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Category Archives: Transhuman News

DNA not sent for testing; judge orders release of two capital murder suspects – WFAA

Posted: July 5, 2017 at 10:47 pm

Judge releases capital murder suspects

Tanya Eiserer, WFAA 3:48 PM. CDT July 05, 2017

A Dallas County district judge has ordered the release of two capital murder suspects after prosecutors failed for more than a year to send the DNA of one of the defendants to the lab to be tested.

On Monday the judge ordered that Leonte Stone, 24, and Konkun Tarpeh, 25, be released on electronic monitoring and house arrest.

The only thing keeping the two men in jail currently are holds from other counties. Tarpeh is being held on a Tarrant County violation on a protective order charge from Tarrant County. Stone is being held from Hunt County for evading arrest and child endangerment charges.

By state law, prosecutors have 90 days to announce that they're ready for trial from the day that a person is arrested. That's to keep indigent defendants from just being held in jail in perpetuity. In this case, prosecutors had failed to send Stones DNA to the lab to be tested against evidence collected in the case.

District Judge Brandon Birmingham ordered their release on a personal recognizance bond.

The DNA testing also cant be done quickly because of a recent issue with countys new DNA testing kits, which proved to be defective. The county crime lab suspended DNA testing in cases set for trial. The lab plans to restart testing in September with new testing kits.

Stone and Tarpeh are accused of killing Taydren Young and Dmydric Williams at an apartment complex on Forest Lane last March. Police said Young and Williams had gone there to buy marijuana.

Stone has been in jail since April. Tarpeh was picked up again in December. Their bail in the capital murder case had been set at $1 million each.

I am highly, highly upset, says Shokee Clay, Youngs mother. I'm very upset about the whole situation that there's even talk of anybody being released. There aren't words to explain how I feel about that.

Clay is angry that prosecutors did not tell her there was an issue with the case. She says the prosecutor on the case had assured her that she would keep her informed.

My son may not matter to them, but he matters to me, and I'm going to fight to the end for my son and I'm not going to let this ride, she says. I'm going to be up there tomorrow because I need some answers... because I need to know why I wasn't notified and how did they let DNA slip through.

She worries that if Stone and Tarpeh are released, they will just cut their ankle monitors and disappear.

The DAs office says that they will continue to vigorously pursue prosecution in the case. They said they could not comment further due to the ongoing nature of the case.

Shokee still cries every day over the loss of her son.

A video of Young freestyle dancing brought a smile to his mom's face. She misses his goofy, fun-loving personality.

I just wish I could reach in here and grab him out, but I know I can't, she says. Every day that go on, you know that he really, really not coming back.

Shokee and her husband had moved their boys out of Dallas to keep them safe.

Her middle son -- who is one year younger than Young -- is in college. Their other son is finishing high school.

Young's future had also looked bright.

He had graduated with honors from John Horn High School in Mesquite. He had a scholarship to Texas Southern University. He attended for two semesters before dropping out.

Young gravitated to a rougher crowd once back in Dallas.

On the day he died, Clay said she called her son. He asked her to pick him up in North Dallas. She told him she would pick him up after work. An hour later, Young was killed. He left behind an infant son.

I did everything I could, she said. Its not about how you raise your boys. It's about the company they keep.

As painful as it was, Shokee was there when they cremated Young.

This is all I have left of him, she says pointing to the wooden box containing his ashes. I walk by it every day and this is what I have and no mother should have to have one of these.

2017 WFAA-TV

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Microsoft’s DNA-Powered Server Cost $2 Billion — but Prices Could Drop Over 99.9% – Madison.com

Posted: at 10:47 pm

A few years ago, Harvard professor and bio-engineering rockstar George Church was a guest on The Colbert Report. As many of the talk show's guests did, he presented host Stephen Colbert with a copy of his book, which he'd co-authored with Ed Regis. Well, sort of. He actually handed Colbert 20 million copies of his book -- and they all fit in his front pocket.

