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Anti-Wrinkle Drug May Treat Stomach Cancers: Study

Posted: August 21, 2014 at 5:11 pm

WASHINGTON, Aug. 20 (Xinhua) -- Botox, the popular wrinkle eraser, could also be effective in treating stomach cancers, a new study said Wednesday.

The study, published in the U.S. journal Science Translational Medicine, showed that the drug slows cancer growth by eliminating the signals sent by nerves that are linked to cancer stem cells.

Researchers have thus far tested the procedure on mice, and will soon start testing on humans.

"This study shows that nerves control cancer stem cells," said the study led by Duan Chen, professor of Norwegian University of Science and Technology, and Timothy Wang, professor of the Columbia University.

"We found that by removing the effect of the nerve, the stem cells in the cancer tumor are suppressed, leading to cancer treatment and prevention," Chen said.

The study found that nerves promote tumor growth through the release of a neurotransmitter.

The researchers tried four methods to cut the connection between the nerves and the tumor: surgically by cutting the gastric vagus nerve (vagotomy), by local injection of Botox to block the release of neurotransmitter from the vagus nerve, by giving a drug to block the receptor of the neurotransmitter, and by knocking out of the receptor gene. All procedures suppressed the tumor growth.

"But we found that the anti-cancer effects were remarkable, especially with local vagotomy or by injecting Botox. It actually surprised us. The finding that Botox was highly effective was particularly exciting," Chen said.

Botox is made from a toxin produced by the bacterium Clostridium botulinum and is well known to the public as a beauty treatment, but it is also used for different medical indications.

"We believe this treatment is a good treatment because it can be used locally and it targets the cancer stem cells. The Botox can be injected through gastroscopy and it only requires the patient to stay in the hospital for a few hours," said Chen.

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Anti-Wrinkle Drug May Treat Stomach Cancers: Study

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West Virginia (Stem Cell) – what-when-how

Posted: August 21, 2014 at 5:11 pm

On July 18, 2006, the U.S. Senate convened to vote on a proposed bill (H.R.810) that would amend the Public Health Service Act and provide federal funding for research on human embryonic stem cells. This bill was passed by the Senate but was later vetoed by President George W. Bush. The two West Virginia Senators, Democrats Robert C. Byrd and Jay Rockefeller, both voted in support of the bill.

As of early 2008, the only hospital offering blood stem cell transplants for therapeutics in the state of West Virginia was the West Virginia University Hospital System, under the leadership of Solveig G. Ericson, M.D., Ph.D. Ericson is the director of the Blood and Marrow Transplant and Hematologic Malignancy Program. This program offers blood stem cell transplants, clinical trials, and access to both national and international stem cell registries.

At the West Virginia University School of Medicine, Sreekumar Othumpangat, Ph.D., working in the laboratories of Laura Gibson, Ph.D., and Giovanni Piedimonte, M.D., in the Department of Pediatrics, studies embryonic stem cell differentiation.

In the Division of Exercise Physiology, Ming Pei, Ph.D., is the director of the Tissue Engineering Laboratory; he works to study how synovium-derived stem cells could be a starting point for engineering of new tissue to repair damaged knee joints. The synovium is a soft tissue in the joints that lines the noncartilaginous regions. Pei is also investigating the use of small intestinally derived stem cells and mesenchymal stem cells for this same purpose. He is funded by a number of sources, including the National Institutes of Health.

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Stem cell treatment for copd

Posted: August 21, 2014 at 5:11 pm

Patricia

Thanks for the update. I went to Dr F on March 19th and my treatment was identical to yours. I have noticed improvements but for the first month I was getting over a nasty cold that started the day BEFORE treatment so I was unable to notice many changes for the first 6 weeks. Two weeks ago, I went out with my husband for brunch and shopping and was able to walk around for two hours without being short of breath (yes I was still using my oxygen). That was the start of seeing improvements. This past week, I had two days where I was able to walk up and down the aisles in Walgreens, get back in the car and go over to the pet store and walk around there for another 30 minutes without any shortness of breath. It was like a miracle for me. I hadn't felt that good for well over a year if not longer. Unfortunately, the rest of the week I've been back to not feeling as great, but I did go to brunch today and then shopping without any trouble. I am having more and more days of feeling stronger, breathing better and my O2 Saturation is a few points higher than it has been. Showering isn't a big ordeal anymore.

I also have ulcerative colitis and have not needed to take my pills for over a month now. This is the first time since last February that I am pain free and not needing meds.

