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Rejuvenating gonads with stem cells – Fertility Lab Insider

Posted: October 15, 2017 at 9:01 am

Harvard scientist Jon Tilly proposed a radical new idea about how eggs are produced that called for the existence of ovarian stem cells which could continually produce new eggs. Stem cells are accepted as essential to sperm production in males. In men, the sperm stem cells (called spermatogonia) produce daughter cells that either make the final end product (new sperm cells) or make more stem cells in a continuing cycle of renewal.

Although accepted as dogma in the male system, the dogma regarding the ovary denied the existence of a renewable stem cell that could continually produce new eggs. The existing dogma was that every baby girl is born with all the eggs she will ever have and her eggs continually die off with age and are lost monthly after puberty. The ovarian stem cells was believed to only produce a defined number of eggs for a short time during fetal development but then became dormant for the rest of the females lifespan.

The problem with this dogma was that Tillys accounting of eggs lost in his experimental systems always ended up with more eggs than expected. The only way he could reconcile this discrepancy was to allow for the existence of a small population of ovarian stem cells which were capable of reactivating and contributing some eggs to the total. Most of his science colleagues were sure that he was wrong. It took him four years to prove the existence of these reactivated stem cells in the ovary by showing that stem cells he recovered from an aging ovary could be induced to make eggs again.

Tilly used cells from aged mouse ovaries, exposing them to the cellular environment of younger mouse ovaries and reactivating or rejuvenating the old stem cells which then started to produce eggs again. If the same could be done in humans, old ovaries could be reawakened to produce eggs. This would be a huge advance in the treatment of infertility since ovarian aging is considered irreversible. The only current treatment option for old ovaries which no longer produce eggs is to do IVF using eggs from a younger donor.

Unfortunately, it will likely be years, if not decades, before these scientific findings in a mouse model are converted to clinical treatments for patients. The typical path for moving a scientific discovery from bench to bedside treatment is excruciatingly slow because the clinical treatment must be proven to be both effective and safe. For reproductive treatments which produce children, the safety and health of those children is the primary concern.

First, treatments must be shown to be safe for both mother and offspring in other animal models, especially other primates like rhesus monkeys and chimpanzees. In vitro experiments with rare donated human ovarian tissue would also be necessary. If all the animal research and in vitro human tissue work still looks promising, clinical trials might start in humans, if institutional review boards give approval for the proposed research in humans. Because in vitro fertilization research is not funded by NIH, and stem cell funding is subject to erratic funded by NIH or individual states, this research will be slower to yield new clinical treatments compared to other non-controversial areas like cancer research.

Although anyone reading this today is unlikely to benefit personally from this research, it still opens a small door to the possibility of new treatments for advanced maternal age that dont involve giving up the genetic link between mother and child.

You can read more about Tillys research in this BioTechniques article Where do babies come from?.

Another scientist, Karim Nayernia, professor of stem cell biology at Newcastle Universitys Institute of Human Genetics, is researching the use of spermatogonial stem cells to revive fertility in the male, after chemotherapy or disease. In mouse studies, he was able to use stem cells from bone marrow and coax it to become sperm stem cells called spermatogonia. Transplants of these new stem cells into mice whose testicles were depleted of stem cells allowed the mice to father offspring. In 2009, his research team reported that they successfully produced human sperm-like cells from embryonic stem cells in vitro. There remain questions about the health of the mice offspring so this research is a long way from clinical use, but offers the possibility of new treatments for male infertility.

Another researcher, Richard Behringer, professor of genetics at the University of Texas MD Anderson Cancer Center has been using stem cells to understand what makes us male or female. His research may one day allow same sex couples to have genetic children together. First, he took stem cells from male mice, cultured them in such a way to cause the X and Y chromosomes to separate in culture, creating some daughter cells that were XO, a genetic type that creates a female genotype due to lack of a Y chromosome. Genetic material from these XO cells was used to replace the genetic material inside a mouse blastocyst. A surrogate mother mouse carried the XO blastocyst and gave birth to a female pup. The ovary of the pup produced eggs that contained DNA from the feminized male stem cell. This female offspring mated naturally with male mice to produce offspring from (essentially) two males.

Dr. Behringer is also investigating techniques to introduce a second X chromosome into an XO cell, creating a female egg cell from a male stem cell. There are decades of basic biology research to be done here which will provide insights into how sex differentiation works. These preliminary experiments are decades away from clinical use and may never be implemented if society as a whole remains uncomfortable with using science to circumvent male-female procreation.

Reproductive research has always been controversial. IVF was considered amoral and possibly dangerous in the beginning and yet is widely accepted today. Public opinion tends to come around if a new medical intervention is effective and causes no harm. If nothing else, stem cell research is unlocking the most basic secrets nature has and although we cant predict what new fertility treatments, if any, might arise, it is certainly worth understanding reproduction at the cellular and molecular level. Stem cells are proving extremely useful for reproductive research.

2011, Carole. All rights reserved.

Posted on January 12, 2011 at 2:03 pmhttp://fertilitylabinsider.com/2011/01/rejuvenating-gonads-with-stem-cells/http://fertilitylabinsider.com/2011/01/rejuvenating-gonads-with-stem-cells/trackback/Categorised under : Ethical Issues , Fertility Preservation , Inside the Lab , Repro Bio 101Tagged with : eggs from stem cells , reproductive research , sperm from stem cells , stem cell research

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Sponsors World Stem Cell Summit