How was that possible? Church had programmed 20 million copies of his book into DNA, which is known, rightly so, as the "information molecule" in biology. The incredible density of information that can be stored in DNA, and the potential to use it much like a traditional hard drive, has not been lost on technology companies scrambling to keep up with society's exponentially growing need for data storage.

Perhaps due to its having let the future pass it by on one too many occasions, Microsoft (NASDAQ: MSFT) is going all-in on the idea. It plans to deploy a proto-commercial, DNA-powered storage device about the size of a commercial Xerox copier by the end of the decade in one of its data centers. Even though it would cost billions using today's DNA synthesis technologies and only serve a niche application, the technology developed in the next three years will go a long way to ushering in digital-bio hybrid computing machines. It could be big for investors, too -- if it works.

Image source: Getty Images.

Microsoft and the rest of the information technology industry has spent billions of dollars on data centers to date in an endless battle to scale with the needs of consumers and growing demand for cloud computing. The most expensive part of a data center is power consumption, since it takes a lot of power to keep arrays of servers cool. That has become especially painful as traditional storage media have begun hitting their limits, which means tech companies won't be able to wring any further cost reductions out of scaling storage capacity with today's technology.

That's what makes DNA so intriguing, on paper at least. Volume for volume, it can store 10 million times more information than the magnetic tape drives commonly used today, which would drastically reduce power consumption per TB or square foot of space in a data center. One copy of your genome, held in just one of your body's cells, holds approximately 1.5 GB of information. And since your body contains trillions of cells, all of the DNA in all of your body's cells stores trillions of GB of information -- more than all of the digital data storage capacity in the entire world (although it's getting close).

There is one massive obstacle to commercializing this technology, however: cost. Consider that state-of-the-art technology today can produce synthetic DNA for genetic engineering applications at costs of about $0.05 per base pair, and experts I've spoken to attest it could be two orders of magnitude lower for DNA data storage applications. (The end use affects the cost of DNA because each application has different requirements for accuracy, length, and yield.)

Image source: Getty Images.

Either way, even with the best technology today, it would take several months and hundreds of thousands of dollars to synthesize an equivalent amount of DNA held in a single cell of E. coli -- something the bacterium does for free in about 20 minutes.

The good news is the cost has fallen quickly -- it was $1 per base pair not long ago. The not-so-good news is Microsoft estimates costs would need to fall by a factor of 10,000 before DNA data storage could really take off.

The company will likely be powerless to drive down the cost of DNA synthesis without outside help from biotech companies (supply) and fellow tech peers (demand). That's why Microsoft has partnered with the University of Washington and DNA synthesis leader Twist Bioscience, which has received investments from Illumina and Applied Materials, among others.

Earlier this year the trio made significant progress developing the basic technology required for DNA data storage, such as error-free read and write capabilities. The early-stage work also shows which areas need drastic improvement:

The biggest cost reductions will come from synthesizing DNA as close to free as possible (nature does this pretty efficiently), although improvements in technologies allowing us to more fully tap into the awesome storage density of DNA will greatly improve the cost-benefit ratio as well.

Put it all together and today's DNA synthesis and DNA data storage technologies would enable digital data storage devices at a cost of between $2 billion and $4 billion per TB. That's awfully expensive, but tremendous cost reductions -- more than 99.9% -- are possible with the proper effort and investments.

It may seem ridiculous, but investors should know there is precedent for dropping costs of biotechnologies over 99.9%. The amazing success of the Human Genome Project, which was initiated to spur innovation in DNA sequencing ("reading genes"), serves as a great example of what's possible. The cost of sequencing a human genome fell from $3 billion at the start of the project to just $1,000 today. Illumina thinks it can reduce that to $100 in the near future.

The recently announced Genome Write Project, which aims to spur innovation in DNA synthesis and construction ("writing genes"), is the logical follow-up to the Human Genome Project. Catalyzing a similar cost reduction to its scientific predecessor would drop DNA data storage costs from $2 billion to $4 billion per TB today to market-ready prices in the next 15 to 20 years, perhaps much sooner for data-center applications when power consumption and footprint costs are factored in.

