Yearly Archives: 2019


Maltese abroad: the best-selling author with roots in Gozo – Times of Malta

Marianne Curley is a Maltese-Australian author best known for her Guardians of Time Trilogy and Old Magic books. She has had to overcome tremendous difficulties that are of inspiration to many.

My Dad was born in Gozo and moved to Australia when he was only 15. He eventually settled on the Hawkesbury River in New South Wales. He returned to Gozo when the war ended and met my mother. They married within three months and moved to Australia.

Mum became homesick and they moved back. But Dad was a farmer and longed for the open spaces and green fields of Australia. In August of 1957, as a family of five, they returned to the Hawkesbury River property. Two years later I was born.

My teen daughters asked me to write a book for their age. I had attempted to write commercial romance, with no success. I was about to start another romance when my thirteen-year-old daughter complained there were not enough books for her age to read. Her sister, older by one year, agreed and that is how I started writing books for young adults.

I found I loved writing for young adults. It was challenging and exciting with more complex plot lines and themes I could explore, and young adult readers appeared to enjoy my writing style.

I find inspiration almost anywhere if Im looking for it. I listen to music, look through photographs or glance at passing scenery in a car or train. Our world is full of ideas. They surround us wherever we go.

The plot for Old Magic, my first published novel, came to me while I was having lunch in a park with friends on Dorrigo Mountain. Our children were walking across a field together when a mist rolled in from behind them. I watched as the mist caught up and continued to roll past, making the children almost invisible. It struck me how magical the scene was.

My readers are my proudest achievements, through their emails and messages, that have given many reasons to be most proud of them. My readers have let me know how my books, the characters and stories within, have affected them, inspired them, assisted them in tough times, and changed their lives.

Surviving my type of cancer was a miracle that I thank God for every day. The odds were not in my favour, I had a 30-35 per cent chance of surviving, and without a successful transplant I would have died within two months of my diagnosis. I am thankful for my sister Therese for giving me her stem cells and for the prayers and support I received from my friends and relatives.

I could not write for years. Weeks after surviving my transplant, and on the way to recovering, I sustained a fall in my hospital room, that broke my back. My bones were week from the chemotherapy, my spine crumbled, and I lost several vertebrae. My spine wasnt strong enough for any supportive treatment. The pain when I moved was unimaginable. Because of this, I was unable to write again for a few years.

Only focus on today. Whatever you are facing, life can become complex and at times overwhelming. You think you cant cope. Dont think of all you have yet to do, just think about what you have to do today. Only today. Tomorrow will come, theres no doubt about that. Think of what you must do tomorrow, when it is tomorrow.

I dream of visiting Malta. I had planned to visit Malta as a reward after my cancer battle, but by then Id had the fall which made travelling difficult. So sadly, Ive never had the chance to visit Malta, which just makes me miss it more. My hope is that one day I can overcome my physical difficulties enough for a long visit.

Are you a Maltese person living abroad? Contact malteseabroad@timesofmalta.com

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Maltese abroad: the best-selling author with roots in Gozo - Times of Malta

Exosome Technologies Market Report- Capricor Therapeutics Inc , Evox Therapeutics Ltd , ReNeuron Group Plc , Stem Cell Medicine Ltd and more – Hitz…

Latest report, Exosome Technologies Market: Recent Surge in R&D with Capricor, Codiak and Evox Therapeutics among Key Players, explores the application of exosome technologies within the pharmaceutical and healthcare industries. Exosomes are small cell-derived vesicles that are abundant in bodily fluids, including blood, urine and cerebrospinal fluid as well as in in vitro cell culture.

Get FREE PDF Sample of the Report @ https://www.reportsnreports.com/contacts/requestsample.aspx?name=1781607

Top Company Analysis in this Report:Capricor Therapeutics Inc , Evox Therapeutics Ltd , ReNeuron Group Plc , Stem Cell Medicine Ltd , Tavec Inc. , Codiak Biosciences Inc., Therapeutic Solutions International Inc., ArunA Biomedical Inc., Ciloa and more

These vesicles are being used in a variety of therapeutic applications, including as therapeutic biomarkers, drug delivery systems and therapies in their own right. Research within this area remains in the nascent stages, although a number of clinical trials have been registered within the field. Exosomes have several diverse therapeutic applications, largely centering on stem cell and gene therapy. Exosomes have been identified as endogenous carriers of RNA within the body, allowing for the intercellular transportation of genetic material to target cells.

As such, developers have worked to engineer exosomes for the delivery of therapeutic miRNA and siRNA-based gene therapies. As RNA is highly unstable within the body, a number of different biologic vector systems have been developed to enhance their transport within the circulation, including viruses and liposomes. Similarly, exosomes derived from stem cells have also been identified for their therapeutic applications, particularly in the treatment of cancer and cardiovascular disease. Exosome technologies offer several advantages over existing biologic-based drug delivery systems.

They have a long circulatory half-life as a result of their high stability and ability to avoid breakdown by the mononuclear phagocyte system and reticuloendothelial systems. Moreover, exosomes have several functional properties that favor their use in therapeutic delivery. Exosomes can be engineered to incorporate targeting ligands, allowing them to deliver cargo selectively to cells. Their small size allows them to penetrate the blood-brain barrier for the delivery of central nervous system therapies, whereas in cancer they can accumulate within the tumor via enhanced permeability and retention effects.

