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Bioethics second midterm
Bioethics second midterm
Bioethics second midterm
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Bioethics of Gene Therapy
A genome is all of the DNA in a given organism. The DNA is split up into smaller groups of nucleotides called genes. Every gene contains the information for the production of a different protein. The human genome was once thought to have over 100,000 genes but it was recently found to have around 30,000 genes. The proteins produced by the genes determine different characteristics of the organism such as hair color, the ability to fight infection, some aspects of behavior, all enzymes, hormones, and almost all other characteristics of the organism. Genes are passed down from generation to generation.
There is a two step process involved in order for the genes to be used. The first half of this process is called transcription. DNA is made up of four nucleotides: adenine, cytosine, guanine, and thiamin. These nucleotides are in pairs in the DNA and their order is very important because it dictates how the gene will be expressed. During transcription RNA, a similar molecule to DNA, comes in and makes the compliment copy of the DNA sequence. The second half of this process is called translation. During translation the RNA is used to make amino acids, which are then used to make a protein. Not all of the RNA is used to make the amino acids, only the sections which are between the start and stop signals. Then sets of three nucleotides called codons are used to make specific amino acids. Different sets of amino acids code for different proteins.
So why is the genome so important? Because it is not only what determines many every day characteristics, it is also what determines genetic diseases that affect so many people. Therefore increasing knowledge of the genome will give us more knowledge not only about these diseases but how to cure them. In 1990, a project called the U.S. Human Genome Project was launched in order to discover all the genes in human DNA as well as the sequences of the nucleotides that make up DNA. With this knowledge we hope to accomplish many things, one of which is gene therapy.
Gene therapy is a new approach to treating diseases by changing a person’s genes. Not only does gene therapy hope to be used to cure genetic diseases, but there are also promises of disease prevention. There are two types of gene therapy somatic and germline. Somatic gene therapy hopes to change the gene of the patient, but this change of expression in the gene will not be passed down to the next generation.
Gene therapy is the application of the technique where the defect-causing "bad" genes are replaced by correct "good" genes. The idea of gene therapy is to treat the disease by correcting the "bad" DNA (Deoxyribonucleic acid) rather than the current me thod of providing drugs, or proteins not produced by the defective gene. Gene therapy addresses the problem first hand by directly working with the genetic information causing the disease. From the book Shaping Genes, Dr. Darryl Macer says "It is like f ixing a hole in the bucket, rather than trying to mop up the leaking water." There are two kinds of gene therapy, somatic cell gene therapy and germline gene therapy.
In this paper, I will argue that genetic therapies should be allowed for diseases and disabilities that cause individuals pain, shorter life spans, and noticeable disadvantages in life. I believe this because everyone deserves to have the most even starting place in life as possible. That is no being should be limited in their life due to diseases and disabilities that can be cured with genetic therapies. I will be basing my argument off the article by “Gene Therapies and the Pursuit of a Better Human” by Sara Goering. One objection to genetic therapies is that removing disabilities and diseases might cause humans to lose sympathy towards others and their fragility (332). However, I do not believe this because there are many other events and conditions in society that spark human compassion and sympathy towards others.
Human gene therapy is a method used in the medical field that treats diseases at a molecular level, by solving the source of the problem; our genes. Today, diseases and disorders are commonly treated by solving the symptoms, the surface of the problem. Many disorders and diseases are caused by defective proteins and within those defective proteins are damaged and defective genes. These defective genes can be treated through gene therapy. Gene therapy is not new and has been developed and improved by researchers for the past couple years. Being an experimental technique, gene therapy also has its pros and cons, but so far is showing positive and rising success rates.