However, the Genome Write Project's main problem is a lack of funding: Other than a $250,000 grant from Autodesk, there isn't much funding to speak of, despite interest in DNA data storage for data centers from across the industry. If Microsoft is serious about delivering DNA data storage technology to the market, it may want to consider funding the public research project in addition to its in-house R&D. Otherwise, it may be difficult to drum up support from tech peers -- who represent future synthetic DNA demand.

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DNA testing – on the road to regenerative medicine – VatorNews

Posted: at 10:47 pm

We recently had Dr. Craig Venter speak at our Splash Health 2017 event. Dr. Venter is the first person to sequence a human genome, simply put: the instructions and information about human development, physiology, and evolution. In his interview, he points out that 15 years ago, sequencing a human genome would have cost $100 million and take over nine months.

Oh how far weve come. Today, there are a number of companies helping us to analyze our genes, or basically our DNA, which make up genes, to understand our physiology. Advances in sequencing the human genome have been the foundation for this knowledge, and is ultimately paving the path toward personalized medicine - therapies that are personalized to a persons genetic code, and its cousin regenerative medicine - therapies that replace or enable damaged cells, organs to regenerate.

One company, Orig3n, is doing both. Boston-based Orig3n started out in 2014 collecting blood samples to conduct regenerative medicine studies, but later added in the ability to conduct DNA testing to learn more about a persons intelligence, or predisposition to learning languages, to knowing what vitamins theyre deficient in.

Its an interesting an unique funnel the company has created for itself on its way to solve big problems with regenerative medicine, which seems more in its infancy than DNA testing.

To that end, Orig3ns DNA testing business has taken off.

In order to be tested, you take a cotton swab and swab the inside of your cheek to collect DNA samples from the cells inside your mouth. Alternatively, one could spit in a tube, which is how 23andMe collects samples of DNA.

From there, Orig3n breaks down the cells to open up the DNA, which is inside the nucleus of the cell. The DNA is then purified and put into a genetic test panel. Your DNA is then analyzed against other DNA that have been collected and studied.

The analysis of the DNA is pretty standard. What differentiates its products, according to Robin Smith, Founder and CEO, is how the analysis is packaged and how quickly the results are turned around. The whole genome sequencing world has been around for 15 years and is fairly commoditized, said Smith. The same thing is happening with DNA detection. The biggest differentiator for Orig3n is that it delivers the data in ways that are understandable, said Smith.

For instance, on Orig3n, tests focus on an analysis of your skin to perfect your skincare routine, or about your strength and intelligence. Tests range from $20 to $100.

On Everlywell, you can take a DNA test to measure your sensitivity to foods. Or for around $239, it appears you can test to see if you have HIV, Herpes Type 2 and other sexual diseases.

On 23andMe, you can pay $199 to learn what proportion of your genes come from 31 populations worldwide, or what your genetic weight predisposes you to weigh vs an average and what are some healthy habits of people with your genetic makeup [though personally these habits seem to be good for anyone regardless of genetic makeup].

But for Orig3n, the DNA tests are just a good business while also a funnel to the bigger problem theyre trying to solve, and for which they recently raised $20 million for: Regenerative medicine.

Before offering the DNA tests, Orig3n was taking and continues to take blood samples, reprogramming cells to go back to a state three days prior. And from there, they can grow certain tissues. The purpose of Orig3n is to create cell therapies for various diseases and disorders.

In the next fives year, there will be real live therapies to repairing the degeneration of your eyes or performing some cardiac repair, Smith predicted. It feels like 1993 when I used a phone line to dial into the Internet, then seven years later we had the boom. We think regenerative medicine - getting your body to induce itself to rejuvenate parts that are broken - is where the Internet was in 1993.

