Scientists identify chain reaction that shields breast cancer stem cells from chemotherapy – Medical Xpress

February 22, 2017 Micrograph showing a lymph node invaded by ductal breast carcinoma, with extension of the tumour beyond the lymph node. Credit: Nephron/Wikipedia

Working with human breast cancer cells and mice, researchers at Johns Hopkins say they have identified a biochemical pathway that triggers the regrowth of breast cancer stem cells after chemotherapy.

The regrowth of cancer stem cells is responsible for the drug resistance that develops in many breast tumors and the reason that for many patients, the benefits of chemo are short-lived. Cancer recurrence after chemotherapy is frequently fatal.

"Breast cancer stem cells pose a serious problem for therapy," says lead study investigator Gregg Semenza, M.D., Ph.D., the C. Michael Armstrong Professor of Medicine, director of the Vascular Biology Program at the Johns Hopkins Institute for Cell Engineering and a member of the Johns Hopkins Kimmel Cancer Center. "These are the cells that can break away from a tumor and metastasize; these are the cells you most want to kill with chemotherapy. Paradoxically, though, cancer stem cells are quite resistant to chemotherapy."

Semenza says previous studies have shown that resistance to chemotherapy arises from the hardy nature of cancer stem cells, which are often found in the centers of tumors, where oxygen levels are quite low. Their survival is made possible through proteins known as hypoxia-inducible factors (HIFs), which turn on genes that help the cells survive in a low-oxygen environment.

In this new study, described Feb. 21 in Cell Reports, Semenza and his colleagues conducted gene expression analysis of multiple human breast cancer cell lines grown in the laboratory after exposure to chemotherapy drugs, like carboplatin, which stops tumor growth by damaging cancer cell DNA. The team found that the cancer cells that survived tended to have higher levels of a protein known as glutathione-S-transferase O1, or GSTO1. Experiments showed that HIFs controlled the production of GSTO1 in breast cancer cells when they were exposed to chemotherapy; if HIF activity was blocked in these lab-grown cells, GSTO1 was not produced.

Semenza notes that GSTO1 and related GST proteins are antioxidant enzymes, but GSTO1's role in chemotherapy resistance did not require its antioxidant activity. Instead, following exposure to chemotherapy, GSTO1 binds to a protein called the ryanodine receptor 1, or RYR1, that triggers the release of calcium, which causes a chain reaction that transforms ordinary breast cancer cells into cancer stem cells.

To more directly assess the role of GSTO1 and RYR1 in the breast tumor response to chemotherapy, the researchers injected human breast cancer cells into the mammary gland of mice and then treated the mice with carboplatin after tumors had formed. In addition to using normal breast cancer cells in the experiments, the team also used cancer cells that had been genetically engineered to lack either GSTO1 or RYR1. Loss of either GSTO1 or RYR1, the researchers report, decreased the number of cancer stem cells in the primary tumor, blocked metastasis of cancer cells from the primary tumor to the lungs, decreased the duration of chemotherapy required to induce remission and increased the duration of time after chemotherapy was stopped that the mice remained tumor-free.

Although the study showed that blocking the production of GSTO1 may improve the efficacy of chemotherapy drugs, such as carboplatin, GSTO1 is only one of many proteins that are produced under the control of HIFs in breast cancer cells that have been exposed to chemotherapy. The Semenza lab is working to develop drugs that can block the action of HIFs, with the hope that HIF inhibitors will make chemotherapy more effective.

Explore further: Toughest breast cancer may have met its match

More information: Haiquan Lu et al. Chemotherapy-Induced Ca2+ Release Stimulates Breast Cancer Stem Cell Enrichment, Cell Reports (2017). DOI: 10.1016/j.celrep.2017.02.001

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Scientists identify chain reaction that shields breast cancer stem cells from chemotherapy - Medical Xpress

VetStem Biopharma, Inc., Announces The Opening Of Its GMP Cell Therapy Manufacturing Facility – Laboratory Network

VetStem constructed and validated a state-of-the-art GMP stem cell manufacturing plant at its headquarters laboratory in Poway, California

Poway,CA (PRWEB)- VetStem Biopharma, Inc., announced the opening of its GMP cell therapy manufacturing facility at its headquarters laboratory in Poway, California. Based upon 12 years of knowledge gained by following GTP laboratory guidelines and utilizing the experience of both in-house personnel and consultants, VetStem constructed and validated a state-of-the-art GMP stem cell manufacturing plant. This clean room facility has already produced three registration batches of stem cell product and those batches have been officially released for use in pivotal FDA studies of safety and efficacy.

