Saturday, March 16, 2013

Obama heads to Middle East with low expectations

FILE -- In this Monday, May 18, 2009 file photo, Israeli Prime Minister Benjamin Netanyahu, right, looks towards President Barack Obama as he speaks to reporters in the Oval Office of the White House in Washington. President Barack Obama?s vow to take his message straight to the public during his first presidential visit to Israel next week will be a tough sell with many Israelis who consider him naive, too soft on the nation?s enemies and even hostile to Prime Minister Benjamin Netanyahu. (AP Photo/Charles Dharapak, File)

FILE -- In this Monday, May 18, 2009 file photo, Israeli Prime Minister Benjamin Netanyahu, right, looks towards President Barack Obama as he speaks to reporters in the Oval Office of the White House in Washington. President Barack Obama?s vow to take his message straight to the public during his first presidential visit to Israel next week will be a tough sell with many Israelis who consider him naive, too soft on the nation?s enemies and even hostile to Prime Minister Benjamin Netanyahu. (AP Photo/Charles Dharapak, File)

FILE -- In this Sunday, June 14, 2009 file photo, an Ultra Orthodox Jewish man walks past posters depicting US President Barack Obama wearing a traditional Arab headdress, in Jerusalem, Sunday, June 14, 2009. President Barack Obama?s vow to take his message straight to the public during his first presidential visit to Israel next week will be a tough sell with many Israelis who consider him naive, too soft on the nation?s enemies and even hostile to Prime Minister Benjamin Netanyahu. (AP Photo/Sebastian Scheiner, File)

File - In this March 10, 2013 file photograph, Israeli Prime Minister Benjamin Netanyahu attends the weekly cabinet meeting in his Jerusalem office. Netanyahu signed a coalition deal Friday March 15, 2013, with rival parties to form the next government, a spokesman said, in an agreement that was stalled for weeks due to tough negotiations. (AP Photo/Sebastian Scheiner, File)

(AP) ? When President Barack Obama steps into the Middle East's political cauldron this coming week, he won't be seeking any grand resolution for the region's vexing problems.

His goal will be trying to keep the troubles, from Iran's suspected pursuit of a nuclear weapon to the bitter discord between Israelis and Palestinians, from boiling over on his watch.

Obama arrives in Jerusalem on Wednesday for his first trip to Israel as president. His first priority will be resetting his oft-troubled relationship with now-weakened Israeli Prime Minister Benjamin Netanyahu and evaluating the new coalition government Netanyahu laboriously cobbled together.

The president also will look to boost his appeal to a skeptical Israeli public, as well as to frustrated Palestinians.

"This is not about accomplishing anything now. This is what I call a down payment trip," said Aaron David Miller, an adviser on Mideast peace to six secretaries of state who is now at the Woodrow Wilson International Center.

For much of Obama's first term, White House officials saw little reason for him to go to the region without a realistic chance for a peace accord between the Israelis and Palestinians. But with the president's one attempt at a U.S.-brokered deal thwarted in his first term and the two sides even more at odds, the White House has shifted thinking.

Officials now see the lowered expectations as a chance to create space for frank conversations between Obama and both sides about what it will take to get back to the negotiating table. The president will use his face-to-face meetings to "persuade both sides to refrain from taking provocative unilateral actions that could be self-defeating," said Haim Malka, a senior fellow at the Center for Strategic and International Studies.

The trip gives Obama the opportunity to meet Netanyahu on his own turf, and that could help ease the tension that has at times defined their relationship.

The leaders have tangled over Israeli settlements in the Palestinian territories, and Netanyahu has questioned Obama's commitment to containing Iran's nuclear ambitions. Netanyahu also famously lectured the president in front of the media during a 2011 meeting in the Oval Office, and later made no secret of his fondness for Republican challenger Mitt Romney in last year's presidential campaign.

Beyond Mideast peace, the two leaders have similar regional goals, including ending the violence in Syria and containing the political tumult in Egypt, which has a decades-old peace treaty with Israel.

The president's trip comes at a time of political change for Israel.

Netanyahu's power was diminished in January elections and he struggled to form a government. He finally reached a deal on Friday with rival parties, creating a coalition that brings the centrist Yesh Atid and pro-settler Jewish Home parties into the government and excludes the ultra-Orthodox Jewish parties for the first time in a decade.