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Turning point: Single-cell mapper – Nature.com

Posted: at 10:47 pm

Mike Liskay

Biotechnologist Andrew Adey developed a high-throughput method for mapping the genomes of single cells. The advance, reported in January, allows for the identification of diverse cell populations in tumours, and so paves a path towards precision medicine. To develop it, Adey, now at Oregon Health & Science University in Portland, relied on HeLa cells, a prolific cancer-cell line biopsied in the 1950s from Henrietta Lacks, who had cervical cancer, and used widely in biomedical research without her consent.

How has single-cell biology advanced?

In the mid-2000s, next-generation sequencing was just starting, so today's version of single-cell biology was non-existent. Today, researchers can look at genome-wide properties or other aspects of single cells.

How did you use HeLa cells?

I knew nothing about the history of HeLa, just that it was a cancer-cell control line that grew really well. We wanted to understand how different copies of chromosomes influence cells. Once we developed technology to do this in normal cells, we set out to see how those copies act in cancer cells, and so applied it to HeLa. We learned more about HeLa notably, that multiple copies of a genome can act differently and worked out the genomic changes that enable an aggressive cancer to reproduce so readily.

What was your role in the privacy debate over publishing HeLa sequence information?

As we were readying a paper in 2013 (A. Adey et al. Nature 500, 207211; 2013), we didn't know how we were going to publish genetic information that could have consequences for Lacks's descendants. Ultimately, the US National Institutes of Health reached an agreement with the Lacks family that accompanied our paper, and that granted researchers access to the cells while maintaining the Lacks's privacy. HeLa is a unique case one not only at the forefront of medical advances but also about the ethical informed consent that is crucial to medical practice.

Can you explain the technique put forth in your January paper?

Initially, our platform could fully sequence only the portion of the genome that regulates gene expression in single cells (S. A. Vitak et al. Nature Meth. 14, 302308; 2017). We wanted to progress to whole-genome sequencing from single cells. But when you target regulatory elements, you typically have access to only 14% of the genome. We had to work out how to free up the DNA to convert the entire genome into sequenceable molecules.

What were the main obstacles?

At one point, it seemed like we were playing 'whack-a-mole'. Every time we altered one fixed property of the protocol, something else that had been working fine would stop. It was challenging, because the genome is packed nicely into nuclei. We needed to destroy the proteins that packaged the DNA inside the nucleus, without destroying everything else. Most of the time, everything would just explode and we'd lose the ability to look at single cells.

What's next?

We've already improved our method from what we published in January. It's even more reproducible, and we can get more data from single cells. Half of my lab does technology development; the other half applies those methods to answer questions of interest. This method was the first step to examining other aspects at the single-cell level. We're now using these technologies to explore cell identity. For example, how does a cell respond when treated by a cancer drug?

How will your method affect cancer treatment?

With a single-cell focus, we can start to profile an individual's tumour and identify molecularly distinct subpopulations in a tumour. If we can then profile large cohorts and tumours at the single-cell level, we can learn how certain subpopulations will respond to specific drugs to better home in on effective treatments.

This interview has been edited for length and clarity.

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Scientists are questioning the idea that the human lifespan has a limit – Yahoo News

Posted: at 10:47 pm

An elderly man swims

(Al Bello/Getty Images)

Jeanne Calment, the French woman who holds the record for the longest verified lifespan, died in 1997 at 122 years old.

Few people, of course, everbecome supercentenarians 110 years old or older and even fewer hit 115.

So few people have exceeded that age, in fact, that a group of researchers published an analysis in the journal Nature last year arguing that the human species' lifespan plateaus around115.

But a number of scientists are now rebutting that analysis with five separate commentaries published in Nature on June 28.

The authors of these piecesargue that the original analysis relied onstatistics that were incomplete or analyzed in a way that led to a falseconclusion. They suggesttwo alternatives: We either don't have enough data to know if the human lifespan has a limit, or theplateau is closer to125 than 115.

"The available data are limited, there aren't that many supercentenarians," Maarten Pieter Rozing, a professor at the University of Copenhagenwho co-authoredone commentary, told The Scientist. "And I think there are no strong arguments that show there is a decline [in the rate at whichlifespans areincreasing]."

