GE3LS Digest - November 4, 2008

The GE3LS Digest
A compendium of news and research from around the country and around the world

Date: November 4, 2008
 
This news digest is published by GE3LS at Genome Alberta. Feel free to forward to your colleagues. If you would like to be added/ removed from the distribution list, please email rhyde-lay@genomealberta.ca 
   
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NEWS
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CANADA

Canadian, Japanese scientists team up to accelerate work on stem cell therapies – October 16, 2008
http://healthandfitness.sympatico.msn.ca/News/ContentPosting?newsitemid=100309042&feedname=CP-HEALTH&show=False&number=0&showbyline=True&subtitle=&detect=&abc=abc&date=True
Canadian and Japanese stem cell researchers are joining forces in a bid to more quickly translate scientific discoveries from the lab into treatments for people with such diseases as autism and cystic fibrosis. The University of Toronto and Japan's Kyoto University signed a research-sharing agreement in Tokyo on Thursday that will bring together world-renowned stem cell researchers in Toronto with the Japanese lab of Dr. Shinya Yamanaka. Yamanaka shook the science world last year by converting normal adult cells into embryonic-like stem cells. Embryonic stem cells have the ability to differentiate into any type of tissue in the body, from heart and liver to brain and skin. But the idea of harvesting stem cells from human embryos is ethically contentious. Yamanaka's discovery would allow scientists to get around restrictions regarding generation of stem cells from embryos, meaning research should move at a faster pace. "Shinya Yamanaka and his team have developed some of the world's most important technology in stem cell research, and the team at U of T is among the best at differentiating cells to produce innovative therapies," Bill Stanford, associate director at the university's Institute for Biomaterials and Biomedical Engineering, said in a statement. "Together, we'll share patient samples, technologies and protocols to get basic science to the clinic much faster."

B.C. court issues injunction in class-action over sperm, egg donor births – October 28, 2008
http://healthandfitness.sympatico.msn.ca/News/ContentPosting?newsitemid=41913026&feedname=CP-HEALTH&show=False&number=0&showbyline=True&subtitle=&detect=&abc=abc&date=True
A British Columbia judge hearing the case of a woman who wants to know the identity of her sperm donor father has issued an injunction against the destruction or transfer of any records concerning artificial insemination. The case involves Olivia Pratten, 26, who has launched a class-action lawsuit on behalf of children conceived via sperm, egg or embryo donation. Pratten said Tuesday she feels that the rights of those born through artificial insemination are have been neglected. "My mom received donor sperm treatment," she said in a telephone interview from New York. "But I'm not treatment, I'm a person."
The B.C. Supreme Court order issued Tuesday applies to any records of the identity, medical history or social history of donors in such births, not just Pratten's.
The class-action lawsuit against B.C.'s attorney general and the province's College of Physicians and Surgeons claims the law discriminates against people who were conceived as a result of so-called gamete donation.


INTERNATIONAL

Scientists find 26 genes promoting lung cancer – October 16, 2008
http://healthandfitness.sympatico.msn.ca/abc/News/ContentPosting.aspx?isfa=1&feedname=CP-HEALTH&showbyline=True&newsitemid=36739024
In the largest effort of its kind, scientists have identified 26 genes that, when damaged, appear to promote lung cancer. It's a step toward developing new treatments that can be tailored to specific patients. The federally funded project was the largest ever to screen genes for mutations in the most common form of lung cancer, called adenocarcinoma. The results more than double the catalogue of genes implicated in that condition.
The findings, from scientists at a dozen institutions in the United States and Germany, appear in Thursday's issue of the journal Nature. Lung cancer is the leading cancer killer in the United States, Canada and worldwide. The study focused on tumours that originated in the lung and were surgically removed. But researchers also hope to study whether the same mutations appear in lung tumours that spread elsewhere.
The scientists sampled 188 tumours. They examined the makeup of 623 genes to look for those that were the most often mutated. The idea is that if a gene is mutated in so many tumours, it probably plays a role in the disease. The mutations clearly arose in the cancers because they did not appear in healthy tissue from the cancer patients. New public