Posted: October 15, 2017 at 9:00 am

Cellular Dynamics

Cellular Dynamics International (CDI), a FUJIFILM company, is a leading developer and manufacturer of human cells used in drug discovery, toxicity testing, stem cell banking, and cell therapy development. The Company partners with innovators from around the world to combine biologically relevant human cells with the newest technologies to drive advancements in medicine and healthier living. CDIs technology offers the potential to create induced pluripotent stem cells (iPSCs) from anyone, starting with a standard blood draw, and followed by the powerful capability to develop into virtually any cell type in the human body. Our proprietary manufacturing system produces billions of cells daily, resulting in inventoried iCell products and donor-specific MyCell Products in the quantity, quality, purity, and reproducibility required for drug and cell therapy development. Founded in 2004 by Dr. James Thomson, a pioneer in human pluripotent stem cell research, Cellular Dynamics is based in Madison, Wisconsin, with a second facility in Novato, California. For more information, please visit http://www.cellulardynamics.com, and follow us on Twitter @CellDynamics.FUJIFILM Holdings Corporation, Tokyo, Japan brings continuous innovation and leading-edge products to a broad spectrum of industries, including: healthcare, with medical systems, pharmaceuticals and cosmetics; graphic systems; highly functional materials, such as flat panel display materials; optical devices, such as broadcast and cinema lenses; digital imaging; and document products. These are based on a vast portfolio of chemical, mechanical, optical, electronic, software and production technologies. In the year ended March 31, 2015, the company had global revenues of $20.8 billion, at an exchange rate of 120 yen to the dollar. Fujifilm is committed to environmental stewardship and good corporate citizenship. For more information, please visit: http://www.fujifilmholdings.com.

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Stem Cell Therapy – Cendant Cellular Therapies – Denver …

Posted: October 15, 2017 at 9:00 am

Harnessing stem cells to cure disease is the hottest topic in joint injury, knee pain and arthritis treatment today. By using the adult stem cells found in our own bodies, we can amplify and speed up the natural healing process as well as grow new bone and cartilage to rebuild joints without the need for artificial replacements.

At Cendant Stem Cell Centerin Denver and our new Milwaukee Wisconsin clinic, we provide our patients with the most recent technological advancements available for treating orthopedic injuries and conditions. Our Stem Cell therapy procedureprovides treatment to repair damaged cartilage, restore function, eliminate hip, shoulder, back and knee pain and to prevent further joint destruction.

The patients adipose (fat) derived Stem Cells and/or bone marrow derived Stem Cells are injected alongwith Platelet Rich Plasma into the joint capsule space. These components are put on top of an Extracellular Fiber Matrixwhich is injected into the joint capsule before the introduction of Stem Cells. This FDA approved fiberis a major advancement in the Stem Cell procedure which gives Stem Cells a structure to bind and growupon inside the joint space. The technology allows us to treat older patients and patients with more aggressive joint disease who are facing replacement surgery or suffering from chronic pain.

The Stem Cell procedureis virtually painless, takes 3 hours and is performed under local anesthesia. It requires little to no downtime and is effective, fast and safe. Please visit our Video Testimonials page to hear from our patients and why they choose our Denver and Milwaukee stem cell clinics for their medical needs.

Ourunique approach to stem cell therapy does not offer a single franchised solution. Cendants multiple technologies provide case-driven stem cell treatment options to address individual patient needs.

Medical researchers are reporting remarkable results using platelet rich plasma and stem cellsin the treatment of common injuries, including:

What should patients expect after Stem Cell Therapy?

The noticeable regeneration of the joint tissue and cartilage typically starts to occur within 3 weeks. Most of our patients report asubstantialreduction in pain and improved function within 4-6 weeksafter treatment. Many report total pain elimination within 10-12 weeks. Within 3-5 daysafter the procedure, most patients can return to work and resume normal daily activities. Patients cannot start stressful activity or begin strenuous exercise for six weeks. Returning to stressful activity before six weeks may result in incomplete healing of the treated tissue.

Is this therapy safe?

Yes. Autologous PRP therapy and Stem Cell therapy has been used for over 10 years in surgical and orthopedic procedures. There are many research articles published on the safety of these therapies. Because a patients own blood and cells are used, there is little risk of a transmissible infection, no side effects and a very low risk of allergic reaction.

How many treatments are required?

We treat most patients aggressively upon the first visit with a mix of PRP, Extracellular Fiber Matrix and Stem Cells which all work together to create yourregenerative injection. Most patients need only 1 treatment but you could potentially have a follow up pure PRP injection which is thought of as a booster shot, the primary function of which is to stimulate continual stem cell growth.

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Cell Science, Stem Cell Research & Regenerative …

Posted: October 15, 2017 at 9:00 am

Overview

Cell scienceis an emerging field of therapeutics and as well as stem cell therapyalso. In this Stem cells are playing widal role to develop into a newregenerative medicineof modern era in the globe. Most researchers believe thatStem Cellsare play a major role in future generations and give the big global business market across the world. This event leads us to build a great opportunity to fulfill the global needs and human welfare.

1.Molecular and Cellular Physiology and of Structural Biology

The cell structure is an important target structure for drugs and bacterial pathogens. It is composed of different protein filaments that are continuously remodeledto construct a dynamic cellular scaffold. The cytoskeleton is a scaffold that gives cells their diverse and adaptable shapes and that organizes their internal structures.The cytoskeleton plays a fundamental role in all aspects of cell mechanics, such as cell adhesion and motility, cell division, intracellular transport, the establishment of cell polarity and the organization of cells in tissues and organs.Many drugs and bacterial toxins act by blocking or activating cytoskeletal regulatory proteins.We primarily investigate the regulation of the cytoskeleton in the context of cancer and bacterial infections.

2.Cell Biology of Vertebrates, Microbes and Parasites

Vertebrates are multicellular, heterotrophic eukaryotes with tissues that develop from embryonic layers. Biologists have identified 1.3 million living species of animals. Estimates of the total number of animal species run far higher, from 10 to 20 million to as many as 100 to 200 million.in general vertebrates are all motile, heterotropic, and multicellular .Animals are ingestive heterotrophs unlike plants, who store their food as starch,and animals store their food as glycogen. Vertebrates cells lack of cell walls that provide structural support for plants and fungi .The multicellular bodies of animals are held together by extracellular structural proteins especially collagen. Vertebrate cells are made up of cells organized into tissues .each tissue specialized to some specific functions .vertebrates have their unique types of intracellular junctions, including tight junctions, desmosomes. And gap junctions together. Microbes are member of the group of eukaryotic organisms that includes unicellular microorganisms such as yeasts and molds, as well as multicellular fungi that produce familiar fruiting forms known as mushrooms. These organisms are classified as a kingdom, Fungi, which is separate from the other eukaryotic life kingdoms of plants and animals.