Ben Rhodes, Obama's deputy national security adviser, acknowledged that with a new government, "you don't expect to close the deal on any one major initiative." But he said starting those conversations now "can frame those decisions that ultimately will come down the line."

Among those decisions will be next steps in dealing with Iran's disputed nuclear program.

Israel repeatedly has threatened to take military action should Iran appear to be on the verge of obtaining a bomb. The U.S. has pushed for more time to allow diplomacy and economic penalties to run their course, though Obama insists military action is an option.

The West says Iran's program is aimed at developing weapons technology. Iran says its program is for peaceful energy purposes.

Another central difference between the allies on Iran is the timeline for possible military action.

Netanyahu, in a speech to the United Nations in September, said Iran was about six months away from being able to build a bomb. Obama told an Israeli television station this past week that the U.S. thinks it would take "over a year or so for Iran to actually develop a nuclear weapon."

Michael Oren, the Israeli ambassador to the U.S., tried to play down any division on the Iranian issue ahead of Obama's trip. He said Friday that "the United States and Israel see many of the same facts about the Iranian nuclear program and draw many similar conclusions."

Obama's visit to Israel may quiet critics in the U.S. who interpreted his failure to travel there in his first term as a sign that he was less supportive of the Jewish state than his predecessors. Republican lawmakers levied that criticism frequently during last year's presidential campaign, despite the fact that GOP President George W. Bush did not visit Israel until his final year in office.

The centerpiece of Obama's visit will be a speech in Jerusalem to an audience mainly of Israeli students. It's part of the president's effort to appeal to the Israeli public, particularly young people.

He will make several cultural stops, all steeped in symbolism, in the region. They include the Holocaust memorial Yad Veshem; Mount Herzl, where he'll lay wreaths at the graves of Theodor Herzl, the founder of modern political Zionism, and the Prime Minister Yitzhak Rabin; and the Church of the Nativity in Bethlehem, a revered site for Christians.

Traveling to the West Bank, Obama will meet with Palestinian Authority President Mahmoud Abbas and Prime Minister Salam Fayyad in Ramallah. Obama and Fayyad will visit a Palestinian youth center, another attempt to reach the region's young people.

Obama will make a 24-hour stop in Jordan, an important U.S. ally, where the president's focus will be on the violence in neighboring Syria. More than 450,000 Syrians have fled to Jordan, crowding refugee camps and overwhelming aid organizations.

The White House said Obama had no plans to visit a refugee camp while in Jordan, though he will be discussing with government officials how the U.S. can increase its assistance.

In his talks with Jordan's King Abdullah, Obama also will try to shore up the country's fledgling attempts to liberalize its government and stave off an Arab Spring-style movement similar to the ones that have taken down leaders elsewhere in the region.

The president's final will be at Petra, Jordan's fabled ancient city.

___

Follow Julie Pace at http://twitter.com/jpaceDC

___

Online:

White House: http://tinyurl.com/a9r3lej

Associated Press

Source: http://hosted2.ap.org/APDEFAULT/3d281c11a96b4ad082fe88aa0db04305/Article_2013-03-16-US-Obama-Mideast/id-7203e69cf6924507a273760bb803f733

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ShaqIsDope ? Vintage Paris (Prod. By Melrose Zee) + Dirty California (Prod. By LSMi)

To provide a quick introduction, here?s couple tracks from ?20-year-old Toronto native ShaqIsDope. The kid can definitely rap and a mixtape is currently in the works, set to be released later this year. Until then, listen to ?Vintage Paris? and ?Dirty California.?

Source: http://youheardthatnew.com/2013/03/shaqisdope-vintage-paris-prod-by-melrose-zee-dirty-california-prod-by-lsmi/

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Restore Your Natural Sitting and Standing Posture and Get Rid of Back and Neck Pain

Restore Your Natural Sitting and Standing Posture and Get Rid of Back and Neck PainRestore Your Natural Sitting and Standing Posture and Get Rid of Back and Neck Pain Not only are we killing ourselves by sitting all day, we're probably sitting all wrong. Esther Gokhale, who has studied the posture of people in less industrialized places (where back pain is virtually unknown), shows us in this video what natural ("primal") posture looks like for standing and sitting.

Essentially, you want to have a "ducky butt, not tucky butt," she says in a profile of her work on SF Gate. Instead of tucking your tailbone in, stick your butt out, because good posture relies much on the pelvis.

