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stem cell research F6373525 B9FE 40FF 8A84 11B056987500 – Video

Posted: January 15, 2014 at 5:40 pm


stem cell research F6373525 B9FE 40FF 8A84 11B056987500

By: Olivia Woodson

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Art of Science: Montage of Stem Cells by Peter Tonge – Video

Posted: January 15, 2014 at 9:46 am


Art of Science: Montage of Stem Cells by Peter Tonge
A montage of stem cells called "All for One - One for All" by Peter Tonge.

By: Mount Sinai Hospital

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HealthWACH – Banking baby's stem cells – Video

Posted: January 15, 2014 at 9:46 am


HealthWACH - Banking baby #39;s stem cells
For the latest news weather and sports visit: http://www.wach.com Like WACH Fox on Facebook: http://www.facebook.com/wachfox Follow WACH Fox on Twitter: http...

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New breast cancer stem cell findings explain how cancer spreads

Posted: January 15, 2014 at 9:46 am

Jan. 14, 2014 Breast cancer stem cells exist in two different states and each state plays a role in how cancer spreads, according to an international collaboration of researchers. Their finding sheds new light on the process that makes cancer a deadly disease.

"The lethal part of cancer is its metastasis so understanding how metastasis occurs is critical," says senior study author Max S. Wicha, M.D., Distinguished Professor of Oncology and director of the University of Michigan Comprehensive Cancer Center. "We have evidence that cancer stem cells are responsible for metastasis -- they are the seeds that mediate cancer's spread. Now we've discovered how the stem cells do this."

First, on the outside of the tumor, a type of stem cell exists in a state called the epithelial-mesenchymal transition (EMT) state. These stem cells appear dormant but are very invasive and able to get into the bloodstream, where they travel to distant parts of the body.

Once there, the stem cells transition to a second state that displays the opposite characteristics, called the mesenchymal-epithelial transition state (MET). These cells are capable of growing and making copies of themselves, producing new tumors.

"You need both forms of cancer stem cells to metastasize and grow in distant organs. If the stem cell is locked in one or the other state, it can't form a metastasis," Wicha says.

The findings, which are published in the January issue of Stem Cell Reports, raise a number of questions about how to treat or prevent metastatic breast cancer. Researchers must now understand whether new therapies must attack both forms of the stem cell to be successful. Different pathways regulate each type of stem cell, which suggests that effective therapies must be able to target multiple pathways.

In addition, current tests that look at tumor cells circulating in the blood to help determine whether the cancer is spreading do not appear to capture the EMT stem cells, which are the cancer cells that travel through the blood. U-M researchers are working with colleagues from the U-M College of Engineering to develop new tools to isolate the EMT stem cells from the blood of cancer patients.

"Now that we know we are looking at two different states of cancer stem cells, we can use markers that distinguish these states to get a better sense of where the cancer stem cells are and to determine the effectiveness of our treatments," Wicha says.

The study looked specifically at breast cancer stem cells but the researchers believe the findings likely have implications for other cancer types as well.

Breast cancer statistics: 234,580 Americans will be diagnosed with breast cancer this year and 40,030 will die from the disease, according to the American Cancer Society.

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Research Advancements Made in Diabetes-Induced Blindness

Posted: January 15, 2014 at 9:45 am

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Newswise LOS ANGELES (January 15, 2014) Investigators at the Cedars-Sinai Regenerative Medicine Institute have identified new molecular abnormalities in the diabetic cornea that could contribute to eye problems in affected patients. With this new knowledge, investigators aim to accelerate the process of healing and repair in damaged corneas to ultimately reverse the effects of diabetes-induced eye complications.

We observed small but significant changes in the gene expressions between normal and diabetic corneas, said Mehrnoosh Saghizadeh Ghiam, PhD, assistant professor of biomedical sciences and neurosurgery, a researcher in the Regenerative Medicine Institute Eye Program and the lead author of the study published in the journal PLOS ONE. These slight alterations may contribute to disease progression and cause cascading effects on the cellular functions that prevent wound healing and eventually contribute to vision impairment.

Diabetes is a systemic disease affecting all parts of the body, including the eye and may lead to vision loss. Roughly 50 to 70 percent of diabetic patients suffer from corneal complications that include alterations in vital corneal stem cells, causing lasting defects and eventually, vision impairment.

Investigators identified gene expression regulators, microRNAs, in normal and diabetic human corneas. They then successfully confirmed that several of these regulators were expressed differently in the diabetic corneas. These differently expressed microRNAs may contribute to stem cell and epithelial (tissue cells) abnormalities in diabetic corneas. Researchers are working on the manipulation of these microRNAs by gene therapy to normalize these corneas.

No previous studies have addressed the role of microRNAs in the corneas of patients with diabetes, said Alexander Ljubimov, PhD, director of the Eye Program at the Regenerative Medicine Institute and co-author of the paper. This first-of-a-kind study will allow researchers to better understand the roles of microRNAs in corneal diseases.

