Courtesy National Institutes of HealthRecord numbers of women are opting for a test that checks if their genetic make-up makes them stronger candidates for breast cancer. Last year about 100,000 women were tested. Doctors generally recommend against testing anyone under the age of 25, the same age that mammograms are first recommended. That’s because little can be done to screen or prevent breast cancer before that age.
But a growing movement among young women wants to find out how their genetic make-up could impact their risk for breast cancer. And they want to find out that news at an earlier age.
It’s a hot ethical question in clinics across the country today, which is explained in full detail here.
On the one side, pro-testing people point out that young people armed with this information could make lifestyle choices that could reduce their cancer risk. There is some evidence that young women with a positive genetic test have quit smoking, for example. Others have limited alcohol intake or avoided using birth control pills, two other factors that can raise breast cancer risk.
On the other side of the debate, researchers say that young women have enough health issues to deal with at an early age. Ringing alarms for something they can’t be “officially” tested for until later in life is just one more worry that they really don’t need to deal with at the time.
The tests themselves cost around $3,000. More and more medical insurance companies are providing coverage for the test.
If the test shows a faulty gene, the patient’s risk of developing breast cancer is three to seven times higher. In a few cases, parents have tested the genes of their pre-adolescent children. One girl test was just four years old.
What do you think? Is this good genetic curiosity or being a genetic busy-body? Is it important to find out this information if nothing can be done to treat the situation for a number of years? Share your thoughts here with other Buzz readers.
Courtesy Thomas HawkOops. I forgot y’all are too cool to read the word “poopy” now and again. Maybe next time I’ll drop an S-bomb on y’all. Or I could write “sulfurous compounds,” or skatole, or indole. But where would that get us? Nowhere very graphic, certainly.
So, how would you like it if it was your job to sniff out human feces?
Well, I’m sorry, but the job has already been taken. Taken, no less, by a member of a group whose mission in this country seems to be to take jobs from honest, upstanding Americans. That’s right: dogs.
This particular dog is named Sable Sheets, and he hails from Lansing, Michigan. (He doesn’t actually have a last name, being a dog, so I gave him one.) Sable is a professional sniffer of crap. If sniffing human feces were an Olympic sport, Sable would be a gold medalist, if it were a martial art, Sable would be a ninja. It is a serious pursuit—Sable sniffs for the government.
Since he was a puppy, Sable has been trained to recognize certain smells: the odors of water contaminants. Earlier this week, we went over just how great at smelling dogs are. Sable needs to be a great smeller, because not only does he have to recognize chemical contaminants, like those that come from household detergents, but he also has to be able to distinguish animal feces from human feces. A little animal feces in the water is gross, but if Sable can detect human feces it’s a sign that there could be a failed and leaking septic system nearby. Aside from the other obvious issues involved with poop in your water, leaking septic systems can lead to E. coli contaminating rivers and streams. And we don’t want that.
Municipal governments hire Sable and his handler, a former K-9 officer, to check out catch basins, outflows, and manhole covers. If Sable gets a hint of duke, he barks and looks at his handler.
E. coli bacteria can, of course, be detected without the help of a dog, but only with the help of laboratory equipment. To find and test all possible sources of E. coli contamination in a water system would take a tremendous amount of time and effort. A dog like Sable—who, at the moment, might be one of a kind—can speed up the effort greatly. He’s like a miniature, mobile, furry lab. Based on the sample’s that have been sent to the lab on account of Sable’s barks, the dog is about 87 percent accurate.
His handler adds that Sable is “getting better; getting more refined.” Sort of like a connoisseur of fine wines, really, but with… you know.
Scooby, whose real name (I’m guessing) is being withheld for his own safety, is believed to have been present when his 59-year old owner was hung from the ceiling of her Paris apartment.
The death was initially supposed to be a suicide, but the dead woman’s family demanded a murder investigation. During the preliminary trial, the dog was lead to the witness box to see how it reacted to a suspect. Scooby is reported to have started “barking furiously” as he neared the suspect.
The judge has yet to decide whether there’s enough evidence to launch a full murder inquiry, but was very impressed with Scooby.
In addition to the outburst at the witness, however, several crotches and one butt have been added to the list of suspects.
Soooo… How can this be a science story? Well, let us consider the olfactory prowess of your average dog, and how that could possibly be considered as evidence in a case that would put a person in jail for, no doubt, a long, long time.
I don’t know if you live in an area where skulls—preferably mammal skulls—are readily available. If you do have a local skull store or skull pit, however, do yourself a favor and grab a skull or two. If you check out the nose hole (don’t use that term on any skull-themed tests, by the way), you’ll see a bunch of thin, bony, scroll-shaped plates. Air passing through the nose hole (again…) is spread out over the surface of these plates. The chemicals that give inhaled air its odor are dissolved into the mucus produced by the spongy tissue covering the plates. The chemicals (or odors) in the mucus are then detected by little antlered nerve cells (keep that one off the test too). These nerve cells run pretty much directly to the brain, where the detected chemicals are analyzed. The brain can then decide if you’ve just smelled triple berry pie, or, say, a French murderer.