Carolyn Wrightson, Ph.D., VP of Operations, stated, This facility is the culmination of six years of planning and research, supported by over 12 years of commercial stem cell laboratory operations by VetStems experienced cell therapy team. We believe this is the first dedicated veterinary-specific cell therapy facility in the United States. It will provide all the stem cell products for use in VetStem FDA product development programs. The facility operates under FDA GMP guidelines and is designed to produce commercial products, once approved by the FDA.

Quality is a critical element necessary to bring stem cell therapy into mainstream veterinary practice. VetStem has been committed to quality since its founding and has worked directly with the FDA Center for Veterinary Medicine since 2003 to assure our products and services adhere to the strictest guidelines for safety and efficacy, saidBob Harman, DVM, MPVM, CEOof VetStem. VetStem offers tours of this unique facility via large viewing windows in an exterior corridor and veterinarians are amazed at the high tech approach to veterinary cell therapy including the specialized approach to donor selection, disease screening, clean room cell culture and final packaging of the product in specialized cell product vials.

Stem cell therapy is a truly novel and natural approach to treatment of acute and chronic diseases in animals that have few or less efficacious therapeutic options. Using donor derived allogeneic stem cells provides cell therapy in a ready to use format without the need for tissue collection, or processing thus expanding the availability to more animals. VetStem is dedicated to providing affordable stem cell therapy for diseases of dogs, cats and horses, especially in areas of unmet needs, according to Harman.

About VetStem Biopharma VetStem Biopharma is a veterinarian-lead company that was formed in 2002 to bring regenerative medicine to the profession. This privately held biopharmaceutical enterprise, based near San Diego (California), currently offers veterinarians an autologous stem cell processing service (from patients own fat tissue) among other regenerative modalities. With a unique expertise acquired over the past 14 years and 12,000 patients treated by veterinarians for joint, tendon or ligament issues, VetStem has made regenerative medicine applications a therapeutic reality beyond the realm of research. The VetStem team is focused on developing new clinically practical and affordable veterinary solutions that leverage the natural restorative abilities present in all living creatures. The companys stated mission is to extend and enhance the lives of animals by improving the quality of recovery in acute conditions, but also by unlocking ways to slow, stop and ultimately revert the course of chronic diseases. In addition to its own portfolio of patents, VetStem holds exclusive global veterinary licenses to a portfolio of over 70 issued patents in the field of regenerative medicine.

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VetStem Biopharma, Inc., Announces The Opening Of Its GMP Cell Therapy Manufacturing Facility - Laboratory Network

Stem Cell Therapy Could Reverse Hearing Loss – Seeker

Humans have about 15,000 inner ear-hair cells, each one picking up sound vibrations, converting them to electric signals and sending them to the brain for processing.

Over time, loud noise, medications and old age combine to kill these cells and their microscopic hairs called stereocilia which leads to hearing loss. Unlike other animals, however, humans and mammals can't regrow them. But a group of scientists based in Boston say they've figured out a way to switch on the body's cellular factories and possibly reverse hearing loss.

"The biology is there, we just need to awaken it," said Jeffrey Karp, associate professor at Brigham and Women's Hospital, Harvard Medical School and an author on the new study appearing Tuesday in the journal Cell Reports. "For some reason there are brakes that we need to release for a short period of time to allow new hair cells to be produced."

RELATED: Can We Reverse Hearing Damage?

Karp and colleagues were able to regrow the hair cells by activating a stem cell in the cochlea called Lgr5 with a small molecule drug treatment. A similar stem cell is found in the human intestine and allows the body to regrow the exterior lining of the organ every five days.

The team also obtained a human cochlea from a patient who suffered from cancer and were able to regrow hair cells with their drug treatment.

"We don't want to provide false hope, but we are highly encouraged by this work. And our ability to produce bona fide functional hair cells is very compelling," Karp said.