3.Current Research in Cell and Molecular Biology

Cell biology is playing a vital role in current scientific research oriented studies. Current situation is all about cell biology leads to invention of regenerative medicine and receptor and antibody mediated medicine. Stem cells are using as a therapy for diseases include bone marrow transplantation ,cancer therapy and treating in Alzheimers disease and cardiac treatments etc. The cell science research is mainly target to to achieve the diagnostic and therapeutic uses for the people across the global. Currently it has emerged as a rapidly diversifying field with the potential to address the worldwide organ shortage issue and comprises of tissue regeneration and organ replacement. Regenerative medicine save public health bodies money by reducing the need for long-term care and reducing associated disorders, with potential benefits for the world economy as a whole.

4.Nanotechnology: Stem Cells & Cancer

Nanotechnology in medicine offers some exciting possibilities. Some techniques are only imagined, while others are at various stages of testing, or actually being used today. Nanotechnologies in medicine involve applications of nano particles currently under development, as well as longer range research that involves the use of manufactured nano-robots to make repairs at the cellular level. Nanotechnology in medicine currently being developed involves employing nano particlesto deliver drugs, heat, light or other substances to specific types of cells (such as cancer cells). Particles are engineered so that they are attracted to diseased cells, which allow direct treatment of those cells. This technique reduces damage to healthy cells in the body and allows for earlier detection of disease.

5.Molecular and Cellular Basis of Growth and Regeneration

Cell growth is used in the biological cell development and cell reproduction. Where a cell, known as the mother cell, grows and divides to produce two daughter cells. In the cell development cytoplasmic and organelle volume increase and genetic material also. Regeneration is the process of renewal, restoration, and growth that makes genomes, cells,organisms, and ecosystems resilent to natural fluctuations or events that cause disturbance or damage.

6.Stem Cells, Self-Assembly, Tissue Growth and Regeneration

Stem cells have the remarkable potential to develop into many different cell types in the body during early life and growth. In addition, in many tissues they serve as a sort of internal repair system, dividing essentially without limit to replenish other cells as long as the person or animal is still alive. When a stem cell divides, each new cell has the potential either to remain a stem cell or become another type of cell with a more specialized function, such as a muscle cell, a red blood cell, or a brain cell.

7.Germline Stem Cells

Germ cells are specialized cells which are involved in reproduction. The most well-known examples of this type of cell are gametes, the sperm and eggs which come together to create a zygote which can develop into a foetus. In addition to gametes, a number of other cells involved in reproduction are also germ cells, including gonocytes, the cells which regulate the production of eggs and sperm. All germ cells carry the germ line, the genetic material which an organism can pass on to its offspring. In humans, these cells are haploid, meaning that they carry only half the number of chromosomes necessary to create an organism. When germ cells from two different people meet, their haploid genetic material combines to create diploid cells which can replicate themselves through cell division, ultimately building a baby.

8.Cellular And Molecular Medicine

Regenerative medicines have the ability to repair, replace, and regenerate tissues and organs affected due to injury, disease, or natural aging process. These medicines are capable of restoring the functionality of cells & tissues and are applicable in a wide range of degenerative disorders such as dermatology, Neurodegenerativediseases, cardiovascular and orthopaedic applications. Researchers focus on developing technologies based on biologics, genes, somatic as well as stem cells. Stem cells are capable of proliferation and differentiation owing to which they are of importance in this field.

9.Computational Biology and Drug Designing

Computational Biology is the science of using biological data to develop algorithms and relations among various biological systems. Computational biology is different from biological computation, which is a sub field of computer science and computer engineering using bio engineering and biology to build computers, but is similar to bioinformatics, which is an interdisciplinary science using computers to store and process biological data. Computer-aided drug design methods have played a major role in the development of therapeutically important small molecules for over three decades. The field is broadly defined and includes foundations in computer science, applied mathematics, animation, statistics, biochemistry, chemistry, biophysics, molecular biology, genetics, genomics, ecology, evolution, anatomy, neuroscience, and visualization.

10.Cell Signaling Technology

Cell signalling is major part of communication that coordinates basic activities of cells and perform cell actions. The ability of cells to perceive and correctly respond to their micro environment on the basis of development, tissue reform, and immunity as well as normal tissue homeostasis. Damage in cellular information processing are responsible for diseases such as cancer, autoimmunity, and diabetes. By understanding cell signalling, diseases may be treated more effectively and, theoretically, artificial tissues may be created. Cell signalling has been most studied in human diseases. Cell signalling may also occur between the cells of two different organisms. In mammals, early embryo cells exchange signals with cells of the uterus.

11.Tissue Engineering

Tissue engineering evolved from the field of bio material development and describes the practice of combining scaffolds, cells, and biologically active molecules into functional tissues. The goal of tissue engineering is to assemble functional constructs that restore, maintain, or improve damaged tissues or whole organs. Artificial skin and cartilage are examples of engineered tissues that have been approved by the FDA. This field continues to evolve. In addition to medical applications, non-therapeutic applications include using tissues as biosensorsto detect biological or chemical threat agents, and tissue chips that can be used to test the toxicity of an experimental medication.

12.Cell Rejuvenation and Wound Healing

Cell Rejuvenation is described as the reforming of a damaged cell. Skin compartments, epidermis, and hair follicles house stem cells that are indispensable for skin homeostasis and regeneration. The stem cells also contribute to wound repair, resulting in restoration of tissue integrity and function of damaged tissue. Unsuccessful wound healing processes often lead to non-healing wounds. Chronic wounds are caused by depletion of stem cells and a variety of other cellular and molecular mechanisms, many of which are still poorly understood. Current chronic wound therapies are limited, so the search to develop better therapeutic strategies is on going.Adult stem cells are gaining recognition as potential candidates for numerous skin pathologies. Emerging concepts offer some perspectives on how skin tissue-engineered products can be optimized to provide efficacious therapy in cutaneous repair and regeneration.