Genome database to spark research, unease – October 19, 2008
http://www.biotechniques.com/default.asp?page=news&subsection=article_display&id=300
Ten volunteers are preparing to share with the world what is arguably their most personal possession: their decoded DNA, along with medical history, ethnic background, and other traits. These pioneers are participating in the Personal Genome Project (PGP), a Harvard University–based research group whose initiative is to provide more openly available genetic information in order to further genetic and medical research.Because the common issues surrounding privacy have been sidestepped by gaining complete consent from the “PGP 10,” as they call themselves, the database—which the project hopes to expand to include 100,000 participants—will include phenotypic information, which has typically been avoided in other databases due to privacy concerns. Complete, open access to this type of data is expected to help researchers better understand how outward traits and genes are linked.In allowing the partial genomes of the 10 volunteers to remain openly accessible, the PGP hopes to also confront the stigma surrounding the concept of a public genome. It is, as the New York Times aptly described, “[a]s much a social experiment as it is a scientific one.” Dr. George M. Church, a human geneticist at Harvard, who is the leader of the PGP and also a participant, concedes that it is unknown how the availability of this information will affect its participants. “We don’t yet know the consequences of having one’s genome out in the open, but it’s worth exploring,” he told the Times.
Others are not so swift to agree. “There will be new uses of this data that people can’t anticipate,” said Kathy Hudson, director of the Genetics and Public Policy Center at Johns Hopkins University, “and they can’t do anything to get it back.”

Biotech cash crunch threatens new medicines: UK expert – October 21, 2008
http://www.reuters.com/article/healthNews/idUSTRE49Q21720081027
The global credit crunch, which has already pushed some small biotechnology companies to the wall, could seriously delay the discovery of new life-saving medicines, a British expert warned on Monday. David Wield, director of the Economic and Social Research Council's Edinburgh-based Innogen Center, said the cash crisis now looming for many firms had wider implications for society. "Drug discovery depends on long-term finance with high risk of failure -- and lots of it," he said in remarks prepared for a conference in London. "What will happen to investment in biotech research if finance cannot even be found for relatively everyday expenses, which are increasingly becoming more of a struggle?" Many biotech companies are desperate to find new funds as investors shun the notoriously risky sector, leading to severe financial problems on both sides of the Atlantic. In addition to the impact on the basic research performed at biotech companies, development of drugs by large pharmaceutical firms has also been hit by the credit crunch, with several having laid off staff or closed research units, Wield said.

New Zealand approves pig-human tissue transplants for diabetics—October 21, 2008
http://www.physorg.com/news143787874.html
New Zealand on Tuesday gave the green light for clinical trials involving the transplantation of pig cells into humans in a potential breakthrough treatment of diabetes.
Health Minister David Cunliffe said the process, known as xenotransplantation, had huge potential for diabetes sufferers. "This is critical new technology that could well make New Zealand a world leader in both the treatment of diabetes and in the use of xenotransplantation," he said. Biotech entrepreneur Living Cell Technologies Ltd (LCT) wants to transfer cells from the pancreas of pigs to produce insulin in type-1 diabetes sufferers. Though the technology could produce significant benefits for patients, it is highly controversial given the potential for a pig virus to be transferred that could then became capable of spreading as an infection in people. "It remains clear to me that any such trial will always carry a very low residual risk, so the key issue has always been whether this risk is sufficiently small and can be successfully managed," Cunliffe said.

Drought Resistance Is the Goal, but Methods Differ – October 22, 2008
http://www.nytimes.com/2008/10/23/business/23drought.html?_r=1&ref=science&oref=slogin
To satisfy the world’s growing demand for food, scientists are trying to pull off a genetic trick that nature itself has had trouble accomplishing in millions of years of evolution. They want to create varieties of corn, wheat and other crops that can thrive with little water. Skip to next paragraphAs the world’s population expands and global warming alters weather patterns, water shortages are expected to hold back efforts to grow more food. People drink only a quart or two of water every day, but the food they eat in a typical day, including plants and meat, requires 2,000 to 3,000 quarts to produce. For companies that manage to get “more crop per drop,” the payoff could be huge, and scientists at many of the biggest agricultural companies are busy tweaking plant genes in search of the winning formula. Monsanto, the biggest crop biotechnology company, says its first drought-tolerant corn will reach farmers in only four years and will provide a 10 percent increase in yields in states like Nebraska and Kansas that tend to get less rainfall than eastern parts of the Corn Belt.

Nuffield Council on Bioethics launches personalised healthcare study – October 22, 2008
http://www.phgfoundation.org/news/4378/
The Nuffield Council on Bioethics has launched a study which will consider the ethical issues raised by new technologies that make healthcare more personalised (see press release). A Working Party has been formed which will examine the ethical issues raised by new technologies such as whole body CT or MRI scans, personal genomics and telemedicine, with the aim of producing a report and recommendations on policy and practice. The Working Party chaired by Professor Christopher Hood will hold a public consultation in Spring 2009 and aims to produce a report with recommendations on policy and practice by early 2010. Many of the issues associated with personalised health care (see previous news) have already been raised in relation to personalised genomics (see previous news). This includes questions about informed consent and data confidentiality, the usefulness of such information to the individual, how it will affect lifestyle choices, regulation of direct-to-consumer tests, and the impact of such information on insurance policies and the NHS as people seek follow-up support. Although the NHS already utilises some forms of the technologies that the project is focusing on, their application as tools for ‘personalised’ healthcare is at present primarily offered by commercial companies.

