Monday, December 3, 2012

Drug makers step up search for hearing loss medicines ? Business ...

ZURICH/LONDON ? When Swiss biotech firm Auris Medical wanted to recruit patients to test its experimental hearing loss drug, it decided to enlist partygoers deafened by firecrackers on New Year?s Eve.

In the weeks leading up to Dec. 31, 2005 it advertised in the subway and on radio stations in Munich and Berlin, urging victims of sudden firecracker-induced hearing loss to turn up at designated clinics for treatment on January 1.

?We had just one single day of enrolment, we didn?t know how many people would show up,? Thomas Meyer, managing director of Auris, told Reuters.

Luckily, his gamble paid off and the small private company is now one of the leaders in what has been an empty space for the pharmaceutical industry.

Auris managed to recruit enough people to show that its compound AM-111 posed no safety risk and has since successfully completed a mid-stage trial in acute sensorineural hearing loss, or sudden deafness, involving 210 patients.

While there is no guarantee that its drug, which is injected through the eardrum, will pass muster in final-stage tests, the progress by Auris and a clutch of rival biotech firms is making large pharmaceutical companies sit up and take notice.

There are currently no approved disease-modifying drugs for hearing loss, which affects nearly a third of people aged 65 to 74 and half of those over 75.

But the science is developing and investor interest is growing, piqued by the huge commercial success of recent new treatments for sight loss, such as Lucentis from Novartis and Roche and Eylea from Regeneron and Bayer.

British charity Action on Hearing Loss conservatively puts the potential Western market for new drugs at $4.6 billion a year ? a figure that could grow quickly as ageing populations swell the ranks of those with hearing problems.

NEGLECTED FIELD

?It?s one of the few areas that, as yet, hasn?t really been tackled by the drugs industry,? said Kate Bingham, managing partner at SV Life Sciences Advisers, a venture capital firm with investments in new drugs for both eyes and ears.

Bingham sits on the board of Autifony Therapeutics ? a hearing loss firm spun out of GlaxoSmithKline in which the British drugmaker retains a stake.

Historically, hearing loss has received little attention from Big Pharma, given the lack of obvious targets for drug intervention, the difficulties of running clinical trials and a widespread belief that most deafness could not be reversed.

Now the big companies are getting involved, although the work is early-stage.

?A drug that is therapeutic and priced right could be quite a blockbuster. That?s why they?ve put their toe in the water,? said Jonathan Kil, chief medical officer at Seattle-based Sound Pharmaceuticals, which is enrolling young iPod users in a trial of an oral drug for noise-induced hearing loss.

U.S. giant Pfizer is arguably the most advanced of the big players, with a drug in initial Phase I clinical testing trial for age-related sensorineural hearing loss that looks to enhance the function of existing hair cells.

Some of its biggest rivals are laying bets, too. Last year French drugmaker Sanofi inked a two-year research deal with privately held Dutch biotech firm Audion Therapeutics to develop small molecule drugs to improve hearing.

In October, Roche joined forces with venture capital firm Versant Ventures and biotech Inception Sciences to find molecules targeting ear hair cell protection and regeneration in the cochlea, the spiral-shaped cavity in the inner ear.

Cross-town competitor Novartis, meanwhile, struck a 2010 deal potentially worth more than $213 million with U.S. biotech GenVec to develop gene-based treatments to replace hair cells in the ear that transmit sound.

?We?re looking at restoration as our main line of work and we?re interested in whether there are chemicals that might also play this role instead of having to introduce a gene,? said Novartis research head Mark Fishman.

?This is an area that?s a bit more futuristic and ultimately restoring the hair cells will be the cure.?

EYES AND EARS

Unlike new eye drugs, which work by inhibiting an unwanted process, hearing drugs will need to restore damaged function ? a more difficult proposition.

Experts say the first drugs will target niche areas, such as damage caused by loud noise or as a result of chemotherapy.

?Hearing loss is not just one condition. It?s like cancer ? there are lots of different types and there is work to be done to segment the market,? said Ralph Holme, head of biomedical research at Action on Hearing Loss.

Heading the field for noise-induced hearing loss is South Illinois University, which has launched a late-stage trial with the U.S. military for a drug to increase protection for people exposed to very noisy environments like soldiers.

Canada?s Adherex also has a late-stage trial to test a drug that may protect against hearing loss caused by platinum-based anti-cancer agents in children.

While protective treatments could become available within the next few years, regenerative approaches ? such as injecting stem cells into the ear or chemically intervening to switch on genes that control cell growth ? are much further off.