If you don't have time for the entire video, go to the 4:25 mark to see a sitting exercise that will help you get back into your primal posture.

Back to Primal Posture | YouTube via ZDNet

Source: http://feeds.gawker.com/~r/lifehacker/full/~3/BqJfnjcBfc4/restore-your-natural-sitting-and-standing-posture-and-get-rid-of-back-and-neck-pain

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Friday, March 15, 2013

The Weirdest Thing on the Internet Tonight: A Story About Robots

It was only as he slowly wound down did the robot finally realize, "What is love? Baby don't hurt me, don't hurt...me no...mo..." More »


Source: http://feeds.gawker.com/~r/gizmodo/full/~3/0t0gwltZDrY/the-weirdest-thing-on-the-internet-tonight-a-story-about-robots

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Agawi Partners With NVIDIA To Deliver Ready-To-Stream Gaming ...

Game streaming might be a common feature of ISP packages for bundled Internet, if Agawi has anything to say about it. The cloud gaming startup has outlasted rival OnLive, which still exists in name after a nasty bankruptcy, and Gaikai, which was picked up by Sony to power its?upcoming?PS4 cloud-based features, and now it wants to give ISPs and carrier networks a chance to regain their place as providers of content.

Internet providers have been demoted to dumb tubes with the advent of services like Netflix, iTunes, Spotify and others, which is not where they want to be. Serving up piping hot content to customers is the way to own a more complete relationship, one that?s likely to result in longer-term commitment and deeper revenue pockets. If you control both the channel and what?s on it, you?re winning both ways, after all.?Agawi, which has spent the past few years building its cloud gaming infrastructure, is now pursuing its plans of making that tech, code named VG36, commercially available to ISPs, with a ready-to-roll white label solution they can pass on to their customers.

Agawi is partnering with NVIDIA to make this happen, after the two worked together on building their ?True Cloud? gaming architecture in February. The combination of Agawi?s existing tech with servers based on Nvidia?s Grid processors is designed to help stream multiple games at the same time from a single server, thereby bypassing or at least?minimizing the upfront equipment costs that proved extremely troublesome to OnLive.

I spoke to Agawi executive chairman Peter Relan about the launch of the new platform, which will be opening up to general availability in July. It?s being announced now because of the long lead times a lot of Agawi?s target customers have when implementing services like this one, Relan said. The point is to make potential partners aware that Agawi is ready do deploy this tech as soon as the second half of this year, with data center partners lined up around the globe.

?Everybody has been waiting for MNVOs, MSOs, the?telecom?guys, the cable guys, to bring new services to market,? he said. ?They offer voice, they offer Internet, they offer television, so what?s the next big content area? Gaming. Almost all the major telecom operators and cable operators want to do trials this year with introducing gaming services, and the?easiest?way to bring them to market is through cloud gaming, because the alternative is to put the equivalent of an iPad inside their set-top box.?

Once Agawi begins deployments in earnest, any service provider that participates should be able to offer games direct to existing subscribers through the hardware they already have it ? be it computers, mobile devices or even connected TVs. Reland says it can also help with licensing of specific content, and will offer three tiers (casual, mid-core and AAA) to appeal to all types of gamers.

Targeting the folks who manage the pipes is a good strategy for Agawi, not only because providers are looking around for content?opportunities, but because cloud gaming has the potential to be very bandwidth-intensive for consumers. If carriers are providing the service, however, they can presumably also offer some way of making sure that bandwidth used to stream games doesn?t count across their monthly totals, the way Comcast?s video service doesn?t count against its caps. Whatever the arrangement between providers and clients ends up being, Agawi still has to sell its offering to telcos and ISPs first.

Source: http://techcrunch.com/2013/03/14/agawi-partners-with-nvidia-to-deliver-ready-to-stream-gaming-architecture-to-isps-and-telcos/

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Thursday, March 14, 2013

Will Alternative Energy Growth Tank During New Fossil-Fuel Glut? [Slide Show]

NATIONAL HARBOR, Md.?The artificial leaf promised to revolutionize the world by bringing reliable modern energy to those mired in poverty. But the company founded to commercialize the research?Sun Catalytix?has found that it needs to concentrate its efforts on something likely to make money in the nearer term, namely the kind of flow batteries that might provide large amounts of energy storage on the U.S. electric grid.

