March 19, 2009
UNIT 3: GeneticsMedical Technology — The Genetic Forefront
A patient is rushed to emergency care following an adverse drug reaction.
A college student comes down with the flu. Worried about missing class, he goes to an emergency clinic and is given a prescription for an antiviral flu drug. Thirty minutes after taking the first pill, he is gasping for breath and his heart is racing. He is rushed to the hospital, where doctors tell him he has had an adverse reaction to his antiviral medication.
A Cure Worse than the Disease
Usually, medications cause only mild side effects, such as drowsiness, headaches, or nausea. Occasionally, patients are allergic to medicines and break out in hives or go into shock. But sometimes reactions to drugs are more serious. In the United States, about 2.2 million patients per year are hospitalized because of adverse drug reactions, and 100,000 die. Of course, no doctor intends for a drug’s side effects to be worse than the disease it is meant to cure. Nonetheless, the current process of prescribing drugs based on medical and family history is one of trial and error.
Customized Drugs
An emerging field called pharmacogenomics is about to revolutionize the prescription process. Pharmacogenomics is the study of how genetic variations can cause different people to react in different ways to the same drugs. In most cases, for example, genetics determines the way in which—and the speed at which—a person’s body breaks down a medication. If a person’s body metabolizes a drug too quickly, the drug may not be effective. If the drug is metabolized too slowly, a standard dose may be too much.
In the future, a patient in need of a prescription could have a blood test, and health care workers could run the blood test results through a computer using biochip, or microarray, technology. In hours, a patient’s doctor could have enough information about the person’s genetic background to predict how the patient would respond to a certain drug and decide whether the dose should be changed. Individuals may even be able to have their genomes mapped and put onto cards that they can take to every doctor visit. Biochip technology is not yet available in most doctors’ offices, but some oncologists (cancer specialists) are already screening patients for particular genotypes before prescribing medications.
Gene Therapy
While pharmacogenomics can provide doctors with more information about their patients, gene therapy may someday provide them with another tool. Some diseases, such as Alzheimer’s disease and hemophilia, have a strong genetic basis. Researchers hope to replace disease-causing alleles with normal ones.
The field of gene therapy is developing slowly because it requires researchers to accomplish several feats. First, they must alter an existing virus—or some other agent that can carry genetic material—so it no longer causes disease; then they insert normal human DNA into it. Next, they must test this virus to make sure that it is safe for humans. Finally, they must test the therapy itself, to see if the virus can carry human DNA to the cells that need it. Much of this research is still being done in animals, but there have been a few successful gene therapy trials in humans.
Other Uses
A scientist examines different types of genetically modified rice plants.
New uses for DNA technology offer both solutions and hard choices. Some of the more difficult questions involve the following kinds of projects:
- Researchers can alter the DNA of viruses to make them harmless and then use the harmless version of the virus as a vaccine.
- Scientists are developing transgenic animals that can be used as medical supply factories. For example, researchers hope to breed pigs that have organs that could be used for human transplants.
- Researchers are engineering crops that contain vaccines that could be administered orally. These vaccines would be easier to grow and distribute in developing countries than are current vaccines.
Unanswered Questions
The Human Genome Project has generated a lot of excitement about its potential use for pharmacogenomic applications. However, many challenges must be addressed before pharmacogenomics can have widespread clinical application.
- Many of the current studies of patients’ responses to different drugs have conflicting results, probably due to small sample sizes, different criteria for measuring a good response, and different population groups.
- Patients’ responses to a drug may be caused by many genes. Scientists will need to study the effect of multiple genes to determine response.
- Genotype testing may increase short-term healthcare costs, which raises questions about who will pay and who will have access to the technology.
UPDATES: Straight from the Headlines
- Frankenfoods or Good Nutrition? GMOs Created but Not Regulated
- Controlling Parkinson’s with Gene Therapy
- Gene Mutations Linked to Spontaneous Cases of Schizophrenia
- Discovery and Use of Glowing Protein Leads to Nobel Prize for Three Scientists
- “Astronaut Food Approach” to Medical Testing
- Vaccines Delivered By A Smoothie
Technology
Biochips
To provide truly individualized medicine, doctors would have to analyze a patient’s DNA using biochip technology. A biochip is a solid surface to which tiny strands of DNA are attached. It allows thousands of biological reactions to occur within a few seconds. When this type of screening becomes clinically feasible, it will take several steps.
- DNA will be extracted from the patient’s blood.
- A biochip will be used to map the patient’s genome. Computer software could scan the genome looking for single nucleotide polymorphisms (called SNPs, or "snips"), places where human DNA is more variable.
- A doctor will then compare the patient’s genomic results with the latest available medical research. Ideally, the resulting prescription should be customized to the patient. If a patient has a variation that is found in a small percentage of the population, however, the doctor is unlikely to have enough data about possible reactions.
Careers
Cancer Geneticist in Action
Dr. Olufunmilayo Olopade
Title: Director, Center for Clinical Cancer Genetics, University of Chicago
Education: M.D., University of Ibadan, Nigeria
Breast cancer occurs in many different forms. It has been most widely studied in Caucasian women but takes a very different form in women of African ancestry. Breast cancer hits women of African ancestry earlier and more aggressively than it does Caucasian women. Dr. Olufunmilayo Olopade wants to learn why. Working with scientists in her native Nigeria, Dr. Olopade compared gene expression in samples of cancer tissue from African women with samples of cancer tissue from Canadian women. She found that cancer cells from the African women often lacked estrogen receptors. This finding means that many of the standard treatments are not effective for this group of women.
Dr. Olopade’s work will have a huge impact on breast cancer screening and treatment in women of African ancestry. "Cancer doesn’t start overnight," she says. "We can develop strategies for preventing it."
Comments
Comment from: drake
September 3, 2008 06:21 PM [#]
cool
Comment from: brianna
August 30, 2009 10:41 AM [#]
this was an excellent article
Comment from: noodle
September 23, 2009 09:31 AM [#]
that was mad intresting
Comment from: Jocellia
November 12, 2009 08:33 AM [#]
THIS IS SOO MAD AWESOME!
Comment from: BRii
November 12, 2009 08:33 AM [#]
this was very like able an intresting i would love to learn more about it.
Comment from: Joanna
November 23, 2009 03:44 PM [#]
This was a cool article. "Vaccines delivered by a Smoothie" LOL!
Thanks for this Mrs. K. It was very educational... I don't know why I just said that... That's kinda the whole point of having a "class" ROFL! This was a cool article. Last thing I'm gonna say... =D
Comment from: Mark
March 8, 2010 10:06 PM [#]
very interesting! :D
Comment from: Hades
March 9, 2010 06:51 PM [#]
nice article...