Despite recent promising tests in gerbils, the potential to replicate this in humans is still uncertain, said Pascal Senn, an ear specialist at the University of Berne.

?If something grows inside the ear, you must be sure that it doesn?t grow excessively or form tumours. There are a lot of roadblocks that need to be overcome in this field. It?s highly risky, but I think it?s also the hottest area,? he said.

One intriguing possibility for the future is the convergence of future drugs and devices. Hearing aid manufacturers have certainly not been deaf to the noises from the pharma sector.

Sonova, the world?s largest maker of hearing aids, has invested in two start-up companies ? one in the United States for drugs to protect hearing and another Swiss biotech working on a treatment for acute tinnitus.

It bought U.S. cochlear implant manufacturer Advanced Bionics in 2009 in a bid to increase its focus on the inner ear and understand how drug treatments could work with implants.

?It will be interesting whether the innovation will be driven by pharma companies moving in or whether the hearing aid companies will branch out,? said Auris? Meyer.

?

Source: http://bangordailynews.com/2012/12/03/health/drug-makers-step-up-search-for-hearing-loss-medicines/

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Scientists at Scripps Research Institute discover how 2 proteins help keep cells healthy

Scientists at Scripps Research Institute discover how 2 proteins help keep cells healthy [ Back to EurekAlert! ] Public release date: 2-Dec-2012
[ | E-mail | Share Share ]

Contact: Mika Ono
mikaono@scripps.edu
858-784-2052
Scripps Research Institute

The work has implications for cancer drug development

LA JOLLA, CA December 2, 2012 Scientists at The Scripps Research Institute (TSRI) have determined how two proteins help create organelles, or specialized subunits within a cell, that play a vital role in maintaining cell health. This discovery opens the door for research on substances that could interfere with the formation of these organelles and lead to new therapies for cancer.

The study, published online ahead of print on December 2, 2012, by the journal Nature Structural & Molecular Biology, focuses on the structure and function of the two proteins, ATG12 and ATG5. These proteins need to bond correctly to form an organelle called the autophagosome, which acts like a trash bag that removes toxic materials and provides the cell with nutrition through recycling.

"Our study focuses on one of the big mysteries in our field," said Takanori Otomo, the TSRI scientist who led the effort. "These proteins are linked, but no one has explained why clearly. We're very excited to have determined the structure of these linked proteins so that the information is available to do the next level of research."

Asking Questions, Finding Answers

At the beginning of the study, Otomo and colleagues knew that many proteins work together to form autophagosomes as part of the process known as autophagy, which breaks down large proteins, invasive pathogens, cell waste, and toxic materials. As part of this process, one key protein, LC3, attaches to a lipid, or fat molecule, on the autophagosome membrane. Yet LC3 cannot attach to a lipid without the help of ATG12 and ATG5, and a cell will only form an autophagosome if the linkage, or conjugate, between these two molecules has been established.

Otomo and colleagues set out to determine the shape of the ATG12-ATG5 conjugate, and to find out why it was needed for LC3 lipidation.

Using a method called X-ray crystallography, the scientists were able to unveil the details of this conjugate. When ATG12 and ATG5 come together, they form a rigid architecture and create a surface area that is made up of evolutionarily conserved amino acids and facilitates LC3 lipidation. The researchers confirmed this finding by mutating those conserved amino acids , which prevented an autophagosome from forming.

Otomo and colleagues also identified a surface on the ATG12-ATG5 conjugate that binds to ATG3, another enzyme required to attach LC3 to the lipid.

Toward Better Understanding and New Cancer Treatments

With this new knowledge, the researchers hope to design molecules that inhibit autophagosome formation, a direction of research that has implications for cancer treatment. A drug that directly inhibits ATG3 binding, for example, could be used in coordination with current therapies to make cancer treatments more effective, preventing a cancer cell from recycling nutrients and prolonging its survival.

"Ultimately, we'd like to understand the molecular mechanisms of each step of autophagy," he said, "As we make progress toward this goal, we will have a better idea of how to manipulate the pathway for therapeutic purposes. This field is still young and there are a lot of unknowns. This work is just the beginning."

###

In addition to Otomo, authors of the paper, "Structure of the human ATG12~ATG5 conjugate required for LC3 lipidation in autophagy," include Chinatsu Otomo and Zoltan Metlagel of TSRI, and Giichi Takaesu of Keio University in Tokyo, Japan.

This research was supported by National Institutes of Health (NIH) grant GM092740 and by funds from Japan Science and Technology Agency through the Keio Kanrinmaru Project.


