Category Archives: Stem Cell Medical Center


Stem cell advance offers hope for infertility

By The Wall Street Journal

February 26, 2012

BOSTON -- Researchers said they have transformed stem cells isolated from women's ovaries into viable-looking eggs, a provocative experiment that might suggest new ways for treating infertility.

Biologists have long held that women are born with a finite supply of eggs that gets depleted with age. The latest experiment, published in Nature Medicine, describes how rare stem cells found in the ovary could potentially be coaxed into rejuvenating the natural egg supply.

Men produce sperm all their life. Now, women "are no longer faced with the idea that there's a fixed bank account of eggs at birth with only withdrawals and no deposits," said Jonathan Tilly, a reproductive biologist at Massachusetts General Hospital in Boston and lead author of the paper. The study was funded by the National Institutes of Health and other groups.

The research is at an early stage, and the quest for practical applications could founder on many obstacles. The human egg is an unstable cell prone to genetic error. Creating eggs from stem cells could enhance those risks.

"When you amplify stem cells in culture they can become unstable," said David Albertini, a reproductive biologist at the University of Kansas Medical Center, who was not involved in the study. "There's a difference between Mother Nature doing this" and attempting it in a lab.

Underpinning the new approach is Tilly's discovery that the ovaries of reproductive-age women harbor tiny quantities of stem cells that can potentially be isolated and then cultured in the lab to become oocytes, or normal, immature egg cells.

The goal would be that instead of freezing and storing a woman's eggs for use at a later date, doctors would extract and freeze a small piece of her ovarian tissue containing stem cells -- a potentially less-invasive and faster procedure. Freezing and thawing could also damage stem cells less than they would eggs, which hold a lot more water.

Infertility affects seven million, or 12 percent, of all women in the US, according to the Centers for Disease Control and Prevention. About half seek treatment, few get it, and not all are successful. Some procedures can be lengthy, expensive and unpleasant.

The ovary of a female fetus at five months holds seven million eggs, but that number drops to one million at birth and 300,000 or fewer by puberty. The supply keeps falling and gets exhausted at menopause, typically when a woman is in her late 40s or early 50s. Biologists have believed there was no way to increase the supply of eggs.

Read more: http://online.wsj.com/article/SB10001424052970204653604577247363486004218.html

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Stem cell advance offers hope for infertility

BrainStorm Featured on CNBC

NEW YORK & PETACH TIKVAH, Israel--(BUSINESS WIRE)--

BrainStorm Cell Therapeutics Inc. (OTCBB: BCLI.OB - News), a developer of innovative stem cell technologies for neurodegenerative disorders, announced that NurOwn™, its autologous stem cell therapy for amyotrophic lateral sclerosis (ALS), or Lou Gehrig's Disease, was profiled yesterday on CNBC. In the Feature Story about the impact of Iran's nuclear threat, Israeli business and scientific leaders were interviewed about Israel's thriving economy and cutting edge technologies. Among those leaders that met with CNBC were Brainstorm’s President Mr. Chaim Lebovits and Prof. Dimitrios Karussis, Principal Investigator of Brainstorm's Phase I/II clinical trial currently underway at the Hadassah Medical Center in Jerusalem.

Brainstorm recently announced positive initial results from the clinical trial, resulting in approval from Hadassah's Helsinki committee to proceed with the trial. Accordingly, additional patients have been enrolled in the study, and Brainstorm will announce additional results in the coming months.

To see the video online, follow the link at: http://video.cnbc.com/gallery/?video=3000074883

To read the Feature Story online, follow the link at: http://www.cnbc.com/id/46484576

Safe Harbor Statement
Statements in this announcement other than historical data and information constitute "forward-looking statements" and involve risks and uncertainties that could cause BrainStorm Cell Therapeutics Inc.'s actual results to differ materially from those stated or implied by such forward-looking statements. The potential risks and uncertainties include risks associated with BrainStorm's limited operating history, history of losses; minimal working capital, dependence on its license to Ramot's technology; ability to adequately protect the technology; dependence on key executives and on its scientific consultants; ability to obtain required regulatory approvals; and other factors detailed in BrainStorm's annual report on Form 10-K and quarterly reports on Form 10-Q available at http://www.sec.gov. The Company does not undertake any obligation to update forward-looking statements made by us.

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BrainStorm Featured on CNBC

Maven Semantic: Embryonic Stem Cells Research Database

DUBLIN--(BUSINESS WIRE)--

Maven Semantic (http://www.mavensemantic.com) announces updates to their Embryonic Stem Cells research database.

The new database is now available to marketing, business development, competitor intelligence, KOL, medical affairs and related departments in the life sciences sector.

The database currently tags 27,000 individuals working in Embryonic Stem Cells. http://bit.ly/zc0cU4.

