Tag Archives: innovation

$2.4 Million in Funding Awarded to Chemistry and Biochemistry Faculty | CSUF News – CSUF News

In 2023, eight faculty members in the Department of Chemistry and Biochemistry received more than $2.4 million in external funding to support research with Cal State Fullerton students.

National Science Foundation:

U.S. Department of Energy:

National Institutes of Health:

U.S. Department of Defense:

American Chemical Society:

Social Science Research Council:

Scott-Jewett Fund for Innovation and Student Success

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$2.4 Million in Funding Awarded to Chemistry and Biochemistry Faculty | CSUF News - CSUF News

Rare disorder causing extra fingers and toes identified – EurekAlert

image:

The foot of one of the children in the study, showing an extra toe

Credit: University of Leeds

A rare disorder which causes babies to be born with extra fingers and toes and a range of birth defects has been identified in new research co-led by the University of Leeds.

The disorder, which has not yet been named, is caused by a genetic mutation in a gene called MAX. As well as extra digits polydactyly - it leads to a range of symptoms relating to ongoing brain growth, such as autism.

The research marks the first time this genetic link has been identified. It has also found a molecule that could potentially be used to treat some of the neurological symptoms and prevent any worsening of their condition. However, more research is needed to test this molecule before it can be used as a treatment.

Published in the American Journal of Human Genetics, the paper focuses on three individuals with a rare combination of physical traits, namely polydactyly, and a much larger than average head circumference known as macrocephaly.

The individuals share some other characteristics, including delayed development of their eyes which results in problems with their vision early in life.

The researchers compared the DNA of these individuals and found they all carried the shared genetic mutation causing their birth defects.

The latest research was co-led by Dr James Poulter from the University of Leeds; Dr Pierre Lavigne at Universit de Sherbrooke in Qubec and Professor Helen Firth at Cambridge University.

Dr Poulter, UKRI Future Leaders Fellow and University Academic Fellow in Molecular Neuroscience, said: Currently there are no treatments for these patients. This means that our research into rare conditions is not only important to help us understand them better, but also to identify potential ways to treat them.

In this case, we found a drug that is already in clinical trials for another disorder meaning we could fast track this for these patients if our research finds the drug reverses some of the effects of the mutation.

It also means that other patients with a similar combination of features can be tested to see if they have the same variant we have identified in our study.

The study team has highlighted the importance of interdisciplinary research into rare diseases in giving understanding and hope of a treatment to families who often face many years of uncertainty about their childs condition and prognosis.

Dr Poulter added: These are often under-represented conditions that have a huge impact on patients and their families. These families go through a long and complex diagnostic odyssey. The time from their first doctors visit as babies to getting a diagnosis can take more than 10 years.

It is important that these patients and their families discover the cause of their condition and if they can access a therapy based on their genetic diagnosis, that could be life changing.

Dr Lavigne said: Finding out the impact of the mutation on the function of MAX is the first step towards the development of a treatment for these children.

The researchers now plan to look for additional patients with mutations in MAX to better understand the disorder and investigate whether the potential treatment improves the symptoms caused by the mutation.

The research was carried out in collaboration with the Leeds Teaching Hospitals Trust, the NHS Wales All Wales Medical Genomics Service and Radboud University Medical Center, The Netherlands.

It used data from the Deciphering Developmental Disorders study, which was led by the Wellcome Sanger Institute.

Professor Firth said: The DDD study recruited across the UK from 2011-2015. Its exciting that in 2024, were still making new discoveries. This new finding is a diagnosis for our DDD patients. Furthermore, this publication will now enable other children worldwide to be diagnosed with this novel disorder.

Further information

A recurrent de novo MAX p.Arg60Gln variant causes a syndromic overgrowth disorder through differential expression of c-Myc target genes is published in American Journal of Human Genetics.

Email University of Leeds press officer Lauren Ballinger on l.ballinger@leeds.ac.uk with media enquiries.

This work was funded by a UK Research & Innovation Future Leaders Fellowship to James Poulter and a Canadian Institutes of Health Research project grant (PL). The genetic sequencing was undertaken as part of the DDD (Deciphering Developmental Disorders) study which presents independent research commissioned by the Health Innovation Challenge Fund [grant number HICF-1009-003]. This study makes use of DECIPHER , which is funded by the Wellcome Trust and hosted by EMBL-EBI [grant number WT223718/Z/21/Z].

University of Leeds

The University of Leeds is one of the largest higher education institutions in the UK, with more than 38,000 students from more than 150 different countries. We are renowned globally for the quality of our teaching and research.

We are a values-driven university, and we harness our expertise in research and education to help shape a better future for humanity, working through collaboration to tackle inequalities, achieve societal impact and drive change.

The University is a member of the Russell Group of research-intensive universities, and plays a significant role in the Turing, Rosalind Franklin and Royce Institutes. http://www.leeds.ac.uk

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American Journal of Human Genetics

A recurrent de novo MAX p.Arg60Gln variant causes a syndromic overgrowth disorder through differential expression of c-Myc target genes

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EU funding for pioneering research on the treatment of gliomas – EurekAlert

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Dr. Anne Rgnier-Vigouroux, coordinator of the GlioLighT project funded by the EU

Credit: : Anne Rgnier-Vigouroux

Gliomas are the most common type of brain tumors and are difficult to treat because they tend to be diffuse and are often located deep within the brain. A very promising and innovative technique for the therapy of gliomas will be investigated in a new EU project and should pave the way for clinical use. "We are convinced that our research will help to significantly improve the treatment of gliomas," said the coordinator of the project, Dr. Anne Rgnier-Vigouroux of Johannes Gutenberg University Mainz (JGU). The other project partners are Aston University in Birmingham, the University of Barcelona, LMU Munich, the Finnish laser manufacturer Modulight, and MODUS Research and Innovation Ltd., a British not-for-profit organization providing advice to secure research funding. Through its Pathfinder program, the European Innovation Council (EIC) supports the exploration of highly innovative and speculative new technologies at the very earliest phase of their development. The new GlioLighT project will receive funding of approximately EUR 2.2 million over the next three years.

Using extremely toxic singlet oxygen to combat gliomas

Gliomas are an extremely deadly form of cancer, mainly due to the inaccessibility of the brain and the widespread dissemination of the tumor cells. These diffuse cells are often anchored too deeply in the brain to be removed completely using current therapeutic techniques, such as resection, irradiation, or chemotherapy. A promising alternative to eliminate glioma cells is to generate reactive oxygen species (ROS) directly at the affected sites. Currently, ROS can only be produced through photodynamic therapy, which has been employed for decades but involves potentially toxic photosensitizers. To avoid detrimental side effects of this type of treatment, the GlioLighT partners propose a different approach involving direct light therapy. This method will entail the direct generation of ROS using laser light at a wavelength of 1,267 nanometers, which is in the near-infrared range. The irradiation of light will produce singlet oxygen, which destroys cancer cells.

"Assuming we can reach the tumor cells directly with laser light, we will no longer need photosensitizers as amplifiers. We will have a minimally invasive and selective procedure, representing a completely new strategy for glioma treatment," said Dr. Anne Rgnier-Vigouroux. The benefits of this approach include improved efficacy of treatment, earlier intervention, and reduced costs. Currently, the precise cancer-inhibiting mechanism of direct light therapy and the safety of the procedure itself are not well understood.