[ Back to EurekAlert! ] [ | E-mail | Share Share ]

?


AAAS and EurekAlert! are not responsible for the accuracy of news releases posted to EurekAlert! by contributing institutions or for the use of any information through the EurekAlert! system.


Scientists at Scripps Research Institute discover how 2 proteins help keep cells healthy [ Back to EurekAlert! ] Public release date: 2-Dec-2012
[ | E-mail | Share Share ]

Contact: Mika Ono
mikaono@scripps.edu
858-784-2052
Scripps Research Institute

The work has implications for cancer drug development

LA JOLLA, CA December 2, 2012 Scientists at The Scripps Research Institute (TSRI) have determined how two proteins help create organelles, or specialized subunits within a cell, that play a vital role in maintaining cell health. This discovery opens the door for research on substances that could interfere with the formation of these organelles and lead to new therapies for cancer.

The study, published online ahead of print on December 2, 2012, by the journal Nature Structural & Molecular Biology, focuses on the structure and function of the two proteins, ATG12 and ATG5. These proteins need to bond correctly to form an organelle called the autophagosome, which acts like a trash bag that removes toxic materials and provides the cell with nutrition through recycling.

"Our study focuses on one of the big mysteries in our field," said Takanori Otomo, the TSRI scientist who led the effort. "These proteins are linked, but no one has explained why clearly. We're very excited to have determined the structure of these linked proteins so that the information is available to do the next level of research."

Asking Questions, Finding Answers

At the beginning of the study, Otomo and colleagues knew that many proteins work together to form autophagosomes as part of the process known as autophagy, which breaks down large proteins, invasive pathogens, cell waste, and toxic materials. As part of this process, one key protein, LC3, attaches to a lipid, or fat molecule, on the autophagosome membrane. Yet LC3 cannot attach to a lipid without the help of ATG12 and ATG5, and a cell will only form an autophagosome if the linkage, or conjugate, between these two molecules has been established.

Otomo and colleagues set out to determine the shape of the ATG12-ATG5 conjugate, and to find out why it was needed for LC3 lipidation.

Using a method called X-ray crystallography, the scientists were able to unveil the details of this conjugate. When ATG12 and ATG5 come together, they form a rigid architecture and create a surface area that is made up of evolutionarily conserved amino acids and facilitates LC3 lipidation. The researchers confirmed this finding by mutating those conserved amino acids , which prevented an autophagosome from forming.

Otomo and colleagues also identified a surface on the ATG12-ATG5 conjugate that binds to ATG3, another enzyme required to attach LC3 to the lipid.

Toward Better Understanding and New Cancer Treatments

With this new knowledge, the researchers hope to design molecules that inhibit autophagosome formation, a direction of research that has implications for cancer treatment. A drug that directly inhibits ATG3 binding, for example, could be used in coordination with current therapies to make cancer treatments more effective, preventing a cancer cell from recycling nutrients and prolonging its survival.

"Ultimately, we'd like to understand the molecular mechanisms of each step of autophagy," he said, "As we make progress toward this goal, we will have a better idea of how to manipulate the pathway for therapeutic purposes. This field is still young and there are a lot of unknowns. This work is just the beginning."

###

In addition to Otomo, authors of the paper, "Structure of the human ATG12~ATG5 conjugate required for LC3 lipidation in autophagy," include Chinatsu Otomo and Zoltan Metlagel of TSRI, and Giichi Takaesu of Keio University in Tokyo, Japan.

This research was supported by National Institutes of Health (NIH) grant GM092740 and by funds from Japan Science and Technology Agency through the Keio Kanrinmaru Project.


[ Back to EurekAlert! ] [ | E-mail | Share Share ]

?


AAAS and EurekAlert! are not responsible for the accuracy of news releases posted to EurekAlert! by contributing institutions or for the use of any information through the EurekAlert! system.


Source: http://www.eurekalert.org/pub_releases/2012-12/sri-sas112912.php

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Sunday, December 2, 2012

The Lovers' Legacy

The Lovers' Legacy

" Because his soul will always find mine, whatever lifetime we may be in "

Owner:

Game Masters:

This topic is an Out Of Character part of the roleplay, ?The Lovers' Legacy?. Anything posted here will also show up there.

Topic Tags:

Forum for completely Out of Character (OOC) discussion, based around whatever is happening In Character (IC). Discuss plans, storylines, and events; Recruit for your roleplaying game, or find a GM for your playergroup.


May I reserve first female angel?