Finally, clinical trials have shown relatively large-scale production to be possible and indicate that exosome therapies can be safely administered to humans. Additionally, exosomes are being investigated for their potential as prognostic and diagnostic biomarkers for several different disease indications. Exosomes make good candidates for biomarker research because of two unique characteristics: their presence in various accessible bodily fluids, and their resemblance to their parent cells of origin. R&D in exosome technologies has increased markedly in recent years. This report provides detailed information on the various healthcare applications of exosomes, and assesses the pipeline, clinical trial and company landscapes.

Scope of the Report:

Reasons to buy this Report:

Direct Purchase Report $ 2995 @ https://www.reportsnreports.com/purchase.aspx?name=1781607

Table of Contents in this Report:

1 Table of Contents 41.1 List of Tables 61.2 List of Figures 7

2 Exosomes in Healthcare 82.1 Overview of Exosomes 82.2 Drug Delivery Systems 92.2.1 Modified Release Drug Delivery Systems 92.2.2 Targeted Drug Delivery Systems 102.2.3 Liposomes 122.2.4 Viruses 142.2.5 Exosomes 172.3 The Exosome Lifecycle 182.4 Exosomes in Biology 182.5 Exosomes in Medicine 192.5.1 Biomarkers 192.5.2 Vaccines 202.6 Exosomes as a Therapeutic Target 202.7 Exosomes as Drug Delivery Vehicles 212.8 Therapeutic Preparation of Exosomes 212.8.1 Isolation and Purification 222.8.2 Drug Loading 222.8.3 Characterization 232.8.4 Bioengineering 232.8.5 Biodistribution and In Vivo Studies 232.8.6 Advantages of Exosome Therapies 242.8.7 Disadvantages of Exosome Therapies 242.9 Exosomes in Therapeutic Research 252.9.1 Exosome Gene Therapies 252.9.2 Exosome in Stem Cell Therapy 262.10 Exosomes in Oncology 272.10.1 Immunotherapy 272.10.2 Gene Therapy 282.10.3 Drug Delivery 292.10.4 Biomarkers 302.11 Exosomes in CNS Disease 302.11.1 Tackling the Blood-Brain Barrier 302.11.2 Exosomes in CNS Drug Delivery 312.11.3 Gene Therapy 322.12 Exosomes in Other Diseases 332.12.1 Cardiovascular Disease 332.12.2 Metabolic Disease 33

3 Assessment of Pipeline Product Innovation 363.1 Overview 363.2 Exosome Pipeline by Stage of Development and Molecule Type 363.3 Pipeline by Molecular Target 373.4 Pipeline by Therapy Area and Indication 383.5 Pipeline Product Profiles 383.5.1 AB-126 ArunA Biomedical Inc. 383.5.2 ALX-029 and ALX-102 Alxerion Biotech 393.5.3 Biologics for Autism Stem Cell Medicine Ltd 393.5.4 Biologic for Breast Cancer Exovita Biosciences Inc. 393.5.5 Biologics for Idiopathic Pulmonary Fibrosis and Non-alcoholic Steatohepatitis Regenasome Pty 393.5.6 Biologic for Lysosomal Storage Disorder Exerkine 393.5.7 Biologics for Prostate Cancer Cells for Cells 403.5.8 CAP-2003 Capricor Therapeutics Inc. 403.5.9 CAP-1002 Capricor Therapeutics Inc. 413.5.10 CIL-15001 and CIL-15002 Ciloa 423.5.11 ExoPr0 ReNeuron Group Plc 423.5.12 MVAX-001 MolecuVax Inc. 433.5.13 Oligonucleotides to Activate miR124 for Acute Ischemic Stroke Isfahan University of Medical Sciences 443.5.14 Oligonucleotides to Inhibit KRAS for Pancreatic Cancer Codiak BioSciences Inc. 443.5.15 Proteins for Neurology and Proteins for CNS Disorders and Oligonucleotides for Neurology Evox Therapeutics Ltd 443.5.16 TVC-201 and TVC-300 Tavec Inc. 45

4 Assessment of Clinical Trial Landscape 484.1 Interventional Clinical Trials 484.1.1 Clinical Trials by Therapy Type 484.1.2 Clinical Trials by Therapy Area 494.1.3 Clinical Trials by Stage of Development 504.1.4 Clinical Trials by Start Date and Status 504.2 Observational Clinical Trials 514.2.1 Clinical Trials by Therapy Type 514.2.2 Clinical Trials by Therapy Area 514.2.3 Clinical Trials by Stage of Development 524.2.4 Clinical Trials by Start Date and Status 534.2.5 List of All Clinical Trials 54

and more

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Exosome Technologies Market Report- Capricor Therapeutics Inc , Evox Therapeutics Ltd , ReNeuron Group Plc , Stem Cell Medicine Ltd and more - Hitz...

Tulane team researching ways to end opioid addiction – News from Tulane

Michael J. Moore, center, a professor of biomedical engineering in the Tulane School of Science and Engineering, is leading a team of researchers on a project called the HEAL Initiative, or Helping to End Addiction Long-term Initiative. Researchers include Jeffrey Tasker, the Catherine and Hunter Pierson Chair in Neuroscience, left, and James Zadina, director of the Neuroscience Laboratory at the Veterans Administration Medical Center and an adjunct professor of medicine at the Tulane School of Medicine. (Photo by Matthew Hinton)

A Tulane University researcher is joining more than 40 universities from across the United States in looking for ways to improve treatment of chronic pain and ultimately achieve long-term recovery from opioid addiction.