Janus-headed macrophages: Anti-inflammatory potential promotes tumor growth

The laser radiation will also affect the cells of the immune system which are expected to fight tumor cells. "We will be paying special attention to the effects on tumor cells but also on immune cells, particularly the macrophages," emphasized Rgnier-Vigouroux. Macrophages are scavenger cells that take up pathogens and render them harmless. They can trigger inflammatory reactions and thus contribute to the bodys immune response and the fight against tumor cells. However, they can also have anti-inflammatory activities and thus prevent other immune cells from attacking the tumor.

"Macrophages can kill tumor cells, but they can also be recruited and manipulated by them, resulting in tumor growth." It is this second possibility that Dr. Anne Rgnier-Vigouroux aims to prevent: "We need to eliminate the tumor cells and, at the same time, trigger the immune cells in their vicinity to exert toxic effects on them."

Other aspects that the GlioLighT researchers will investigate include the type of tumor cell death induced by the laser light, the effect of laser light exposure on healthy cells in the brain, such as the neurons, and the determination of a safe dosage that can be administered without harming healthy cells. The project partners will work on innovative ultrashort pulse lasers to optimize the optical penetration through tissue and to minimize potential risks, ensuring that direct light therapy is suitable for clinical application. Ultimately, the development of a preclinical GlioLighT delivery and sensing system (pcGlio-DSS) should improve glioma treatment.

EIC Pathfinder program provides support for visionary and high-risk technologies in their early stages of development

The GlioLighT Next Generation Glioma Treatments using Direct Light Therapy project is being financed through the future-oriented EIC Pathfinder program under the aegis of the European Union's Horizon Europe program. The EU will provide a total of EUR 2.2 million in financial support to the project, of which approximately EUR 770,000 is earmarked for the research to be undertaken at Johannes Gutenberg University Mainz. The purpose of the EIC Pathfinder Open program of the European Innovation Council is to identify radically new technologies that have the potential to create new markets. Grants are thus awarded to groundbreaking and highly speculative projects that are still in an early stage of development. The participants in a project that has been awarded EIC Pathfinder support are typically visionary and entrepreneurial-minded specialists and researchers at universities, research institutes, start-ups, high-tech SMEs, and individuals working in the industrial realm who have a particular interest in investigating and creating technological innovations.

Project coordinator Dr. Anne Rgnier-Vigouroux has been research group leader at JGU's Institute of Developmental Biology and Neurobiology since January 2013. Her group focuses on the study of cerebral anti-tumor immunity, particularly on the role of microglia and macrophages in brain tumor biology.

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Tackling the Poor Sleep Pandemic: FRENZ Brainband by Earable Neuroscience Announces Global Sales After CES … – PR Newswire

FRENZ Brainband, a pioneering AI-powered sleep wearable initially introduced as a prototype at CES 2023, is now available for global delivery, heralding a new era in sleep tech and digital therapeutics for home use. FRENZ was early funded by Founders Fund and Samsung Ventures.

BOULDER, Colo., Jan. 14, 2024 /PRNewswire/ -- Following its CES Innovation Award for Aging Technology, Earable Neuroscience announced the global sales of FRENZ Brainband, a groundbreaking AI-powered sleep tech wearable designed to help people sleep better. FRENZ Brainband, paired with the complimentary FRENZ AI Sleep Science app, has been clinically proven to help people fall asleep 24 minutes faster on average, as published on Nature Scientific Report. FRENZ is now ready for shipping globally from frenzband.com. The product is currently trending in the Fitness & Activity Monitors category on Amazon.

FRENZ Brainband represents a significant advancement in sleep technology, offering precise tracking and real-time brain activity stimulation using non-invasive audio therapy. Its unique comfortable design includes bone-conduction speakers and sophisticated AI algorithms to promote quicker sleep onset and longer deep sleep periods. This year, Earable showcased this revolutionary product at CES Eureka Park and was among the finalists for the CTA Foundation Pitch.

Prof. Tam Vu, Founder and CEO of Earable Neuroscience and former professor at the University of Colorado and the University of Oxford, passionately presented the Brainband at CES. "FRENZ is a comprehensive, comfortable, all-in-one sleep wearable that provides real-time, direct stimulation with precise data to effectively address sleep issues. FRENZ's science-backed audio therapies are especially beneficial for individuals who struggle to fall asleep or return to sleep after waking up at night, particularly those suffering from stress, anxiety, and running thoughts," said Vu. He highlighted the Brainband's proven efficacy in large-scale trials, with an 89% precision rate compared to the gold standard Polysomnography (PSG), and its significant impact on reducing sleep onset time.

Vu further shared, "As the CES Innovation Honoree for Aging Tech, we have received numerous accolades and interest from forward-thinking healthcare providers in the States this year. With mass production at Foxconn underway, we are poised to scale up the sleep tech market significantly. We are actively seeking strategic B2B partnerships and investments for market expansion in the healthcare and digital therapeutics space."

The Brainband is designed for a broad user base, from wellness enthusiasts to the elderly with chronic sleep issues, to those with mild sleep difficulties. It retails as a wellness device with an MSRP of $490, which includes lifetime access to the standard Fast Sleep and Back to Sleep CBT-i library. Premium content and features are anticipated for future release.

To order a FRENZ Brainband, visit http://www.frenzband.com

About Earable NeuroscienceEarable Neuroscience is a US deep tech company dedicated to delivering scalable and human-centric solutions. The FRENZ Brainband by Earable is the world's first sleep tech wearable capable of tracking and stimulating brain activities through audio therapy to promote better sleep quality.

Media Contact: [emailprotected]

Kimi Doan [emailprotected] +16178555995

SOURCE Earable Neuroscience

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Novel Genetic Priority Score Unveiled to Enhance Target Prioritization in Drug Development – Mount Sinai

Driven by the need for a better way to prioritize targets for drug development, the Icahn School of Medicine at Mount Sinai has led the development of a novel genetic priority score (GPS) that will integrate various types of human genetic data into a single easy-to-interpret score.

The findings were described in the January 3 online issue of Nature Genetics [DOI: 10.1038/s41588-023-01609-2].

Studies have shown that drugs have an increased likelihood of success in clinical trials when the genes they target have been demonstrated to have genetic support. The new tool integrates multiple lines of genetic evidence to prioritize these drug targets.

The score measures the general ability of a gene to be targeted by drugs; genes with a high score in the new tool are more likely to succeed as a drug target. The score identifies both known drug gene targets as well as potential novel therapeutic targets.

We built a genetic priority score that was inspired by the realization that diverse human genetic data provides insights into drug targets, yet there was an absence of a cohesive strategy for integrating these various data types into an easily interpretable score. So we developed a computational score to prioritize drug targets for enhanced drug discovery," says Ron Do, PhD, senior study author and the Charles Bronfman Professor in Personalized Medicine at Icahn Mount Sinai. Remarkably, several genes with high GPS were already known to be targeted by approved drugs, providing validation for the new tool.

The GPS, with its potential to streamline target prioritization, is positioned to have a significant impact on drug development. It offers a valuable resource for researchers seeking to optimize the selection of drug gene targets for enhanced efficiency in the drug development process, say the investigators.

The rising cost of developing therapeutics, in the billions, is primarily due to high clinical trial failures, underscoring inefficiencies in drug development pipelines. Improving early-stage target prioritization is critical. Studies consistently show that drug indications with human genetic support are more likely to succeed in trials and gain approval, says study first author Aine Duffy, a PhD candidate in the lab of Dr. Do.

The researchers are encouraged by the developments but emphasize this represents only a first step for prioritization and the need for careful follow-up and further investigation of gene targets with high scores. Next, the investigators plan to refine the model by incorporating additional genetic features and evaluating more sophisticated algorithms for constructing the GPS.