Top 10 Countries for Embryonic Stem Cells Research (ranked by number of senior researchers)

Leading organisations in Embryonic Stem Cells research include:

Albert Einstein College of Medicine Baylor College of Medicine Brigham and Women's Hospital California Institute of Technology Chinese Academy of Sciences Cornell University Dana-Farber Cancer Institute Duke University Medical Center Fred Hutchinson Cancer Research Center Genome Institute of Singapore Harvard Medical School Howard Hughes Medical Institute Hubrecht Laboratory Indiana University School of Medicine Institut Pasteur Institute for Frontier Medical Sciences Institute of Human Genetics Institute of Molecular Embryology and Genetics Johns Hopkins University School of Medicine Karolinska Institute Keio University School of Medicine Lund University Mount Sinai Hospital New York University School of Medicine Seoul National University University College London University of Cambridge University of Chicago University of Massachusetts Medical School University of Michigan University of Pennsylvania University of Toronto University of Tsukuba Weill Medical College of Cornell University Zhejiang University

The database also includes pharmaceutical companies, biotech companies, CROs, hospitals, government labs and other organisations active in the Embryonic Stem Cells research field.

Sample companies in database include:

AgResearch Ltd Amgen Inc Axiogenesis AG Cellartis AB Cellular Dynamics International, Inc Chugai Pharmaceutical Co., Ltd DNAVEC Corporation ES Cell International Pte Ltd F. Hoffmann-La Roche Ltd Genentech, Inc GENPHARM INTERNATIONAL, INC Geron Corporation Hayashibara Biochemical Laboratories, Inc Illumina, Inc Ingenium Pharmaceuticals AG Invitrogen Corporation Japan Science and Technology Corp KENNEDY KRIEGER, INC Regeneron Pharmaceuticals, Inc

What is Maven:

- Largest database of international medical professionals, with over 6,000,000 people and over 500,000 medical organisations;

- All records are downloadable to excel or in-house database, with email, postal address and phone contacts;

- Profile and segment the entire database using over 47,000 diseases and therapeutic areas

For more information visit http://www.mavensemantic.com/

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Maven Semantic: Embryonic Stem Cells Research Database

Memory formation triggered by stem cell development

Public release date: 23-Feb-2012
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Contact: RIKEN Brain Science Promotion Division
pr@brain.riken.jp
81-484-679-757
RIKEN

Researchers at the RIKEN-MIT Center for Neural Circuit Genetics have discovered an answer to the long-standing mystery of how brain cells can both remember new memories while also maintaining older ones.

They found that specific neurons in a brain region called the dentate gyrus serve distinct roles in memory formation depending on whether the neural stem cells that produced them were of old versus young age.

The study will appear in the March 30 issue of Cell and links the cellular basis of memory formation to the birth of new neurons -- a finding that could unlock a new class of drug targets to treat memory disorders.

The findings also suggest that an imbalance between young and old neurons in the brain could disrupt normal memory formation during post-traumatic stress disorder (PTSD) and aging. "In animals, traumatic experiences and aging often lead to decline of the birth of new neurons in the dentate gyrus. In humans, recent studies found dentate gyrus dysfunction and related memory impairments during normal aging," said the study's senior author Susumu Tonegawa, 1987 Nobel Laureate and Director of the RIKEN-MIT Center.

Other authors include Toshiaki Nakashiba and researchers from the RIKEN-MIT Center and Picower Institute at MIT; the laboratory of Michael S. Fanselow at the University of California at Los Angeles; and the laboratory of Chris J. McBain at the National Institute of Child Health and Human Development.

In the study, the authors tested mice in two types of memory processes. Pattern separation is the process by which the brain distinguishes differences between similar events, like remembering two Madeleine cookies with different tastes. In contrast, pattern completion is used to recall detailed content of memories based on limited clues, like recalling who one was with when remembering the taste of the Madeleine cookies.

Pattern separation forms distinct new memories based on differences between experiences; pattern completion retrieves memories by detecting similarities. Individuals with brain injury or trauma may be unable to recall people they see every day. Others with PTSD are unable to forget terrible events. "Impaired pattern separation due to the loss of young neurons may shift the balance in favor of pattern completion, which may underlie recurrent traumatic memory recall observed in PTSD patients," Tonegawa said.

Neuroscientists have long thought these two opposing and potentially competing processes occur in different neural circuits. The dentate gyrus, a structure with remarkable plasticity within the nervous system and its role in conditions from depression to epilepsy to traumatic brain injury -- was thought to be engaged in pattern separation and the CA3 region in pattern completion. Instead, the MIT researchers found that dentate gyrus neurons may perform pattern separation or completion depending on the age of their cells.