Prostates Grown from Stem Cells: New proof that the mouse prostate contains stem cells could aid cancer research – October 23, 2008
http://www.technologyreview.com/biomedicine/21594/
A single adult stem cell from the prostate of a mouse can develop into an entire functional organ, scientists reported online yesterday in Nature. The finding proves that a population of stem cells exists in the adult prostate, as many have long suspected, and it could provide insight into how prostate cancer develops. "It's extremely exciting, the concept that you can reconstitute an entire prostate from a single cell," says Tyler Jacks, director of the David H. Koch Institute for Integrative Cancer Research, at MIT, who was not involved in the work. "That's impressive stuff." Unlike embryonic stem cells, which can potentially develop into any cell type in the body, adult stem cells are tissue-specific. Many organs are believed to house populations of adult stem cells, but in most cases their existence remains unproven. Known adult stem cells, however, can give rise to all the cell types that characterize the organs in which they're found. Ban on mixed emrbyos of human DNA and animal eggs to remain.

Ban on mixed emrbyos of human DNA and animal eggs to remain – October 24, 2008
http://www.theaustralian.news.com.au/story/0,25197,24543817-30417,00.html
The ban in Australia on producing embryos that fuse human DNA and empty animal eggs will remain, despite a British vote legalising the inter-species creations for stem cell research. Parliamentary Secretary for Health Jan McLucas said yesterday "cybrid" embryos were illegal and were likely to stay so."We are not considering making any changes at this time," Senator McLucas said.Britain's lower house of parliament yesterday voted 355 to 129 to permit the creation of cybrids to overcome a shortage of human eggs. The eggs are central to therapeutic cloning, a procedure devised to create the embryonic stem cells used in medical research. As ES cells can grow into any type of cell, scientists see them as a vital tool for teasing out the mechanisms of diseases and for developing new therapies. Two British research teams began working to make cybrids this year. One group succeeded, giving legislators an extra push to tidy up existing administrative arrangements in Britain. While Britain still bans other human-animal hybrid embryos, it has exempted the cybrids because the ES cells produced ended up 99.9 per cent human.

Scientist leaves UK due to lack of focus on adult stem cell research –October 27, 2008
http://www.biotechniques.com/default.asp?page=news&subsection=article_display&id=317
A renowned stem-cell researcher plans to leave the UK to pursue his research in France, claiming that the British government gives more precedence to embryo experiments over more “ethical” options. Colin McGuckin, a professor of regenerative medicine at Newcastle University, told Times Higher Education that his motivation for leaving the UK is to “cure and treat more people,” and that France offered a “much better environment” to do so. “[France] is very supportive of adult stem cells because they know that these are the things that are in the clinic right now and will be more likely in the clinic,” he said. “A vast amount of money in the UK from the Government has gone into embryonic stem-cell research with not one patient having been treated, to the detriment of [experimentation into] adult stem cells, which has been severely underfunded.” He added that France has kept a “much more reasoned balance” between endorsing both adult and embryonic stem-cell research, unlike the UK, which he says focuses more on embryonic research. According to the Times Online, McGuckin—after three years at Newcastle University—has decided to move to the University of Lyon in January with his research team of about 10 members and research partner Nico Forraz, to develop the world’s largest institute dedicated to cord blood and adult stem-cell research.

Purple 'super tomato' that can fight against cancer – October 27, 2008
http://www.dailymail.co.uk/sciencetech/article-1080695/Purple-super-tomato-fight-cancer.html
It looks like a cross between an orange and a black pudding, but this genetically modified purple 'super tomato' could be the latest weapon in the fight against cancer. The fruit, which tastes and smells like a normal red tomato, has been given two genes from a snapdragon flower that produce the dark colour. The distinctive hue is created by antioxidant pigments that protect against diseases including cancer, heart problems and diabetes. British scientists behind the crop believe their purple tomato is the respectable face of genetic modification and could help convince the public of the benefits of GM food. But critics say the potential health benefits are a distraction from the harmful environmental side effects of GM farming. The tomato  -  developed by the John Innes Centre in Norwich  -  contains high concentrations of anthocyanins, pigments found in blackberries and cranberries