The paper is titled Development of a human genetics-guided priority score for 19,365 genes and 399 drug indications. Please see [DOI:10.1038/s41588-023-01609-2] to view competing interests.

The remainingauthors, all with Icahn Mount Sinai except where indicated, are Ben Omega Petrazzini (Associate Bioinformatician); David Stein (PhD candidate); Joshua K. Park (MD/PhD candidate); Iain S. Forrest, PhD (and MD candidate); Kyle Gibson (MD candidate); Ha My Vy, PhD; Robert Chen Park (MD/PhD candidate); Carla Marquez-Luna, PhD; Matthew Mort, PhD (Cardiff University, UK); Marie Verbanck, PhD (Universite Paris Cite and Icahn Mount Sinai); Avner Schlessinger, PhD; Yuval Itan, PhD; David N. Cooper, PhD (Cardiff University, UK), Ghislain Rocheleau, PhD; and Daniel M. Jordan, PhD.

The study was funded by the following: the NIH T32 Postdoctoral Research Award (5T32HL00782424); the National Institute of General Medical Sciences of the NIH (R35-GM124836); the National Heart, Lung and Blood Institute of the NIH (R01-HL139865) and (R01-HL155915); the French National Research Agency (ANR) (ANR-21-CE45-0023-01); the Leducq Foundation (21CVD01); The Charles Bronfman Institute for Personalized Medicine, Icahn School of Medicine at Mount Sinai; and the Helmsley Foundation Award (2209-05535).

About the Icahn School of Medicine at Mount Sinai

The Icahn School of Medicine at Mount Sinai is internationally renowned for its outstanding research, educational, and clinical care programs. It is the sole academic partner for the eight- member hospitals* of the Mount Sinai Health System, one of the largest academic health systems in the United States, providing care to a large and diverse patient population.

Ranked 14th nationwide in National Institutes of Health (NIH) funding and among the 99th percentile in research dollars per investigator according to the Association of American Medical Colleges, Icahn Mount Sinai has a talented, productive, and successful faculty.More than 3,000 full-time scientists, educators, and clinicians work within and across 44 academic departments and 36 multidisciplinary institutes, a structure that facilitates tremendous collaboration and synergy.Our emphasis on translational research and therapeutics is evident in such diverse areas as genomics/big data, virology, neuroscience, cardiology, geriatrics, as well as gastrointestinal and liver diseases.

Icahn Mount Sinai offers highly competitive MD, PhD, and Masters degree programs, with current enrollment of approximately 1,300 students.It has the largest graduate medical education program in the country, with more than 2,000 clinical residents and fellows training throughout the Health System.In addition, more than 550 postdoctoral research fellows are in training within the Health System.

A culture of innovation and discovery permeates every Icahn Mount Sinai program.Mount Sinais technology transfer office, one of the largest in the country, partners with faculty and trainees to pursue optimal commercialization of intellectual property to ensure that Mount Sinai discoveries and innovations translate into healthcare products and services that benefit the public.

Icahn Mount Sinais commitment to breakthrough science and clinical care is enhanced by academic affiliations that supplement and complement the Schools programs.

Through the Mount Sinai Innovation Partners (MSIP), the Health System facilitates the real-world application and commercialization of medical breakthroughs made at Mount Sinai. Additionally, MSIP develops research partnerships with industry leaders such as Merck & Co., AstraZeneca, Novo Nordisk, and others.

The Icahn School of Medicine at Mount Sinai is located in New York City on the border between the Upper East Side and East Harlem, and classroom teaching takes place on a campus facing Central Park. Icahn Mount Sinais location offers many opportunities to interact with and care for diverse communities.Learning extends well beyond the borders of our physical campus, to the eight hospitals of the Mount Sinai Health System, our academic affiliates, and globally.

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*Mount Sinai Health System member hospitals: The Mount Sinai Hospital; Mount Sinai Beth Israel; Mount Sinai Brooklyn; Mount Sinai Morningside; Mount Sinai Queens; Mount Sinai South Nassau; Mount Sinai West; and New York Eye and Ear Infirmary of Mount Sinai.

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Novel Genetic Priority Score Unveiled to Enhance Target Prioritization in Drug Development - Mount Sinai

Colchicine Not the Answer for Recurring Arrhythmias After Ablation – Medpage Today

For patients undergoing catheter ablation for atrial fibrillation (Afib), there was no signal that a brief course of colchicine reduced atrial arrhythmia recurrence or improved clinical outcomes when taken for 10 days starting right before the procedure, a small pilot trial found.

By 14-day Holter monitoring, colchicine did not prevent atrial arrhythmia recurrence immediately after ablation (31% vs 32% with placebo; HR 0.98, 95% CI 0.59-1.61), nor at 3 months (14% vs 15%; HR 0.95, 95% CI 0.45-2.02), reported Alexander Benz, MD, MSc, of the Population Health Research Institute at McMaster University in Hamilton, Ontario, and colleagues.

The anti-inflammatory drug also did not reduce the composite of emergency department visits, cardiovascular hospitalizations, cardioversions, or repeat ablations during a median follow-up of 1.3 years (29 vs 25 per 100 patient-years; HR 1.18, 95% CI 0.69-1.99).

Yet IMPROVE-PVI was "not sufficiently powered to definitively exclude a clinically significant benefit with colchicine," Benz and team cautioned in their report published in Circulation: Arrhythmia and Electrophysiology.

They highlighted the finding that the incidence of post-ablation chest pain suggestive of pericarditis was reduced with colchicine (4% vs 15%; HR 0.26, 95% CI 0.09-0.77).

"This reduction was observed within days following catheter ablation, suggesting anti-inflammatory effects of short-term treatment with colchicine. This finding is in line with evidence on the efficacy of colchicine in the prevention and treatment of pericarditis and postpericardiotomy syndrome following cardiac surgery," Benz and colleagues wrote.

"Although our definition of pericarditis differed from more stringent definitions, the observed beneficial effect of colchicine on post-ablation chest pain in this placebo-controlled, double-blind trial was clinically meaningful," they argued.

Colchicine is a widely prescribed anti-inflammatory agent that is known to have cardiovascular prevention benefits.

Given that the success of catheter ablation via pulmonary vein isolation is often marred by recurrent atrial arrhythmias, and such arrhythmias are predicted by inflammatory biomarkers, the trialists had hypothesized that colchicine would be of help.

As expected, colchicine therapy resulted in diarrhea as a side effect in IMPROVE-PVI. Yet the incidence of diarrhea was particularly high in this trial (26% vs 7% with placebo; HR 4.74, 95% CI 1.95-11.53) compared with prior observations.

"Possible reasons for the discrepancy in diarrhea incidence between our and other studies include differences in outcome definitions and patient characteristics, as well as potential interaction of colchicine with concomitant medications," the authors suggested.

The present trial had been conducted at a single center and enrolled patients scheduled for catheter ablation. Those with contraindications to colchicine, namely those taking certain medications or those with serious gastrointestinal disease, overt hepatic disease, or severe renal disease were excluded.

Participants were randomized to colchicine 0.6 mg twice daily or placebo for 10 days, starting within 4 hours before ablation.

Recurring atrial arrhythmia was defined as Afib, atrial flutter, or atrial tachycardia >30 seconds on two 14-day Holters performed immediately and at 3 months following ablation.