Michael J. Moore, professor of biomedical engineering in the Tulane School of Science and Engineering, is part of a $945 million National Institutes of Health project called the HEAL Initiative, or Helping to End Addiction Long-term Initiative.

In 2016, an estimated 50 million U.S. adults suffered from chronic pain and in 2018, an estimated 10.3 million people 12 years and older misused opioids, including heroin.

This is indeed an exciting opportunity to work on a problem of great public health significance to our nation.

Tulane biomedical engineering professor Michael J. Moore

Its clear that a multi-pronged scientific approach is needed to reduce the risks of opioids, accelerate development of effective non-opioid therapies for pain and provide more flexible and effective options for treating addiction to opioids, NIH Director Francis S. Collins said in a statement. This unprecedented investment in the NIH HEAL Initiative demonstrates the commitment to reversing this devastating crisis.

Moores share of the project is $1.2 million. He will be teaming up with Jeffrey Tasker, the Catherine and Hunter Pierson Chair in Neuroscience, and James Zadina, director of the Neuroscience Laboratory at the Veterans Administration Medical Center and an adjunct professor of medicine at the Tulane School of Medicine.

This is indeed an exciting opportunity to work on a problem of great public health significance to our nation, Moore said.

The management of pain both acute and chronic can be a frustratingly futile endeavor for both patients and clinicians, Moore said. Desperate attempts at treatment with opioids and other narcotics has led to a heartbreaking and calamitous epidemic of addiction to prescription painkillers.

The epidemic has prompted federal agencies and the pharmaceutical industry to work toward identifying the next generation of painkillers. Unfortunately, Moore said, there are few adequate model systems currently in use to enable rapid screening of the analgesic properties of drug candidates.

Moores proposal seeks to develop the first model of pain that utilizes living human cells on a computer chip, mimicking the transmission of pain and enabling the evaluation of the cellular basis of tolerance to certain drugs. Moore said the model will eventually enable experimental drugs to be screened in a way that is faster, less expensive and more effective.

He and his team are collaborating with Randolph Ashton, an associate professor of biomedical engineering at the University of Wisconsin, and Swaminathan Rajaraman, an assistant professor of electrical and computer engineering at the University of Central Florida. Ashton is developing human stem-cell derived spinal neurons, and Rajaraman is developing specially-made microelectrodes for taking electrical measurements from the cells.

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Tulane team researching ways to end opioid addiction - News from Tulane

The most amazing medical breakthroughs of 2019 – New York Post

Richard Berry had tried nearly everything to fight his prostate cancer: surgery, radiation and chemotherapy. But after two years of treatment, his cancer had metastasized. The opportunity to participate in a clinical trial was his last hope.

I wasnt ready to die, Berry, 75, of Keene, NH, tells The Post. I didnt want to mess around.

In 2015, he connected with Dr. Christopher Sweeney, an oncologist at Bostons Dana-Farber Cancer Institute, who was leading a trial in which the drug enzalutamide an androgen-receptor inhibitor that stops the growth of cancer cells was being used in conjunction with testosterone suppression to treat metastasized prostate cancer.

Berry became one of 1,125 patients involved in the trial. Remarkably, hes now cancer-free.

Hes one of the most dramatic cases to date, Sweeney tells The Post of Berrys progress. Hes in a deep remission. This is what I had hoped to see. However, the magnitude of the effect and the early results were a surprise and delight.

So far, Sweeney says, hes seen a handful of deep remissions like Berrys and that the results were positive sooner than we anticipated. The study was published in July in the New England Journal of Medicine.

The drug, which is already FDA-approved for other uses, is currently under FDA review to make it more widely available for metastasized prostate cancer patients and not just for use in clinical trials.

Approval is anticipated any day now, according to Dana-Farber Cancer Institute reps.

Meanwhile, Berrys scans continue to be clear a year after he stopped the treatment.

I dont even think about [the cancer] anymore, Berry says. I feel good. I have energy again, and, overall, Im just happy.

Here, six more amazing medical breakthroughs that could be a reality and soon.

A blood test for breast cancer

Researchers at the University of Nottingham in England have created a blood test that could potentially detect breast cancer up to five years before a lump or other symptoms appear. The test, which would be much cheaper and easier to conduct than a mammogram, looks for autoantibodies (produced by the body in reaction to cancer cells) in the blood.

The researchers said in a statement that another larger study is planned, and, if all goes well, the test could be on the market within the next five years.

The discovery was presented at the UKs National Cancer Research Institutes annual conference in early November, which showcases the worlds biggest cancer advances. A similar test for lung cancer is currently being studied in Scotland.

A new cystic fibrosis find

After two clinical trials, a new drug, Trikafta, a triple combination therapy, was found to cause significant improvements in cystic fibrosis patients respiratory health and lung function, leading the FDA to fast-track its approval in October.

The trials results were published in the Lancet and the New England Journal of Medicine.

Trikafta is now available to patients 12 and older who have the most common cystic fibrosis mutation, which could affect almost 90% of people with the disease, or about 27,000 people in the US.

A promising Alzheimers drug

Early disappointing results halted studies, but after a comprehensive review of the data, researchers are excited once again about an Alzheimers drug called aducanumab.

After 18 months of taking the drug, participants showed lowered cognitive decline (about 15% to 27%) on memory and cognitive ability tests compared to a placebo. The results were published in late October in the journal Nature.

Due to these results, the drug manufacturer is currently seeking FDA approval for aducanumab to treat Alzheimers disease soon after diagnosis.