The MIT researchers assessed pattern separation in mice who learned to distinguish between two similar but distinct chambers: one safe and the other associated with an unpleasant foot shock. To test their pattern completion abilities, the mice were given limited cues to escape a maze they had previously learned to negotiate. Normal mice were compared with mice lacking either young neurons or old neurons. The mice exhibited defects in pattern completion or separation depending on which set of neurons was removed.

"By studying mice genetically modified to block neuronal communication from old neurons -- or by wiping out their adult-born young neurons -- we found that old neurons were dispensable for pattern separation, whereas young neurons were required for it," co-author Toshiaki Nakashiba said. "Our data also demonstrated that mice devoid of old neurons were defective in pattern completion, suggesting that the balance between pattern separation and completion may be altered as a result of loss of old neurons."

###

The work was supported by the RIKEN-MIT Center for Neural Circuit Genetics, Howard Hughes Medical Institute, Otsuka Maryland Research Institute, Picower Foundation and the National Institutes of Health.

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Memory formation triggered by stem cell development

Carrboro man to get stem cell transplant

Published: Feb 22, 2012 02:00 AM
Modified: Feb 20, 2012 10:41 PM


Carrboro man to get stem cell transplant
Treatment a first at UNC

BY ELIZABETH SWARINGEN, Special to The Chapel Hill News

CHAPEL HILL - Three infusions of your own stem cells - each infusion over a 21-day hospitalization - can seem daunting. But, when it's your best chance for beating a recurrence of testicular cancer, you look forward to it."It doesn't seem intimidating to me at all," said David Alston, 42, of Carrboro. "You don't normally think of stem cell bone marrow transplants as treatment for testicular cancer, but it has been done in New York with success. I'm pleased it's available to me here at UNC Hospitals."This month Alston is having the first triple-tandem transplant done in an adult at UNC Hospitals.The process involves harvesting and freezing his own stem cells, receiving high-dose chemotherapy to attack the cancer, then having the stem cells infused over three back-to-back hospitalizations."He's young and otherwise healthy, and we think this is the right thing for him," said Dr. Paul M. Armistead, assistant professor of medicine in the Division of Hematology/Oncology, a member of the UNC Lineberger Comprehensive Cancer Center and leader of Alston's transplant team. "This is his best chance for being cured."Alston, a Charlotte native, was diagnosed with aggressive testicular cancer in March 2011 after experiencing an "avalanche of symptoms.""I didn't have a lump, but I had some weird back pain and loss of feeling in one leg," David said. "By the time I had some scans, we found lymph node involvement in a lot of places. Essentially, the cancer had gone on vacation all over my body."Testicular cancer is one of the more curable cancers, often cured in the first round of chemotherapy, said Dr. Kim Rathmell, associate professor of medicine, a member of UNC Lineberger Comprehensive Cancer Center and Alston's medical oncologist.Aggressive chemotherapy sent the cancer into remission, and by August Alston returned to his long-time job at Weaver Street Market in Chapel Hill's Southern Village.Routine blood test results in December surprised everyone: the cancer was back."Because of the way David's cancer came back, a more aggressive approach than chemotherapy alone was needed," said Rathmell, adding how hard it was knowing Alston faced treatment again. "I shop that store, and I had seen him back at work."Dr. Matthew Milowsky, who participated in the development of the triple-tandem transplant for testicular cancer at Memorial Sloan Kettering in New York City, joined UNC Lineberger Comprehensive Cancer Center last fall as co-director of UNC's urologic oncology program. Rathmell quickly recruited him to Alston's team."We have everything we need here at UNC to treat David," Rathmell said. "Had David come to us five years ago, when this recommended treatment was newer and we didn't have local expertise, I would likely have referred him elsewhere. Today, we are very comfortable doing this transplant here. And it's a total team approach."In January, Alston began receiving two types of chemotherapy to mobilize his stem cells in preparation for collection.This chemotherapy featured one less drug than what he endured after initial diagnosis and yielded fewer side effects."It was night and day difference," he said, remembering the physical and mental side effects that sent him into the ICU last spring. "By comparison, what I'm doing in preparation for the transplant has been rather effortless."But the process is complicated and has many moving parts."David will have five chemotherapy infusions administered by two separate medical teams that have to work together through a lot of logistics about what happens when," said Armistead. "That David is organized and intelligent and sends a lot of questions to Dr. Rathmell and me via email, he's helping himself stay on top of things. Having a patient who is fully aware of what's going on has kept us on our toes and helped us develop and coordinate a more fool-proof system."Still, as a single, stubbornly independent man, Alston needed help and support. Luckily, his mother, Barbara Alston, a retired medical professional from Concord, is by his side.Both are staying at SECU Family House, the 40-bedroom hospital hospitality house minutes from UNC Hospitals for seriously ill adult patients and their family member caregivers.The Alstons will stay at Family House during the nine weeks total that David is expected to be hospitalized. He will join her between transplants and for post-transplant monitoring."It's a comfort being here at Family House," Barbara Alston said. "If we need something, it's taken care of, both here and at the hospital. I'm assured David's getting the care he needs. I'm helping him whenever and wherever I can."SECU Family House will play an even larger role in Alston's recovery post-transplant, both Rathmell and Armistead agreed."This treatment is intense, and David will be more in the hospital than out," Rathmell said. "He will need a solid support system, and he has that with his mother. It's a fragile time, and she has his best interest at heart.""Post-transplant David will need to be monitored closely because his immune system will be very weak," Armistead said. "His mother's medical background is a bonus. The Family House folks are used to immune-suppressed patients and can get them to the hospital quickly if needed."Alston has kept himself swimming in information to minimize the fear and mystery. Barbara has been the great translator when his own efforts didn't yield the level of detail he needed."The constant learning gives it all a degree of routine that took some of the scariness away," Alston said. "But you can't be too independent or too brainy when you have cancer."Cancer blows you out of the water, but it leaves you with valuable insight," he said. "How you deal with cancer is self-guided and you learn things about yourself and your personality that you never knew. It's the ultimate in snatching the silver lining from a cloud."