DG Sanco debates consumer reception of new technologies – October 29, 2008
http://www.foodnavigator.com/Legislation/DG-Sanco-debates-consumer-reception-of-new-technologies
A conference taking place in Brussels is examining how best to deal with emerging technologies like cloning and nanotechnology, and to ensure that consumer confidence is addressed. Called Delivering for Tomorrow’s European Consumers, the Directorate General for Health and Consumers (DG Sanco) conference sets out to map future challenges for consumer health and protection, and will be used to finalise a strategic paper on action areas before the new Commission. DG Sanco has just published a draft paper 'Future Challenges: 2009-2014’, setting out the most important challenges it expects to face in the coming years. The paper, which gives a basis for the broad topics at the conference, is the result of two years’ of discussions, and takes account of wide-ranging stakeholder comments. This morning’s session took case studies of technologies that have already elicited some response from consumers. In addition to the questions over the use of animals for meat and other derivatives, and whether the safety nanotechnology has been established, it also looked at consumer views of genetically modified foods.

TIME's Best Inventions of 2008 - November 3, 2008
http://www.time.com/time/specials/packages/article/0,28804,1852747_1854493_1854113,00.html
1.The Retail DNA Test
Before meeting with Anne Wojcicki, co-founder of a consumer gene-testing service called 23andMe, I know just three things about her: she's pregnant, she's married to Google's Sergey Brin, and she went to Yale. But after an hour chatting with her in the small office she shares with co-founder Linda Avey at 23andMe's headquarters in Mountain View, Calif., I know some things no Internet search could reveal: coffee makes her giddy, she has a fondness for sequined shoes and fresh-baked bread, and her unborn son has a 50% chance of inheriting a high risk for Parkinson's disease.
Learning and sharing your genetic secrets are at the heart of 23andMe's controversial new service — a $399 saliva test that estimates your predisposition for more than 90 traits and conditions ranging from baldness to blindness. Although 23andMe isn't the only company selling DNA tests to the public, it does the best job of making them accessible and affordable. The 600,000 genetic markers that 23andMe identifies and interprets for each customer are "the digital manifestation of you," says Wojcicki (pronounced Wo-jis-key), 35, who majored in biology and was previously a health-care investor. "It's all this information beyond what you can see in the mirror."

No consensus on when human life begins – November 3, 2008
http://www.bionews.org.uk/new.lasso?storyid=4049
An international poll has shown a range of opinions about when human life begins biologically. It comes ahead of a proposed constitutional amendment in Colorado, US, which could confer legal rights to embryos at the point of fertilisation. The poll was commissioned by Reproductive Biology Associates, an IVF clinic in Atlanta, Georgia. Respondents were asked when human life begins and given a dozen answers, ticking the one they most agreed with. Overall, 23.5 per cent of voters selected detection of fetal heartbeat as the point when human life begins. Just under 23 per cent selected fertilisation, and implantation of the embryo in the womb lining came third, with 15 per cent. Around 650 people were polled. Colorado's constitutional amendment proposes that fertilisation is when human life begins, and also that this is when someone becomes a person, deserving the same legal rights and protection under the US constitution as any child or adult citizen. If it gets voted for, it could make it easier for abortion to be outlawed in Colorado, and encourage similar amendments to be made in other US states.

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CONFERENCES/CALL FOR PAPERS 
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Genome Quebec and Cambridge Healthtech Institute 2nd International Congress; Pharmacogenomics Now: Minimize risks and maximize economic benefits
November 5-6, 20008
Montréal, Québec
http://www.pharmacogenomicsnow.com

Imaging Science: An Artistic Exploration of Science, Society and Social Change Public Exhibition at the Art Gallery of Alberta

November 14, 2008-February 1, 2009
Edmonton, Alberta
http://www.festivalofideas.ca/details.cfm?ID_event=15980
http://www.festivalofideas.ca/details.cfm?ID_event=15979

5th International DNA Sampling Conference: The Age of Personalized Genomics
September 16-19, 2009
Banff, Alberta
For more information contact: robyn.hyde-lay@genomealberta.ca
  
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PAPERS/REPORTS/BOOKS/BLOGS  
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Achievements of the National Plant Genome Initiative and New Horizons in Plant Biology
http://dels.nas.edu/dels/rpt_briefs/plant_genome.pdf
The National Academies have released a new primer on the achievements and promise of plant genome sciences. Based on an expert consensus report from the National Research Council, the booklet explores the potential of the National Plant Genome Initiative -- a federal multiagency project that coordinates research in plant sciences to understand and ultimately harness plants' properties to help meet agriculture, nutrition, energy, and human health needs. For example, by knowing how plants cope with less water, rising temperatures, and other environmental stresses, scientists could develop crops that withstand changing climate conditions. Sections of the booklet examine mutations and manipulation of food crops, the promise and challenges of biofuels, environmental stewardship, biomedical advances, and how scientists can maximize the use of plant sciences. Free electronic and hard copies of the booklet are available at http://nas.edu/plant_genome/