Life expectancy has crept up fairly steadily over the past 150 years or so. But Xiao Dong, Brandon Milholland, and Jan Vijg, the authors of the original analysis, argue that comparing the life expectancy of supercentenarians to theage at whichthey died can reveal thenatural limit ofthe human lifespan.

(iStock)

The scientists used data on maximum reported age at death split into two sets based on supercentenarians from the US, UK, Japan, and France. Thefirst set covered deathsfrom 1968 to 1994 a period when the maximum age was inchingup. But bythe time covered in the next dataset, from 1995 to 2006, the ageseemed to plateau or even slightly be on the decline (exceptions like Calment aside).

Life expectancy, however, rose throughout both time periods.The scientists therefore concludedthatbecause humans' maximum age didn't keeprising with life expectancy, it appeared a limit had been reached.

Even if we were to cure various diseases like cancer or Alzheimer's, those scientists still claimed thathumans would probablybe unlikely to live past 115. And they put thechances ofa person live past 125 atless than 1 in 10,000.

elderly chinese couple

(David Gray/Reuters)

The authors of the recent rebuttals say that because there are so few supercentenarians out there, the number of deaths for this age group between 1995 and 2006 is too small to yield reliableconclusions. There just haven't been enough supercentenarians to really pinpoint amaximum age.

As people live longer, it's likely that more will push past that supposed limit, the authors of the rebuttals argue it'll just take time toget there.

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"[T]he idea of a set limit to human longevity is not strongly supported by what is being discovered about the biology of ageing," Rozing and his co-authors wrote in their commentary. "The continuing increase in human life expectancy that has occurred over recent decades was unforeseen. It provides evidence for greater malleability of human ageing than was originally thought."

Over the span of human history, many of the lifespan increases we've seen would have been unimaginable at some point. Thoseliving200 years ago, for example, would have thought it wascrazy that peoplecould regularly liveto be80. Yet here we are.

Rozing told The Scientistthat there'san easy way to find out whose hypothesis is correctabout the maximum lifespan.

"[W]e can just wait and see who's right," he said.

NOW WATCH: Scientists just discovered the world's oldest shark, and it's ancient

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Dr. Cannaday’s eczema cure, part 2 – Sedalia Democrat

Posted: at 10:46 pm

Sedalia dermatologist Dr. Julian Cannaday achieved fame and wealth treating eczema, a skin disease marked by rough, itchy, scaly patches on the skin. In the book he wrote advocating his treatment for eczema, he questioned the currently available treatments and the doctors who prescribed them. He also offered his own cure.

Cannaday proposed that eczema was difficult to cure because most physicians treated the effects and ignored the cause. He believed he knew the cause, which he claimed was the buildup of acid in the blood and the inability of the body to cleanse the blood, forcing the acid to be excreted through the skin, which developed itchy patches where the acid seeped out. His explanation, and the certainty with which he pronounced it, is interesting, in that the exact cause of eczema remains unknown.

The website of the prestigious Mayo Clinic suggests several contributing factors, including dry irritable skin caused by too much exposure to hot or cold water or harsh cleaning agents, allergies to dyes or perfumes in soaps or lotions, and environmental conditions such as exposure to hot dry air. Cannaday explains that these factors may aggravate eczema by irritating skin already damaged by the acid excreted through the skin.

Some treatments offered during the early 20th century tried to kill germs that were found in the scabs that developed on the skin. Cannaday believed the germs were carried by the fingers of the patient who scratched the intensely itching skin and were not the cause of the disease. In addition, the things prescribed to treat the skintar, zinc, carbolic acid, corrosive sublimates [used] to kill the germs were so strong they injured the skin

Cannaday dismissed some of the treatments proposed by other doctors, such as cod liver oil, though a deficiency of Vitamin D, a substance found in cod liver oil, may contribute to eczema. Cannaday also dismissed ointments prescribed by other doctors.

Cannadays treatment consisted of the use of a diet that avoided foods that build up acid during digestion. His prescribed a special diet that he said would allow the patient to eat enough food to keep hunger away while not building up acid.