I will keep everyone updated of any changes/improvements. I have not had a PFT since treatment (plan to in Sept) but my peak flow meter reading has gone from from 150 to 190 in the past two weeks.

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Stem cell treatment for copd

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Wisconsin Stem Cell Now Stem Cells in Wisconsin

Posted: August 21, 2014 at 5:10 pm

What is regenerative medicine, and what role does it play in the field of medical research?

For centuries, medical research has sought to treat injuries and degenerative diseases that lead to organ failure and chronic health conditions. Many of these conditions are genetic, and have been a leading cause of pain, suffering, and even death for generations of Americans. From the time of the first blood transfusions in the eighteenth century, medical researchers have sought to replace diseased or damaged tissue through organ transplantation. Although some initially opposed the concept of organ transplantation on religious grounds, on the basis that it altered the human body as God had made it, nonetheless millions of lives have been saved by heart, lung, kidney and other organ transplant surgeries. The vast majority of Americans consider it commonplace and entirely moral to alleviate suffering by replacing diseased human tissue with healthy donor tissue.

Organ transplantation has been hampered by long waiting lists for donor organs and difficulties in overcoming the human bodys natural tendency to reject foreign tissue. As a result, researchers have developed mechanical and synthetic devices that can function as artificial organs and tissues. These advances were also criticized by a vocal minority on religious grounds, on the basis that the transplantation of artificial organs into patients diminished the dignity of the human body. However, once again the vast majority of Americans hailed breakthroughs like artificial hearts and insulin pumps for the countless lives that they saved and for the human suffering that they alleviated.

Unfortunately, artificial medical devices are not a complete substitute for the healthy organs that they are designed to replace. In addition, despite advances in nanotechnology, researchers are still struggling to artificially replace human biological functions that occur at a cellular level. Today the search continues for ways to completely cure damaged and diseased human organs and tissue through artificial replacements.

Meanwhile, beginning in the 1970s, significant progress was made in the field of recombinant DNA. Researchers used strands of human DNA inserted into bacteria to manufacture drugs, proteins and artificial hormones that exactly mimic their parallels in the human body. For example, for decades diabetics stayed alive by replacing the human insulin that their bodies no longer made with insulin harvested from slaughtered pigs. Scientists now insert strands of human DNA into bacteria in order to manufacture artificial insulin that is genetically identical to human insulin. The insulin must still be injected into the patient several times a day, so it is a poor second best to replacing the patients damaged pancreas. However, the genetically manufactured insulin is superior to the pig insulin. Cancer treating drugs, such as those that boost red blood cell production during chemotherapy, are also manufactured using recombinant DNA.

The field of regenerative medicine promises to become the endpoint of this long history of medical research. Regenerative medicine applies tissue engineering, stem cell therapy, medical devices and other techniques in order to repair damaged or diseased tissues and organs. Stem cell research allows us to understand the process of human biology at a cellular level, and is therefore one way that researchers hope to learn how to repair or replace human organs and tissues. New cells can be created either through the transformation of one type of specialized cell into another or through the growth of specialized cells out of undifferentiated stem cell lines. The creation of new human organs and tissues, if successful, would mean that seriously ill Americans could be treated with therapies that completely cure their conditions rather than merely treat their symptoms. It is likely that, as with other medical advances over the centuries, there will still be a minority of Americans who react to these advances out of fear or by making claims that medical researchers are playing God. However, just as was the case with blood transfusions, organ transplantation and recombinant DNA, the majority of Americans fully support these medical advances that have the potential to so greatly improve the quality of life for themselves and their loved ones.

What are stem cells?

Stem cells are unspecialized cells that can generate healthy new cells, tissues, and organs. They are the master cells of the human body that can transform themselves into more specialized cells, that in turn perform a specific bodily function such as making the heart beat or secreting a particular hormone. In a human embryo, stem cells form four or five days after fertilization of the egg, and they are the precursor of all of the other cell types that will later be necessary for human development. After birth, stem cells remain in some of our organs, continuing to create specialized cells to replace cells that are damaged or wear out.

A stem cell line is comprised of a group of stem cells that are isolated from either an early stage embryo called a blastocyst or from adult tissue. These stem cells are then placed into a growth culture in a petri dish and induced to self-replicate, generating a colony of cells that continually replaces itself. Researchers then begin the hard work of learning what factors cause the stem cells to transform into one type of cell versus another. Although a relatively new area of scientific inquiry, the study of stem cells has already greatly increased our understanding of human cell biology.

