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A Scientific Approach To Biotechnology

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A Scientific approch to biotechnology between_pic_1 Biotechnology between_pic_2 Biotechnology Help
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Understanding Biotechnology


What is Biotechnology

Overview of Biotechnology

  Then and Now of Biotechnology
 

History of Biotechnology

  Gene Technology
  What is a gene
  Gene Technology Techniques
  Genetic modification myths
  Genes code for proteins
  What is DNA
  Where is DNA
  The Full Set
  What does DNA look like
  What does DNA work
  DNA Unknown

Why do we do biotechnology?


  Why do we do biotechnology?
  Biotechnology for ourselves

Biotechnology for the environment

Biotechnology for food and agriculture

How do you do biotechnology?

  How do you do biotechnology
Finding the gene you want
  Cutting and pasting genes
  Moving genes
  Reading and interpreting genes
  Cloning a gene
  Cloning plants
  Cloning animals
Biotechnology Applications

  Human Uses
  Fighting infectious diseases
  Antibiotics
  Producing human products
  Reproductive technologies
  The human genome project
  Genetic disorders
  Gene therapy
  Cloning
  Stem cells
  Transplantation
  DNA profiling
  Environment
  Biological control of pests
  Protecting threatened species
  Resurrecting extinct species
  Cleaning up and managing
  Researching new products
  Food and Agriculture
  Feed Me
  A problem with weeds
  A problem with insects
  Other reasons to modify crops
  The international scene
  Genetically modified food labeling
  Health and Medical
  Biotechnology in medicines
  Clinical trials
  Gene therapy
  Genes and cancer
  What are ethics
Benefits & Risks of Biotechnology

  Arguments for and against gene
  A nutritionist's view on GM foods
  Balance sheet 2020
  Sustaining the Food supply
Biotechnology Resources

  Ethics of biotechnology
  Conferences and events
  Forums and Communities
  Biotechnology Websites
  Glossary of terms
   
 
 

 

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Genes and Cancer

  All cancers are the result of genetic mutations, although only 5-10% of these mutations are heritable – that is, passed on through families.

The majority of cancers (90-95%) are not inherited and cannot be predicted, nor can their exact cause be identified. However, advances in genetic science are revealing that a heightened susceptibility to some cancers can be inherited.

This knowledge is enabling physicians to identify people at higher risk of developing cancer and to prescribe screening regimes and other measures to increase their chances of avoiding the disease or detecting its onset as early as possible. Researchers are also developing ways to use the genetic basis of cancer as a means to treat the disease.

 
 

Cancer - cells growing out of control

  The cells that make up all living things continually renew themselves through the process of cell division. When a cell divides into two new cells, the DNA that makes up the genes of  the original cell is copied. Normally, the two new cells are formed, each with a complete and exact copy of that DNA, but mistakes in copying can occur. Most are corrected naturally or have no ill effect. However, if many small mutations accumulate over time they can significantly alter the way a cell behaves.

Mutations can occur due to ageing, and environmental factors such as UV radiation from sunlight, poor diet, tobacco smoking, and exposure to some chemicals.

The types of mutations most likely to lead to cancer are those which occur in genes that regulate the process of cell division and gene copying. If a mutation occurs in one of these control genes, cell division in subsequent generations of cells is likely to be more loosely regulated. This could lead to more mutations, eventually leading to cells growing and dividing abnormally. Then they become one of the more than a hundred kinds of cancer which share one trait: cells multiplying out of control to supplant or destroy healthy tissue. Often, these cancer cells become “immortal” – they  multiply out of control, lose their programming to die like normal cells, or both.

There are three types of genes which are collectively known as cancer control genes.  When these genes are mutated, they may no longer be able to prevent the development of cancer, or they may actively promote it.

  • Tumour suppressor genes act as brakes on uncontrolled cell growth.  If mutations render these genes inactive, a tumour may result.
  • Oncogenes, when mutated, can accelerate cell division to the point where a tumour results.
  • Mismatch repair genes find and repair mistakes that occur when genes are copied during cell division.  If these genes are mutated so that they no longer perform their corrective function, further mutations in genes may result, leading to tumour formation.

It is important to note that cells do not usually become cancerous due to a single mutation or loss of function in one control gene. Cancer is due to the build-up of mutations in a number of different control genes. This usually makes cancer development slow and complex.

 
 

What is a predisposition and what does it mean?

  Mutations in control genes can be passed from parents to their children. Although cancers sometimes appear to run in families, this may be due to coincidence (because cancer is a relatively common disease) or because family members are exposed to the same environmental influences. There may not be a common inherited mutation.

An inherited mutation in a control gene increases the risk that cancer will develop but it does not mean that cancer will certainly develop. If subsequent generations of cells do not accumulate further mutations in their critical control genes then cancerous growth can be averted.

 
 

How can I know if I have inherited a predisposition?

  Genetic testing involves the examination of a person’s DNA or the proteins and enzymes the DNA produces (see Genetic Testing). Results of these tests may confirm or eliminate suspicion of a genetic mutation, or abnormality in a protein product. They may show that a person is predisposed to developing a particular disorder. It is also possible to determine the probability that a person will develop a disorder, such as cancer, based on the presence of the mutation, long before any symptoms are apparent.

The effects of a faulty gene are determined by factors such as the type of mutation, the location of a mutated gene in a person’s genome, and its impact on the enzyme or protein that the gene causes a cell to produce.

Although genetic testing for predisposition genes can be useful for some cancers, it is not always of benefit. It is also essential to undergo suitable counselling before undertaking genetic testing.

 
 

Using genes to treat cancer

  As our understanding of the genetic basis of cancer has improved, so has our ability to modify genes in cells, giving rise to opportunities to use gene therapy to treat cancer (see Gene Therapy).

Research in this area has progressed to the stage where small-scale clinical trials involving human subjects have been conducted around the world. Australian researchers have conducted gene therapy trials involving patients suffering from melanoma, prostate and lung cancer, generally recording significant but inconsistent improvements in survival rates.

All gene therapies are currently experimental, and most have not progressed beyond trials using animal subjects. Clinical trials of gene therapies for cancer involving human subjects have so far been limited to early-phase trials involving small numbers of subjects who are usually suffering from advanced stage cancer.  All clinical trials that involve the introduction of genetic material into human subjects must be considered by the Gene and Related Therapies Advisory Panel (GTRAP) prior to approval by a Human Research Ethics Committee.

 
   
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