13.Stem Cell Therapeutics in Modern era

Stem-cell therapy is the use of stem cells to treat or prevent a disease or condition. Bone is the most widely used stem-cell therapy, but some therapies derived from umbilical cord blood are also in use. Research is underway to develop various sources for stem cells, and to apply stem-cell treatments for neurodegenerative diseases and conditions such as diabetes, heart disease, and other conditions. Stem-cell therapy has become controversial following developments such as the ability of scientists to isolate and culture embryonic stem cells, to create stem cells using somatic cell nuclear transfer and their use of techniques to create induced spluripotent stem cell. This controversy is often related to abortion politics and to human cloning. Additionally, efforts to market treatments based on transplant of stored umbilical cord blood have been controversial.

14.Cancer Cell Biology

Cancer stem cells are cancer cells that possess characteristics associated with normal stem cells, specifically the ability to give rise to all cell types found in a particular cancer sample. CSCs are therefore tumorogenic , perhaps in contrast to other non-tumorigenic cancer cells. CSCs may generate tumours through the stem cell processes of self-renewal and differentiation into multiple cell types. Such cells are hypothesized to persist in tumours as a distinct population and cause relapse and metastasis by giving rise to new tumours. Therefore, development of specific therapies targeted at CSCs holds hope for improvement of survival and quality of life of cancer patients, especially for patients with metastatic disease.

15.Bioethical Issues in Cell and Stem Cell Biology

The main Bioethical issues associated with human stem cells involve their derivation and use for research. Although there are interesting ethical issues surrounding the collection and use of somatic adult stem cells from aborted foetuses and umbilical cord blood, the most intense controversy to date has focused on the source of human embryonic stem (hES) cells. At present, new ethical issues are beginning to emerge around the derivation and use of other hES celllike stem cells that have the capacity to differentiate into all types of human tissue. In the near future, as the stem cell field progresses closer to the clinic, additional ethical issues are likely to arise concerning the clinical translation of basic stem cell knowledge into reasonably safe, effective and accessible patient therapies. This Review summarizes these and other bio ethical issues of the past, present and future of stem cell research.

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Spotlights Archive | The University of North Carolina at …

Posted: October 15, 2017 at 8:54 am

A life of purpose

For more than two centuries, the University of North Carolina at Chapel Hill has prepared the states lawyers, business leaders, journalists, teachers, politicians and doctors. But the University experience, Gov. Roy Cooper said, does more than just prepare students for the workforce. This University is second to none in preparing students to make a career

Carolinas University Day celebration will be available at 11 a.m.on Oct. 12 via livestream onunc.edu. University Day marks the 1793 laying of the cornerstone of Old East, the nations first state university building, and the beginning of public higher education in the United States. Chancellor Carol L. Folt will preside over the event. Gov. Roy

Dear Campus Community, Fall is always an exciting time on campus. We just launched the most ambitious fundraising campaign in Carolinas history, and tomorrow we will welcome Gov. Roy Cooper to deliver the keynote address at our celebration marking our Universitys 224thbirthday. In this video, I provide an overview of our bold $4.25 billion, university-wide

For the Ackland Art Museum, 2017 has already been a phenomenal year. In January, Carolina graduate Sheldon Peck and his wife, Leena, made a $25 million commitment to the Ackland Art Museum. That gift included an $8 million endowment and a $17 million art gift that included seven works by Rembrandt. The year got even

In this weeks episode, we look back on the founding of the University with history professor Jim Leloudis.

With the Institute for Convergent Science, Carolina will lead the world in bringing scientific expertise together to improve peoples lives, Chancellor Carol L. Folt said. The UNC Institute for Convergent Science will be at the heart of that vision, giving proven convergent thinkers both here and around the globe the tools and space they need

Both the children of career Marines, Steve and Debbie Vetter know the struggles facing Carolinas military dependents. We grew up as military brats and then came to the University, Debbie said. Our parents helped when they could, but we had to struggle to make it through financially working full time and going to school.

Shawn Hingtgen and his research team at Carolina developed a pioneering cancer treatment method that turns skin cells to cancer-fighting stem cells able to hunt down and eradicate tumor remnants. But Hingtgen wouldnt be here if Carolina hadnt first hunted him down at Harvard Medical School and convinced him to trade the Ivy League for

Carolina has launchedFor All Kind: the Campaign for Carolina, an ambitious fundraising drive that seeks to raise $4.25 billion over the next five years. Chancellor Carol L. Folt, along with Board of Trustees Chair Haywood Cochrane and Vice Chancellor for Development David Routh, announced the launch on Polk Place on Oct. 6, in a tent

One of the most destructive hurricanes in the past decade, Hurricane Matthew drenched North Carolina with 350 millimeters of rain over the course of just 24 hours. It caused $1.5 billion in flood damage to 100,000 houses, businesses and government buildings, took the lives of 28 North Carolinians, forced more than 4,000 people to evacuate,

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Center for Applied Proteomics and Molecular Medicine

Posted: October 15, 2017 at 8:52 am

What is Personalized Medicine?

Every individuals disease is different. Personalized medicine strives to provide the right medicine for the right patient with the lowest toxicity. Personalized cancer therapy using proteomics involves molecular profiling of the patients cancer cells to map the susceptible drug targets and thereby guide therapy. Research, like that being done by the Center for Applied Proteomics and Molecular Medicine, provides strategies for personalized treatment with the goal of providing physicians key missing molecular information about the disease in each of their patients and improving the quality of life for patients.