What is involved in stem cell research?

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Wisconsin Stem Cell Now Stem Cells in Wisconsin

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Novel Gene Predicts Both Breast Cancer Relapse and Response to Chemotherapy

Posted: August 21, 2014 at 5:10 pm

Despite advancements in cancer treatment, breast cancer remains the most common cancer among Singapore women[1]. Thirty percent[2] of early breast cancer patients in the world experience relapse due to metastasis, or the spread of cancer cells to other organs in the body. Some patients also do not respond well to chemotherapy. The inability to forecast relapses or the effectiveness of chemotherapy has led to a pressing need to identify predictive markers, which doctors can use to tailor appropriate treatment for each breast cancer patient at an early stage.

In a study published recently in the Journal of Clinical Investigation, a top-tier journal for discoveries in basic and clinical biomedical research, the team of scientists jointly led by Dr Vinay Tergaonkar, Principal Investigator at IMCB and Dr Alan Prem Kumar, Principal Associate at CSI Singapore and Assistant Professor at the Department of Pharmacology, NUS Yong Loo Lin School of Medicine, uncovered a gene, DP103, which is activated in metastatic breast cancer. DP103 acts as a master regulator, which expresses two sets of unfavourable proteins - one leads to metastasis and the other causes patients to be unresponsive to chemotherapy. Consequently, doctors can predict the probability of metastasis by examining the levels of DP103 in breast cancer patients. The same gene could also be used to predict whether a patient would respond to chemotherapy.

"Doctors are unable to tell if a breast cancer patient will respond to chemotherapy until six months after the treatment has been prescribed. It is very worrisome as the ones who are not responsive to chemotherapy usually also suffer relapses due to metastasis. This DP103 gene that we found explains the link and will facilitate doctors in selecting suitable treatments for different cases of breast cancer," said Dr Tergaonkar.

In addition, the study revealed that reducing the levels of DP103 could contain the cancer, shrink the tumour and make patients more amenable to chemotherapy. All the findings in the study have been validated with samples of breast cancer patients from Singapore, Canada, China and the USA.

"DP103 is a novel biomarker that could help doctors select appropriate treatments for breast cancer patients at an early stage. It is also a therapeutic target which could be explored further to develop drugs that suppress breast cancer growth, as well as metastasis," said Dr Kumar, who first discovered DP103's oncogene potential to drive breast cancer metastasis. He is also the Principal Inventor to a patent application on this discovery and is currently looking into ways to regulate DP103 levels in a variety of cancer types at CSI Singapore.

[1] Top 10 cancers affecting Singapore women: http://bit.ly/VEg7F8 [2] Lancet 365:1687-1717, 2005 - Early Breast Cancer Trialists' Collaborative Group: Effects of chemotherapy and hormonal therapy for early breast cancer on recurrence; 15-year survival: An overview of the randomised trials

Notes to Editor:

The research findings described in this media release can be found in the Journal of Clinical Investigation Journal, under the title, "DEAD-box Helicase DP103 Defines Metastatic Potential of Human Breast Cancers" by Eun Myoung Shin 1,2, Hui Sin Hay 1,2,3, Moon Hee Lee 4, Jen Nee Goh 1,3, Tuan Zea Tan 1, Yin Ping Sen 5, See Wee Lim 5, Einas M. Yousef 6, Hooi Tin Ong 7, Aye Aye Thike 8, Xiangjun Kong 9, Zhengsheng Wu 9, Earnest Mendoz 10, Wei Sun 10, Manuel Salto-Tellez 1,11,12, Chwee Teck Lim 10,13,14, Peter E. Lobie 1,3,15, Yoon Pin Lim 16, Celestial T. Yap 17,18, Qi Zeng 2,16, Gautam Sethi 1,3, Martin B. Lee 19, Patrick Tan 1,20,21, Boon Cher Goh 1,18,22, Lance D. Miller 23, Jean Paul Thiery 1,2,16,18, Tao Zhu 9, Louis Gaboury 6, Puay Hoon Tan 8, Kam Man Hui 7, George Wai-Cheong Yip 5, Shigeki Miyamoto 4, Alan Prem Kumar 1,3,18,24,25, Vinay Tergaonkar 2,16.