The study cohort consisted of 199 patients (median age 61 years, 22% women, 70% undergoing their first ablation procedure) who had either received radiofrequency ablation using the Carto 3 system from Biosense Webster (79%) or cryoballoon ablation with Medtronic's Arctic Front system (21%).

Antiarrhythmic drugs were prescribed at discharge for 75% of patients. At 6-month follow-up, the proportion of patients off antiarrhythmic therapy was 62.2% and 57.0% of the colchicine and placebo groups, respectively.

One person died of sepsis in the colchicine group, whereas there were no deaths in the placebo group.

Benz and colleagues acknowledged that on top of the small sample, they did not look for recurrent arrhythmias using implantable loop recorders, likely resulting in an undercounting in both treatment groups.

Since IMPROVE-PVI was conducted, another technology for catheter ablation, pulse field ablation (PFA), was FDA approved. Medtronic's PulseSelect PFA system was approved last week, while rival PFA system Farapulse from Boston Scientific has yet to be given the green light.

Unlike conventional catheter ablation for Afib, PFA avoids thermal damage to the esophagus or phrenic nerve.

Nicole Lou is a reporter for MedPage Today, where she covers cardiology news and other developments in medicine. Follow

Disclosures

The trial was supported by the Hamilton Health Sciences' New Investigator Fund and the Innovation Fund of the Alternative Funding Plan for the Academic Health Sciences Centres of Ontario.

Benz reported a personal research grant from the German Heart Foundation and lecture fees from Bristol Myers Squibb.

Primary Source

Circulation: Arrhythmia and Electrophysiology

Source Reference: Benz AP, et al "Colchicine to prevent atrial fibrillation recurrence after catheter ablation: a randomized, placebo-controlled trial" Circ Arrhythm Electrophysiol 2023; DOI: 10.1161/CIRCEP.123.012387.

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Colchicine Not the Answer for Recurring Arrhythmias After Ablation - Medpage Today

Bugs that help bugs: How environmental microbes boost fruit fly reproduction – EurekAlert

image:

Drosophila oogenesis process

Credit: Osaka university

Osaka, Japan For many of us, when we think of microbiomes, our first thoughts are probably about the beneficial microorganisms that live in our guts. But now, researchers from Japan and US have discovered how the microbes living in fruit flies can enhance their reproduction.

In a recently published study in Communications Biology, the research group has revealed that microbes in the fruit fly microbiome are involved in controlling the germline stem cells that form eggs, as well as subsequent egg maturation, in female fruit flies.

The microbiomethe community of microorganisms that live together in and on a hosthas a huge role in facilitating functions that are necessary for survival. This includes metabolic regulation, intake of nutrients, and reproduction, including improving fertility in conditions of inadequate nutrition. However, the specific molecular mechanisms enabling microbes to control the maturation of the germline (the lineage of cells within an organism that gives rise to eggs and sperms) are still a mystery.

We propose that microbes control various stages of oogenesis, which leads the production of eggs in the ovary, says lead author of the study Ritsuko Suyama. They may do this by modifying hormone levels and their successive pathways and can therefore promote host fertility in conditions of poor nutrition.

The researchers investigated the effects of microbes on oogenesis in fruit flies, Drosophila melanogaster. Using genetic analysis, the team revealed that microbes boost oogenesis by both accelerating the division of ovarian cells and suppressing programmed cell death, as well as increasing the production of germline stem cells (GSC) by enhanced cell division and eventually increasing the number of mature eggs in females.

We discovered that the microbes enhancement of reproductive function was controlled by the activation of the hormonal pathways for ecdysone and juvenile hormones in the germline stem cellsthe cells that develop into eggs, explains Toshie Kai, senior author.

Ecdysone is a steroid hormone that regulates moulting in insects. The researchers found that the ecdysone pathway may be an important mediator for a microbe-induced increase of GSCs and egg maturation. Meanwhile, the juvenile hormone pathway is involved only in GSC proliferation, which indicates that the hormonal pathways are activated during different stages of oogenesis.

Our results show that environmental microbes can improve host reproduction by controlling hormone release and increasing oogenesis in their hosts, says Suyama.

These new discoveries about host-microbe interactions could present new avenues for improvements in reproductive health, for example via new treatments involving probiotics. Specifically, the findings from this study will contribute to the understanding of how microbes boost their hosts reproductive processes, which will open the door for new methods to improve fertility and infertility treatment.

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The article, Microbes control Drosophila germline stem cell increase and egg maturation through hormonal pathways, was published in Communications Biology at DOI:10.1038/s42003-023-05660-x

About Osaka University

Osaka University was founded in 1931 as one of the seven imperial universities of Japan and is now one of Japan's leading comprehensive universities with a broad disciplinary spectrum. This strength is coupled with a singular drive for innovation that extends throughout the scientific process, from fundamental research to the creation of applied technology with positive economic impacts. Its commitment to innovation has been recognized in Japan and around the world, being named Japan's most innovative university in 2015 (Reuters 2015 Top 100) and one of the most innovative institutions in the world in 2017 (Innovative Universities and the Nature Index Innovation 2017). Now, Osaka University is leveraging its role as a Designated National University Corporation selected by the Ministry of Education, Culture, Sports, Science and Technology to contribute to innovation for human welfare, sustainable development of society, and social transformation.

Website: https://resou.osaka-u.ac.jp/en

Communications Biology

Experimental study

Animals

Microbes control Drosophila germline stem cell increase and egg maturation through hormonal pathways

21-Dec-2023

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Pediatric Drugs Market Size Expected to Reach USD 363.86 Billion by 2032 – GlobeNewswire

Ottawa, Dec. 21, 2023 (GLOBE NEWSWIRE) -- The global pediatric drugs market size accounted for USD 129.13 billion in 2023 and grew to USD 144.36 billion in 2024, expanding at a healthy CAGR of 12.2% between 2023 and 2032.

In March 2023, WHO released the first list of priority pediatric antibiotic compositions, enabling more concentrated research and development activities that tackle the specific requirements of infants and children.

Pharmaceutical companies are now working more on making medicines specifically for pediatrics, considering age, weight, and how their bodies develop. This is because children have unique traits that can affect how medicines work for them. The market for these pediatric drugs is growing because more kids are getting sick, and there are better ways to design drugs. But there are challenges, like figuring out the right amount of medicine for different ages and dealing with smaller groups of patients, which can make the drugs more expensive. Organizations like the European Medical Agency (EMA) and the Food and Drug Administration (FDA) are making rules to encourage research and ensure that medicines for children are safe and work well.

The market for pediatric drugs is growing because kids often face health issues like stomach, allergy, and respiratory problems due to their weaker immune systems. This market includes drugs for conditions like breathing disorders, autoimmune diseases, stomach issues, heart-related problems, and others. Medicines can be taken orally, applied on the skin, injected, or through other ways. This market spans North America, Europe, Asia-Pacific, the Middle East, Africa, and Latin America, with specific data for 17 countries.

Download a short version of this report https://www.towardshealthcare.com/personalized-scope/5074

Individuals aged 2 to 12 receive pharmaceutical interventions specifically designed for pediatric use. The approach to pediatric therapy is fundamentally different from that of adults, primarily stemming from the imperative to tailor dosage regimens to the unique requirements of pediatric patients. Additionally, differentiation is imperative because the physiological response of a child to a given drug may diverge significantly from that observed in an adult population. Thus, the distinct nature of pediatric therapy is essential for ensuring optimal efficacy and safety in this specific age group. Furthermore, the market experiences a positive impetus due to the expanding landscape of clinical trials aimed at introducing novel pediatric pharmaceutical products. This multifaceted synergy of elements substantiates the robust growth trajectory observed in the pediatric drugs market.