Crispr for everything

Crispr is a gene-editing tool that allows scientists to modify DNA and genes.

The technique is being used in numerous ways, from medical research to growing crops. Some of its proposed innovations destroying superbugs, eradicating malaria and curing HIV are quite far off.

Still, the progress is exciting. A patient has been successfully treated for sickle cell disease using the technology, and clinical trials using Crispr to treat cancers such as non-Hodgkins lymphoma are currently recruiting. Next month, at the American Society of Hematology meeting in Orlando, Fla., scientists will present the results of a three-person cancer study where Crispr was used to treat two people with multiple myeloma and one with sarcoma.

Another sickle cell breakthrough

The first patient in an ongoing clinical trial for sickle cell disease, Manny Johnson, 22, who used to require monthly blood transfusions, has been symptom-free for more than a year after undergoing treatment in Boston. Another sufferer, Jennelle Stephenson, 28, reported showing no signs of sickle cell anemia in March after undergoing a yearlong treatment in DC.

The treatment, which is based on 70 years of research, uses a novel gene therapy treatment an infusion of the patients own reworked bone marrow to help the body produce normal red blood cells consistently.

Clinical trials are ongoing around the country. The results of the first adolescent participant, a 16-year-old girl, are expected next month from Dana-Farber.

Peanut allergy promise

A new study out of Stanford University showed that after one injection of the antibody, etokimab, which is already being studied to treat other immune issues such as asthma and eczema, people with severe peanut allergies were able to eat peanut protein just two weeks later.

The study was published Nov. 14 online in the journal JCI Insight.

Currently, the only available treatment for the potentially deadly allergy is oral immunotherapy, where patients eat small doses in graduating scales under medical care. The process can take up to a year and can cause allergic reactions.

A larger study is planned to shore up dosing, timing and hopefully be used to treat other food allergies.

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The most amazing medical breakthroughs of 2019 - New York Post

Precision Medicine and Personalized Treatments Shifting the Tide in Mantle Cell Lymphoma – Curetoday.com

While resistance can often make it a challenge to treat mantle cell lymphoma, therapies have come a long way in recent years thanks to the emergence of personalized treatment and the use of BTK inhibitors, according to one expert.

Ruan, a hematologist and oncologist from Weil Cornell Medicine in New York City, recently sat down with OncLive, CUREs sister publication, to discuss the treatment trends in this disease space.

We're moving toward precision medicine and personalized treatment (in MCL), said Ruan. The objective is to overcome resistance and come up with treatment plans that address the underlying disease biology and take personal factors about the patients into consideration.

When asked about the novel agents that are currently showing promise in MCL, Ruan explained that BTK inhibitors have resulted in highoverall response rates (ORRs), more complete remissions (CRs) and a lower number of side effects in this patient population.

Since the approval of Revlimid (lenalidomide) in 2013, a number of newer BTK inhibitors have been approved, with first-generation Imbruvica (ibrutinib) standing out as the top choice for many. So far, this class of agents has the best single-agent activity in MCL to date, explained Ruan. For example, ibrutinib would give about a 65% to 67% ORR, and about 20% of that would be CRs. In contrast, lenalidomide would give you about a 30% ORR and up to about 8% CR.

A newer BTK inhibitor, Calquence (acalabrutinib), is considered just as effective as Imbruvica with an overall response rate of 81% and complete response in 40% of patients who took it during the phase 2 study that led to its approval. That's quite remarkable for a single agent for patients who have relapsed/refractory MCL, Ruan said.

The field continues to grow with the testing of new agents, including BCL-2 inhibitor, Venclexta (venetoclax), which is currently approved in chronic lymphocytic leukemia and other indolent B-cell non-Hodgkin lymphomas. In MCL, we have data to suggest that it has promising activity as a single agent, she said. Currently, it's being studied in combination with a variety of other agents, including BTK inhibitors. They seem to work very well and are helping to move treatment away from chemotherapy.

However, treating MCL can be challenging because of treatment resistance, explained Ruan. All of the agents are being introduced, tested, and approved in the setting of relapsed disease, said Ruan. That is a big challenge for a sizable portion of patients who do not respond maybe they have a genetic mutation that is not responsive to targeted therapy or they develop a secondary mutation in the process of being treated and then they become resistant.

The issue of resistance is important to consider when treating MCL, according to Ruan. We have to provide novel agents that are sensitive to the disease at every stage of the evolution and come up with additional therapies that can overcome the resistance, she said.

In the future, Ruan predicts the shift toward precision medicine and personalized treatment will continue. The objective is to overcome resistance and come up with treatment plans that address the underlying disease biology and take personal factors about the patients into consideration, she said. This is important for us to understand MCL individually.

This precise approach would mean doing more genetic analysis to determine what type of disease is being treated in order to create a treatment plan that would provide the most benefit for the patient.

If we could know (about mutations) ahead of time, we could have the treatment designed and tailored to maximize treatment effectiveness and minimize adverse events, said Ruan.

It doesn't make sense to subject patients to all of the cytotoxicity associated with conventional intensive chemotherapy while other options, such as participation in clinical trials with novel agents, could be very effective.