Food Biotechnology: A Study of U.S. Consumer Attitudinal Trends, 2008 REPORT
http://www.ific.org/research/biotechres.cfm
The 2008 Food Biotechnology: A Study of US Consumer Trends Survey, commissioned by the International Food Information Council is the 13th annual nationally representative survey designed to gain insights into consumer perspectives on food biotechnology. This research provides the opportunity to track public awareness and perceptions of plant and animal biotechnology, determine confidence in the U.S. food supply and understand attitudes about food labeling, determine consumer opinions regarding potential benefits associated with biotechnology, and uncover emerging opinions on sustainable food production. This survey has again found that biotech foods do not make the top-of-mind list of things Americans are avoiding.  In addition, awareness of food biotechnology continues to correlate with favorability. Therefore, the need for communication of credible, science-based information about food biotechnology remains strong.
Also, the likelihood to purchase biotech foods for special benefits remains high and stable.  Across the board, awareness of these benefits drives favorability.

BLOGS

Genetic Privacy: An Outdated Concern? –October 21, 2008
http://www.technologyreview.com/blog/editors/22156/
The vote was unanimous. Every one of the PGP-10--the first 10 volunteers for the Personal Genome Project--decided to make the genomic information he or she has received so far public, along with his or her medical and other trait information. (For background on the project, check out yesterday's "Genomes on Display.") The group revealed its decisions at a press conference at Harvard Medical School on Monday afternoon….Before the PGP-10 revealed its decisions to the world, the group spent the day discussing some of the issues that the unique project raises--especially the issue of privacy. The plan for the PGP is to make all aspects as open as possible, from the technology that is developed to the medical and genetic information of the participants. The rationale is that it is difficult to promise research subjects anonymity when the data being collected includes genetic information--the ultimate personal identifier--so it's better to make everything open from the get-go.

Stem-cell law goes to the polls: The 4 November election will settle more than who sits in the White House – October 29, 2008
http://www.nature.com/news/2008/081029/full/4551154a.html
Last year Sean Morrison, a stem-cell scientist at the University of Michigan in Ann Arbor, received an e-mail from a woman wanting to donate extra embryos from her in vitro fertilization procedure towards his research into Parkinson's disease. He had to say no. According to Michigan law, the woman could donate the embryos to another state or throw them away — but not give them to a local researcher to derive new stem-cell lines. Michigan's scientific reputation could change on 4 November. Voters will not only choose the next US president (see Nature 455, 442–453; 2008) but also say yes or no to a state ballot measure on stem-cell research, known as Proposal 2 — one of several initiatives across the country (see map). If passed, the proposal would amend a 1978 state law banning research on live human embryos, which currently prevents Michigan researchers from deriving new human embryonic stem-cell lines, and which they see as limiting their research.The initiative would also mean that, instead of having to discard embryos left over from fertility treatment, women could legally donate them directly to state stem-cell research centres. The state's ban on using somatic-cell nuclear transfer to produce a human embryo would still hold, and buying and selling human embryos would also become illegal.

Genome scans for the whole family: 23andMe research director talks about genotyping her kids – October 31, 2008
http://scienceblogs.com/geneticfuture/2008/10/genome_scans_for_the_whole_fam.php
One of the ethical quandaries raised by direct-to-consumer genetic testing is the possibility that customers may send in DNA samples for analysis from other people who haven't provided informed consent - prospective spouses, for instance, a la Gattaca - and then use that genetic information for nefarious purposes. In the past, personal genomics company 23andMe has responded to this possibility by arguing that it's not really the company's responsibility to prevent its customers from performing illegal acts; they have also (quite convincingly) pointed out the difficulties of extracting 2 mL of saliva from an unwilling victim without arousing suspicion. However, there is one class of potential customers who are legally unable to provide informed consent, but who could usually be convinced quite easily to give up a tube full of spit: customers' children. And in this case 23andMe's view seems to be extremely relaxed - they even have a non-judgmental warning about the difficulty of collecting the required saliva from infants under 3. In fact, judging from a recent entry on 23andMe's corporate blog The Spittoon, the company is actively encouraging customers to bring their own kids into the happy 23andMe family. This is a bold move, and one that is likely to provoke considerable controversy (and outrage). But rather than shying away from this debate 23andMe seems determined to confront the issues head-on.