The following factors propel the pediatric drugs market growth

Innovation in Pediatric Drugs Expands Market Growth

The expansion of the pediatric drugs market is driven by several factors, such as advancements in pediatric research, the broadening range of clinical trials, and increased investment in developing medications personalised for children. This trend creates substantial business prospects for pharmaceutical and biotechnology companies specialising in pediatric drug formulations. For instance, in August 2023,Aurobindo Pharma Ltd announced the release of their HIV triple combination medicine to pediatric patients in around 123 low- and middle-income countries.

Additionally, companies offering contract manufacturing services for pediatric pharmaceuticals stand to benefit. Collaborative research ventures, innovative drug delivery methods, and strategic partnerships with healthcare providers further facilitate market growth. Overall, these developments present promising opportunities for growth in the pediatric drugs market.

You can place an order or ask any questions, please feel free to contact us at sales@towardshealthcare.com

Some of the Recent Pediatric Oncology Drug Approvals by FDA:

Specialised Pharmaceutical Drugs is the Driving Force behind the Growth of the Pediatric Drugs Market

The wider utilization of off-label drugs in the pediatric population underscores the need for specialised pharmaceuticals customised to pediatric drug requirements, fueling innovation and expansion in the pediatric drug market. The expansion of the pediatric drug market is primarily driven by the increasing prevalence of health issues in children, including obesity, diabetes, asthma, and neurological disorders.

This has led to a rising demand for specialised pharmaceuticals personalised to the unique needs of the pediatric population. Recognising children's distinct physiological and developmental characteristics, the pharmaceutical industry increasingly focuses on research and developing drugs specifically designed for them.

The heightened awareness among parents, caregivers, and healthcare practitioners regarding the importance of addressing children's healthcare needs has fueled the demand for pediatric medications. This advocacy has prompted governments and regulatory bodies to introduce incentives, such as market exclusivity and extended patent protection for pediatric drugs, encouraging research in this field. Consequently, these initiatives have attracted pharmaceutical investments and fostered innovation. The surge in pediatric health issues is propelling the growth of the pediatric drug market, underscoring its crucial role in safeguarding and improving the well-being of children globally.

Respiratory Disorders Dominate Pediatric Drugs Market

The pediatric drugs market is anticipated to be predominantly influenced by the respiratory disorder drugs segment, which holds the largest market share. This is primarily attributed to factors such as compromised immunity, heightened pollution levels, and increased exposure to various allergens, leading to chronic respiratory disorders like Chronic Obstructive Pulmonary Disease (COPD). COPD, a significant contributor to the global pediatric healthcare burden, has seen a surge in demand for effective treatments. According to the World Health Organization (2021),COPD ranked as the third leading cause of global mortality in 2019, causing 3.23 million deaths.

The segments growth is driven by the escalating prevalence of rare autoimmune disorders linked to various cancers, genetic disorders, and other autoimmune conditions. The market is further propelled by initiatives to develop drugs for rare diseases, exemplified by the FDA's approval of RUZURGI (amifampridine) tablets from Jacobus Pharmaceutical Company in May 2019. These prescription drugs, though associated with high costs, are contributing to the rapid growth of the global pediatric drugs market.

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Rising Prevalence of Diseases in the Pediatric Population Expands the Pediatric Drugs Market Growth

The variance between the high rate of childhood illness, roughly 60%, and the narrow focus of pharmacological trials, about 12%, highlights the unrealized potential in the pediatric medication market. This disparity, coupled with a greater understanding of the particular healthcare requirements of children, has spurred more focus and funding for pediatric medication research. The growth of the pediatric medication business has also been aided by regulatory incentives, including pediatric exclusivity and an understanding of the moral need to address children's health. As a result, pharmaceutical companies are working harder on research and development projects to close this gap and satisfy the unique therapeutic needs of the diseases. They are mostly prevalent with childhood cancer in North America.

According to the Nationwide Childrens Hospitals May 2023 estimates,in the U.S., around 90% of 17,000 paediatrics are diagnosed with cancer every year. 1,000+ Medical research grants at 150 institutions, 240+ Ongoing clinical trials funded each year. The increasing incidence of chronic disorders, encompassing conditions such as anorexia, asthma, congenital disabilities, growth deficiencies, diabetes, childhood cancer, juvenile diabetes, and attention deficit hyperactivity, is projected to positively impact the growth trajectory of the market. This surge in chronic disorders is a primary factor contributing to heightened demand for pediatric drugs, consequently influencing the market dynamics throughout the forecast period from 2022 to 2032.

Obesity is one of the most prevalent conditions among children. For instance, according to data from the 2020-2021 National Survey of Children's Health (NSCH),17% of children aged 10 to 17 in the United States are obese. Obesity is a major problem that leads to several diseases like Type 2 Diabetes, Hypertension, Hyperlipidemia, Liver and kidney diseases, Hypertension, Cancer Risk and others.

Advancement in Healthcare Infrastructure Foster the Pediatric Drugs Market Growth

The escalation of healthcare investment plays a pivotal role in shaping the trajectory of the pediatric drug market. A substantial determinant contributing to market growth is the surge in healthcare expenditure, facilitating the enhancement of healthcare infrastructure. Notably, government bodies are proactively augmenting this development by allocating increased funding to bolster healthcare facilities, exerting a profound impact on market dynamics.

Moreover, the concerted efforts of both public and private entities to raise awareness, coupled with a notable uptick in childhood obesity cases, are poised to further propel the pediatric drugs market. This phenomenon is further accentuated by evolving lifestyle patterns and a burgeoning population, collectively fostering the expansive growth of the pediatric drugs sector. The convergence of these factors delineates a landscape where healthcare investments, governmental initiatives, and societal changes converge to drive advancements in pediatric pharmaceuticals.

Challenges Posed by Limited Market Exclusivity in Pediatric Drug Development

The abbreviated duration of market exclusivity poses a significant obstacle to the growth of the pediatric drugs market. In contrast to pharmaceuticals customised for adults, pediatric medications often face shorter market exclusivity and patent protection periods. This diminishes the financial allure for pharmaceutical companies to invest in pediatric drug development, as they are inclined towards markets where research and development investments can be recouped with substantial profits. The pediatric sector encounters challenges due to smaller patient populations and limited exclusivity periods, making it more difficult to justify allocating resources for research and development. This limitation mainly affects the development of drugs for rare pediatric diseases, where patient numbers are exceptionally restricted.

Consequently, a considerable number of children resort to off-label use of medications intended for adults, posing potential risks to safety and effectiveness. Addressing this constraint necessitates policy and regulatory reforms that offer enhanced incentives for pediatric drug development, ensuring children can access secure and efficacious treatments.

Drug Type Segment Holds a Substantial Market Share

The paediatrics drugs market is categorized by type, encompassing analgesic and antipyretic, central nervous system drugs, especially antibiotics, gastrointestinal drugs, respiratory drugs, and vaccines. The segment held a significant market share, driven by children's lower immunity, increasing pollution, and allergen exposure leading to chronic respiratory disorders, including Chronic obstructive pulmonary disease. Montelukast is notably employed for asthma prevention in children 2 years and older, particularly for exercise-induced bronchoconstriction. The Autoimmune Disorders segment is anticipated to exhibit substantial growth, attributed to the rising incidence of genetic disorders, cancers, and cystic fibrosis. In addition, mental health problems sucg as anxiety, depression, ADHD, and behavioural problems are also common among children aged 5-27 years.