Elizabeth Swaringen wrote this article for UNC Health Care.

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Carrboro man to get stem cell transplant

Cancer Stem Cell Research Drives Growth in RBCC’s Target Market

NOKOMIS, Fla.--(BUSINESS WIRE)--

Research into Cancer Stem Cells (CSC) is on the rise, fueling industry growth that Rainbow Coral Corp. (OTCBB: RBCC.OB - News) expects to translate into demand for n3D cell growth technologies.

RBCC is finalizing an equity funding agreement with n3D Biosciences, the maker of a revolutionary new system that allows scientists to grow three-dimensional cell cultures more easily than ever before. The device, called the Bio-Assembler, could have an extraordinary impact on cell research worldwide, and RBCC expects to find a strong market for the device once its funding agreement with n3D is finalized.

Many cancers, including breast, prostate, pancreatic, colon, brain, and lung cancers, contain a subset of stem-like cells understood to play a critical role in the development and progression of the disease. Research suggests that these cells, called Cancer Stem Cells, are able to “seed” new tumor formation and drive metastasis.

Because these cells are believed to be at the root of the development and spread of cancer, they’re quickly becoming the center of cancer diagnostics and biomarkers. CSCs are resistant to a number of chemotherapy drugs and radiotherapy, and approximately 20 different strategies are currently being pursued in the hope of selectively targeting CSCs. This creates a huge opening for new companies and technologies dedicated to streamlining cellular research.

RBCC believes that the Bio-Assembler could allow researchers to dramatically shorten the development timeline for new CSC drugs and treatments, potentially proving very lucrative to the company.

For more information on Rainbow BioSciences, please visit http://www.rainbowbiosciences.com/investors.

Rainbow BioSciences will develop new medical and research technology innovations to compete alongside companies such as Celgene Corp. (NASDAQ: CELG), Cardinal Health, Inc. (NYSE: CAH), Abbott Laboratories (NYSE: ABT) and Affymax, Inc. (NASDAQ: AFFY).

Follow us on Twitter at www.twitter.com/RBCCinfo.

About Rainbow BioSciences

Rainbow BioSciences is a division of Rainbow Coral Corp. (OTCBB: RBCC). The company continually seeks out new partnerships with biotechnology developers to deliver profitable new medical technologies and innovations. For more information on our growth-oriented business initiatives, please visit our website at [www.rainbowbiosciences.com]. For investment information and performance data on the company, please visit www.RainbowBioSciences.com/investors.

Notice Regarding Forward-Looking Statements

Safe Harbor Statement under the Private Securities Litigation Reform Act of 1995: This news release contains forward-looking information within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended, including statements that include the words "believes," "expects," "anticipate" or similar expressions. Such forward-looking statements involve known and unknown risks, uncertainties and other factors that may cause the actual results, performance or achievements of the company to differ materially from those expressed or implied by such forward-looking statements. In addition, description of anyone's past success, either financial or strategic, is no guarantee of future success. This news release speaks as of the date first set forth above and the company assumes no responsibility to update the information included herein for events occurring after the date hereof.

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Cancer Stem Cell Research Drives Growth in RBCC’s Target Market

Editor’s move sparks backlash

Bioethicist Glenn McGee’s new job raised questions of conflict of interest at the journal he founded.

J. WILSON/KRT/NEWSCOM

The field of bioethics is embroiled in a period of soul-searching, sparked by a startling career move by one of its biggest names.