Gene therapy works in three ways; it works to replace a missing or defective gene with a normal one, replace a faulty gene so that it will function properly and it works to activate and deactivate a gene, allowing it to “switch” on and off. Gene therapy is done by the deliverance of a gene to a cell via a carrier, or vector, such as a virus. Scientists lean more towards using a virus because they can seek out particular cells and transfer pieces of deoxyribonucleic acid into them. Scientists also take advantage by deactivating their harmful characterizes and modifying them to carry particular gene into designated cells. After gene therapy is done, the genes can then stimulate the production needed for standard functioning, allowing that gene to return to its previous normal state. Therefore, if a patient were to be in the beginning stages of cancer, gene therapy would seek out the cancerous gene and replace it with a healthy one and minimizes the disease from
Although the highly technical aspects of human gene therapy are somewhat complex, the basic concept is very straight forward. The goal of gene therapy is to correct mistakes that have occurred within the genetic material, or DNA, of the living cell. In very simple terms, DNA is often thought of as the "language" of the biological functioning of organisms. This language is organized by letters (nucleotide pairs), words (codons), sentences (genes), and books (genomes). Before being able to repair the damaged or defective genetic material, the location of the gene or genes causing the dysfunction in the individual must be determined.
Gene therapy gives people who suffer from genetic diseases a chance to lead a normal life. Dangerous diseases, such as AIDS, SCID, Thalassemia and ADA can be cured successfully. In September 5, 2006, two people with advanced melanoma received Gene therapy and they got recovery soon. This is a breakthrough in cancer gene therapy. Gene therapy uses patients own cells to cure diseases, and, therefore, no rejection to their bodies. Furthermore, patients could get permanent cure from gene therapy without recurrence.
Gene therapy is a provisional technique that is the insertion of normal genes into the cells where there is a missing or miscoded gene to fix a genetic disorder. In the 1960s and early 1970s,
Gene therapy focuses on the replacement of defective genes with modified functioning genes. Many diseases are caused by a defective gene meaning the body is incapable of producing essential proteins or enzymes. In its simplest form, gene therapy aims to identify the defective gene and fix this gene with the replacement of a normal gene (Senn).
"The aim is to decrease the fear of a brave new world and to encourage people to be more proactive about their health. It [Gene therapy] will help humans become better physically and even mentally and extend human life. It is the future” (Hulbert). Dr. Hulbert, a genetic engineer, couldn’t be anymore right; more time, money, and research needs to be put into gene therapy and genetic engineering, since it can cure certain illness and diseases that are incurable with modern medicine, has fewer side-effects than conventional drugs or surgery, and allows humans to be stronger physically and mentally at birth. Gene therapy or genetic engineering is the development and application of scientific methods, procedures, and technologies that permit direct manipulation of genetic material in order to alter the hereditary traits of a cell, organism, or population (NIH). It essentially means that we can change DNA to make an organism better. Genetic engineering is used with animals and plants every day; for example with genetic...
Imagine if there was a cure for cancer right at our fingertips… Gene therapy is attempting to achieve that goal by replacing a mutated gene, such as a cancer gene, with a healthier copy of it. However gene therapy is still very new in the medical field and as such comes with plenty of risks with one being that it may cause a tumor to grow. How can gene therapy act as a potential cure for cancer and what are the potential harms that can come out of treatment?
“A gene is a segment of DNA or a sequence of nucleotides in DNA that code for a functional product,” Tortora. Microbiology. p. 575. The syllable of the syllable. These genes not only affect our outlook, but also play a role.
[Cover: discussion about how risks are balanced during risk assessment, why this is a difficult task -> proposing a set of principles and practical measures that might assist both researchers and patients, to enable more informed decisions about risk]
Genes are made of DNA – the code of life (Gene Therapy- The Great Debate!). The changes in genes may cause serious problems, which we called genetic disorder. In theory, the only method to cure genetic disorders is gene therapy, which basically means the replacement of genes in order to correct the loss or change in people’s DNA. Although gene therapy gives patients with genetic disorders a permanent cure, it is controversial because it has safety and efficacy problems, and raises ethical issues.
Due to the fact that the field of biotechnology is very serious and potentially dangerous, rules must be set down in order to keep the research in check. The high risk research of genetic therapy needs guidelines that have to be followed in order to keep the study just. The articles that are discussed in this essay focus on ethical issues and ideas that should be followed in the field in order to keep research safe and valid.
...ring deadly diseases and preventing abortions. In order for gene therapy to one day become effective much more research needs to be done to discover the consequences of altering specific genes. Also the technology of gene therapy needs to be cost effective so people who need help are able to get help. In the end gene therapy in humans needs to come a long ways before it will be widely accepted but there is great potential in the technology and it needs to be pursued.