The Center for Applied Proteomics and Molecular Medicines mission is to: a) create new technologies and make basic science discoveries in the field of disease pathogenesis b) apply these discoveries and technologies to create and implement strategies for disease prevention, early diagnosis and individualized therapy. The primary emphasis of our disease research is cancer, but new technologies developed in the center are being applied to a number of important human diseases including cardiovascular disease, diabetes, and obesity, as well as liver, ocular, neurodegenerative and infectious diseases.

The 7th Global Reverse Phase Protein Array Workshop will be hosted in Dublin, Ireland on September 14-16, 2017. RPPA technology is a powerful multiplexed immunoassay that can quantitatively measure hundreds of proteins and post-translationally modified proteins from a limited number of cells or a fraction of a biopsy.In the last decade, RPPA has been extremely useful to:1) focus on the role of functional proteomics in the aetiology and pathogenesis of any disease.2) focus on translational-clinical biomarker research.3) design clinical trials of established and novel treatments to identify, validate and advance understanding of baseline and pharmacodynamic predictive biomarkers of drug effectiveness as well as of drug resistance mechanisms.This is only the start. Every day a growing number of basic research scientists, biomedical and pharmaceutical companies around the world find new applications for this constantly evolving technology. Regardless of whether you are a pioneer of the technology, an experienced user or a researcher interested in incorporating the technology into your portfolio, join us to discuss the next applications of this technology. These range from advances in personalized medicine to the identification of therapeutic targets and discovery and validation of biomarkers.This year in Dublin, we will continue to build on the knowledge exchanged at the previous meetings in Houston (USA) 2011, Edinburgh (UK) 2012, Kobe (Japan) 2013, Paris (France) 2014, Manassas (USA) 2015, and Tubingen (Germany) 2016.

The Side-Out Metastatic Breast cancer trial was announced at the annual meeting of the American Society of Clinical Oncology (ASCO) and is expected to expand into phase two this month.

ASCO Poster Presentation

The pilot study was the first of its kind to utilize novel protein activation mapping technology along with the genomic fingerprint of cancer as a way to find the most effective treatment. Results indicate that while prior standard chemotherapy failed the 25 women who participated in the 2.5 year pilot study, nearly half of the patients enrolled in the Side-Out trail had at least a 30 percent increase in progression-free survival.

This molecular approach creates opportunities for new therapies. For example, if a breast tumor shares the same protein pathway activation shared with lung cancer, then the drug developed to hit that target for lung cancer can be used now for breast cancer. The pilot study included only FDA-approved drugs currently on the market. Additional studies are expected to fold in new drugs as they become available with experimental drug.

Hear what patients and a treating physician has to say: Funded by Volleyball Tournaments, Breast Cancer Pilot Study Succeeds

Based on the results of this trial, CAPMM and the Side-Out Foundation are expanding this study to a new trial that is set to launch within the next month.

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Stem Cells to Relieve Low Back Pain? WebMD

Posted: October 14, 2017 at 2:21 am

By Brenda Goodman

HealthDay Reporter

FRIDAY, April 12 (HealthDay News) -- Medical researchers are trying a new treatment for low back pain. Their hope is that harvesting and then re-injecting the body's own bone marrow -- which is rich in stem cells -- may repair worn-out discs in the spine.

In a small new study, the approach appeared to be safe -- and none of the patients reported that their pain got worse after the procedure.

But both the doctors who are testing the technique and outside experts say much more research is needed before they can say whether the treatment offers real relief.

"I tell everybody that this is experimental, with a capital E," said Dr. Joseph Meyer Jr., an anesthesiologist and pain medicine specialist at the Columbia Interventional Pain Center, in St. Louis. "We don't know if it works. I do believe that it's safe, but it might not do anything for you."

For the study, Meyer and his colleagues reviewed the case histories of 24 patients who were injected with their own bone marrow aspirate cellular concentrate (BMAC). Bone marrow concentrate contains adult stem cells, which have been called the body's own repair kit because they can change into -- and potentially heal -- different kinds of tissues.

Meyer's patients reported suffering from chronic low back pain for anywhere from three months to 12 years. Imaging tests showed that all the patients had some evidence of degeneration, or damage, to the discs that cushion the bones of the spine. Disc degeneration is common with age, and it is thought to be a major cause of low back pain.

Many times, exercise and weight loss can help people with persistent low back pain. But if conservative approaches fail and the pain becomes debilitating, Meyer said, the next option is invasive spinal fusion surgery.

"Fusion is a big, big step with questionable effectiveness," he said. "Often, you're back in the same boat a year later."

Meyer said he offered patients the bone marrow treatment as something to try before resorting to surgery.

For the procedure, he used a long needle to extract bone marrow from the back of the hip. The bone marrow was spun in a centrifuge to concentrate the cells and then injected into the space around a damaged disc. Meyer said the treatment costs a few thousand dollars and is not covered by insurance.

Of the 24 patients who initially received the bone marrow injections, half went on to have other procedures over the next 30 months, making it impossible to know what might have affected their back pain.

Of the 12 who had no other kinds of treatment, 10 reported that their pain lessened in the two to four months after their injections. After a year, eight patients were still reporting significant pain relief, while three said their back pain had not improved. One patient had not yet reached the 12-month mark. After two years, five said their back pain was better, and three had no improvement. For the other four, it was still too early to tell.

Meyer said none of the 24 patients who tried the technique had complications from their procedures, but injections always carry the risk of infection.

The study was scheduled for Thursday presentation at the annual meeting of the American Academy of Pain Medicine in Fort Lauderdale, Fla. Studies presented at scientific conferences usually haven't been scrutinized by independent experts, and their results are considered preliminary.

An expert who was not involved in the study said people with back pain shouldn't get too excited about these results, particularly since there was no control group used for comparison.

"Low back pain often gets better over time," said Dr. Richard Deyo, a professor of evidence-based medicine and a back pain expert at Oregon Health and Sciences University, in Portland. "Even patients who have chronic pain, their symptoms tend to wax and wane and fluctuate. They seek care when their symptoms are worst, and very often they drift back to their average level of pain, which looks like improvement."