The alternative energy landscape is in tumult, judging by the recent fourth annual summit of the Advanced Research Projects Agency for Energy, or ARPA?E. A glut of cheap natural gas threatens to sweep all other energy sources before it. The so-called "shale gale," as Alaska Sen. Lisa Murkowski put it at the recent ARPA-E energy summit, is forcing a rethink of energy strategy. "Before this so-called shale gale came upon us, groupthink had most of us focusing on energy scarcity," Murkowski noted. "The consensus now is that we have abundant energy. We can't fall into the trap of groupthink again."

Funding for alternative energy?whether from the federal stimulus bill or venture capitalists?has dried up. "We're here because it's ARPA?E, and they have some resources," says Saul Griffith of OtherLab, a research and design firm that has received funding from the agency for researching uniquely shaped tanks for natural gas. "We all suffer from a lack of resources. We all have ambitions that want to go faster and bigger." Or as retired Marine Corps Gen. James L. Jones put it as part of a talk about the link between national security and energy security: "A vision without resources is a hallucination."

More than 250 exhibitors came to show their wares alongside ARPA?E efforts ranging from Smart Wire Grid's power-flow controllers for electricity transmission lines to OPX Biotechnologies's modified microbe that builds liquid fuels from hydrogen and carbon dioxide. "After three years have there been home runs?" asked retiring Secretary of Energy Steven Chu at the summit. "Maybe not, but there are people rounding second or third base."

View a slide show of future energy efforts.

The question becomes: Will energy alternatives falter in the face of a new abundance of fossil fuels as happened in the 1970s and 1980s? "Today we have the gas," observed financier T. Boone Pickens of BP Capital Management, who has been pushing for increased use of natural gas since 1988. "We're fools if we don't use it."

Even ARPA-E has begun to shift its limited funding into projects to enhance the use of natural gas, such as the Methane Opportunities for Vehicular Energy, or the MOVE program, as well as an effort to convert natural gas to liquid fuels via microbes or chemistry. "We can meet U.S. demand for liquid transportation fuels over the next 50 years," argues biological engineer Ramon Gonzalez, ARPA?E program director.

Or is there enough momentum behind alternative energy that the renewables revolution has become unstoppable, thanks to progress in making solar power cheap and the proliferation of wind farms as well as the possibility of electric cars displacing gasoline-powered vehicles? Tennessee Sen. Lamar Alexander drove to the conference in his Nissan LEAF and urged scientists to work on making battery technology cost less. "We are more likely to see electric vehicles as a second car for many Americans when it's cheaper. Most of that cost is in the battery."

The goal of ARPA?E remains to encourage innovation so that sustainable energy solutions, however defined, become the cheapest and therefore most common options. But how many of these exhibitors, like Sun Catalytix, will be showcasing different wares in future? "In the energy domain, we need to get to what is right faster," added OtherLab's Griffith. "That means getting things wrong faster." Follow Scientific American on Twitter @SciAm and @SciamBlogs. Visit ScientificAmerican.com for the latest in science, health and technology news.
? 2013 ScientificAmerican.com. All rights reserved.

Source: http://news.yahoo.com/alternative-energy-growth-tank-during-fossil-fuel-glut-200100216.html

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Study shows how vitamin E can help prevent cancer

Study shows how vitamin E can help prevent cancer [ Back to EurekAlert! ] Public release date: 14-Mar-2013
[ | E-mail | Share Share ]

Contact: Ching-Shih Chen
chen@pharmacy.ohio-state.edu
614-688-4008
Ohio State University

COLUMBUS, Ohio Researchers have identified an elusive anti-cancer property of vitamin E that has long been presumed to exist, but difficult to find.

Many animal studies have suggested that vitamin E could prevent cancer, but human clinical trials following up on those findings have not shown the same benefits.

In this new work, researchers showed in prostate cancer cells that one form of vitamin E inhibits the activation of an enzyme that is essential for cancer cell survival. The loss of the enzyme, called Akt, led to tumor cell death. The vitamin had no negative effect on normal cells.

"This is the first demonstration of a unique mechanism of how vitamin E can have some benefit in terms of cancer prevention and treatment," said lead author Ching-Shih Chen, professor of medicinal chemistry and pharmacognosy at The Ohio State University and an investigator in Ohio State's Comprehensive Cancer Center.

The study appears in the March 19, 2013, issue of the journal Science Signaling.

