DNA Technology in Medicine

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DNA Technology in Medicine

4th of April 2002

The intervention of humans in nature has increased dramatically as the years have gone by. As we start this millennium, a very powerful new technology with much potential is being unravelled that will allow humans to continue unearthing nature’s secrets, and to continue tinkering with them: DNA technology. With the human genome fully sequenced, the possibilities to apply DNA technology in a field such as medicine are tremendous. Imagine: drugs tailored to your DNA, that work the first time round leaving no side effects; predictive medicine that will tell you what diseases you might some day suffer, and the gene therapy that is best suited to curing them; the elimination of a genetic disease you have even before your birth; medical checks that involve but a blood test. The possibilities are indeed great. The risks are also great as this technology goes through its baby-steps. Will its benefits be accessible to everyone?   Is it dangerous to play with nature?  Will its use be adequate to our real needs? Just how far should we go with it? If we go too far, what will the consequences be? These are the types of questions that must be answered in making a judgment on how beneficial DNA technology is, and may prove, for humans. DNA technology in medicine, which in some cases is already being applied, will have immense effects on plausibly every facet of human life while raising many pointed questions in fields such as technology, economic factors of medicine, and ethics.

DNA technology has already started benefiting humans in the field of medicine. A representative example is that of gene therapy and predictive medicine on “Mendelian” diseases (illnesses that are caused by the breakdown of a single gene, and follow the rules of inheritance) and “polygenic” disorders (illnesses where several genes are involved).  This technology has developed from the findings of the Human Genome Project which has as its primary aim the improvement of human health.  The dream is finally becoming a reality. A recent example is that of an eighteen month old baby who was cured of severe combined immunodeficiency (SCID). By means of gene therapy, a faulty gene on his X chromosome was genetically engineered to produce T cells (which his body was not developing), vital to the functions of the immune system.  Although this is still a new technology, the procedure will be tried on several more children and provides hope for many more. However, the fact that it is a new technology also makes it a dangerous one.  It is only until now that scientists are making gene therapy work. Only a few years ago, the history of this technology was one of failure. In 1999, a boy died undergoing gene therapy for a rare metabolic disease in the University of Pennsylvania. In one gene therapy study at Boston hospital, three of the six patients involved died.  In another case an error in an operation caused patients being treated for brain tumours to suffer from partial paralysis and speech impairment. Today, the failures far outweigh the successes, but it is only a matter of time before this technology is improved, and people can begin to confidently undergo gene therapy operations.

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The industry of medicine through DNA technology is based on investigating the human genome, finding genes, and understanding how they work in order to take a line of action against a disease. Unfortunately, this is no easy task, yet companies are willing to invest billions in these investigations as they believe their investment will turn into profit in the future.  The difficulty lies in that 98% of DNA is “junk” (endless lines of DNA that apparently code for nothing; introns). Although many systems have been created to find functional genes in the human genome, they are still extremely expensive ...

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