Glenn McGee is the editor-in-chief of the American Journal of Bioethics (AJOB), the most cited bioethics journal, which he founded in 1999. Since December 2011, he has also been president for ethics and strategic initiatives at CellTex Therapeutics in Houston, Texas, a controversial company involved in providing customers with unproven stem-cell therapies. A CellTex press release says that “Dr McGee’s responsibilities will include ensuring that all of the firm’s work, centered on adult stem cells, will meet the highest ethical standards of the medical and scientific communities.”

Although McGee has said he will leave the journal on 1 March, many bioethicists have criticized him, the journal’s editorial board and its publisher, London-based Taylor and Francis. They argue that in holding both posts, McGee has a conflict of interest between his responsibilities to the journal and his new employer’s desire to promote the clinical application of stem-cell treatments that are not approved by the US Food and Drug Administration.

“Imagine if the Editor of the New England Journal of Medicine took a job as Vice President at Merck, and the Mass Medical Society asked him to stay on as Editor, opining that the conflicts of interest would be manageable. One might rightly wonder, ‘What are these people smoking?’,” says John Lantos, director of the Children’s Mercy Bioethics Center in Kansas City, Missouri, and a past president of the American Society for Bioethics and Humanities.

More broadly, bioethicists are questioning whether it can ever be acceptable to work for companies, which, they argue, may be using the appointment to present a veneer of ethical probity. The episode brings to a head concerns that have emerged among bioethicists over the past decade, says Insoo Hyun, a stem-cell bioethicist at Case Western Reserve University in Cleveland, Ohio. “It’s a perfect storm,” he says.

McGee is a leading voice on one side of the debate, arguing that bioethics must have practical relevance. For the past three years he has been chair of bioethics at the non-profit Center for Practical Bioethics in Kansas City, where he ran a course for those who might go on to chair hospital ethics committees or serve as ethical advisers to corporations.

But during McGee’s tenure as editor-in-chief of the AJOB, four editors are known to have resigned from the editorial board because of differences in opinion over how the journal handles conflicts of interest. Two left this month, including Lantos, who wrote on his blog that he will no longer work with the journal because of McGee’s simultaneous employment at the AJOB and CellTex, and frustration over the lack of a clear conflict-of-interest policy at the AJOB. In response to Nature’s questions about the situation, Taylor and Francis responded that it “is grateful for Dr McGee’s editorship of AJOB” and “supportive of Glenn’s decision to step down”.

On 17 February, McGee announced that he is merely acting in an advisory capacity at the journal until 1 March, when its new editors-in-chief take over. They are David Magnus, director of the Center for Biomedical Ethics at Stanford University, California, and Summer Johnson McGee, director of graduate studies at the Center for Practical Bioethics and the journal’s current executive editor. She is also Glenn McGee’s wife.

“Mainstream bioethics is no longer speaking truth to power.”

Responding to questions from Nature, Summer Johnson McGee says that the journal has a conflict-of-interest policy that requires editors to withdraw from reviewing a manuscript if they perceive a conflict. She calls allegations that her appointment results from her relationship with her husband “baseless and sexist”. “David Magnus and I were hired by our publisher, not by my husband.” Magnus says that at least a dozen editorial board members have supported his and Summer Johnson McGee’s appointments. Two even indicated that Glenn McGee should have been able to retain an advisory or editorial role.

Other bioethicists’ blogs and Twitter feeds about the episode have expressed concerns, however. Leigh Turner of the University of Minnesota, Minneapolis, called on the entire editorial board of the AJOB to resign for allowing the situation to persist. And many say that McGee’s move illustrates a broader problem. “Mainstream bioethics is no longer speaking truth to power,” complains Jan Helge Solbakk at the University of Oslo. “Instead it has become the handmaiden of the medico-industrial complex, and of bioscience and technology.”

So how should companies get their advice on bioethics? Magnus never takes cash from industry for advising or speaking — “I’m a hardass about that” — but he believes that bioethicists can work for industry as long as they give up their academic positions, including posts on journal editorial boards.

Working for a respected company may be acceptable to some bioethicists, but McGee’s new employer comes with a great deal of baggage. CellTex, which was founded last year and as yet has no website, licenses stem-cell technology from Seoul-based RNL Bio. The South Korean company has made a business out of taking fat cells from people, processing them in a way that they say increases the number of mesenchymal stem cells, and then reinjecting them in an effort to treat conditions such as spinal cord injury.

McGee already had a connection with RNL Bio. In 2010, two patients died following injections of RNL’s cells. McGee, working for stem-cell lobby group the International Cellular Medicine Society, based in Salem, Oregon, helped to conduct an investigation into the company. This concluded that only one of the two cases was likely to be related to the injections, and because the patient understood the risk the company was not culpable.