The second part of Cannadays treatment was a blood tonic taken as either pills or liquid form three times per day. He believed the tonic would improve digestion.

The third part of his treatment was the use of a special wash for the affected skin.

Cannadays book does not list the foods allowed on his diet, nor does it give any hints as to the composition of the tonic or the wash. For the treatment, one had to pay $12.50 ($308 in todays purchasing power) for two months worth of tonic, powder to mix with water to make the wash, and a written copy of the diet.

We still do not know the exact nature of Cannadays cure. Perhaps someday, someone will find in the attic a copy of the diet, a tonic pill or two, and some of the wash power so they can be analyzed for their content.

http://www.sedaliademocrat.com/wp-content/uploads/2017/07/web1_Chalfant_-RhondaCMYK.jpg

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How To Treat Eczema on Your Face – Men’s Health

Posted: at 10:46 pm


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How To Treat Eczema on Your Face
Men's Health
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Hopkins joins gene cloning project to advance medicine development – Baltimore Sun

Posted: at 10:46 pm

Scientists at Johns Hopkins, Rutgers and Harvard universities, as well as the University of Trento in Italy, have created a new technique that allows thousands of genes in a DNA sequence to be cloned at once.

Researchers hope the advance in gene cloning will allow them to more quickly identify markers for diseases and discover new medicines.

Until now genes had to be cloned individually in a time-consuming process. The new molecular method allows thousands of the long DNA strands that make up genes to be isolated and cloned at the same time.

The discovery was published June 26 in Nature Biomedical Engineering.

"Our goal is to make it cheap and easy for any researcher in any field to clone and express the entire set of proteins from any organism," said Ben Larman, an assistant professor of pathology in the Johns Hopkins School of Medicine and the study's co-senior author, in a statement. "Until now, such a prospect was only realistic for high-powered research consortia studying model organisms like fruit flies or mice."

The scientists call their technique for capturing DNA strands that make up genes the LASSO method, for long adapter single-stranded oligonucleotid. They also liken it to capturing cattle with a rope.

The new process speeds up the genes' creation of proteins, which manage cell activity, compared to the old process of cloning individual genes.

To test the method, the scientists sought to capture more than 3,000 DNA strands from the E. coli bacterial genome, commonly used as a model organism, and were successful with most of the targets. They also were able to use the strands to analyze what the gene's proteins do.

"We're very excited about all the potential applications for LASSO cloning," Larman said. "Our hope is that by greatly expanding the number of proteins that can be expressed and screened in parallel, the road to interesting biology and new therapeutic biomolecules will be dramatically shortened for many researchers."

The next step, already underway, is improving the cloning process and building libraries of proteins from DNA samples for use in research, said Biju Parekkadan, an associate professor in the Department of Biomedical Engineering at Rutgers University-New Brunswick.

Funding for the research came from the Shriners Hospitals for Children, the Prostate Cancer Foundation and the National Institutes of Health.

Larman, Parekkadan and a Harvard scientist on the project have sought a patent for the method, which is pending.

meredith.cohn@baltsun.com

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Asthma drug shows promise in treating obesity and diabetes – University of Michigan Health System News (press release)

Posted: at 10:46 pm

ANN ARBOR, Mich. -- After 12 weeks of taking an anti-inflammatory asthma drug, obese patients with type 2 diabetes showed a clinically significant drop in blood glucose.

The drug amlexanox, prescribed in Japan to treat asthma, appeared to free the metabolic system to burn more energy. A subset of patients had improved fatty liver disease and insulin sensitivity, a response seen among those who started the clinical trial with higher levels of inflammation in their fat tissue than others.

While the discovery at Michigan Medicine and the University of California at San Diego is not ready for the clinic, it reveals an inflammatory link between obesity and type 2 diabetes.

Inflammation is the bodys natural response to injury and illness, but chronic inflammation caused by obesity is believed to promote insulin resistance, a main feature of diabetes.