The study was conducted by a team of Cedars-Sinai researchers including Saghizadeh Ghiam, Ljubimov, Vincent Funari, PhD, director of the Cedars-Sinai Genomics Core in the Department of Biomedical Sciences, and research associates Michael Winkler and Jordan Brown.

The research was supported by the following National Institutes of Health (NIH) grants: NIH R21 EY022771 and R01 EY13431, as well as the Cedars-Sinai Regenerative Medicine Institute.

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Stem cell guru walks out on Spanish science

Posted: January 15, 2014 at 9:45 am

A world leader in stem cell research is leaving the cutting-edge center he helped create in Barcelona due to a lack of support from the authorities in both Catalonia and Spain.

Juan Carlos Izpisa, a Spanish biochemist who teaches at the Salk Institute in California and has earned numerous awards for his research into organ and tissue development, had helped found the Barcelona Regenerative Medicine Center (CMRB) in 2004, bringing Spain to the forefront of stem cell research.

But now Izpisa is resigning from his director's post due to a lack of financial and political support from his two major public sponsors, the government of Spain and the regional government of Catalonia.

Sources in the scientific community are blaming the move on "the cuts, political mediocrity and a lack of empathy from Madrid." They also note that Catalan premier Artur Mas met with Izpisa 18 months ago and assured him that he would put all available means at his disposal.

Sources in the scientific community are blaming the move on "the cuts, political mediocrity and a lack of empathy from Madrid"

According to sources familiar with the months-long negotiations, the decision to let Izpisa go originated in the Catalan government, although Madrid did nothing to stop it. The explanation supplied was that, as an undesirable effect of cutbacks, the government was no longer in a condition to keep funding the center "at the quality levels required" by its director.

While his departure will not bring about the immediate closure of the center, the CMRB will lose many of its lines of research, since 18 of the 21 scientific projects it is currently carrying out are the intellectual property of Izpisa, who will take them with him.

The move also underscores how the crisis has meant further cuts for scientific projects in Spain, which is seeing many researchers move abroad to find jobs and financial support.

Shortly after the crisis hit Spain in 2008, the then-Socialist government announced a shift away from construction as the basis of the countrys economic growth. But so far this has failed to translate into any significant investment in other fields.

Over the last decade, the CMRB has published more than 200 papers, including some seminal work in the emerging field of regenerative medicine. One of Izpisa's projects, the development of "micro-kidneys" from stem cells, was described by Science magazine as one of the great advances of 2013.

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Stem Cells Could Prove Effective in Treating Brittle Bone Disease

Posted: January 15, 2014 at 9:44 am

Durham, NC (PRWEB) January 14, 2014

A new study released in STEM CELLS Translational Medicine indicates that stem cells can be effective in treating a debilitating and sometimes lethal genetic disorder called brittle bone disease.

Brittle bone disease, or osteogenesis imperfecta (OI), is characterized by fragile bones causing some patients to suffer hundreds of fractures over the course of a lifetime. In addition, according to the OI Foundation, other symptoms include muscle weakness, hearing loss, fatigue, joint laxity, curved bones, scoliosis, brittle teeth and short stature. Restrictive pulmonary disease occurs in the more severe cases. Currently there is no cure.

OI can be detected prenatally by ultrasound. In the study reported on in STEM CELLS Translational Medicine, an international team of researchers treated two patients for the disease using mesenchymal stem cells (MSCs) while the infants were still in the womb, followed by stem cell boosts after they were born.

We had previously reported on the prenatal transplantation for the patient with OI type III, which is the most severe form in children who survive the neonatal period, said Cecilia Gtherstrm, Ph.D., of the Karolinska Institutet and Karolinska University Hospital, Stockholm, Sweden. She and Jerry Chan, M.D., Ph.D., of the Yong Loo Lin School of Medicine and National University of Singapore, and KK Womens and Childrens Hospital, led the study that also included colleagues from the United States, Canada, Taiwan and Australia.

The first eight years after the prenatal transplant, our patient did well and grew at an acceptable rate. However, she then began to experience multiple complications, including fractures, scoliosis and reduction in growth, so the decision was made to give her another MSC infusion. In the two years since, she has not suffered any more fractures and improved her growth.

She was even able to start dance classes, increase her participation in gymnastics at school and play modified indoor hockey, Dr. Gtherstrm added.

The second child, which was experiencing a milder form of OI, received a stem cell transfusion 31 weeks into gestation and did not suffer any new fractures for the remainder of the pregnancy or during infancy. She followed her normal growth pattern just under the third percentile in height until 13 months of age, when she stopped growing. Six months later, the doctors gave her another infusion of stem cells and she resumed growing at her previous rate.