Jin Han Hong, the then president of RNL’s US subsidiary, admitted in 2010 that there was no clinical-trial evidence proving that these treatments are effective (Nature 468, 485; 2010). As treatment with RNL’s stem cells is not approved in the United States or South Korea, for the procedures the company sends patients to China or Japan, where regulations are less strictly enforced. Using RNL’s methods, CellTex is banking stem cells that have gone on to be used in a number of patients, including Rick Perry, governor of Texas (Nature 477, 377–378; 2011). CellTex says that it does not conduct medical procedures itself.

When Nature contacted McGee to put the criticisms to him, he directed us to previous statements indicating that he wants to put CellTex on firmer ethical ground by having it conduct clinical trials that meet standards set by the International Society for Stem Cell Research, based in Deerfield, Illinois, which represents most mainstream stem-cell researchers around the world.

Hyun warns that working directly for business can be fraught with danger, however good a bioethicist’s intentions. In 2005, he helped to craft the informed consent procedure for egg donations used in a cloning procedure by disgraced Korean stem-cell scientist Woo Suk Hwang. Following Hwang’s claim, later proved fraudulent, that he had cloned human embryos and harvested stem cells from them, it emerged that he had ignored the consent procedure for egg donations (Nature 438, 536–537; 2005), leading to embarrassment for Hyun.

“I know first hand how difficult it is to separate conflict of interest — to maintain the role of bioethicist,” says Hyun. “I know you need to not be too chummy with enterprises trying to speed ahead in stem cells.”

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Editor’s move sparks backlash

Russian Press – Behind the Headlines, February 20

Moskovskiye Novosti

Church Calls for Ban on Stem Cell Research

The Russian Orthodox Church has called for recognizing fetuses as human life and for banning medical research that involves biological material procured from abortion procedures.

The church has sent a series of amendments to the cell technology bill, which iscurrently in the works, to Healthcare Minister Tatyana Golikova in the hope that “the ministry will heed its opinion.” “We, in turn, are ready for dialogue and discussion on each proposal,” said Bishop Panteleimon, head of the the Synodal Department for Church Charity and Social Ministry.

Incidentally, the clerics cite “enlightened” European policies on this issue. In October 2011, the European Court of Justice outlawed the patenting of stem cell research that destroys a human embryo as immoral. Russia’s Healthcare Ministry supported that decision and said the cell technology bill they were working on embraced similar ethical principles. Deputy Minister Veronika Skvortsova said the new bill would ban the use of a human fetus, embryo or gamete in preparing cell lines.

According to Bishop Panteleimon, this means that the government is ready to agree that a fertilized ovum constitutes a person. Therefore, it would only remain to legalize this statement. That would make it possible to refer to an embryo as a “child,” which in turn would make the 1959 Children’s Rights declaration applicable to the embryo, thus guaranteeing the “child” legal protection “before and after birth.”

One proposal would include church officials on the ministry’s expert council on biomedical ethics. The church has had a similar council since 1998.

“The ministry’s bill cites advanced cell technology that is not widely used in Russia,” a church official said. “At the same time, there are simpler technologies which also use fetal cells as biological material, and these are quite widespread.”

The letter sent to Minister Golikova mentions valid patents for using fetal cells in anti-aging treatments, mesotherapy and fetal tissue implants.

The bill, drafted by the Ministry of Healthcare, is currently in the public discussion stage, and could be submitted to the lower house this spring. Given current legislative trends, the church may well expect that its proposals will be heeded. However, Russian scientists involved in stem cell research fear that the bill would entirely halt research in this area.

According to Sergei Kiselyov from the Human Stem Cells Institute, very few cell technologies are actually used in medicine. The bill would drastically limit the current research and could affect projects that are already underway. This would lead to Russia’s lagging even further behind Western biotechnology, he said.

Kommersant

Russia Joins OECD Convention Against Bribery

The Russian Foreign Ministry notified the Organization for Economic Cooperation and Development (OECD) on Friday that Russia has joined the OECD Convention on Combating Bribery of Foreign Public Officials in International Business Transactions. Experts believe that joining the convention will stimulate the fight against corruption. Russia will be the 39th state party to the convention as of April 17.

The State Duma ratified the convention on January 13, 2012, and President Dmitry Medvedev signed it into law on February 1. Medvedev said at a judiciary meeting, “Accession will harmonize our legal system with international standards in the fight against corruption.”

“We have not joined this convention to please anybody,” First Deputy Foreign Minister Andrei Denisov clarified. “Joining is important in terms of our internal anti-corruption policy.”

Denisov added that ratifying the convention, a three-year process, is a condition for OECD accession. Russia, he said, will seek to join the organization in 2013, but the country will have to ratify 160 other conventions and instruments in 22 categories, including the introduction of international standards for economic statistics. Joining the anti-bribery convention requires Russia to pay annual dues of about 100,000 euros per year to the OECD Working Group on Bribery in International Business.

