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Risky treatment halts MS

Posted: Published on April 4th, 2013

As a third-year medical student Alex Normandin expected to be learning about patients, not become one himself. But then, the Montrealer and aspiring doctor noticed some alarming symptoms fatigue, numbness and problems with balance and coordination. Researchers at the Montreal Neurological Institute confirmed he has a particularly aggressive form of multiple sclerosis, an unpredictable and degenerative disease that affects the central nervous system. Most patients with MS do not become severely disabled because the illness moves slowly. But in Normandins case, the destruction was so fast that doctors expected him to need a wheelchair within months. Normandin, however, learned of a cutting-edge treatment run by Mark Freedman and Harry Atkins at the Ottawa General Hospital an experimental bone-marrow stem-cell transplant as a last resort for patients who fail to improve on drug therapy. Normandin became patient 19 of 24. His transplant took place in Ottawa in December 2008. The procedure is risky because it relies on toxic chemotherapy to wipe out the patients immune system in preparation for the stem-cell transplant, which re-boots the immune system. One patient died in an earlier phase of the trial. Normandin survived and spoke to the Gazette in April 2009, five months after having … Continue reading

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Ottawa doctors optimistic about new MS treatment

Posted: Published on April 4th, 2013

Ottawa doctors have developed a new treatment for multiple sclerosis that they say has eliminated the disease in 70 per cent of their patients. Multiple sclerosis, or MS, is a disease where the body's immune system attacks itself, causing damage to the spinal cord and brain. A team of doctors from the Ottawa Hospital are to publish findings in a yet-to-be-determined medical journal on a new treatment that uses stem cell transplants and high doses of chemotherapy. The doctors have tested 24 people over the past 13 years, starting as an experimental study for patients with severe symptoms who did not improve using drug therapy. Dr. Harold Atkins, a bone-marrow transplant expert, has helped lead the study. He said a large majority of the patients have gained long-term freedom from evidence of further MS. "These transplants are pushing the limits of technology," Atkins said. "We have to use very high doses of chemotherapy to get rid of the old immune system that's attacking the patient's brain that has a lot of side effects." Atkins admitted the side effects of chemotherapy can lead to infection or organ failure. He also said some patients have irreparable damage to their brain, and one … Continue reading

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Christian Pope, M.D.: Assessing the risks of hormone – replacement therapy

Posted: Published on April 4th, 2013

The Women's Health Initiative (WHI) was a major 15-year research program to address the most common causes of death, disability and poor quality of life in postmenopausal women cardiovascular disease, cancer, and osteoporosis. The WHI was launched in 1991 and consisted of a set of clinical trials and an observational study, which together involved 161,808 generally healthy postmenopausal women. The clinical trials were designed to test the effects of postmenopausal hormone therapy, diet modification, and calcium and vitamin D supplements on heart disease, fractures, and breast and colorectal cancer. The hormone trial had two studies: the estrogen-plus-progestin study of women with a uterus and the estrogen-alone study of women without a uterus. (Women with a uterus were given progestin in combination with estrogen, a practice known to prevent endometrial cancer.) In both hormone therapy studies, women were randomly assigned to either the hormone medication being studied or to placebo. Those studies have now ended and the data has been analyzed. Though it was found and generally agreed upon that women who took combined hormone replacement therapy (estrogen and progesterone) to lessen their hot flushes and insomnia symptoms increased their chances of breast cancer slightly, many studies suggested that the cancer … Continue reading

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UW stem cell pioneer Thomson earns innovation award