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Precision Medicine and Personalized Treatments Shifting the Tide in Mantle Cell Lymphoma - Curetoday.com

Low-Concentration PTX And RSL3 Inhibits Tumor Cell Growth Synergistica | CMAR – Dove Medical Press

Jing Ye, Xiaohua Jiang, Zhihuai Dong, Sunhong Hu, Mang Xiao

Department of Otolaryngology Head and Neck Surgery, Sir Run Run Shaw Hospital, College of Medicine, Zhejiang University, Hangzhou, Zhejiang, Peoples Republic of China

Correspondence: Mang XiaoDepartment of Otolaryngology Head and Neck Surgery, Sir Run Run Shaw Hospital, College of Medicine, Zhejiang University, East Qingchun Road Nr.3, Hangzhou, Zhejiang 310016, Peoples Republic of ChinaEmail joelxm@zju.edu.cn

Introduction: RSL3-induced ferroptosis is a cell death pathway dependent upon intracellular iron and is characterized by accumulation of lipid hydroperoxides. Glutaminolysis, a glutamine-fueled intracellular metabolic pathway, is an essential pathway of ferroptosis in cancer cells. Recent findings showed low-concentration paclitaxel (PTX) could inhibit cell death by upregulating p53 expression; downregulating glutaminolysis-related genes.Methods: The therapeutic effect of RSL3 plus low-concentration PTX combination therapy was investigated in HPSCC cells harboring mutant p53 (mtp53). Relative cell viability, ferroptosis-specific lipid peroxidation and relevant protein expression were evaluated.Results: We demonstrated that neither PTX nor RSL3 in low concentration caused significant cell death; however, the combination therapy is shown to induce ferroptosis and significant cell death in mtp53 HPSCC. We discovered that low-concentration PTX enhanced the RSL3-induced ferroptosis by upregulating mtp53 expression. Furthermore, mtp53-mediated transcriptional regulation of SLC7A11 could be the key determinant.Discussion: Although gain-of-function of p53 variants remains to be characterized, our findings provide new insight into the synergistical cell death by regulating ferroptosis and p53.

Keywords: HPSCC, ferroptosis, low-concentration paclitaxel, RSL3, synthetic cell death, mtp53, SLC7A11, GOF p53 variants

This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution - Non Commercial (unported, v3.0) License.By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms.

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Low-Concentration PTX And RSL3 Inhibits Tumor Cell Growth Synergistica | CMAR - Dove Medical Press

THUMPD3-AS1 Is Correlated With Non-Small Cell Lung Cancer And Regulate | OTT – Dove Medical Press

Jia Hu, Youfang Chen, Xiaodong Li, Huikai Miao, Rongzhen Li, Dongni Chen, Zhesheng Wen

Department of Thoracic Oncology, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Sun Yat-Sen University Cancer Center, Guangzhou 510060, Peoples Republic of China

Correspondence: Zhesheng Wen Email wenzhsh@sysucc.org.cn

Background: Of all malignancies, lung cancer is the leading cause of death, and non-small cell lung cancer (NSCLC) accounts for 8085% of all lung cancers. In this study, the long non-coding RNA (lncRNA) THUMPD3-AS1 was observed to be highly expressed in NSCLC and correlated with TNM stages and relapse, suggesting that THUMPD3-AS1 is involved in the regulation of NSCLC.Methods: The aim of this study was to investigate the regulatory function and mechanism of THUMPD3-AS1 in NSCLC cells by cellular function and molecular biology experiments.Results: Overexpression and knockdown analysis revealed that THUMPD3-AS1 promoted tumor progression by increasing cell proliferation and self-renewal of NSCLC cells. Moreover, THUMPD3-AS1 may act as an endogenous sponge of microRNA-543 (miR-543) which can regulate the target gene ONECUT2 in NSCLC cells.Conclusion: Our study indicated that THUMPD3-AS1 regulated NSCLC cell self-renewal by regulating the expression of miR-543 and ONECUT2, and THUMPD3-AS1 can potentially act as a biomarker or therapeutic target in NSCLC.

Keywords: non-small cell lung cancer, self-renewal, THUMPD3-AS1, miR-543, ONECUT2

This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution - Non Commercial (unported, v3.0) License.By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms.

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THUMPD3-AS1 Is Correlated With Non-Small Cell Lung Cancer And Regulate | OTT - Dove Medical Press

Teen ready to get back on the field after risky tumor surgery – KFOR Oklahoma City

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NORMAN, Okla. (KFOR) - A love of sports runs deep for 14-year-old Xander Brayfield from Norman.

Basketball, soccer, E-sports, and even a friendship with OU Linebacker Kenneth Murray are all things that bring out this teenager's famous grin.

But in quiet moments last May, Xander started feeling a troubling pain he couldn't ignore.

His mother, Kirsten De Beurs recalled, "When it came time to sit down and do his homework, he said my back is hurting so bad I can't take it."

"It was not the best summer," agreed Xander.

Not the best, because of what scans revealed.

Xander had a large tumor, wrapped around his aorta, lodged and growing between his heart and his spine.

"I couldn't listen to the doctors the first week because all I did was cry and I couldn't process the information," said Xander's mother.

Dr. Kisha Beg from Jimmy Everest Cancer Center shakes her head when asked about Xander's treatment for neuroblastoma cancer.

"You get a whole kitchen-sink of treatment," she acknowledged.

She says she's been very impressed by how Xander takes charge of his treatment plan.

"He picked up all the chemotherapy papers, he wanted me to talk to him about all the terms, all the side-effects, and he had GREAT questions," Dr. Beg said.

Chemotherapy did not erase the tumor, and the Brayfields eventually traveled to Michigan to a specialist who collaborated with Jimmy Everest Center doctors and performed an extremely risky operation.

Xander shows how the incision wraps around from his ribs to his shoulder blades.