1 Cancer Science Institute of Singapore, National University of Singapore, Singapore 2 Institute of Molecular and Cellular Biology, A*Star, Singapore Departments of 3 Pharmacology, 5 Anatomy, 11 Pathology, 16 Biochemistry, and 17 Physiology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore 4 McArdle Laboratory for Cancer Research, Department of Oncology, University of Wisconsin-Madison, Wisconsin, USA 6 Institute for research in immunology and cancer (IRIC), University of Montreal, Quebec, Canada 7 Division of Cellular and Molecular Research, Humphrey Oei Institute of Cancer Research, National Cancer Centre, Singapore 8 Department of Pathology, Singapore General Hospital, Singapore 9 Hefei National Laboratory for Physical Sciences at Microscale and School of Life Sciences, University of Science and Technology of China, Hefei, Anhui, P.R. China 10 Division of Bioengineering and Department of Mechanical Engineering, National University of Singapore, Singapore 12 Centre for Cancer Research and Cell Biology, Queen's University Belfast, United Kingdom 13 Mechanobiology Institute, National University of Singapore, Singapore 14 NUS Graduate School for Integrative Sciences and Engineering, National University of Singapore, Singapore 15 Liggins Institute, University of Auckland, New Zealand 18 National University Cancer Institute, Singapore 19 Renal Center, National University Hospital, Singapore 20 Cancer and Stem Cell Biology, Duke-NUS Graduate Medical School, Singapore 21 Genome Institute of Singapore, A*Star, Singapore 22 Department of Haematology-Oncology, National University Hospital, Singapore 23 Department of Cancer Biology, Wake Forest University School of Medicine, Winston-Salem, North Carolina, USA 24 School of Biomedical Sciences, Faculty of Health Sciences, Curtin University, Western Australia 25 Department of Biological Sciences, University of North Texas, Denton, Texas, USA.

Full text of the Journal of Clinical Investigation paper can be accessed online from: http://www.ncbi.nlm.nih.gov/pubmed/25083991

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Novel Gene Predicts Both Breast Cancer Relapse and Response to Chemotherapy

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Grants fund UW technology projects on the road to commercialization

Posted: August 21, 2014 at 5:10 pm

Aug. 15, 2014

A coordination-retraining device was awarded first-round funding from the universitys Discovery to Product program. One key step to commercialization will be to test the device with stroke patients with varying levels of disability.

Photo: Kreg Gruben

An exercise machine that helps stroke victims walk. An advanced technology for assessing the progress of prostate cancer. A faster process for making neural stem cells to investigate new treatments for injury and disease. A cheaper, more beautiful LED light bulb. A game to teach meditation.

These projects, and a dozen more, are beneficiaries of the first round of awards by the University of Wisconsin-Madisons Discovery to Product, or D2P, program, which began operating in March. The 17 grants announced this week will support innovations in many fields of research at the university, from food engineering and medicine to stem cell biology and biomedical engineering.

None have yet reached the company stage. All have proven technology. And all have the potential to advance quickly to the market, says John Biondi, director of D2P. Our goal is to achieve commercialization by June 2015, defined as reaching a licensing agreement or creating a startup company that has a high probability of getting funded.

A new technology to create large quantities of nerve cells is also being funded by D2P.

Photo: Jeff Miller

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Grants fund UW technology projects on the road to commercialization

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Wyoming (Stem Cell) – what-when-how In Depth Tutorials …

Posted: August 21, 2014 at 5:10 pm

THE STATE of Wyoming does not have a law specifically addressing human cloning. Neither is there is a law specifically permitting or forbidding research on embryos or fetuses; however, the state does expressly prohibit the sale, donation, or distribution of an embryo, an aborted viable fetus, or a live child for the purposes of what it calls experimentation. Thus, effectively, any human embryonic stem cell research is forbidden.

At the University of Wyoming, Dr. David S. Fay investigates hormonal control of germline stem cell proliferation using the nematode Caenorhabditis elegans as a model organism. Scientists and other members of the University of Wyoming campus have access to seminars, symposia, and discussion groups focused on stem cell research and its ethical considerations.

On July 18, 2006, the United States Senate convened to vote on a proposed bill (H.R.810) that would amend the Public Health Service Act and provide federal funding for research on human embryonic stem cells. This bill was passed by the Senate but was later vetoed by President George W. Bush. In the vote, the two Wyoming senators voted against the bill: Republicans Mike Enzi and Craig L. Thomas. The group Right to Life Wyoming is strongly opposed to embryonic stem cell research and advocates alternate sources of stem cells such as amniotic fluid or adult stem cells.