The next step is taking the experimental data and starting a human clinical trial. Karp and Robert Langer of MIT are co-founders in a small startup firm, Frequency Therapeutics, that's working toward a phase I trial in the next 18 months, according to Karp.

A possible drug treatment for hearing loss could help the 360 million people worldwide who suffer from the condition.

RELATED: Why Does Loud Music Cause Hearing Loss?

"Their proposal is very novel and essentially by activating these supporting cells, a natural process will take over and a certain percentage would become hair cells capable of playing a role in the encoding of sound," said Nicolas Reed, an instructor in otolaryngology at the Johns Hopkins School of Medicine. "I don't see any obvious negative indications right now."

Hearing loss can lead to big problems as we age, including the onset of Alzheimer's disease, falls and social isolation, according to Larry Medwetsky, chairman of our Department of Hearing, Speech and Language Sciences at Gallaudet University.

"It is not a minor matter," Medwetsky said. "Hearing loss can affect you mentally and emotionally. If you can prevent or remediate it than you can also you can restore quality of life and avoid some of these issues."

WATCH: How Did Human Hearing Evolve?

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Stem Cell Therapy Could Reverse Hearing Loss - Seeker

Health Beat: Stem cell therapy for osteoarthritis – WFMZ Allentown

Health Beat: Stem cell therapy for...

CHICAGO - As a professional photographer, climbing up step ladders and walking down stairs are part of the daily grind for 65-year-old Linda Schwartz.

"There's constant activity; you're moving the whole time, really," Schwartz said

But the pain of osteoarthritis in both of her knees was making all that activity a little harder.

"I tried cortisone shots. I had something called Euflexxa," Schwartz detailed. "I was sent to physical therapy twice. I mean, I did try acupuncture in my knees, but it didn't really seem to make a difference."

"It's like the rubber on the tire, so as you start to lose the rubber in your tire and the rim hits the road, that's what happens when you have bone on bone arthritis and you've lost all the cartilage in your knee," explained Dr. Adam Yanke, an orthopedic surgeon at Rush University Medical Center in Chicago.

Yanke enrolled Schwartz in an experimental new therapy that involved injecting amniotic fluid that contained stem cells donated by healthy mothers into the knees of osteoarthritis patients.

"Between the two of those, they're a potent anti-inflammatory and they also have growth factors that help promote healing or healthy growth of tissue," Yanke said.

It was, by far, the most effective pain treatment that Schwartz has tried. Unlike cortisone shots, there are no side-effects. The pain relief has so far lasted up to a year.

Research summary - Stem cell therapy for osteoarthritis

"It was a very gradual feeling of it's a little bit better, it's a little bit better, and then realizing, wow, it's really pretty good," said Schwartz.

The one drawback is the therapy is not for patients whose arthritis is so bad it requires knee replacement surgery. Even though it's still in the experimental stage, Yanke offers the stem cell treatment to his patients, but at a cost of $2,200 a shot, it is not yet covered by insurance.

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Health Beat: Stem cell therapy for osteoarthritis - WFMZ Allentown

Angels’ Garrett Richards Among Pitchers Using Stem Cell Treatment Over Tommy John Surgery – CBS Local


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Angels' Garrett Richards Among Pitchers Using Stem Cell Treatment Over Tommy John Surgery
CBS Local
This, combined with new advances in stem cell technology, gave Richards the option to avoid going under the knife and instead undergo stem cell treatment. This and much more on the topic of stem cell research and its role in baseball was revealed in a ...

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Angels' Garrett Richards Among Pitchers Using Stem Cell Treatment Over Tommy John Surgery - CBS Local

Risky treatment can stop multiple sclerosis for years – BBC News


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Risky treatment can stop multiple sclerosis for years
BBC News
A multiple sclerosis treatment being tested in patients can stop the disease for at least five years, say doctors. The risky therapy involves wiping out the person's immune system with strong cancer drugs and then rebooting it with a stem cell ...
Radical stem cell treatment for MS could stop the disease in its tracks for 5 years and even allow some sufferers to ...Daily Mail
Stem Cell Transplants May Help Some With Multiple SclerosisDoctors Lounge
Resetting the Immune System, A Risky Treatment But Proven Solution To Stop Multiple Sclerosis For 5 YearsScience Times
Edition Time -iTech Post
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Risky treatment can stop multiple sclerosis for years - BBC News

Better Stem Cell Tx Outcomes for Younger MS Patients – Doctors Lounge

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Results support additional trials of autologous hematopoietic stem cell transplantation

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MONDAY, Feb. 20, 2017 (HealthDay News) -- Stem cell transplants may halt the progression of aggressive multiple sclerosis (MS) in nearly half of those with the disease, but selecting the right patients for the treatment is key, according to a study published online Feb. 20 in JAMA Neurology.