He explained, "She went through my ribs, and took out the tumor somehow."

This tricky surgery was successful but is just the start of a checklist of needed medical procedures.

Dr. Beg explained, "He has to go through a transplant, stem-cell transplant, radiation, then maintenance."

All this difficult news has been balanced by incredible support from his medical team, his school, and the community.

Xander says he stays on track mentally by "just staying strong and knowing you're going to get back to your normal stuff if you just keep on going."

He added, "I love playing soccer, so as soon as I'm ready for it I'm going to get on the field and practice, get a physical trainer and get back in shape."

Xander is always ready with a smile, ready to reclaim his old life.

If you would like to help kids like Xander fight cancer, consider donating to JECFriends.org.

Kids with Courage is sponsored by Friends of the Jimmy Everest Center.

35.222567-97.439478

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Teen ready to get back on the field after risky tumor surgery - KFOR Oklahoma City

Breaking News: Cardiol Therapeutics Announces Clinical Steering Committee for Phase 2 International Trial in Acute Myocarditis Using CardiolRx(TM) 100…

Cardiol Therapeutics Inc. (TSX: CRDL) (OTCQX: CRTPF), a leader in the production of pharmaceutical cannabidiol (CBD) products and in the development of innovative cannabidiol medicines for heart disease, is pleased to announce the formation of the Clinical Steering Committee (CSC) for a Phase 2 international trial in acute myocarditis using the Companys CardiolRx100 cannabidiol formulation.

The CSC, which comprises key opinion leaders in acute myocarditis from North America and Europe, recently met during the American Heart Associations Scientific Sessions in Philadelphia held November 16th to 18th. The role of the CSC is to advise on the trial design, provide overall supervision of the trial, and ensure that it is being conducted in accordance with the principles of Good Clinical Practice. The CSC has oversight of the protocol, any protocol amendments, and provides advice to the investigators on all aspects of the trial.

Acute myocarditis is characterized by inflammation of the heart muscle (myocardium). The most common cause is viral infection of the heart tissue which is initially responsible for the inflammation. In a significant number of cases, perhaps due to an autoimmune process, the inflammation persists with ongoing myocardial damage and depressed heart function. Although the symptoms are often mild, myocarditis remains an important cause of acute and fulminant heart failure and is the most common cause of sudden cardiac death in people less than 35 years old. In addition, some patients proceed to develop chronic dilated cardiomyopathy which continues to be the leading indication for cardiac transplantation. Symptoms include chest pain, fatigue, shortness of breath, and arrhythmias. Because of the progressive damage to heart cells, heart failure develops (defined as the inability of the heart to pump sufficient blood to meet the needs of the body). The study will use left ventricular ejection fraction (LVEF) as one measure of heart function.

CardiolRx100 is Cardiol Therapeutics pure pharmaceutically (cGMP) produced high concentration cannabidiol formulation that is THC free (<10ppm). Based on the large body of experimental evidence of the anti-inflammatory and cardioprotective properties of cannabidiol in models of cardiovascular disease, Cardiol believes there is an opportunity to develop a potential breakthrough therapy for acute myocarditis that would be eligible for designation as an orphan drug. In the United States, an orphan drug designation is granted for pharmaceuticals being developed to treat medical conditions affecting fewer than 200,000 people. These conditions are referred to as orphan diseases. In the U.S. and the European Union, orphan drugs are eligible for accelerated marketing approvals and companies developing orphan drugs typically receive other incentives, including a prolonged period of market exclusivity that can extend over seven years, during which the drug developer has sole rights to market the drug.

Cardiol has assembled eight highly distinguished thought leaders in cardiology from North America and Europe to oversee and guide our acute myocarditis trial that is being planned at world leading heart institutes, including the Cleveland Clinic, the Mayo Clinic, the Houston Methodist DeBakey Heart and Vascular Center, the University of Ottawa Heart Institute, and Charit University Medicine Berlin, stated David Elsley, President and CEO of Cardiol Therapeutics. The U.S. orphan drug program was successfully utilized to accelerate the first FDA approval of cannabidiol for the treatment of two pediatric epilepsy orphan diseases. We see a similar opportunity with our international trial in acute myocarditis to fast track the development of our CardiolRx formulation for a serious cardiovascular orphan disease for which there is currently no accepted standard of care.

Members of Cardiols Acute Myocarditis CSC include:

Dennis M. McNamara, MD (Chair)

Dr. Dennis McNamara is a Professor of Medicine at the University of Pittsburgh. He is also the Director of the Heart Failure/Transplantation Program at the University of Pittsburgh Medical Center. Dr. McNamara received his undergraduate/graduate education at Yale University, New Haven, Connecticut, and Harvard Medical School, Boston, Massachusetts, respectively. He completed his internship, residency, and cardiology fellowship at Massachusetts General Hospital in Boston. McNamaras current research interests include etiology and pathogenesis of dilated cardiomyopathies; inflammatory syndromes of cardiovascular disease; myocardial recovery in recent onset non-ischemic primary cardiomyopathy; etiology and management of peripartum cardiomyopathy; and genetic modulation of outcomes in cardiovascular disease.