Call me... ?????or Hallowed... If you dare. :3

User avatar
Hallowed777
Member for 0 years


Hey guys, just wanted to stop by as I normally do with romance-based RPs and make sure that everyone is familiar with our Rules! No one is in trouble in any way, this is just a friendly reminder so that someone doesn't join the game and do something that will get the game shut down and ruin the fun for everyone.
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Be reminded: Adult content is permitted on RolePlayGateway. It must 1) be tagged appropriately, and 2) be collaboratively written so as not to clutter the story. Sexually explicit (kissing, fondling, etc.) interactions must be concluded immediately in the responding author's post and must be separated by at least 5 posts of other non-adult writing. Help keep RolePlayGateway smut-free by working together with your game's players to meet this requirement.

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Jag
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Member for 3 years


May I please reserve Gabriel? :)
I'll fill a sheet out for him, either today or tomorrow :)

User avatar
Nami L'Chi
Member for 0 years



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Pets Up For Adoption At Whiskers In Wonderland Event ? CBS New ...

(Photo Credit: NYCFCI/Maggie O'Neill)

(Photo Credit: NYCFCI/Maggie O?Neill)

NEW YORK (CBSNewYork) ? More than 300 cats, kittens and rabbits were up for adoption Sunday from more than 20 rescue groups and shelters at the Whiskers in Wonderland holiday pet adoption event.

The event, hosted by the Mayor?s Alliance for New York City?s Animals, was to be in progress through 5 p.m. Sunday at five Manhattan Petco stores:

? Union Square (880 Broadway at 17th Street);
? 86th Street & Lexington Avenue;
? Columbus Square (805 Columbus Avenue at 98th Street);
? Kips Bay (560 Second Avenue at 30th Street);
? 92nd Street & Broadway.

Cats and kittens were available at all sites, but rabbits were only available at Union Square, 86th and Lexington, and Columbus Square.

?We?re just really hoping that people come out at this time of year, and bring home a four-footed, furry, family member, because we have a lot of cats most of the time who are looking for great new homes, but particularly because of Sandy,? said Jane Hoffman, president of the alliance.

Hoffman told WCBS 880 many Sandy victims were grateful that the city put on the event.

?Many of the people who were displaced or homes were destroyed by Sandy, unfortunately, had to end up relinquishing their pets,? she said, ?but at least they had the consolation that their pets were going to groups that would find them great new homes.?

Rock & Rawhide was to collect donations of pet toys and clean linens for shelter animals.

Please leave your comments below?

Source: http://newyork.cbslocal.com/2012/12/02/pets-up-for-adoption-from-rescue-groups-at-whiskers-in-wonderland-event/

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Saturday, December 1, 2012

Cougar Alert! Ke$ha Would Have Sex with Justin Bieber

After their recent breakup and possible reconcilation, no one is really sure about Justin Bieber and Selena Gomez's current relationship status. But thing is for sure: There are plenty of other ladies lining up to take Selena's place!

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Cornell NYC Tech | Plans Taking Shape | Roosevelt ... - The Real Deal

Plans for Cornell NYC Tech?s office, retail space taking shape

Officials seek complimentary tenants for 300,000 square feet of commercial space at the Roosevelt Island campus

November 30, 2012 03:30PM
By Guelda Voien

A rendering of the planned Cornell NYC Tech campus on Roosevelt Island

The Cornell NYC applied sciences campus will boast 300,00 square feet of commercial space?including offices, a hotel and a conference center?and executives involved with the project said last night they are seeking tenants from the fields of technology, venture capital and intellectual property law, among others.

The 2 million-square-foot campus, a collaboration between Cornell University and Technion-Israel Institute of Technology, is slated to transform both Roosevelt Island and New York City?s technology sector as it rises over the next 35 years. The first phase of construction should be completed by 2017.

The event, where executives involved with the project discussed its implications for commercial real estate on Roosevelt Island, was presented by corporate real estate network CoreNet Global?s New York chapter, which hosts monthly summits on topics of interest to the corporate real estate community.

The first phase of construction for the campus includes four buildings, including three to be developed by third parties. Several weeks ago, project officials sent out requests for proposals to find developers for the three towers, as well as a master developer. Cornell plans to select a master developer by next spring.

The first building, a ?loft-like? corporate collocation tower boasting 200,000 square feet of space, will offer 150,000 feet to technology firms, said Karen Backus, president at Backus & Associates, a consultancy working with Cornell on the new campus.

?We are looking at a wide variety of private tenants,? for the building, Backus said, underscoring that the project has a strong ?focus on commercialization,? and hopes to foster collaboration between the private and public sectors within its walls. Tenants in consideration include venture capital firms and intellectual property attorneys, she said.