Chen cautioned that taking a typical vitamin E supplement won't offer this benefit for at least two reasons: The most affordable supplements are synthetic and based predominantly on a form of the vitamin that did not fight cancer as effectively in this study, and the human body can't absorb the high doses that appear to be required to achieve the anti-cancer effect.

"Our goal is to develop a safe pill at the right dose that people could take every day for cancer prevention. It takes time to optimize the formulation and the dose," he said.

Chen has filed an invention disclosure with the university, and Ohio State has filed a patent application for the agent.

Vitamin E occurs in numerous forms based on their chemical structure, and the most commonly known form belongs to a variety called tocopherols. In this study, researchers showed that, of the tocopherols tested, the gamma form of tocopherol was the most potent anti-cancer form of the vitamin.

The scientists manipulated the structure of that vitamin E molecule and found that the effectiveness of this new agent they created was 20-fold higher than the vitamin itself in cells. In experiments in mice, this agent reduced the size of prostate cancer tumors.

These findings suggest that an agent based on the chemical structure of one form of vitamin E could help prevent and treat numerous types of cancer particularly those associated with a mutation in the PTEN gene, a fairly common cancer-related genetic defect that keeps Akt active.

The researchers began the work with both alpha and gamma forms of the vitamin E molecule. Both inhibited the enzyme called Akt in very targeted ways, but the gamma structure emerged as the more powerful form of the vitamin.

In effect, the vitamin halted Akt activation by attracting Akt and another protein, called PHLPP1, to the same region of a cell where the vitamin was absorbed: the fat-rich cell membrane. PHLPP1, a tumor suppressor, then launched a chemical reaction that inactivated Akt, rendering it unable to keep cancer cells alive.

"This is a new finding. We have been taking vitamin E for years but nobody really knew about this particular anti-cancer mechanism," Chen said.

The gamma form was most effective because its chemical shape allowed it to attach to Akt in the most precise way to shut off the enzyme.

Because of how the various molecules interacted on the cell membrane, the scientists predicted that shortening a string of chemical groups dangling from the main body, or head group, of the gamma-tocopherol molecule would make those relationships even stronger. They lopped off about 60 percent of this side chain and tested the effects of the new agent in the prostate cancer cells.

"By reducing two-thirds of the chain, the molecule had a 20 times more potent anti-tumor effect, while retaining the integrity of vitamin E's head group," Chen said. This manipulation enhanced the anti-tumor potency of the molecule by changing its interaction with the cell membrane, so that the head group was more accessible to Akt and PHLPP1.

When mice with tumors created by these two prostate cancer cell lines were injected with the agent, the treatment suppressed tumor growth when compared to a placebo, which had no effect on tumor size. Chemical analysis of the treated tumors showed that the Akt enzyme signal was suppressed, confirming the effects were the same in animals as they had been in cell cultures.

The animal study also suggested the experimental agent was not toxic. Chen's lab is continuing to work on improvements to the molecule.

###

This work was supported by the National Institutes of Health.

Co-authors include Po-Hsien Huang, Hsiao-Ching Chuang, Chih-Chien Chou, Huiling Wang, Su-Lin Lee, Hsiao-Ching Yang, Hao-Chieh Chiu, Naval Kapuriya, Dasheng Wang and Samuel Kulp of the Division of Medicinal Chemistry and Pharmacognosy at Ohio State. Huang and Chen also are affiliated with National Cheng-Kung University, Yang with Fu-Jen Catholic University, and Chiu with National Taiwan University, all in Taiwan; and Kapuriya with Saurashtra University in Gujarat, India.

Contact: Ching-Shih Chen, (614) 688-4008; chen@pharmacy.ohio-state.edu (Email is the best way to contact Chen.)

Written by Emily Caldwell, (614) 292-8310; Caldwell.151@osu.edu


[ 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.


Study shows how vitamin E can help prevent cancer [ Back to EurekAlert! ] Public release date: 14-Mar-2013
[ | E-mail | Share Share ]

Contact: Ching-Shih Chen
chen@pharmacy.ohio-state.edu
614-688-4008
Ohio State University

COLUMBUS, Ohio Researchers have identified an elusive anti-cancer property of vitamin E that has long been presumed to exist, but difficult to find.

Many animal studies have suggested that vitamin E could prevent cancer, but human clinical trials following up on those findings have not shown the same benefits.