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Coronary arteries hold heart-regenerating cells

Posted: August 21, 2014 at 1:45 am

Endothelial cells residing in the coronary arteries can function as cardiac stem cells to produce new heart muscle tissue, Vanderbilt University investigators have discovered.

The findings, published recently in Cell Reports, offer insights into how the heart maintains itself and could lead to new strategies for repairing the heart when it fails after a heart attack.

The heart has long been considered to be an organ without regenerative potential, said Antonis Hatzopoulos, Ph.D., associate professor of Medicine and Cell and Developmental Biology.

"People thought that the same heart you had as a young child, you had as an old man or woman as well," he said.

Recent findings, however, have demonstrated that new heart muscle cells are generated at a low rate, suggesting the presence of cardiac stem cells. The source of these cells was unknown.

Hatzopoulos and colleagues postulated that the endothelial cells that line blood vessels might have the potential to generate new heart cells. They knew that endothelial cells give rise to other cell types, including blood cells, during development.

Now, using sophisticated technologies to "track" cells in a mouse model, they have demonstrated that endothelial cells in the coronary arteries generate new cardiac muscle cells in healthy hearts. They found two populations of cardiac stem cells in the coronary arteries -- a quiescent population in the media layer and a proliferative population in the adventitia (outer) layer.

The finding that coronary arteries house a cardiac stem cell "niche" has interesting implications, Hatzopoulos said. Coronary artery disease -- the No. 1 killer in the United States -- would impact this niche.

"Our study suggests that coronary artery disease could lead to heart failure not only by blocking the arteries and causing heart attacks, but also by affecting the way the heart is maintained and regenerated," he said.

The current research follows a previous study in which Hatzopoulos and colleagues demonstrated that after a heart attack, endothelial cells give rise to the fibroblasts that generate scar tissue.

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Trial to use stem cells to repair heart

Posted: August 21, 2014 at 1:45 am

ROCHESTER, Minn. (KTTC) -- Medical officials are talking about a breakthrough clinical trial that could help the heart repair itself.

On Tuesday afternoon, Mayo Clinic and Cardio3 BioSciences officials outlined an FDA-approved clinical trial to be carried out in the United States. A similar trial has already been underway in Europe.

Cardio3 CEO Christian Homsy said stem cells are a major part of this heart-healing process. "What we do is take cells from a patient and we reprogram those cells to become cardiac reparative cells. Those cells have the ability to come and repair the heart." Those stem cells would come from the bone marrow of patients who suffer from heart failure.

This treatment is the result of a Mayo Clinic discovery. In Mayo's breakthrough process, stem cells that are harvested from a cardiac patient's bone marrow undergo a guided treatment designed to improve heart health in people suffering from heart failure.

Cardio3 officials said a manufacturing facility will be the first thing that is needed for this clinical trial, and the rest of the details like staffing will follow.

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Vanderbilt researchers find that coronary arteries hold heart-regenerating cells

Posted: August 21, 2014 at 1:45 am

PUBLIC RELEASE DATE:

20-Aug-2014

Contact: Craig Boerner craig.boerner@vanderbilt.edu 615-322-4747 Vanderbilt University Medical Center

Endothelial cells residing in the coronary arteries can function as cardiac stem cells to produce new heart muscle tissue, Vanderbilt University investigators have discovered.

The findings, published recently in Cell Reports, offer insights into how the heart maintains itself and could lead to new strategies for repairing the heart when it fails after a heart attack.

The heart has long been considered to be an organ without regenerative potential, said Antonis Hatzopoulos, Ph.D., associate professor of Medicine and Cell and Developmental Biology.

"People thought that the same heart you had as a young child, you had as an old man or woman as well," he said.

Recent findings, however, have demonstrated that new heart muscle cells are generated at a low rate, suggesting the presence of cardiac stem cells. The source of these cells was unknown.

Hatzopoulos and colleagues postulated that the endothelial cells that line blood vessels might have the potential to generate new heart cells. They knew that endothelial cells give rise to other cell types, including blood cells, during development.

Now, using sophisticated technologies to "track" cells in a mouse model, they have demonstrated that endothelial cells in the coronary arteries generate new cardiac muscle cells in healthy hearts. They found two populations of cardiac stem cells in the coronary arteries a quiescent population in the media layer and a proliferative population in the adventitia (outer) layer.

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