Fig. Percentage of Children and Adolescents Aged 5-17 Years Who Received Mental Health Medication Counselling or Therapy from a Mental Health Professional Between 2019 and 2022 in the U.S.

Additionally, the Pediatrics Medicine Market growth is further fueled by the inclusion of antibiotics, analgesics, antipyretics, respiratory drugs, gastrointestinal drugs, central nervous system drugs, vaccines, and others in the pediatric disease treatment spectrum. This comprehensive range contributes significantly to the overall market expansion.

The Route of Administration Segment brings Substantial Growth in the Pediatric Drugs Market

The Pediatrics Medicine Market is categorized based on the route of administration, namely topical, oral, parental, and others. In 2020, the Oral segment dominated with the highest revenue share. This is attributed to the preference for non-invasive oral delivery in pediatric patients, minimizing pain and enhancing parental comfort, resulting in improved medication compliance.

This growth is driven by the minimal risk of adverse reactions and drug interactions, along with the ease of administration to children. Additionally, factors such as cost-effectiveness, lower drug quantities, and the concentrated application of antibiotics in affected areas contribute to the growth of this route of administration.

The Distribution Channel Segment expands the Pediatric Drugs Market Growth

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Geographical Landscape:

North America dominates the pediatric drugs market due to rising healthcare spending, supportive regulatory framework, and quick adoption of advanced technologies across the U.S. and Canada. The growth in this region is primarily attributed to its robust healthcare infrastructure, substantial research and development capabilities, and a significant pediatric patient demographic. The region's dominance is further bolstered by favourable regulatory frameworks and government incentives, fostering the development and accessibility of pediatric medications. For instance, in 2021, US FDA approved the Rethymic drug for pediatric patients and used it to treat rare immune disorders. Rethymic is the 1st thymus tissue that is approved in the United States.

The market benefits from North America's dedicated focus on pediatric healthcare heightened awareness among parents and healthcare professionals, and the region's economic strength. Additionally, the presence of leading pharmaceutical companies further solidifies North America's prominent position in the global pediatric drugs market. During the forecast period, the Asia-Pacific region is poised for significant pediatric drug market growth. This expansion is driven by various vital factors, including the region's substantial and expanding pediatric population, leading to an increased demand for specialized healthcare solutions for children. The economic prosperity and expanding middle-class demographic in Asia-Pacific also enhance affordability and accessibility to pediatric medications.

Government initiatives and increased regional healthcare investments are pivotal in fostering market growth. The pharmaceutical industry in Asia-Pacific is channelling more resources towards developing medications tailored for pediatric patients. This concerted effort has positioned the region as a significant influencer in the pediatric drugs market, emerging as a central hub for research, development, and distribution of pharmaceuticals for children.

Competitive Landscape

The pediatric drugs are competitive, with a few big companies leading the way. Some of these companies have a larger share of the market. To stay ahead, some introduce new medicines to tackle existing problems, while others ensure they reach the people needing them.

In the past 10 years, pharmaceutical companies have increasingly chosen external organisations known as CROs, i.e. Contract Research Organisations, for their clinical trial and clinical research. A Tufts University and ICON PLC study predicts that by 2022, about 72% of global clinical trials will be handled by CROs. The combination of research and accessibility strategy allows these companies to stay ahead in the competitive landscape of pediatric medication.

Key Market Players:

Pediatric Drugs Market Segmentation:

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By Route of Administration:

By Distribution Channel

By Geography

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Pediatric Drugs Market Size Expected to Reach USD 363.86 Billion by 2032 - GlobeNewswire

Long COVID Research Is a Bit of a Mess – Technology Networks

Back in March 2020, as the COVID-19 pandemic descended over the world, Naima was a busy tech worker, zipping around London, speaking to clients and jogging on the weekends.

I was very, very busy, she says. I did triathlons and [was] running 10Ks all the time. I was living a normal life, a full life.

Then, like every other person in the UK, her life came to a standstill as the countrys first lockdown began. Only, Naima was even more sedentary than most; she was ill with COVID-19.

I had quite a few symptoms: headache, fever, full-body soreness, sore throat, a bit of a cough and I felt very weak, she explains. That lasted a couple of weeks.

It would have been easy to panic, contracting the very virus that had just shut down the world, but Naima was relatively calm. Because I was so fit, I wasnt too worried, she says. The only real story that was happening was the hospitalizations. The line was: Unless you have underlying conditions or youre much older, youll be fine.

And for a while she was, mostly.

I had this niggling sensation in my chest that would pop up every couple of days, just for a few seconds. And in those few seconds, I couldnt breathe properly. But that didnt develop into anything else for several months.

When it did, Naima wasnt just troubled with a tight chest; she was debilitated with palpitations and crippling fatigue. She could barely walk. My world was turned upside down from that point in October, when those severe symptoms kicked in. I spoke to general practitioners; I said, I cant move at all. It feels like there are bricks on my chest and shooting pains that come whenever I get up. They said, You know, youre so young and fit, but this sounds like a heart attack.

It wasnt. It was long COVID. Naima was part of the first batch of people in the world to develop ongoing, disabling complications following an un-hospitalized COVID-19 infection. And shes still ill, more than three years later.

How could a fit and healthy 26-year-old go from running triathlons to being bed-bound for months, just from a passing viral infection? Why were she and people like her left with life-altering symptoms, while others could move on from their infections, seemingly unchanged? Back in 2020, no one had answers to these questions. No one really knew how to help those struggling with the illness. Research was desperately needed.

And, as 2021 dawned, research arrived. The UK government awarded 18.5 million to four studies that set out to define long COVID. The European Union gave 27.9 million to a larger research initiative, known as ORCHESTRA, to study how COVID-19 was impacting peoples health. And in February 2021, the US National Institutes of Health (NIH) raised the bar and allocated $1.15 billion to research the causes of long COVID and its possible treatments.

So, nearly three years later, what has been learned? Perhaps more importantly, have any treatments been produced?

The short answers: a lot. And not quite.

To begin with, researchers set about defining long COVID as a starting point. Many understood the condition to involve persisting symptoms after a SARS-CoV-2 infection, but that was about it. They didnt know exactly what these symptoms were or who they were affecting. To gather insights, they began profiling patients.

A lot of these patients were actually young and healthy, in their 20s and 30s, says Dr. Ziyad Al-Aly, a clinical epidemiologist at Washington University. And everybody at the time [in March 2020] was telling them that, If youre young and healthy, then SARS-CoV-2, its not a big deal; youll recover. But weeks later, these people were not recovering. So we decided to research long COVID to try to understand what it is.

Al-Aly and his colleagues began by looking at patient medical records. They recently published two years worth of observations in Nature, comparing the medical data of 138,818 individuals who had had a SARS-CoV-2 infection and 5,985,227 who hadnt. There were some stark differences.

Among the non-hospitalized, long COVID took away 80.4 disability-adjusted life years (DALYs), a standard measure of disease burden, per 1,000 people. For comparison, others studies have estimated that chronic obstructive pulmonary disease, for instance, costs between 3.6 and 6.7 DALYs per 1,000 people.

Disability-adjusted life years (DALYs) summarizes the burden of healthy years of life lost due to premature mortality and disability.

Long COVIDs high disease burden is partly explained by its sheer number of possible symptoms; Al-Aly and his colleagues observed more than 80 within the medical records. These included atrial fibrillation, cardiac arrest, anemia, diabetes, fatigue, acute gastritis, myalgia, memory problems and peripheral neuropathy. Just over 30% of these sequalae remained significant in non-hospitalized patients for two years.