Our findings suggest that prenatal transplantation of autologous stem cells in OI appears safe and is of likely clinical benefit and that re-transplantation with same-donor cells is feasible. However, the limited experience to date means that it is not possible to be conclusive, for which further studies are required, Dr. Chan said.

Although the findings are preliminary, this report is encouraging in suggesting that prenatal transplantation may be a safe and effective treatment for this condition, said Anthony Atala, M.D., editor of STEM CELLS Translational Medicine and director of the Wake Forest Institute for Regenerative Medicine.

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The International Society for Stem Cell Research announces its 2014 award recipients

Posted: January 15, 2014 at 9:41 am

PUBLIC RELEASE DATE:

14-Jan-2014

Contact: Michelle Quivey mquivey@isscr.org 224-592-5012 International Society for Stem Cell Research

CHICAGO The International Society for Stem Cell Research (ISSCR) has announced the following 2014 award recipients, who will be formally recognized at its 12th Annual Meeting in Vancouver, taking place June 18-21, 2014:

The McEwen Award for Innovation, supported by the McEwen Centre for Regenerative Medicine, recognizes original thinking and groundbreaking research pertaining to stem cells or regenerative medicine that opens new avenues of exploration toward the understanding or treatment of human disease or affliction. The winner receives $100,000 USD. Past winners include James Thomson, Rudolf Jaenisch, Kazutoshi Takahashi and Shinya Yamanaka.

Award recipient Surani is a world leader in the field of epigenetics and the development of the mammalian germ line. His work on early mammalian development led to his involvement in the discovery of genomic imprinting and ongoing contributions to understanding the mechanistic basis of imprinting. Most relevant to stem cell biology, is his work on the cellular and molecular specification of the mammalian germ cell lineage, which impacted the field's understanding of how the germ line is established and the molecular mechanisms responsible for reprogramming the epigenome in order to generate the totipotent state.

"The ISSCR is thrilled to announce the McEwen Award for Innovation, our most prestigious award, will be presented to Azim Surani," Janet Rossant, ISSCR president, said. "His pioneering research, which has changed the face of epigenetics and advanced the field of stem cell biology, is a rare and significant contribution from a single individual."

The ISSCR-BD Biosciences Outstanding Young Investigator Award recognizes exceptional achievements by an ISSCR member and investigator in the early part of their independent career in stem cell research. The winner receives a $7,500 USD personal award and an opportunity to present at the ISSCR Annual Meeting. Past winners include Marius Wernig, Cdric Blanpain, Robert Blelloch, Joanna Wysocka and Konrad Hochedlinger.

Award recipient Greco established a noninvasive method to directly visualize skin stem cell division in real time in living animals the first of its kind for imaging any stem cell. By combining this method with laser ablation and transgenic lineage tracing, she captured previously inaccessible key information on stem cell behavior during tissue maintenance and regeneration. She demonstrated that the niche location of stem cells dictates their fates, the niche is required for tissue maintenance, and that a -catenin-mediated extrinsic mechanism regulates stem cell activation.

"The ISSCR is looking forward to presenting our Outstanding Young Investigator Award to Valentina Greco," Rossant said. "Her enthusiastic nomination by over a dozen leaders in the field of stem cell research demonstrates the significance of her early-career contributions to stem cell biology and regenerative medicine."

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New tool assists stem cell therapy

Posted: January 15, 2014 at 9:40 am

Published:Tuesday, January 14, 2014

Updated:Tuesday, January 14, 2014 18:01

A new tool that could help facilitate future stem cell therapy has recently been identified by a UVM professor and his colleagues, according to UVMs College of Medicine.

The development of this tool could potentially help more than 700,000 Americans who suffer a heart attack each year.

Because stem cells have the potential to develop into a variety of cell types in the body, they may offer a renewable source of replacement cells to treat diseases, conditions and disabilities, and even regenerate damaged tissue and organs.

However, the field of regenerative medicine has struggled to successfully graft cells from culture back into injured tissue.

UVM Associate Professor of Medicine Jeffrey Spees, Ph.D., collaborated with the Center for Gene Therapy at Tulane University. His research team recently set out to develop ways to enhance graft success.

Dr. Spees and his team focused on a type of bone marrow-derived progenitor cell or biological cell that forms stromal cells or connective tissue cells.

They found that the medium contained Connective Tissue Growth Factor (CTGF) and the hormone insulin, and together, they have a synergistic effect, Spees said to UVMs College of Medicine.

The group found that the protective ligands resulted in improved graft success, breaking the record for engraftment.

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Age Reversal Study – Testimony of Caleb during his 7th injection – Video

Posted: January 14, 2014 at 7:52 am


Age Reversal Study - Testimony of Caleb during his 7th injection
http://a1stemcells.com/anti-aging-2 testimony of Caleb, 36yo, recorded during his 7th injection. It changed Caleb #39;s life. Stem cell rejuvenation program in M...

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