The convention was signed in 1997 and entered into force in February 1999. Most European countries are members, as are some Latin American countries and the United States. The main obligation for the states parties is to track and prosecute their citizens for bribery or attempted bribery of foreign officials and to track foreign officials on their territories who take bribes. The convention recommends not only criminalizing these acts, but also blacklisting the companies found guilty of bribing foreign public officials from tenders for government contracts. The convention discourages the practice of allowing income tax deductions for bribes to officials of foreign states: some companies in developing countries having been implicated in this practice. The convention aims to prevent parties from adding to corruption not only within their borders, but also beyond. However, fewer than 20% of participating countries actively apply the convention's provisions, according to a 2011 Transparency International report.

Even before ratifying the convention, Russia adopted a series of measures to fulfill it. In April 2011, Dmitry Medvedev's anti-corruption package introduced amendments to the Criminal Code, including multiple penalties for giving and receiving bribes, as well as mediation. Foreign officials as well as companies that give bribes to foreign officials or officials of international public organizations will be held liable.

Vladimir Yuzhakov, director of the Department for Administrative Reform at the Center for Strategic Studies, said that the practice of applying the convention will provide additional incentives to fight corruption in the country in general. Yuzhakov expects that the convention will require further steps in developing anti-corruption legislation – in particular, the introduction of more stringent procedures for investigating cases of bribery of foreign public officials.

RIA Novosti is not responsible for the content of outside sources.

 

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Russian Press - Behind the Headlines, February 20

$30M for health care research, education and care at McMaster University – Video

06-02-2012 12:13 The Marta and Owen Boris Foundation is giving $30M to McMaster to accelerate the university's innovations in health research, education and care. Of the total, $24 million is designated to establish The Boris Family Centre in Human Stem Cell Therapies, which will speed the commercial development of discoveries at the McMaster Stem Cell and Cancer Research Institute. The six-year-old institute has had several major breakthroughs, including the ability to turn human skin into blood. An additional $6 million is for a unique clinic which will allow patients with complex health problems to see several specialists and have related tests during one visit. Established in partnership with Hamilton Health Sciences, this patient-oriented clinic will be built in the McMaster University Medical Centre in Hamilton and led by a senior research chair.

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Groundbreaking Clinical Trials Study Cord Blood Stem Cells to Help Treat Brain Injury and Hearing Loss

SAN BRUNO, Calif., Feb. 16, 2012 /PRNewswire/ -- Cord Blood Registry (CBR) is the exclusive partner for a growing number of clinical researchers focusing on the use of a child's own cord blood stem cells to help treat pediatric brain injury and acquired hearing loss. To ensure consistency in cord blood stem cell processing, storage and release for infusion, three separate trials have included CBR in their FDA-authorized protocol—including two at the University of Texas Health Science Center at Houston (UTHealth) working in partnership with Children's Memorial Hermann Hospital, and a third at Georgia Health Sciences University, home of the Medical College of Georgia (MCG). This makes CBR the only family stem cell bank pairing researchers with prospective patients for these studies. 

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"Partnering with a series of specialists who want to research the use of a child's own newborn blood stem cells on a variety of disease states allows CBR to help advance medical research for regenerative therapies by connecting the child whose family banked with CBR to appropriate researchers," said Heather Brown, MS, CGC, Vice President of Scientific & Medical Affairs at Cord Blood Registry.  "The pediatric specialists from UTHealth, Children's Memorial Hermann Hospital, and Georgia Health Sciences University are at the forefront of stem cell research as they evaluate cord blood stem cells' ability to help facilitate the healing process after damage to nerves and tissue."

Hearing Loss and Traumatic Brain Injury Clinical Trials Break New Ground

Sensorineural hearing loss affects approximately 6 per 1,000 children by 18 years of age, with 9 percent resulting from acquired causes such as viral infection and head injury.(1,2,3)  The Principal Investigator of the hearing loss study is Samer Fakhri, M.D., surgeon at Memorial Hermann-Texas Medical Center and associate professor and program director in the Department of Otorhinolaryngology – Head & Neck Surgery at UTHealth.  He is joined by James Baumgartner, M.D., sponsor of the study and guest research collaborator for this first-of-its-kind FDA-regulated, Phase 1 safety study of the use of cord blood stem cells to treat children with acquired hearing loss. The trial follows evidence from published studies in animals that cord blood treatment can repair damaged organs in the inner ear. Clients of CBR who have sustained a post-birth hearing loss and are 6 weeks to 2 years old may be eligible for the year-long study. "The window of opportunity to foster normal language development is limited," said James Baumgartner, M.D.  "This is the first study of its kind with the potential to actually restore hearing in children and allow for more normal speech and language development."