"People grasp at straws, and they shouldn't. We have a long history of treatments that look promising when they start and turn out to be no more effective than placebo interventions," said Deyo, who also is deputy editor of the journal Spine. "We also have a history of treatments that, in some cases, turned out to be harmful. It's really too early to know if this is going to be effective or safe."

The study's authors agreed. They said they hope this pilot project will encourage more research.

"We hope it will get people thinking and hopefully promote a future controlled study," Meyer said.

WebMD News from HealthDay

SOURCES: Joseph Meyer Jr., M.D., Ph.D., anesthesiologist and pain-medicine specialist, Columbia Interventional Pain Center, St. Louis; Richard Deyo, M.D., M.P.H., Kaiser-Permanente endowed professor of evidence-based medicine, department of family medicine, Oregon Health and Sciences University, Portland, Ore.; April 11, 2013, presentation, American Academy of Pain Medicine annual meeting, Fort Lauderdale, Fla.

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First Gene Therapy For An Inherited Disorder Gets Expert …

Posted: October 14, 2017 at 2:18 am

A panel of experts has recommended that the Food and Drug Administration approve a treatment developed by Spark Therapeutics for a rare form of blindness. Spark Therapeutics hide caption

A panel of experts has recommended that the Food and Drug Administration approve a treatment developed by Spark Therapeutics for a rare form of blindness.

Gene therapy, which has had a roller-coaster history of high hopes and devastating disappointments, took an important step forward Thursday.

A Food and Drug Administration advisory committee endorsed the first gene therapy for an inherited disorder a rare condition that causes a progressive form of blindness that usually starts in childhood.

The recommendation came in a unanimous 16-0 vote after a daylong hearing that included emotional testimonials by doctors, parents of children blinded by the disease and from children and young adults helped by the treatment.

"Before surgery, my vision was dark. It was like sunglasses over my eyes while looking through a little tunnel," 18-year-old Misty Lovelace of Kentucky told the committee. "I can honestly say my biggest dream came true when I got my sight. I would never give it up for anything. It was truly a miracle."

Several young people described being able to ride bicycles, play baseball, see their parents' faces, read, write and venture out of their homes alone at night for the first time.

"I've been able to see things that I've never seen before, like stars, fireworks, and even the moon," Christian Guardino, 17, of Long Island, N.Y., told the committee. "I will forever be grateful for receiving gene therapy."

The FDA isn't obligated to follow the recommendations of its advisory committees, but it usually does.

If the treatment is approved, one concern is cost. Some analysts have speculated it could cost hundreds of thousands of dollars to treat each eye, meaning the cost for each patient could approach $1 million.

Spark Therapeutics of Philadelphia, which developed the treatment, hasn't said how much the company would charge. But the company has said it would help patients get access to the treatment.

Despite the likely steep price tag, the panel's endorsement was welcomed by scientists working in the field.

"It's one of the most exciting things for our field in recent memory," says Paul Yang, an assistant professor of ophthalmology at the Oregon Health and Science University who wasn't involved in developing or testing the treatment.

"This would be the first approved treatment of any sort for this condition and the first approved gene therapy treatment for the eye, in general," Yang says. "So, on multiple fronts, it's a first and ushers in a new era of gene therapy."

Ever since scientists began to unravel the genetic causes of diseases, doctors have dreamed of treating them by fixing defective genes or giving patients new, healthy genes. But those hopes dimmed when early attempts failed and sometimes even resulted in the deaths of volunteers in early studies.

But the field may have finally reached a turning point. The FDA recently approved the first so-called gene therapy product, which uses genetically modified cells from the immune system to treat a form of leukemia. And last week, scientists reported using gene therapy to successfully treat patients suffering from cerebral adrenoleukodystrophy, or ALD, a rare, fatal brain disease portrayed in the film Lorenzo's Oil. Researchers are also testing gene therapy for other causes of blindness and blood disorders such as sickle cell disease.

The gene therapy endorsed by the committee Thursday was developed for RPE65-mutation associated retinal dystrophy, which is caused by a defective gene that damages cells in the retina. About 6,000 people have the disease worldwide, including 1,000 to 2,000 people in the United States.

The treatment, which is called voretigene neparvovec, involves a genetically modified version of a harmless virus. The virus is modified to carry a healthy version of the gene into the retina. Doctors inject billions of modified viruses into both of a patient's eyes.

In a study involving 29 patients, ages 4 to 44, the treatment appeared to be safe and effective. More than 90 percent of the treated patients showed at least some improvement in their vision when tested in a specially designed obstacle course. The improvement often began within days of the treatment.

"Many went from being legally blind to not being legally blind," said Albert Maguire, a professor of ophthalmology who led the study at the University of Pennsylvania, in an interview before the hearing.

The improvement varied from patient to patient, and none of the patients regained normal vision. But some had a significant increase in their ability to see, especially at night or in dim light, which is a major problem for patients with this condition.

"What I saw in the clinic was remarkable," Maguire told the committee. "Most patients became sure of themselves and pushed aside their guides. Rarely did I see a cane after treatment."

That was the case of Allison Corona, who's now 25 and lives in Glen Head, N.Y. She underwent the treatment five years ago as part of the study.

"My light perception has improved tremendously," Corona said during an interview before the hearing. "It's been life-changing. I am able to see so much better. I am so much more independent than what I was. It is so much better."

The patients have been followed for more than three years, and the effects appear to be lasting. "We have yet to see deterioration," Maguire says. "So far the improvement is sustained."

The injections themselves did cause complications in a few patients, such as a serious infection that resulted in permanent damage, and a dangerous increase in pressure in the eye. But there were no adverse reactions or any signs of problems associated with the gene therapy itself, the researchers reported.

While this disease is rare, the same approach could work for similar forms of genetic eye disease, Maguire says."There are a lot of retinal diseases like this, and if you added them together it's a big thing because they are all incurable."

If approved, the treatment would be marketed under the name Luxturna.