In this new work, researchers showed in prostate cancer cells that one form of vitamin E inhibits the activation of an enzyme that is essential for cancer cell survival. The loss of the enzyme, called Akt, led to tumor cell death. The vitamin had no negative effect on normal cells.

"This is the first demonstration of a unique mechanism of how vitamin E can have some benefit in terms of cancer prevention and treatment," said lead author Ching-Shih Chen, professor of medicinal chemistry and pharmacognosy at The Ohio State University and an investigator in Ohio State's Comprehensive Cancer Center.

The study appears in the March 19, 2013, issue of the journal Science Signaling.

Chen cautioned that taking a typical vitamin E supplement won't offer this benefit for at least two reasons: The most affordable supplements are synthetic and based predominantly on a form of the vitamin that did not fight cancer as effectively in this study, and the human body can't absorb the high doses that appear to be required to achieve the anti-cancer effect.

"Our goal is to develop a safe pill at the right dose that people could take every day for cancer prevention. It takes time to optimize the formulation and the dose," he said.

Chen has filed an invention disclosure with the university, and Ohio State has filed a patent application for the agent.

Vitamin E occurs in numerous forms based on their chemical structure, and the most commonly known form belongs to a variety called tocopherols. In this study, researchers showed that, of the tocopherols tested, the gamma form of tocopherol was the most potent anti-cancer form of the vitamin.

The scientists manipulated the structure of that vitamin E molecule and found that the effectiveness of this new agent they created was 20-fold higher than the vitamin itself in cells. In experiments in mice, this agent reduced the size of prostate cancer tumors.

These findings suggest that an agent based on the chemical structure of one form of vitamin E could help prevent and treat numerous types of cancer particularly those associated with a mutation in the PTEN gene, a fairly common cancer-related genetic defect that keeps Akt active.

The researchers began the work with both alpha and gamma forms of the vitamin E molecule. Both inhibited the enzyme called Akt in very targeted ways, but the gamma structure emerged as the more powerful form of the vitamin.

In effect, the vitamin halted Akt activation by attracting Akt and another protein, called PHLPP1, to the same region of a cell where the vitamin was absorbed: the fat-rich cell membrane. PHLPP1, a tumor suppressor, then launched a chemical reaction that inactivated Akt, rendering it unable to keep cancer cells alive.

"This is a new finding. We have been taking vitamin E for years but nobody really knew about this particular anti-cancer mechanism," Chen said.

The gamma form was most effective because its chemical shape allowed it to attach to Akt in the most precise way to shut off the enzyme.

Because of how the various molecules interacted on the cell membrane, the scientists predicted that shortening a string of chemical groups dangling from the main body, or head group, of the gamma-tocopherol molecule would make those relationships even stronger. They lopped off about 60 percent of this side chain and tested the effects of the new agent in the prostate cancer cells.

"By reducing two-thirds of the chain, the molecule had a 20 times more potent anti-tumor effect, while retaining the integrity of vitamin E's head group," Chen said. This manipulation enhanced the anti-tumor potency of the molecule by changing its interaction with the cell membrane, so that the head group was more accessible to Akt and PHLPP1.

When mice with tumors created by these two prostate cancer cell lines were injected with the agent, the treatment suppressed tumor growth when compared to a placebo, which had no effect on tumor size. Chemical analysis of the treated tumors showed that the Akt enzyme signal was suppressed, confirming the effects were the same in animals as they had been in cell cultures.

The animal study also suggested the experimental agent was not toxic. Chen's lab is continuing to work on improvements to the molecule.

###

This work was supported by the National Institutes of Health.

Co-authors include Po-Hsien Huang, Hsiao-Ching Chuang, Chih-Chien Chou, Huiling Wang, Su-Lin Lee, Hsiao-Ching Yang, Hao-Chieh Chiu, Naval Kapuriya, Dasheng Wang and Samuel Kulp of the Division of Medicinal Chemistry and Pharmacognosy at Ohio State. Huang and Chen also are affiliated with National Cheng-Kung University, Yang with Fu-Jen Catholic University, and Chiu with National Taiwan University, all in Taiwan; and Kapuriya with Saurashtra University in Gujarat, India.

Contact: Ching-Shih Chen, (614) 688-4008; chen@pharmacy.ohio-state.edu (Email is the best way to contact Chen.)

Written by Emily Caldwell, (614) 292-8310; Caldwell.151@osu.edu


[ 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/2013-03/osu-ssh031413.php

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