Leslie T. Cooper, Jr., MD (Co-Chair)

Dr. Leslie T. Cooper, Jr., is a general cardiologist and the chair of the Mayo Clinic Enterprise Department of Cardiovascular Medicine, as well as chair of the Department of Cardiovascular Medicine at the Mayo Clinic in Florida. Dr. Coopers clinical interests and research focus on clinical and translational studies of rare and undiagnosed cardiomyopathies, myocarditis, and inflammatory cardiac and vascular diseases, such as giant cell myocarditis, cardiac sarcoidosis, eosinophilic myocarditis, and Takayasus arteritis. He has published over 130 original peer-reviewed papers, as well as contributing to and editing books on myocarditis. In addition to his clinical and research work, Dr. Cooper is a fellow of the American College of Cardiology, the American Heart Association, the European Society of Cardiology Heart Failure Association, the International Society for Heart and Lung Transplantation, and the Society for Vascular Medicine and Biology. He is also the founder and former president of the Myocarditis Foundation and continues to serve on its Board of Directors.

Arvind Bhimaraj, MD

Dr. Arvind Bhimaraj is a specialist in Heart Failure and Transplantation Cardiology and is Assistant Professor of Cardiology, Institute for Academic Medicine, at Houston Methodist and at Weill Cornell Medical College, NYC. He has been Co-Director of the Heart Failure Research Laboratory at Houston Methodist since 2016. His area of focus is anti-fibrotic mechanisms and how to promote recovery of a damaged heart. Dr. Bhimaraj was a Heart Failure Fellow at the Cleveland Clinic from July 2010 to September 2011. Dr. Bhimaraj also specializes in Interventional Cardiology, is board certified in Cardiovascular Disease, and the author of numerous cardiovascular publications.

Matthias Friedrich, MD

Dr. Matthias Friedrich is Full Professor with the Departments of Medicine and Diagnostic Radiology at the McGill University in Montreal and Chief, Cardiovascular Imaging at the McGill University Health Centre. He is also Professor of Medicine at Heidelberg University in Germany. Dr. Friedrich earned his MD at the Friedrich-Alexander-University Erlangen-Nrnberg, Germany. He completed his training as an internist and cardiologist at the Charit University Medicine Center, Humboldt University in Berlin. Dr. Friedrich founded one of the first large Cardiovascular Magnetic Resonance centres in Germany at the Charit University Hospital in Berlin. After his move to Canada, from 2004 to 2011, he was Director of the Stephenson Cardiovascular MR Centre at the Libin Cardiovascular Institute of Alberta and Professor of Medicine within the Departments of Cardiac Sciences and Radiology at the University of Calgary, Canada. From 2011 to 2015, he directed the Philippa and Marvin Carsley Cardiovascular MR Centre at the Montreal Heart Institute and was Michel and Renata Hornstein Chair in Cardiac Imaging at the Universit de Montral.

Peter Liu, MD

Dr. Peter Liu is the Chief Scientific Officer and Vice President, Research, of the University of Ottawa Heart Institute, and Professor of Medicine and Physiology at the University of Toronto and University of Ottawa. He was the former Scientific Director of the Institute of Circulatory and Respiratory Health at the Canadian Institutes of Health Research, the major federal funding agency for health research in Canada. Prior to that role, he was the inaugural Director of the Heart & Stroke/Lewar Centre of Excellence in Cardiovascular Research at University of Toronto. Dr. Liu received his MD from the University of Toronto, and postgraduate training at Harvard University. His laboratory investigates the causes and treatments of heart failure, the role of inflammation, and the identification of novel biomarkers and interventions in cardiovascular disease. Dr. Liu has published over 300 peer-reviewed articles in high impact journals and received numerous awards in recognition of his research and scientific accomplishments.

Wai Hong Wilson Tang, MD

Dr. Wai Hong Wilson Tang is the Advanced Heart Failure and Transplant Cardiology specialist at the Cleveland Clinic in Cleveland, Ohio. Dr. Tang is also the Director of the Cleveland Clinics Center for Clinical Genomics; Research Director, and staff cardiologist in the Section of Heart Failure and Cardiac Transplantation Medicine in the Sydell and Arnold Miller Family Heart & Vascular Institute at the Cleveland Clinic. He attended and graduated from Harvard Medical School in 1996, having over 23 years of diverse experience, especially in Advanced Heart Failure and Transplant Cardiology. Dr. Tang is affiliated with many hospitals including the Cleveland Clinic and cooperates with other doctors and physicians in medical groups including The Cleveland Clinic Foundation.

Barry Trachtenberg, MD

Dr. Barry H. Trachtenberg is a cardiologist specializing in heart failure and cardiac transplantation. He is also the director of the Michael DeBakey Cardiology Associates Cardio-Oncology program, an evolving field devoted to prevention and management of cardiovascular complications of cancer therapies such as chemotherapy and radiation. His clinical experience includes heart failure and heart transplantation, mechanical support pumps, and cardio-oncology. He has contributed to multiple publications related to advanced heart failure, cardiac transplantation, regenerative therapies, and ventricular assist devices. Dr. Trachtenberg is a member of the American Heart Association, the International Society for Heart and Lung Transplantation, the Heart Failure Society of America, and the International CardiOncology Society of North America.

Carsten Tschpe, MD

Dr. Carsten Tschpe is Professor of Medicine and Cardiology and Vice Director of the Department of Internal Medicine and Cardiology, Charit University Medicine Berlin. He received his doctorate in medicine in 1993 and has over 140 peer-reviewed publications, including overview and book articles, and 120 international original articles. His research interests include inflammatory cardiomyopathy, diabetic cardiopathy, and ischemic cardiopathy. He also includes diastolic dysfunction, endothelial dysfunction, peptide systems, and experimental and clinical studies in cardiology and stem cells in his research studies. For his outstanding research work, Dr. Tschpe was awarded the prestigious Arthur Weber Prize by the German Cardiac Society Cardiovascular Research.