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Stem Cell Therapy – Colorado Springs Orthopedics

Posted: October 14, 2017 at 2:17 am

STEM CELL THERAPY

Christopher K. Jones, MD

I am very excited to offer stem cell therapy as a treatment for a variety of musculoskeletal conditions. Although stem cell therapy is in its infancy, early research is opening the door for another non-invasive treatment for degenerative arthritis, lateral or medial epicondylitis, patella tendinitis, plantar fascitis, rotator cuff tears, muscle injuries, shin splints as well as a variety of other conditions.

What are Stem Cells?

Stem cells are cells that are able to differentiate (change) into any type of mature cell (i.e. bone, cartilage, tendon, muscle). These cells have the ability to repair injured tissue by transforming into the particular type of cell that is needed in the area of treatment.

How are stem cells obtained?

Stem cells can be obtained from an individual by aspirating bone marrow and centrifuging it in order to separate the stem cells from the other cells such as red blood cells and adipocytes. They can also be obtained from fetal tissue or the amniotic membrane. The amniotic membrane can be sterilely processed and produce an injectable product.

What else does this injection contain?

The amniotic membrane contains over 1 million cells and 44% of these cells are mesenchymal stem cells. It also contains many other vital substances for the healing process, such as growth factors, fibrocytes, epidermal cells and amino acids. These other constituents is what differentiates amniotic products from adult derived mesenchymal stem cells.

What are the advantages of using amniotic derived stem cells over adult derived (bone marrow aspirate)?

Besides the obvious benefit of not having an invasive procedure, which carries all of the inherent risks of surgery, amniotic derived stem cells have been shown to develop into fully functioning cell types. In other words, the cells carry the potential to heal and grow. Further, the procedure is as simple as having a cortisone injection.

How are stem cell injections given?

First, The amniotic derived stem cells are mixed with PRP (Platelet Rich Plasma). The area to be injected is treated with a local anesthetic, and the mixture of local anesthetic and PRP is injected into the part of the body being treated. For many of these injections, I utilize ultrasound in order to guide the needle into the bad tissue or joint. The whole process takes place in my clinic and typically takes less than 30 minutes.

What happens after your treatment?

First and foremost, it is important to create the most optimal environment for the stem cells. This means avoiding the use of non-steroidal anti-inflammatory drugs (ibuprofen, naproxyn, Celebrex, aspirin) and not icing the affected area for the first 4-6 weeks. Additionally, I advise against high impact or vigorous activity during the 6 weeks. It is okay to walk, lift light weights and do low impact activities such as bicycle or elliptical.

What conditions may benefit from stem cell injections?

When will I begin to see some improvement?

Patients typically report some improvement as early as 6 weeks. They also report improvements up to 2 years following the treatment. For some patients, if limited response is seen at 6 months, I may recommend a second injection.

What are the potential complications?

There have been no reported adverse reactions in patients treated with the amniotic stem cell product that I use. There is typically injection site soreness for a few days after the injection, and there is a very low (well less than 1%) risk of infection with any injection.

Does insurance pay for stem cell therapy?

Insurance companies consider stem cell therapy experimental, and therefore, do not pay for this treatment.

What are the results?

The research currently available suggests that approximately 85% of patients respond favorably to stem cell injections. There are several studies evaluating treatment of knee arthritis. These studies show patients to have significant relief up to 2 years following the injection. Further, they noted that those with more severe arthritis will not benefit as much, and will more likely require additional treatments. The results of treating tendinopathies have shown similar success. This therapy is certainly new, but shows incredible promise and will likely be mainstream in the future.

Am I a candidate for stem cell therapy?

If you are suffering from one of the above or other orthopedic conditions, I am happy to have you schedule a consultation and discuss your particular case.

How do I schedule an appointment?

Call my office at 719-632-7669

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Stem Cell Treatments: 6 False-Hope Warning Signs

Posted: October 14, 2017 at 2:15 am

There's a dark side to stem cells: bogus treatments that prey on patients' hopes when mainstream medicine has little to offer.

Stephen Byer stepped far outside typical medical care when his son, Ben, had ALS. He took Ben to China for stem cell-like treatments, and later helped hundreds of people do the same, believing it would help them.

The unproven procedure could have killed Ben. It didn't -- but it also didn't work. Ben later died of ALS. So did the ALS patients Byer now regrets helping get the treatment.

Why take the chance? For Byer, it started with misleading promises online.

"The Internet, while increasing communication, has spawned a horde of charlatans and creeps," Byer says. "We were suckered into one of the earlier forms of stem cell chicanery."

But not everyone who seeks unapproved stem cell treatments feels ripped off. Even though the stem cell treatments Dawn Gusty got in Tijuana, Mexico, didn't ease her multiple sclerosis, she doesn't look back with regret.

That moment -- when hope surpasses science, and when someone claims to be able to bridge that gap -- may be one of the riskiest for patients to handle. And it's one of the most alarming for stem cell experts.

"It is a very dangerous situation," says Joshua Hare, MD, director of the Interdisciplinary Stem Cell Institute at the University of Miami.

Make no mistake: Hare is all for scientific stem cell research. His concern, he says, is "hype" that glosses over an inconvenient fact: There are no new approved stem cell therapies.

The danger becomes clear if you Google "stem cell treatment." You'll get search results from clinics in the U.S. and around the world touting stem cell treatments for conditions ranging from baldness to ALS (Lou Gehrig's disease).

People who pursue those treatments "are spending huge sums of money to get therapies that are completely unproven and unlikely to work," Hare says.

Aaron D. Levine, PhD, a Georgia Institute of Technology bioethics professor, agrees. "A lot of companies are claiming they can do things right now the science can't support," Levine says.

But it's happening anyway. Famous athletes and politicians have sought the treatments. So why shouldn't we?

Twice, Dawn Gusty paid $27,000 for stem cell treatments at a clinic in Tijuana, Mexico. Twice, her care there was completely out of step with accepted medical care for her multiple sclerosis.