Long COVID is literally the long-lasting legacy of this pandemic, Al-Aly says.

Al-Alys study documented, in unprecedented detail, just how wide-ranging the effects of long COVID-19 can be. But what exactly is causing these symptoms? Parallel research has shed some light.

One study found that long COVID patients had 100 times the levels of SARS-CoV-2-specific T cells normally seen in people who recovered from the virus a finding that suggests the virus is still active in the bodies of people with long COVID, surviving in reservoirs, plaguing sufferers for months. Tiny blood clots have been found in patients clots that could be blocking oxygen from reaching cells, starving patients of their energy. The brains of people with long COVID are also more active in certain areas than the brains of those without the post-viral illness an observation that could explain the memory loss and confusion experienced by many with the condition.

Theres a lot going on under the skin of long COVID patients, multiple etiologies affecting multiple organ systems.

And this is where the field of long COVID research gets sticky, because highly variable diseases are difficult to study further. What kind of clinical researcher is best suited to the job? A cardiologist? A neurologist? An infectious disease specialist? Based off the mounting data, it seems like long COVID is a job for all three.

This issue is partly why, more than three years on from when the illness was identified, long COVID research is still stuck in its characterization phase. Have a Google of long COVID research these days and one will still come across new papers decrying how blurry the definition of the disease is and arguing for more thorough studies to detail it better.

But people with this condition cant wait any longer for such preliminary studies. Theyre desperate for interventional clinical trials now. People are hanging their hopes on these trials, says Al-Aly. They want them to be done yesterday. And yet were moving forward at a turtles pace.

Ironically, its the same kind of characterization research that demonstrates this desperation best. Almost one in five UK doctors responding to a recent BMJ survey said that they had lost their ability to work due to their post-COVID ill-health. A US study, published last year, estimated that long COVID potentially accounted for 15% of the countrys whole labor shortage.

Even those who have managed to keep working through their illness report life-altering levels of fatigue (the most common symptom of long COVID), enough to rob them of their prior quality of life. One survey of patients at a long COVID clinic, published in BMJ Open this year, found that, on average, the patients fatigue scores were worse or similar to those of people with severe kidney disease. The respondents quality of life scores were also lower than those of people with stage four lung cancer.

Most concerning of all, due to the toll of the illness, people with long COVID seem to be at a higher risk of suicide. One US patient-led survey found that 45% of respondents had experienced recent suicidal thoughts more than 11 times the national average (4%). Sadly, these data are supported by a growing number of anecdotal reports within the long COVID patient community from grieving loved ones.

So, with no approved treatments for the illness or standardized care plan and a disease duration that can span over three years in certain cases its perhaps no wonder people with long COVID are crying out for trials. Fortunately, a few have been greenlit.

In August 2023, there were 386 trials underway around the world relating to long COVID, according to the ClinicalTrials.govdatabase. A promising figure, one might think. Only 94 of those studies, however, were classed as interventional and were recruiting, and only 12 trials were testing pharmacological interventions; the rest were testing the effects of food supplements, psychological support, acupuncture and other non-drugs.

What are the 12 drug trials testing, though? Well, one led by Yale University is studying whether Paxlovid (a COVID-19 antiviral made by Pfizer) could benefit people with long COVID, perhaps by eliminating any rogue remnants of SARS-CoV-2 that may still be lingering in their bodies. Another led by a private US company is seeing whether a novel drug designed to remove pro-inflammatory nucleic acids could reduce the levels of vascular inflammation observed in long COVID patients, thereby reducing their fatigue.

But perhaps the most highly anticipated trial within the long COVID community is that undertaken by the relatively small biotech company Berlin Cures. The German start-up made headlines back in 2021 when it announced that it had effectively treated four people with long COVID with just a single infusion (per person) of its proprietary drug, BC007. Encouraged by these initial results, the company has since launched a Phase 2 clinical trial of its neutralizing functional auto-antibody formula, which recently completed a Phase 2 open study for heart failure.

We know, and others have shown, that these functional auto-antibodies play a key role in the pathogenesis of various debilitating diseases, says Oliver von Stein, Berlin Cures CEO. Long COVID, we believe, is one of them, heart failure is potentially another.

To be included as a participant in the companys trial, potential patients have to test positive for these pernicious auto-antibodies, so the Berlin Cures team can later test if a reduction in auto-antibody levels correlates with a reduction in fatigue (the prime symptom assessed by the study).

Thanks to this level of rigor built into the trial, and the early results of BC 007, von Stein and his colleagues are expecting promising results by the second half of next year results that they hope will attract a new wave of investment for a Phase 3 trial and, beyond that, other trials for other maladies.

We are optimistic and expect good data from our ongoing Phase 2 study, von Stein says. And, if this is the case, this will provide a lot of momentum to tackle other diseases, similar conditions for example, chronic fatigue syndrome.

Chronic fatigue syndrome or myalgic encephalomyelitis (ME) is the elephant in the long COVID room. For the past three years, much of the media and discussion around long COVID has treated the post-viral condition as an entirely new illness, a view that has been reflected in its research; scientists from around the world have scrambled to study the disease from scratch.

But if ME had been studied more thoroughly or even just believed years ago, much of the foundational work of long COVID research may already have been achieved. Thats certainly the belief of many of those suffering from ME, who often live exceptionally stationary lives due to their condition. Some are bed-bound, quite literally, for decades.

Half of long COVID symptoms are basically equivalent to ME symptoms, says Chris Ponting, a professor at the University of Edinburghs Medical Research Council Human Genetics Unit and lead investigator of its Decode ME project.

If anyone is compensating for these lost years of ME research, its Ponting; he and his colleagues are currently conducting the largest study of ME ever undertaken. By analyzing the DNA samples of 25,000 patients, they hope to identify genetic markers that could underpin a persons susceptibility to the disease. With that information in hand, they could then both validate the existence of the malady and identify targets for future drugs to treat it.

We anticipate that well be able to find a bunch of places in our genomes that scream at us: immunology, or mitochondria or some neurological phenotype in the genome, says Ponting. Then, through joining up the dots, we can make an evidence-based, cogent explanation for what is going wrong.

It all sounds quite promising. But theres an obstacle to follow-up studies, the same one that prevented ME research for decades: funding. Our study was funded prior to the COVID-19 pandemic, Ponting says. There has not been further funding since then.

Contrary to the hopes of many in the ME community, the relative surge of interest in long COVID has not translated into a research boon for other fatigue-inducing, likely post-viral conditions, according to Ponting. There has been a shift in the dial in acceptance of ME, he notes, which has not translated to substantial research funding that this disease deserves.

And unfortunately, at the tail end of 2023, its not just ME thats being starved of vital research. The funding well for long COVID is drying up, too.

All of these scientists, theyre back in the usual hurdles that scientists go through to try and get research up and running in this country. There is no sense of urgency at all, says Margaret OHara, founder trustee of Long Covid Support, a UK-based charity supporting people with long COVID.

OHara liaises with researchers on behalf of the charity. Two years ago, many of the scientists she spoke to were getting their funding from the UKs National Institute for Health and Care Research (NIHR), which launched rounds of commissioned calls that were worth millions in 2021. Now those funding rounds are a distant memory.

Then NIHR said, Right, no more commission calls, says OHara. Long COVIDs not special anymore, and if you want money to research it, you [must] go through the usual channels for example, RFPB [Research for Patient Benefit] and you compete with all the other diseases.' So, what we find now is that [research grant applications] are just getting knocked back.