We are beginning to understand the role this form of internal inflammation plays in the development of chronic diseases like diabetes, says lead study author Elif Oral, M.D., director of the MEND Obesity and Metabolic Disorder Program at Michigan Medicine. Ultimately we may be able to personalize therapy based on the degree of inflammation present at baseline which is a new concept.

Oral is an endocrinologist and translational scientist at Michigan Medicine, the University of Michigans academic medical center where the clinical trial was conducted and analyzed.

Tissue analysis was led by study author Alan R. Saltiel, Ph.D., at U-C San Diego, along with scientists at the Salk Institute for Biological Sciences.

In the Cell Metabolism study, researchers identified a molecular signature in obese patients with type 2 diabetes who responded to the drug amlexanox.

When we looked at the drug-treated group we saw a bimodal distribution, that is, there were some responders and some nonresponders. We didnt understand why, so we did a molecular analysis from biopsies of fat cells we took from patients at the beginning and end of the study, says Saltiel, director of the Institute for Diabetes and Metabolic Health at U-C San Diego

In the responder group, the level of inflammation in fat was higher than in the nonresponder group at the beginning of the study, indicating that there is something about inflammation that predisposes a person to respond. And, what was really amazing was that there were more than 1,100 gene changes that occurred exclusively in the responders.

The glucose-lowering effects of amlexanox were first discovered in mice during research at the University of Michigan where Saltiel served as director of the Life Sciences Institute at the U-M.

Promising results

Amlexanox is an inhibitor of two enzymes, IKK and TBK1. In previous studies, Saltiel and U-M researchers discovered that these two enzymes are induced in obese mice, causing a drop in energy expenditure or reduction in calories burned.

This prompted them to look for inhibitors of these enzymes by screening a library of 150,000 chemicals. They found amlexanox. Giving obese mice the inhibitor caused them to lose weight, while their sensitivity to insulin increased, improving their diabetes and fatty liver disease.

The human trial revealed that gene changes that occurred in the mouse model also happened in the human responder group. Blood sugar in the clinical trial patients went down as genes involved in the expenditure of energy changed.

The proof of concept trial began with an unblinded safety trial of six patients. It was followed by a controlled trial of 42 obese patients with type 2 diabetes.

Half of the patients were randomized to a placebo group while the other half received amlexanox for three months. Blood sugar, insulin sensitivity, weight and liver fat were measured. A biopsy of fat cells from each patients midsection was taken before and after the trial to measure changes in gene expression.

The most exciting part of this is that we have a new drug that has never been studied before, says Saltiel. Its a new mechanism for a diabetes and fatty liver drug. Its promising, but there are a lot of questions that need to be answered still.

Among them: Which gene changes are the most important to target? Whats the right drug dosage? What time of day should it be administered? How often should patients take the drug? Can the percentage of responders be increased? Will the beneficial effects of the drug be sustained for a longer time?

One-third of the participants in the blinded study responded. Among responders with nonalcoholic fatty liver disease, an improvement was also seen.

Researhers are planning follow-up trialsto look at whether its possible tostratify patients who are likely to respond based on the degree of underlying inflammation, and explore if other drug combinations can be used with amlexanox.

We are grateful for patient participation and hope that our patients will respond with the same enthusiasm to our new trials. Without patients volunteering, the sort of study can never happen, says Oral.

Primary support for the research came from the National Institutes of Health High Risk High Reward grant R21DK098776.

Additional authors include Shannon M. Reilly, Andrew V. Gomez, Rasimcan Meral, Laura Butz, Nevin Ajluni, Thomas C. Chenevert, Evgenia Korytnaya, Adam H. Neidert, Rita Hench, Diana Rus, Jeff Horowitz, BreAnne Poirier, Peng Zhao, Kim Lehmann, Mohit Jain, Ruth Yu, Christopher Liddle, Maryam Ahmadian, Michael Downes and Ronald M. Evans.

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Asthma drug shows promise in treating obesity and diabetes - University of Michigan Health System News (press release)

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