Twice, the procedure didn't work. Still, Gusty, of Kingston Springs, Tenn., isn't second-guessing herself. She had gone looking for something better than what her U.S. doctors could offer.

"I was being treated by the book, but I am not a textbook case of MS," Gusty tells WebMD. "It was doing no good."

In Tijuana, Gusty got heavy metal chelation , growth hormone shots, drugs to stimulate the production of blood cells, and chemotherapy . Bone marrow drained from her leg was injected directly into her spine, into her muscle, and infused into her bloodstream.

After her first visit, she felt more energetic, although she was disappointed that her condition didn't improve much. After the second treatment, she says she felt "a slight improvement, and then I settled into the same condition I had been in."

Still, she sees a different kind of value in it. "I learned so much," she says. "It changed my direction and put me on the path I am on now. I am not seeing a traditional neurologist, and not taking standard medicine."

The International Society for Stem Cell Research (ISSCR), a group of established stem cell researchers concerned with the proliferation of unproven treatments, has issued a patient handbook on stem cell therapies.

The ISSCR advises patients to seek only stem cell treatments being tested in clinical trials approved by the FDA (or, if abroad, by a national regulatory agency such as the European Medicines Agency). It also allows for smaller studies approved by an independent Institutional Review Board (IRB) or Ethics Review Board (ERB).

The ISSCR lists these warning signs that a stem cell treatment is not legitimate:

Anyone still considering a therapy after checking all of the above can download the 26-item list of questions the ISSCR recommends asking. Ask a doctor or medical professional to help you understand the answers to these questions about the treatment, scientific evidence behind it, oversight of the clinic and practitioner, safety and emergency plans, patient rights, and costs.

"One of the notorious signs of an unproven therapy is the claim it will treat anything," Levine says. "A lot of people say we have stem cells that will seek out your ailments and cure them, whatever they are, anything from spinal cord injury to autism to heart disease . It is hard to imagine how a single therapy could really be beneficial for all of these things."

In the U.S., the FDA says "stem cells, like other medical products that are intended to treat, cure, or prevent disease, generally require FDA approval before they can be marketed."

However, treatments may avoid FDA regulation if the stem cells:

Transplanting such cells, clinics argue, is a surgical procedure rather than treatment with a drug or biological product. Licensed doctors can perform such transplants if they deem it medically appropriate for a patient.

"It is a gray area," says Mahendra Rao, MD, PhD, director of the National Institutes of Health's Center for Regenerative Medicine. "If you make too many health claims, it is still illegal. But if you do it correctly and there is validation to your work and you make your claims carefully, it is a surgical procedure not regulated by the FDA."

Because it's a gray area, Rao says, "certain groups try to see what they can drive through this window."

The FDA is stepping up its inspections of U.S. stem cell clinics and defending its actions in federal court. However, people can still find doctors and clinics in the U.S. who offer unproven stem-cell treatments.

"This is a very confusing time for patients. They have two questions: 'Can I do it?' and 'Should I do it?'" Hare says. "If the answer to 'Can I do it?' is yes, patients automatically assume the answer to 'Should I do it?' also is yes. And that can be dangerous."

"If you can't establish the benefits, you should not take the risk," Hare says.

Many stem cell clinics advertise that their procedures are safe. Since they are taking your own cells, concentrating them, and giving them back to you, what could be the harm?

"Let's say the therapy itself is completely neutral, no harm and no foul comes from it. You still are going through a medical procedure, going to a doctor's office, being put under anesthesia, getting liposuction, and then having the material injected back into you. And the first rule doctors learn is that there is no such thing as a benign procedure," Hare says.

Every treatment has some risks. So the question comes down to whether the benefits outweigh the risks. And those studies haven't been done yet.

"The most patients can hope for is that the injection triggers some reaction in their bodies that has some benefit. And that is optimistic," Levine says. "The least-bad risk is financial harm from the costs of these treatments. But patients may also wind up sicker, because one thing about injecting cells is they stay in the body and may not do what they want. It's hard to know how harm is being done, because most of these clinics do not follow up on patients and have little incentive to do so."

Many patients claim they are much better or even cured by unorthodox stem cell treatments -- including some who received the same treatment as Ben Byer.

The procedure he underwent was -- and still is -- being advertised to patients, who must travel to China to get the treatment. It's not advertised as a stem-cell therapy, but uses stem-cell-like cells from aborted fetuses.

"The doctor took the cells, nurtured them in a test tube, and then injected them in two places in the brain and in the spinal cord, way up in a dangerous place," Byer says. "Remarkably, Ben survived the surgery."

Not all unapproved stem-cell treatments involve such risky surgery. A common technique gets stem cells from fat removed via liposuction. That's less risky than brain injections but is not without risk.

Byer, too, thought the early improvement he saw in his son meant the treatment was a success.

"I didn't realize it was a time-constrained benefit and that in a short time, Ben would be back to where he was," Byer says. "And during that short time I set up a whole operation to send literally hundreds of people to China. Even when I saw the benefits diminish over four weeks, and in the weeks after that, I didn't believe it. I told myself he'd recover those benefits. Then I told myself something else. By the time I faced up to it, it was too late."

SOURCES:

Stephen Byer.

Dawn Gusty, Kingston Springs, Tenn.

Joshua Hare, MD, director, Interdisciplinary Stem Cell Institute, University of Miami.

Mahendra Rao, MD, PhD, director, Center for Regenerative Medicine, National Institutes of Health, Bethesda, Md.

Aaron Levine, assistant professor, School of Public Policy, Georgia Institute of Technology, Atlanta.

Mary Laughlin, MD, professor of medicine, hematology, and oncology, University of Virginia, Charlottesville; and past president, International Society for Cellular Therapy.

FDA web site.

Sipp, D. Stem Cell Treatment Monitor web site, "More than Minimally Manipulative."

U.S. vs. Regenerative Sciences, LLC: "Order of Permanent Injunction."

News release, Regenexx web site.

IntelliCell web site.

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