Although the neurologic outcome for nearly all types of brain injury (with the exception of abuse) is better for children than adults,(4,5) trauma is the leading cause of death in children,(6) and the majority of the deaths are attributed to head injury.(7) Distinguished professor of pediatric surgery and pediatrics at UTHealth, Charles S. Cox, M.D. launched an innovative study building on a growing portfolio of research using stem cell-based therapies for neurological damage. The study will enroll 10 children ages 18 months to 17 years who have umbilical cord blood banked with CBR and have suffered a traumatic brain injury (TBI) and are enrolled in the study within 6-18 months of sustaining the injury. Read more about the trial here.

"The reason we have become interested in cord blood cells is because of the possibility of autologous therapy, meaning using your own cells. And the preclinical models have demonstrated some really fascinating neurological preservation effects to really support these Phase 1 trials," says Charles S. Cox, M.D., principle investigator of the trial. "There's anecdotal experience in other types of neurological injuries that reassures us in terms of the safety of the approach and there are some anecdotal hints at it being beneficial in certain types of brain injury."

Georgia Health Sciences University (GHSU) Focuses on Cerebral Palsy

At the GHSU in Augusta, Dr. James Carroll, professor and chief of pediatric neurology, embarked on the first FDA-regulated clinical trial to determine whether an infusion of stem cells from a child's own umbilical cord blood can improve the quality of life for children with cerebral palsy. The study will include 40 children whose parents have stored their cord blood at CBR and meet inclusion criteria. 

"Using a child's own stem cells as a possible treatment is the safest form of stem cell transplantation because it carries virtually no threat of immune system rejection," said Dr. Carroll. "Our focus on cerebral palsy breaks new ground in advancing therapies to change the course of these kinds of brain injury—a condition for which there is currently no cure."

Cerebral palsy, caused by a brain injury or lack of oxygen in the brain before birth or during the first few years of life, can impair movement, learning, hearing, vision and cognitive skills. Two to three children in 1,000 are affected by it, according to the Centers for Disease Control.(8)

Cord Blood Stem Cell Infusions Move From the Lab to the Clinic

These multi-year studies are a first step to move promising pre-clinical or animal research of cord blood stem cells into clinical trials in patients. Through the CBR Center for Regenerative Medicine, CBR will continue to partner with physicians who are interested in advancing cellular therapies in regenerative applications.

"The benefits of cord blood stem cells being very young, easy to obtain, unspecialized cells which have had limited exposure to environmental toxins or infectious diseases and easy to store for long terms without any loss of function, make them an attractive source for cellular therapy researchers today," adds Brown. "We are encouraged to see interest from such diverse researchers from neurosurgeons to endocrinologists and cardiac specialists."

About CBR

CBR® (Cord Blood Registry®) is the world's largest and most experienced cord blood bank.  The company has consistently led the industry in technical innovations and supporting clinical trials. It safeguards more than 400,000 cord blood collections for individuals and their families. CBR was the first family bank accredited by AABB and the company's quality standards have been recognized through ISO 9001:2008 certification—the global business standard for quality. CBR has also released more client cord blood units for specific therapeutic use than any other family cord blood bank. Our research and development efforts are focused on helping the world's leading clinical researchers advance regenerative medical therapies. For more information, visit http://www.cordblood.com.

 

(1)  Bergstrom L, Hemenway WG, Downs MP. A high risk registry to find congenital deafness. Otolaryngol Clin North Am. 1977;4:369-399.
(2)  Billings KR, Kenna MA. Causes of pediatric sensorineural hearing loss: yesterday and today. Arch Otolaryngol Head Neck Surg. 1999 May;125(5):517-21.
(3)  Smith RJ, Bale JF Jr, White KR. Sensorineural hearing loss in children. Lancet. 2005;365(9462):879-890.
(4)  Faul M, Xu L, Wald MM, Coronado VG. Traumatic brain injury in the United States: emergency department visits, hospitalizations, and deaths. Atlanta (GA): Centers for Disease Control and Prevention, National Center for Injury Prevention and Control; 2010.
(5)  Schnitzer, Patricia, PH.D., "Prevention of Unintentional Childhood Injuries", American Academy of Family Physicians, 2006.
(6)  Centers for Disease Control and Prevention, "10 Leading Causes of Death, United States, 1997-2007", WISQARS, National Center for Health Statistics (NCHS), National Vital Statistics System
(7)  Marquez de la Plata, Hart et al, National Institutes of Health, "Impact of Age on Long-term Recovery From Traumatic Brain Injury", Arch Phys Med Rehabilitation, May 2008.
(8)  Centers for Disease Control and Prevention, http://www.cdc.gov/Features/dsCerebralPalsy, accessed February 6, 2012

 

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Groundbreaking Clinical Trials Study Cord Blood Stem Cells to Help Treat Brain Injury and Hearing Loss