Now, while I know of several individuals I could probably identify by smell, I’m pretty certain that I couldn’t pull your average French murderer out of a lineup by odor alone. But, then, I’m no dog.
The area of tissue covered with smell receptors in a human’s nose slightly less than a couple square inches—about the size of a big postage stamp. A dog, on the other hand, has enough smell receptors to cover an area of tissue almost as big as a standard sheet of printer paper. And while all dogs are significantly better smellers than humans (that is to say, better at receiving smells, not giving off pleasant ones), certain breeds of dog far outstrip the rest. A human, for instance, has about five million smell receptors. A wiener dog has about one hundred and twenty five million smell receptors, and a German shepherd has two hundred and twenty five million. Bloodhounds have about 300 million smell receptors. What’s more, the percentage of a dog’s brain devoted to analyzing smells is 40 times larger than the same area in a human’s brain. All things considered, it is thought that dogs are perhaps ten thousand times more sensitive smellers than humans. (Or, if you go by Wikipedia, a dog’s sense of smell is as much as one hundred million times more sensitive than a person’s. But I’d keep that off the test too.) Add all this to the notion that individuals may have unique individual odors, and it makes sense that a dog might be able to identify a person who had murdered their companion/owner.
No, we aren’t.
Tiny, naked astronauts were recently exposed to the vacuum environment, harsh temperatures, and dangerous radiation of space for a period of several days. The space travelers went into an almost entirely dormant state for the duration, slowing their metabolisms to .01% of their normal levels.
After they were brought back into the low-orbit space vessel, most of the astronauts were completely revived. (Some died. It was very sad.) Aside from enduring the vacuum of space, and the extreme temperatures outside of a space capsule, the astronauts’ ability to survive the radiation of space most surprised scientists. On the surface of earth, solar radiation (as you no doubt are aware) is strong enough to give us sunburn, and cause genetic damage to our skin cells (leading to skin cancer). The levels of radiation in space are 1,000 times higher, enough to sterilize an organism, yet the astronauts did fine with it, and were even able to successfully reproduce on their return to earth. Scientists hope to isolate whatever mechanism allowed the astronauts to repair the genetic damage they likely incurred while in space. Such research might be applied to radiation therapy techniques.
We salute you, tiny, naked challengers of the unknown.
Using the new induced pluripotent stem cell (iPS) technique, researchers from Harvard Stem Cell Institute produced a robust new collection of disease-specific stem cell lines. Having these disease-specific iPS cells will allow researchers to watch the development of diseases in petri dishes, outside of the patients. HSCI iPS Core will produce these disease-specific cell lines for use by scientists around the world.
The cell lines the researchers produced carry the genes or genetic components for 10 different diseases, including Parkinson’s Disease, Type I diabetes, Huntington’s Disease, Down Syndrome, a form of combined immunodeficiency (“Bubble Boy’s Disease”), Lesch-Nyhan syndrome, Gaucher’s Disease, and two forms of Muscular Dystrophy, among others. Havard Stem Cell Institute Spotlight
The work is described in a paper published in the online edition of the journal Cell. Click here to read the full text of the paper titled, Disease-Specific Induced Pluripotent Stem Cells.The chief researchers were George Q. Daley, associate director of the Stem Cell Program at Children's Hospital Boston, and Chad Cowan and Konrad Hochedlinger of Massachusetts General Hospital.
Click hear to listen to an 08/06/08 press conference with George Daley and Doug Melton (who is also co-chairman of Harvard's new interfaculty Department of Stem Cell and Regenerative Biology).
Courtesy FIR0002New research coming out of Britain shows eating broccoli may reverse damage done by diabetes to heart and blood vessels. I’m always glad to hear anything new about the benefits of broccoli. Not that I have diabetes – I don’t. But broccoli is my favorite vegetable, and besides its potentially new vascular benefits, the leafy vegetable is high in fiber, full of vitamins C and K, and nutrients that have been found to reduce the risk of some cancers. A member of the cabbage family (Brassica), broccoli, along with other vegetables in the genus (including brussel sprouts, cauliflower, turnips, kohlrabi, and mustard seed) has been linked to the reduction of strokes and heart attacks.
Diabetes is a serious metabolic disorder resulting in abnormally high levels of blood sugar (hyperglycemia). The disease can affect nearly every part of the body, and left untreated can lead to blindness, kidney failure, nerve damage, and loss of limb. Diabetics have up to 5 times the risk of suffering from vascular diseases such as heart attacks, strokes because of damaged blood vessels.