Riccardo Saccardi, M.D., from the cell therapy and transfusion medicine unit at Careggi University Hospital in Florence, Italy, and colleagues followed 281 patients with predominantly progressive forms of MS. The patients were from 13 countries and all had undergone autologous hematopoietic stem cell transplant between 1995 and 2006.

The researchers found that 46 percent of the patients experienced progression-free survival at five years after transplant. Younger patients with a relapsing form of MS who were not severely disabled and who hadn't found relief with other treatments fared better than others over five years. Within 100 days of transplant, eight patients died (2.8 percent). The researchers believe these deaths were most likely due to the transplant technology used before 2006, which has since improved.

"Stem cell transplantation cannot be considered a cure for MS," Saccardi told HealthDay. "However, it can be considered a concrete option for patients showing aggressive MS who have not responded to approved treatments."

More than one author disclosed financial ties to pharmaceutical and biotechnology companies, several of which contributed funding for the study.

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Better Stem Cell Tx Outcomes for Younger MS Patients - Doctors Lounge

Connecting the Dots: Stem Cells Provide Valuable Tool for Linking Genes and Disease – Memorial Sloan Kettering Cancer Center (blog)

Summary

MSK researchers are using pluripotent stem cells to create models of disease in the pancreas, including diabetes and pancreatic cancer.

Highlights

The ability to isolate and grow pluripotent stem cells has offered many new opportunities for biological and medical research since the technique was first developed about 20 years ago. These cells are remarkable because they have the ability to develop into any type of cell in the body from liver cells to nerve cells to heart cells and more.

The field of regenerative medicine is based on the premise that doctors may eventually be able to engineer stem cells to replace tissues that have been lost due to injury or disease. Increasingly, pluripotent stem cells are also proving to be a valuable tool in the lab, especially for studying how genetic changes affect cell growth and division.

In a new study published February 9 in the journal Cell Stem Cell, a team of researchers led by Memorial Sloan Kettering developmental biologist Danwei Huangfu has demonstrated the value of using pluripotent stem cells to study how pancreatic cells form in a person. Their research has implications for the study of diabetes a disease characterized by dysfunction in certain types of pancreas cells as well as pancreatic cancer.

A gene-editing technology called CRISPR/Cas9 allows scientists to study the effects of specific molecular changes.

Many diseases have been difficult to recreate in animal models like mice, which makes it hard for us to study them, Dr. Huangfu says. Using pluripotent stem cells to create pancreas cells in a dish is teaching her lab members about the role certain genes play in pancreatic diseases and may lead to new kinds of treatments.

In the new study, the investigators looked at the function of a gene called GATA6 in pancreas cells. In humans, mutations in this gene can cause a range of medical problems that result from the inability of the pancreas to develop and function normally.

To study the gene, the team used a gene-editing technology called CRISPR/Cas9, which acts like a molecular scissors and enables researchers to make precise changes to DNA. Specifically, the MSK researchers used the technology to create pancreas cells that had only one copy of the GATA6 gene rather than the normal two copies, a state called haploinsufficiency. This situation is similar to what is seen in some forms of diabetes.

Our research illustrates the important contribution that human pluripotent stem cells can make in studying common but complex diseases.

Danwei Huangfu developmental biologist

Recreating these defective pancreas cells in a dish has already enabled the researchers to make new discoveries about GATA6 and its interaction with another gene called GATA4 in pancreatic defects, some of which they report in the Cell Stem Cell paper.

We believe this is the first study in human pluripotent stem cells to look beyond diseases caused by relatively rare single-gene mutations, Dr. Huangfu says. Our research illustrates the important contribution that human pluripotent stem cells can make in studying common but complex diseases characterized by multiple genetic factors as well as by potential environmental factors.