Posted: Published on April 4th, 2013

A prestigious scientific honor adds to the legacy of stem cell pioneer James Thomson. James Thomson Thomson, who first derived human embryonic stem cells in 1998 and reprogrammed human skin cells into induced pluripotent stem cells in 2007, has earned the McEwen Award for Innovation from the International Society for Stem Cell Research (ISSCR). He is being honored for his work in isolating human pluripotent stem cells, which revealed new possibilities for basic biology, drug discovery and cell-based therapies. "It's an honor to be recognized with the McEwen Award and I'm pleased that my work-and the work of many key collaborators in this field has created new avenues for understanding and addressing challenges in human health," said Thomson. Thomson is director of regenerative biology at the Morgridge Institute for Research and the James Kress professor of embryonic stem cell biology at the University of Wisconsin-Madison. He also is a John D. MacArthur professor at UW-Madison's School of Medicine and Public Health and a professor in the department of molecular, cellular and developmental biology at the University of California, Santa Barbara. Thomson's regenerative biology lab at the Morgridge Institute for Research focuses on how cells maintain or change identity as well … Continue reading

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For the first time, researchers isolate adult stem cells from human intestinal tissue

Posted: Published on April 4th, 2013

Public release date: 4-Apr-2013 [ | E-mail | Share ] Contact: Les Lang llang@med.unc.edu 919-966-9366 University of North Carolina Health Care CHAPEL HILL, N.C. For the first time, researchers at the University of North Carolina at Chapel Hill have isolated adult stem cells from human intestinal tissue. The accomplishment provides a much-needed resource for scientists eager to uncover the true mechanisms of human stem cell biology. It also enables them to explore new tactics to treat inflammatory bowel disease or to ameliorate the side effects of chemotherapy and radiation, which often damage the gut. "Not having these cells to study has been a significant roadblock to research," said senior study author Scott T. Magness, PhD, assistant professor in the departments of medicine, biomedical engineering, and cell and molecular physiology at UNC. "Until now, we have not had the technology to isolate and study these stem cells now we have to tools to start solving many of these problems" The UNC study, published online April 4, 2013, in the journal Stem Cells, represents a leap forward for a field that for many years has had to resort to conducting experiments in cells from mice. While significant progress has been made using … Continue reading

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Adult stem cells isolated from human intestinal tissue

Posted: Published on April 4th, 2013

Apr. 4, 2013 For the first time, researchers at the University of North Carolina at Chapel Hill have isolated adult stem cells from human intestinal tissue. The accomplishment provides a much-needed resource for scientists eager to uncover the true mechanisms of human stem cell biology. It also enables them to explore new tactics to treat inflammatory bowel disease or to ameliorate the side effects of chemotherapy and radiation, which often damage the gut. "Not having these cells to study has been a significant roadblock to research," said senior study author Scott T. Magness, PhD, assistant professor in the departments of medicine, biomedical engineering, and cell biology and physiology at UNC. "Until now, we have not had the technology to isolate and study these stem cells -- now we have to tools to start solving many of these problems" The UNC study, published online April 4, 2013, in the journal Stem Cells, represents a leap forward for a field that for many years has had to resort to conducting experiments in cells from mice. While significant progress has been made using mouse models, differences in stem cell biology between mice and humans have kept researchers from investigating new therapeutics for human … Continue reading

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NYSCF scientists develop new protocol to ready induced pluripotent stem cell clinical application

Posted: Published on April 4th, 2013

Public release date: 3-Apr-2013 [ | E-mail | Share ] Contact: David McKeon dmckeon@nyscf.org 212-365-7440 New York Stem Cell Foundation NEW YORK, NY (April 3, 2013) A team of New York Stem Cell Foundation (NYSCF) Research Institute scientists led by David Kahler, PhD, NYSCF Director of Laboratory Automation, have developed a new way to generate induced pluripotent stem (iPS) cell lines from human fibroblasts, acquired from both healthy and diseased donors. Reported in PLOS ONE, this cell-sorting method consistently selects the highest quality, standardized iPS cells, representing a major step forward for drug discovery and the development of cell therapies. Employing a breakthrough method developed by 2012 Nobel laureate Shinya Yamanaka, MD, PhD, adult cells are "reprogrammed" or reverted to an embryonic-like state, commonly through viral infection. Reprogramming is a dynamic process, resulting in a mixture of fully reprogrammed iPS cells, partially reprogrammed cells, and residual adult cells. Previous protocols to select promising fully reprogrammed cells rely primarily on judging stem cell colonies by eye through a microscope. Cell colonies selected by qualitative measures could include partially reprogrammed cells, a major concern for clinical applications of cell therapies because these cells could become any other cell type in a patient … Continue reading