This tower will also be ?net-zero,? noted Kyu-Jung Whang, Cornell?s vice president of facilities, meaning it will only use energy generated on site, including solar, geothermal and tidal energy.

The second building will include a 210-room hotel, a 40,000-square-foot conference center, as well as a restaurant, bar and other retail, Backus said.

The third building will be a 250,000-square-foot residential complex.

Whang said construction plans have not changed drastically in the wake of Hurricane Sandy because Cornell had already taken a fairly conservative approach, with all entrances planned for 19 feet above sea level.

?We believe global warming is real. It?s going to get worse and worse,? he said. The university may now require entrances to be slightly higher, he said.

He added that Cornell will have to build some sort of temporary barge to get construction materials to the island, but that there were no plans in the works to increase transportation infrastructure for individuals in anticipation of the campus.

For now, the primary focus remains on moving patients at the island?s Coler-Goldwater Specialty Hospital, which will need to be demolished before the campus can be built, to another facility.

?This is going to transform New York City,? Whang said.

?

?

Source: http://therealdeal.com/blog/2012/11/30/plans-for-cornell-nycs-office-retail-space-taking-shape/

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Manning: Thoughts of suicide, made noose

FORT MEADE, Md. (AP) ? The Army private charged with handing over reams of classified material to WikiLeaks acknowledged Friday that he tied a bedsheet into a noose and contemplated suicide shortly after his arrest.

The pretrial testimony appeared to support the military's argument that it was trying to protect Pfc. Bradley Manning from harming himself by keeping him in strict isolation, taking away his clothes and shackling him when he was outside his cell.

Manning's lawyers argue that the conditions he experienced for nine months at the Marine Corps brig in Quantico, Va., amounted to illegal punishment, lasting well past the time he was having suicidal thoughts, and that the charges against him should be dropped as a result.

Under cross-examination by prosecutor Maj. Ashden Fein, Manning testified that he fashioned the noose while being held in Kuwait soon after he was accused of engineering the biggest leak of classified material in U.S. history.

Manning, 24, said his time in Kuwait was the lowest he felt during his entire confinement.

"I certainly made a noose," the former intelligence analyst said. "The sheet noose in particular."

When he was transferred to the brig at Quantico in July 2010, he said, he wrote on his intake form that he was "always planning and never acting" upon suicidal thoughts. He was classified a suicide risk for eight days, then was upgraded to the less-restrictive "prevention of injury" status.

Manning maintains that neither designation was appropriate because he didn't feel like hurting himself after leaving Kuwait.

Quantico commanders maintained the extra restrictions despite repeated recommendations by brig psychiatrists that they be eased. Among other things, he was given scratchy, suicide-prevention bedding. Sometimes all his possessions, including his underwear and eyeglasses, were removed from his cell.

Manning testified Friday that he stood at naked attention for morning count one day in 2011 after a guard appeared to object to his use of a blanket to cover himself. He said he had been put on "suicide risk" the previous day after making a motion as if to hit himself in the head during a heated discussion with the brig commander about his confinement.

The testimony marked the first time military prosecutors went face-to-face with Manning in court.

The 5-foot-3 soldier looked youthful in his dark-blue dress uniform, close-cropped hair and rimless eyeglasses. He was animated, often speaking in emphatic bursts, swiveling in the witness chair and gesturing with his hands.

On Friday morning, as on previous days, there were more than a dozen Manning supporters in the courtroom.

The mood was lighter than on Thursday, the first time he spoke in public since his arrest in May 2010. Manning appeared relaxed on the stand and frequently smiled. He provoked laughter when he described his grading system for Quantico guards on weekly questionnaires: "decent" when he was unhappy with his treatment, "excellent" or "fine" otherwise.

Manning was an intelligence analyst in Baghdad in 2009 and 2010.

He is accused of sending the secret-spilling website WikiLeaks more than 250,000 diplomatic cables, classified memos, Iraq and Afghanistan war logs, Guantanamo Bay prison records and a 2007 video clip of a U.S. helicopter crew gunning down 11 men later found to have included a news photographer. The Pentagon said its troops mistook the camera equipment for weapons.

Manning is charged with offenses including violating espionage and computer security laws as well as aiding the enemy, which alone is punishable by up to life in prison.

He has offered to plead guilty to eight of the 22 charges against him, but the military judge presiding over the case has yet to decide whether to accept the plea. The government could still prosecute Manning on all counts.

Source: http://news.yahoo.com/gi-charged-wikileaks-case-admits-making-noose-155605657.html

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