About Cardiol Therapeutics

Cardiol Therapeutics Inc. (TSX: CRDL)(OTCQX: CRTPF) is focused on producing pharmaceutical cannabidiol (CBD) products and developing innovative therapies for heart disease, including acute myocarditis and other causes of heart failure. The Companys lead product, CardiolRx, is designed to be one of the safest and most consistent CBD formulations on the market. CardiolRx is pharmaceutically produced, cGMP certified, and is THC free. The Company plans to commercialize CardiolRx in the billion-dollar market for medicinal cannabinoids in Canada and is also pursuing distribution opportunities in Europe and Latin America.

In heart failure, Cardiol is planning an international clinical study of CardiolRx in acute myocarditis, a condition caused by inflammation in heart tissue, which remains the most common cause of sudden cardiac death in people less than 35 years of age. The Company is also developing proprietary nanotechnology to uniquely deliver pharmaceutical CBD and other anti-inflammatory drugs directly to sites of inflammation in the heart that are associated with heart failure. Heart failure is the leading cause of death and hospitalization in North America with associated healthcare costs in the U.S. alone exceeding $30 billion. For further information about Cardiol Therapeutics, please visitwww.cardiolrx.com.

Original post:
Breaking News: Cardiol Therapeutics Announces Clinical Steering Committee for Phase 2 International Trial in Acute Myocarditis Using CardiolRx(TM) 100...

Redruth woman travels over 3,500 miles to meet the stranger who saved her life – Cornwall Live

Ashop assistantfrom Redruthisappealing for people to become bone marrow donors after meeting the stranger who saved her life.

Carol Timmins was diagnosed with aplastic anaemia in January 2014.

The 58-year-old said: "Being told that I had bone marrow failure came as a great shock. I had no idea what it actually meant but soon realised that I was very, very sick.

"Id previously been diagnosed with Chronic Fatigue Syndrome, so feeling tired and lacking energy had been a way of life for several years. The initial treatment that I received was regular blood transfusions until May when I started an Antilymphocyte Globulin treatment.

"By September it was apparent that the treatment was not working and a bone marrow transplant was my best chance of survival."

Carolhad a bone marrow transplant inDecember 2014from a stranger. Patients and donors must remain anonymous for two years after a transplant takes place.

After this period has passed, if both the patient and donor would like to meet, they can contact blood cancer charity Anthony Nolan, who are then able to put them in contact with each other.

In September 2019, Carol and her husband Paul, travelled from Cornwall to Detroit, USA, to meet her lifesaver.

She added: "Ninety days after my transplant I had decided that it was time to thank my donor so I sent an anonymous letter through Anthony Nolan. Within a few weeks I received a reply. We were both overjoyed at receiving such an important piece of mail and he was very pleased that I was making a good recovery."

From that moment she set her sights on thanking her donor in person.

"I knew that it would be a few years before I could travel but I made it my goal. I had to thank the man who had saved my life," Carol said.

As time passed by, the medication reduced and their correspondence increased. There was a turning point in her life when she was told that she had the option to release her personal information, and to request her donors details.

Carol continued: "I decided not to rush into it, as I needed time to comprehend exactly what that would mean. I had come so far, and to be able to correspond with my donor directly would be quite surreal."

Through letter writing, they contemplated at how their paths had crossed and shared stories about their families. In May 2018 she exchanged personal details with her donor.

She said: "It was a truly amazing day learning the name of the man I had written to for four years - Darin."

Through emails they exchanged family photos and started to make plans for her trip. Their friendship blossomed and finally, in September 2019 they met for the first time.

"The welcome that I received at the airport was something that only dreams are made of. After hugs and tears of joy with Darin and his wife Valerie, I was introduced to a local news channel who were delighted to witness and report on such an emotional and inspiring story," added Carol.

Carol and Paul stayed at Darin and Valeries home in Detroit for eight days. During that time they shared their experiences as a donor and recipient, reminiscing about a very surreal time in their lives.

Carol added: "Darin said that if he was asked to donate again he would do it in a heartbeat.

"I consider myself truly blessed to have found a donor who was a perfect match, but to have the opportunity to thank the man who gave me his bone marrow has meant the world to me.

"Please dont wait until it happens to you or yours, people are dying waiting for their perfect match and you can help them by joining the register. Without Darin I probably wouldnt be here today, so if youre a healthy 16-30 year old (or you know someone who is), Anthony Nolan needs you.

"My heartfelt thanks go to Anthony Nolan and to all of the potential donors on the register, as well as the wonderful team of doctors and nurses who treated me."

Anthony Nolan is the charity that finds matching donors for people with blood cancer and gives them a second chance of life.

It also carries out ground-breaking research to save more lives and provide information and support to patients after a stem cell transplant, through its clinical nurse specialists and psychologists, who help guide patients through their recovery.

Henny Braund, chief executive of Anthony Nolan said "Its fantastic to see Carol,living her life to the fullest andDarinshould be incredibly proud of the difference he has made to Carol and her family.

"Our amazing stem cell donors are lifesavers and they continue to give patients with blood cancer a second chance of life. Anyone wanting to find out more can visit our website to join the stem cell register or support our work by making a donation, which will help give someone likeCarola second chance of life in the future. Without you there is no cure."

For more information, visit the Anthony Nolan website here.

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Redruth woman travels over 3,500 miles to meet the stranger who saved her life - Cornwall Live