formed. Many mutations have no effect on the organisms at all. Occasionally mutations result in a different protein being formed that gives the cell or organism an advantage in a particular environment. Sometimes mutations cause problems – these may be in the form of a change that causes a genetic disease or they may result in the uncontrolled cell growth we recognise as cancer.
All of these amazing adaptations are the result of mutations and natural selection.
Point mutations: The mutation of one or a small number of bases within a gene. Changes in the codons of the DNA can affect which amino acids are linked together to make proteins, and so can affect the whole cell.
Chromosomal mutations: Changes in the positions of the genes within a chromosome – the genes may be duplicated, deleted or their positions may be changed around.
All of these mutations have the potential to produce problems in the individual, because they may result in the formation of a different protein that does not function properly in the cell.
Whole chromosome mutations: These usually occur in meiosis, when a whole chromosome is lost or duplicated in the gametes.
Common types of mutations
In multicellular organisms the cell cycle is repeated rapidly in almost all cells during growth and development. In mature organisms it may slow down or stop completely, in some tissues at least. The cell cycle is controlled by a number of chemical signals made in response to different genes. This control is brought about at a number of checkpoints as described on page 4
The transformation of a normal cell to a cancer cell usually involves a series of gene mutations. Mutations are irreversible and are passed on to the daughter cells during mitosis. Certain genes are involved in the maintenance of normal cell growth patterns. Mutations in these genes greatly increase the risk of cancer developing.
Oncogenes have the ability to transform normal cells into cancer cells, but only do so if something happens to switch them on. They are normally switched off but if a mutation switches them on they become the ‘accelerator’ genes of cancer.
Suppressor genes act as ‘brakes’ as they normally control or prevent cell division. Mutations in suppressor genes can result in cells dividing uncontrollably. For example most human tumour cells have a defective p53 gene – one of the most important tumour suppressor genes.
Caretaker genes help keep DNA in a good state of repair, and in so doing prevent the build-up of DNA damage which can accelerate the formation of cancer. Mutations in these genes prevents the repair of potentially cancer-causing mutations in other genes
If cell division is uncontrolled the cells tend to be smaller and undifferentiated. They form a tumour, a mass of undifferentiated cells. Some tumours are malignant or cancerous. Malignant tumours grow and spread into the healthy tissue around them. Some of the cells may detach and be carried around the body in the blood or lymph tissue until they lodge in another organ. There they begin to grow and invade the healthy tissues, forming secondary cancers. This is known as metastasis. Non-malignant tumours are less dangerous than cancers, but they can still cause disease and death depending on where they are growing.
Normal cell division and the development of cancer
Some agents increase the likelihood of cancer-causing mutations occurring in dividing cells. They are known as carcinogens. These include a number of chemicals and ionising radiation, including UV light from the sun. We are exposed to carcinogens in different ways during our lifetime. The longer we live, the more carcinogens we have met and so the higher our risk of developing cancer. If we deliberately chose to raise the number of carcinogens we are exposed to then we increase our risk of developing cancer.
Globally millions of people increase their risk of developing cancers of the lungs, throat and mouth everyday through exposure to the carcinogens in tobacco smoke. (Photo credit: EdBrown05. Licensed under the Public Domain Mark 1.0)