The current research involves the anti-cancer compound sulforaphane, a product of another compound found in broccoli called glucoraphanin. Sulforaphane encourages production of enzymes that protect blood vessels, and reduce levels of cell-damaging molecules. When researchers at the University of Warwick tested the effects of sulforaphane on blood vessels damaged by hyperglycemia (high sugar levels), they noticed a nearly 75% reduction of Reactive Oxygen Species (ROS) molecules in the body. High levels of ROS -the result of increased blood sugar- can damage cells. The researchers noted sulforaphane also protected cells by triggering a protein that activated antioxidant enzymes.
“Our study suggests that compounds such as sulforaphane from broccoli may help counter processes linked to the development of vascular disease in diabetes,” said Professor Paul Thornalley of the University of Warwick. His team’s appears in the journal Diabetes. Thornalley added that he expects future tests of a brassica vegetable-rich diet could yield further health benefits for diabetic patients.
"It is encouraging to see that Professor Thornalley and his team have identified a potentially important substance that may protect and repair blood vessels from the damaging effects of diabetes,” said Dr Iain Frame, director of research at the charity Diabetes UK. "It also may help add some scientific weight to the argument that eating broccoli is good for you."
That brings to mind the time when the first president Bush said since he was president he didn’t have to eat broccoli anymore. (I think the quote was “Read my lips: no more broccoli”) Well, good for him. It just means more of the natural, leafy panacea for the rest of us.
Stephen Hawking has amyotrophic lateral sclerosis (ALS), a disease that destroys motor neurons. So far, progress in understanding this disease has been relatively slow, mainly because it has been difficult to obtain a decent supply of living motor neurons affected by the condition. New research done by John Dimos and Kit Rodolfa from the Harvard Stem Cell Institute has created in the laboratory a plentiful supply of cells that have the same genetic makeup as a patient with a particular disease.
A paper published online in the journal,Science, describes how they created the first stem cell lines from the skin of an elderly sick person, then coaxed these cells to become nerve cells genetically matched to those that had gone bad in a patient's spinal cord. By comparing diseased cells to normal cells in a Petri dish, scientists hope to better understand what causes disease and test new drugs.
This research builds upon the research we posted Jan. 18 titled Human embryo cloned from skin.
Courtesy CDC/Jim Gathany
Did you know back in February scientist and medical professionals selected the influenza virus strains for the upcoming flu season? Now that it is July the pharmaceutical companies are well into manufacturing, purification and testing the vaccine. Meanwhile, it is winter and flu season in the southern hemisphere and the virus is busy mutating. The big question on everyone’s mind is will it mutate so much that the northern hemisphere vaccine will be ineffective?
I agree with Dr. Steven Salzberg remarks in his recent Nature commentary…
"The current system, in which most of the world’s vaccine supply is grown in chicken eggs, is an antiquated, inefficient method requiring six months or more to ramp up production, which in turn means that the vaccine strains must be chosen far in advance of each flu season. More crucially it sometimes prevents the use of the optimal strain, as it did in 2007."
Influenza (the flu) is a serious disease
Each year in the United States, on average:
Some vaccine problems in the past
In recent years the match between the vaccine viruses and those identified during the flu season has usually been good. In 16 of the last 20 U.S. influenza seasons, including the 2007-08 season, the viruses in the influenza vaccine have been well matched to the predominant circulating viruses. Since 1988, there has only been one season (1997-98) when there was very low cross-reaction between the viruses in the vaccine and the predominate circulating virus and three seasons (1992-93, 2003-04, and 2007-08) when there was low cross-reaction (CDC). So after last year’s miscalculation the committee picked three new strains for the vaccine this year. One is a current southern hemisphere vaccine virus which they expect will still be present next year. In addition, they predict a second new Type A strain, known as H1N1/Brisbane/59, to also hit, along with a newer Type B/Florida strain.
Dr. Salzberg feels last year’s miscalculation was a failure…
"The harm was thus twofold; people fell ill and their trust in the vaccine system was undermined. This failure could have been predicted, if not prevented, through a more open system of vaccine design, a stronger culture of sharing in the influenza research community and a serious commitment to new technologies for production. The habits of the vaccine community must change for the sake of public health."
He goes on to suggest…
"The process of choosing flu-vaccine strains needs to be much more open. Other scientists, such as those in evolutionary biology with expertise in sequence analysis, could meaningfully contribute to the selection. At present, external scientists cannot review the data that went into the decision, nor can they suggest other types of data that might improve it."
Even with all of these miscalculations, I still feel getting the vaccine is worth the risk. But that doesn’t mean the process shouldn’t be improved. So once again I will be vaccinated and I will make sure my family is too—but what can we do as citizens to improve this process? What will you do?