The situation seems much the same across the Atlantic. Remember that $1.15 billion the US NIH allocated to long COVID research? Well, its pretty much all been spent, largely on observational, characterization research, according to an analysis by STAT, and theres been no announcement of any follow-up funding, despite calls from US researchers. Some long COVID studies in the country have since relied on charitable donations to keep going.

Why has the money dried up? Fittingly, one could blame fatigue. There is a bitter feeling within the long COVID community that the rest of the world has grown tired of all things COVID and no longer wants to hear from or fund studies affecting those damaged by the virus.

We think theres a bit of a message coming from the top to say, Yeah, lets downplay long COVID because, you know, COVIDs over, says OHara.

Whether accurate or not, this sentiment that the top has lost interest in long COVID is a doubly frustrating one for those researching the disease because, right now, the field could really do with some leadership.

[There is] no coherent approach to studying long COVID. No coherent strategy, says Al-Aly. I liken it to if you have a bunch of musicians, and everybody is singing their own tune, and theres no conductor harmonizing all of this.

Al-Alys exasperation is shared by many of his fellow researchers. At a time of disappearing grants, many say the field needs a conductor some governing body with a comprehensive, coordinated plan of action.

We think there should be a coordinated effort by UKRI [UK Research and Innovation] to say, OK, long COVID is a disease of great interest and we need to coordinate responses, says OHara.

We need to put these scientists together so that theyre not all repeating the same thing.

OHara and her colleagues at Long Covid Support have been calling for this kind of managed response since 2020. The charity recently wrote to the UK government, recommending that it declare long COVID a public health emergency and prioritize research into treatments. These pleas have so far gone unheeded, which may be unsurprising given recent political revelations. In October 2020, when presented with the health departments first guidance on long COVID, the then prime minister Boris Johnson scrawled bo***cks, in capitals, on the document.

But this offensive dismissiveness from the top doesnt mean a top-down research strategy, if coordinated by health departments and research funders, is an impractical suggestion, researchers insist.

The funders will say thats up to the scientists to coordinate, says Ponting. And they would have a point; it has to be from the ground-up mostly rather than from the top-down. But top-down does work.

The response to mad cow disease did come from the top, he adds. There have been international efforts on many different diseases going back decades, including polio. So, the answer that it is up to the scientists to organize ourselves in a competitive world, where we compete for funding because theres so little of it, is missing part of what should happen, which is that we need coordination.

While all this disarray between researchers, funders and governments plays out, long COVID patients watch on, many despondent. Some are relatively new to the illness. Some have been coping with it for over three years with little improvement. Others have improved over time, gaining back enough physical capability to return to work. But this remission is fragile. According to a Long Covid Support survey of people who had recovered from the illness, 60% got long COVID again following a reinfection of COVID-19. This happened to Naima, twice.

To protect herself from worsening symptoms, Naima still practices strict infection protocols. She restricts her socializing. She wears a mask on public transport. She routinely tests for COVID-19 and asks others she sees to do the same. Shes still behaving like many people did in 2020. Without long COVID treatments, she cant afford to change her habits.

Ive been lucky in terms of my life beforehand, she says. I no longer feel that way. I live with fear every day of reinfection.

What does she make of the state of long COVID research, then? Does it give her hope for a return to a normal, fear-free future? Not quite. While she is part of a characterization study being conducted at Imperial College London, and is optimistic that such research will one day bear useful results, she says those who have been struggling with their long COVID for years need better outcomes now.

A lot of studies are moving on to: who is getting this? Im part of a study now with Imperial taking blood samples. Its just [about] understanding: why are we so greatly impacted by this? Is there a specific gene that we have? I think that [answer] would really go a long way to understanding this. And then, of course, treatments for people who have been suffering now for years

She pauses.

I think, because Ive had improvement, she adds. I have more hope because I know that I do have better points and worse points. But some people have not had any good moments; theyve been around for three years and had no improvement. I think we really need to be able to offer something to those people, to all of us.

Those interested in following Naimas journey of long COVID recovery can subscribe to her Substack journal.

For those living with long COVID, links to support groups and symptom management guides can be found at Long Covid Support.

Those with ME can find similar support resources at ME Association.

For those struggling with suicidal ideation in the UK, Papyrus and Samaritans offer 24/7 support. Those living in the US can call the 988 Suicide & Crisis Lifeline.

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Long COVID Research Is a Bit of a Mess - Technology Networks

Researchers find certain cancers can activate ‘enhancer’ in the … – University of Toronto

Researchers at the University of Toronto have found that cancer cells can enhance tumour growth by hijacking enhancer DNA normally used when tissues and organs are formed.

The mechanism, called enhancer reprogramming, occurs in bladder, uterine, breast and lung cancer and could cause these types of tumors to grow faster in patients.

The research was conducted in the lab of Jennifer Mitchell, a professor in the department of cell and systems biologyin the Faculty of Arts & Science, andpublished recently in the journalNucleic Acids Research. It pinpoints the role that specific proteins play in regulating the enhancer region which may lead to improved treatments for these cancer types.

Living cells, even cancer cells, follow instructions in the genome to turn genes on and off in different contexts, says first authorLuis Abatti, a PhD candidate in Mitchells lab.

The genome is like a recipe book written in DNA that gives instructions on making all the parts of the body, Abatti says.

In each organ, only the recipes relevant to that organ should be followed whether its the instructions for lung, breast or some other tissue. Like flipping pages in a recipe book, the DNA containing the instructions for turning genes on in the lung is open and used in the lung, for example, but closed and ignored in other types of cells.

We know that some cancer cells are opening the wrong pages in the recipe book ones that contain the SOX2 gene, which can cause tumours to grow uncontrollably. We wanted to find out: How does the gene become expressed in cancer cells?

The researchers analyzed genome data to look for enhancer DNA that could activate SOX2 in cancer cells. The enhancer they found is open in many different types of patient tumours, meaning this could be a cancer enhancer active in bladder, uterus, breast and lung tumours. Unlike many cancer-causing changes, the enhancer reprogramming mechanism does not arise out of mutation due to DNA damage it is caused by part of the genome opening when it should be staying closed.

The researchers then determined that the enhancer causes increased cancer cell growth because when they removed the enhancer in lab-grown cells, the cancer cells created fewer new tumour colonies.

To figure out why cells have a DNA region that makes cancer worse, the team examined mice without this DNA region and found they do not form a separate passage for air and food in their throat as they develop. Thus, this potentially dangerous cancer-enhancer region is likely in the human genome to regulate airway formation as the human body forms. However, if a developing cancer cell opens this region, it will form a tumour that grows faster and is more dangerous for the patient.

We also found that two proteins known to have a role in the developing airways FOXA1 and NFIB are now regulating SOX2 in breast cancer, says Mitchell, who is associate chair of research in the department of cell and systems biology and is cross-appointed to thedepartment of laboratory medicine and pathobiologyin the Temerty Faculty of Medicine.

The enhancer is activated by the FOXA1 protein and suppressed by the NFIB protein. This means that drugs suppressing FOXA1 or activating NFIB may lead to improved treatments for bladder, uterine, breast and lung cancer.

Now that we know how the SOX2 gene is activated in certain types of cancers, we can look at why this is happening, Mitchell says.

Why did the cancer cells end up on the wrong page of the genome recipe book?

The research received support from the Canadian Institutes of Health Research, the Canada Foundation for Innovation and the Ontario government.

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Researchers find certain cancers can activate 'enhancer' in the ... - University of Toronto