Dr. Huangfus lab is also using gene editing to study the formation of cancer in the pancreas. Because MSK sequences many of our patients tumors, we know a lot about the mutations that are present in cancer, she says. But we dont always know which ones are important.

In cancer, genetic changes in tumors are categorized as driver mutations errors that are important for the formation and growth of tumors or passenger mutations, which just go along for the ride.

Doing experiments with cancer genes inserted into these pancreas models helps us understand the cellular basis of the disease, and to separate the drivers from the passengers, Dr. Huangfu explains. Then we can work toward developing better diagnostic methods and treatments for cancer, based on knowing which mutations come first and which are the most important.

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Connecting the Dots: Stem Cells Provide Valuable Tool for Linking Genes and Disease - Memorial Sloan Kettering Cancer Center (blog)

Early-stage study validates Cellect Bio’s method of stem cell selection; shares ahead 19% – Seeking Alpha

Thinly traded nano cap Cellect Biotechnology Ltd. (APOP +19.4%) jumps on more than a 4x surge in volume in response to its announcement of positive results from a Phase 1 study aimed at validating its proprietary method of stem cell selection called ApoGraft. The process allows for the natural enrichment of stem cells that can be used in cell therapies or transplantation with significantly less risk of rejection.

The study was conducted on blood stem cells donated by 104 healthy subjects. Each sample represented a 5% graft. ApoGraft, used for only a few hours, produced a significant increase in the death of mature immune cells without compromising the quality and quantity of stem cells.

The Companys technology is expected to provide pharma companies, medical research centers and hospitals with the tools to rapidly isolate stem cells for in quantity and quality that will allow stems cell-related treatments and procedures. Cellects technology is applicable to a wide variety of stem cells related treatments in regenerative medicine and that current clinical trials are aimed at the cancer treatment of bone marrow transplantations.

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Early-stage study validates Cellect Bio's method of stem cell selection; shares ahead 19% - Seeking Alpha

BrainStorm seeks early approval for stem cell treatment in Canada – Reuters

TEL AVIV Israel's BrainStorm Cell Therapeutics is seeking early approval in Canada for its adult stem cell treatment for patients with amyotrophic lateral sclerosis (ALS), a neuro-degenerative disease, even before it completes late-stage clinical trials.

BrainStorm said on Tuesday that it had signed an agreement with CCRM, a Canadian not-for-profit organization that supports development of regenerative medicine, to support a market authorization request for its ALS treatment, called NurOwn.

CCRM is helping BrainStorm meet requirements for the Canadian health regulator's early access pathway, which provides rapid review for drugs to treat serious or life-threatening conditions.

If NurOwn qualifies, it could be authorized in Canada for distribution by the start of 2018, the company said.

"We seemingly fit the criteria," BrainStorm Chief Executive Chaim Lebovits told Reuters.

At the same time, BrainStorm will conduct a Phase 3 clinical trial for NurOwn at multiple sites in the United States and Israel. The company in December said the advanced clinical trial is expected to begin enrolling patients in the second quarter of 2017.

BrainStorm also plans to submit an application in Israel that will allow patient access to NurOwn as a treatment that has been granted "Hospital Exemption". This recently approved pathway would permit BrainStorm to partner with a medical center in Israel and be allowed to treat patients with NurOwn for a fee.

Lebovits foresees possible treatments under this pathway as early as the second half of 2017.

BrainStorm is also examining whether it may be eligible for early approval in the United States under new legislation passed in December that supporters say will speed access to new drugs.

According to the ALS Association, 5,600 people in the United States are diagnosed each year with the disease, also known as Lou Gehrig's Disease, which has severely disabled British physicist Stephen Hawking.

(Reporting by Tova Cohen; Editing by Mark Potter)

WASHINGTON Virginia Governor Terry McAuliffe on Tuesday vetoed a bill that would have blocked funding for Planned Parenthood, which provides abortions and other health services.

CHICAGO Tyson Foods Inc in June will switch its retail line of company-branded chicken products to birds raised without any antibiotics, a top executive said on Tuesday, accelerating the meat sector's shift away from the drugs.

GENEVA China has detected an evolution in the H7N9 avian flu virus that is capable of causing severe disease in poultry and requires close monitoring, the World Health Organization (WHO) said on Tuesday.

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BrainStorm seeks early approval for stem cell treatment in Canada - Reuters