Courtesy J.Vinther/YaleResearchers at Yale University are reporting the discovery of pigmentation within the fossilize feather from a bird or dinosaur. Using a powerful electron microscope, paleobiologist Jakob Vinther and his team claim that particles seen in the 100-million-year-old fossil appear to be similar to those seen in the feathers of living birds. This could mean that color - a characteristic long-thought lost in the fossil record - could someday be determined from the remains of pigment.
Vinther’s colleagues included Yale paleontologist Derek E. G. Briggs and Yale ornithologist Richard O. Prum. The results of their study will appear in an upcoming issue of Biology Letters. The research shows that dark stripes in the Cretaceous-aged feather display many similarities to the make-up of black melanin particles found in modern bird feathers. Melanin compounds determine color in plants and animals, a trait useful for such things as camouflage, species identification, and courtship display. In humans, melanin colors our skin and also protects us from overexposure to sunlight.
For a long time, the dark granules seen in fossilized feathers were thought to be the carbon remains of bacteria that had worked at decomposing the organism prior to fossilization. But advances in electron microscope technology have given scientists a closer - and clearer – picture of the feather’s structure, and instead show them to be fossilized melanosomes containing melanin pigment.
"Feather melanin is responsible for rusty-red to jet-black colors and a regular ordering of melanin even produces glossy iridescence,” Vinther said. “Understanding these organic remains in fossil feathers also demonstrates that melanin can resist decay for millions of years."
Under the scope, the lighter bands of the fossilized feather showed only the rock matrix, while the darker bands displayed traces of residue closely resembling the organic compounds found in the feathers of modern birds.
“You wouldn’t expect bacteria to be aligned according to the orientation of the feathers,” said Vinther.
Another bird fossil showed similar organic traces in the feathers surrounding its skull. The 55-million-year-old fossil from Denmark also preserved an organic imprint of the eye that showed structures similar to the melanosomes found in eyes of modern birds.
Nanostructure studies could one day provide paleontologists with evidence of colors other than just black and gray tones, and not just in fossil feathers. Vinther figures other organic remains such as fur from prehistoric mammals or fossil skin impressions from dinosaurs could prove to be the remains of the melanin.
Courtesy FasterDixOkay. Now I know what you’re thinking: “Every scene in Willow is frightening. Each scene is, in fact, somehow the most frightening scene. Will all of that become real too?”
Don’t worry, my doves, don’t worry.
You won’t be pursued through the forest by horrible pig dogs.
You won’t be puked on by a magic baby.
Your ethnicity won’t be slandered by drunks and soldiers.
You will not be captured and molested by hideous little rat men.
Monkeylike trolls will not chase you through derelict castles.
You won’t have to watch one of those awful trolls turn inside out and morph into a dragon. And you will not have to fight that dragon.
A shirtless Val Kilmer will not threaten you.
There will not be epic battles, nor attempted baby sacrifices.
You will not be stabbed by a man with a skull mask and an unspeakable caveman face.
A metal brazier will not chase you around a lightning-lit tower.
No wands will be brandished at you.
The town loudmouth will not belittle you in front of your family.
So, all in all, there’s relatively little to be concerned about. That said, there is one more most frightening scene to consider.
Do you remember when the army of Madmartigan and Airk Thaughbaer first laid siege to the fortress of Nockmark? Before Willow was able to fully control the powers of Cherlindrea’s wand and return Fin Raziel to her human, albeit greatly aged, form? You’ll recall that as soon as Airk, Madmartigan and Sorsha confront Bavmorda at the gates of Nockmark, the evil enchantress turns the whole of the attacking army into pigs. Once they were pigs things don’t seem so bad, but the process of turning into pigs was horrible to watch. There were hoof-hands everywhere, and emerging piggy snouts, and tusks, and oinking, and everybody looked really sweaty. It was very frightening to see, and it’s happening in our own plane of existence: human-pig hybrids have been given the go-ahead in England.
Careful examination of the story clearly indicates that half human, half pig creatures like those in Willow are neither the intent here, nor are they actually possible from these experiments. But I tend to believe what I imagine is the case more than what I’m old is the case.
If you do want to waste your time with what you’re told, however, listen up:
The aim of this research is in no way to create a weird pig man. Or a weird man pig. The goal is actually to put human DNA from skin cells into a pig egg that has had its chromosomes removed, and then let it develop into an embryo. In fact, the scientists involved are attempting to create an embryo with no animal DNA left in it at all (kind of ironic, I suppose).
There’s more to it, of course, but the idea is this: the human DNA put into the eggs will be DNA taken from people with a genetic heart disease. As the scientists observe the transformation from egg to embryo, they hope to better understand the molecular mechanics of the disease. That information could then be used to create better treatments for people living with related heart conditions. None of the “hybrids” will develop past the very first stages of being an embryo (basically a featureless sphere of cells).
Or, if you’re into letting your gut and imagination do your critical thinking for you…prepare yourself for Island of Doctor Moreau Earth.