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Scientists develop new protocol to ready induced pluripotent stem cell clinical application

Posted: Published on April 4th, 2013

Apr. 3, 2013 A team of New York Stem Cell Foundation (NYSCF) Research Institute scientists led by David Kahler, PhD, NYSCF Director of Laboratory Automation, have developed a new way to generate induced pluripotent stem (iPS) cell lines from human fibroblasts, acquired from both healthy and diseased donors. Reported in PLOS ONE, this cell-sorting method consistently selects the highest quality, standardized iPS cells, representing a major step forward for drug discovery and the development of cell therapies. Employing a breakthrough method developed by 2012 Nobel laureate Shinya Yamanaka, MD, PhD, adult cells are "reprogrammed" or reverted to an embryonic-like state, commonly through viral infection. Reprogramming is a dynamic process, resulting in a mixture of fully reprogrammed iPS cells, partially reprogrammed cells, and residual adult cells. Previous protocols to select promising fully reprogrammed cells rely primarily on judging stem cell colonies by eye through a microscope. Cell colonies selected by qualitative measures could include partially reprogrammed cells, a major concern for clinical applications of cell therapies because these cells could become any other cell type in a patient following transplantation. Additionally for drug efficacy assays and toxicity investigations on iPS cells, heterogeneous cell populations can mar the response of representative iPS … Continue reading

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Mapping Eliza: Decoding DNA Secrets

Posted: Published on April 4th, 2013

Genome sequencing is cheap, fast, and poised to revolutionize health care. In the one-hour radio special Mapping Eliza: Decoding DNA Secrets, IEEE Spectrum editor Eliza Strickland gets a glimpse of the medical future by getting her own genome sequenced. She takes listeners on her personal journey as she explores her genes, and investigates just how much they can reveal about her medical destiny. This radio program is presented byPRX, the Public Radio Exchange, and received support fromfrom theAlfred P. Sloan Foundationenhancing public understanding of science, technology, and economic performance. Jump to: Segment One / Segment Two / Segment Three Segment One Eliza Strickland: Have you ever lain awake in the middle of the night and wondered what will kill you in the end? I did a bit of that recently. I mentally scrolled through my family history and counted up the relatives who had died of heart diseaseand then I vowed to go to the gym more often. I thought of an aunt who died of breast cancer and a grandfather who had kidney failure, and I sent internal messages to those body parts: How you doing in there? Stay strong. I need you! I think most of us would … Continue reading

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Genetic vulnerability of lung cancer to lay foundation for new drug options

Posted: Published on April 4th, 2013

Public release date: 4-Apr-2013 [ | E-mail | Share ] Contact: Alex Lyda alex.lyda@utsouthwestern.edu 214-648-3404 UT Southwestern Medical Center DALLAS April 4, 2013 Physician-researchers at UT Southwestern Medical Center have identified a vulnerability of certain lung-cancer cells a specific genetic weakness that can be exploited for new therapies. Although researchers have long known that mutant versions of the KRAS gene drive tumor formation and are key to cell survival in non-small cell lung cancer, the blocking of activated KRAS has proven difficult. For years, investigations have explored stopping lung cancer at this junction, which also would have an impact on many other cancers. KRAS mutations, for instance, account for as much as 50 percent of all colon cancers. "There is an urgent need to identify 'downstream' pathways that are required to sustain and grow non-small cell lung cancer (NSCLC)," said Dr. Pier Paolo Scaglioni, assistant professor of internal medicine and a member of the Harold C. Simmons Cancer Center. "As we focus on the right pathways, we stand a much better chance of chemically blocking them and stopping tumor growth." The team's findings are published in the April edition of Cancer Discovery, a journal of the American Association for Cancer … Continue reading

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