Equillium Announces Closing of $30 Million Registered Direct Offering

LA JOLLA, Calif., Feb. 05, 2021 (GLOBE NEWSWIRE) -- Equillium, Inc. (Nasdaq: EQ) a clinical-stage biotechnology company developing itolizumab to treat severe autoimmune and inflammatory disorders, today announced the closing of its previously announced registered direct offering with life science institutional investment funds managed by Decheng Capital, to purchase 4,285,710 units (the “Units”) from Equillium, with each Unit consisting of one share of common stock and a warrant to purchase 0.3 of a share of common stock. The purchase price per Unit was $7.00, priced above the market under Nasdaq rules. The warrants have an exercise price of $14.00 per share, are immediately exercisable, and will expire on the earlier of (i) the fifth anniversary of issuance, or (ii) the 15th calendar date following the date on which Equillium closes a financing raising a minimum of $25 million at a price per share of no less than $25.00.

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Equillium Announces Closing of $30 Million Registered Direct Offering

Evotec and Medical Center Hamburg-Eppendorf Enter Partnership to Develop iPSC-Based Tissue Therapy for Heart Failure – GuruFocus.com

HAMBURG, GERMANY / ACCESSWIRE / February 4, 2021 / Evotec SE (Frankfurt Stock Exchange: EVT, MDAX/TecDAX, ISIN: DE0005664809) today announced that the Company has entered into a multi-year partnership with the Medical Center Hamburg-Eppendorf ("UKE") for the development of a highly innovative first-in-class cell therapy approach for the treatment of heart failure.

Under the terms of the partnership, Evotec and UKE will leverage their complementary strengths for the development of a new cell therapy approach using Engineered Heart Tissue for the treatment of heart failure. Heart failure is frequently associated with ischemic heart disease and often comes with a poor prognosis. Mortality is comparable to that of the most common cancers, with <50% 4-year survival. Treatment of patients suffering from heart failure is expected to deliver significant patient benefit through improved heart function, ultimately leading to an improved prognosis.

Evotec leverages its industry-leading human induced pluripotent stem cells ("hiPSCs") platform to establish GMP-compatible process development and upscaling for large-scale generation of clinical-grade heart muscle cells known as cardiomyocytes. Evotec will also contribute genetically modified GMP iPSC lines, which contain alterations preventing rejection of the cardiomyocyte-containing product by patient immune systems ("cloaking"), and include additional safety mechanisms to control unwanted proliferation of graft cells. By using these GMP-grade iPSC lines, the project will deliver off-the-shelf products, which can be implanted in broad patient populations with little to no immunosuppression. UKE applies its proprietary Giga Patch Method for the generation of fully functional heart tissue suitable for cardiac transplantation. Further in vivo validation and development activities will be shared jointly between the partners. Evotec will be responsible for GMP and pre-clinical activities as well as for any subsequent partnering of the programme.

Dr Cord Dohrmann, Chief Scientific Officer of Evotec, commented: "We are very excited about this collaboration with the UKE. Both Evotec and UKE have developed and refined their respective technology platforms over a number of years and have now decided to jointly drive this cardiac cell therapy programme towards clinical development. We are confident that this partnership will deliver a new therapeutic option for patients who suffer from heart failure."

Prof. Dr Thomas Eschenhagen, Director of the Institute of Experimental Pharmacology and Toxicology at UKE, added: "We are excited about the new opportunities the partnership with Evotec will create. After having worked on means to repair injured heart by 3-dimensional heart muscle patches for over two decades, joining forces with Evotec and its industrialized hiPSC platform and new cell lines, will bring this development to a new stage. We are aiming at the most efficient and safest therapy in the field."

"We are very happy to see a scientific success story advance to a feat of technology transfer. Translation of scientific insights into therapeutic options is a key mission of our University Medical Center", says Prof. Dr Blanche Schwappach-Pignataro, the Dean of Faculty of Medicine of the UKE.

No financial terms of the agreement were disclosed.

About heart failure Heart failure is a severe global health burden with more than 26 million people suffering with the condition worldwide, disproportionately affecting elderly people. While there are options to treat heart failure both medicinally and with devices, there is currently no treatment that targets the cause of the disease or significantly slows down its progression.

About Evotec and iPSC Induced pluripotent stem cells (also known as iPS cells or iPSCs) are a type of pluripotent stem cell that can be generated directly from adult cells. Pluripotent stem cells hold great promise in the field of regenerative medicine. Because they can propagate indefinitely, as well as give rise to every other cell type in the body (such as neurons, heart, pancreatic and liver cells), they represent a single source of cells that could be used to replace those lost to damage or disease.

Evotec has built an industrialised iPSC infrastructure that represents one of the largest and most sophisticated iPSC platforms in the industry. Evotec's iPSC platform has been developed over the last years with the goal to industrialise iPSC-based drug screening in terms of throughput, reproducibility and robustness to reach the highest industrial standards, and to use iPSC-based cells in cell therapy approaches via the Company's proprietary EVOcells platform.

ABOUT THE MEDICAL CENTER HAMBURG-EPPENDORF (UKE) Since its foundation in 1889, the Medical Center Hamburg-Eppendorf (UKE) has been one of the leading clinics in Europe. With about 13,600 employees, the UKE is one of the largest employers in Hamburg. Each year, the UKE treats around 511,000 patients, 106,000 of whom are inpatients and 405,000 outpatients. The emphasis in UKE's research are the neurosciences, cardiovascular research, care research, oncology, as well as infections and inflammations. Other potential areas of the UKE are molecular imaging and skeletal biology research. The UKE trains about 3,400 medical specialists and dentists. Knowledge, Research, Healing through Shared Competence: The UKE | http://www.uke.de

ABOUT EVOTEC SE Evotec is a drug discovery alliance and development partnership company focused on rapidly progressing innovative product approaches with leading pharmaceutical and biotechnology companies, academics, patient advocacy groups and venture capitalists. We operate worldwide and our more than 3,500 employees provide the highest quality stand-alone and integrated drug discovery and development solutions. We cover all activities from target-to-clinic to meet the industry's need for innovation and efficiency in drug discovery and development (EVT Execute). The Company has established a unique position by assembling top-class scientific experts and integrating state-of-the-art technologies as well as substantial experience and expertise in key therapeutic areas including neuronal diseases, diabetes and complications of diabetes, pain and inflammation, oncology, infectious diseases, respiratory diseases, fibrosis, rare diseases and women's health. On this basis, Evotec has built a broad and deep pipeline of more than 100 co-owned product opportunities at clinical, pre-clinical and discovery stages (EVT Innovate). Evotec has established multiple long-term alliances with partners including Bayer, Boehringer Ingelheim, Bristol Myers Squibb, CHDI, Novartis, Novo Nordisk, Pfizer, Sanofi, Takeda, UCB and others. For additional information please go to http://www.evotec.com and follow us on Twitter @Evotec.

FORWARD-LOOKING STATEMENTS Information set forth in this press release contains forward-looking statements, which involve a number of risks and uncertainties. The forward-looking statements contained herein represent the judgement of Evotec as of the date of this press release. Such forward-looking statements are neither promises nor guarantees, but are subject to a variety of risks and uncertainties, many of which are beyond our control, and which could cause actual results to differ materially from those contemplated in these forward-looking statements. We expressly disclaim any obligation or undertaking to release publicly any updates or revisions to any such statements to reflect any change in our expectations or any change in events, conditions or circumstances on which any such statement is based.

Media Contact Evotec SE: Gabriele Hansen, SVP Head of Global Corporate Communications & Marketing, Phone: +49.(0)40.56081-255, [emailprotected]

IR Contact Evotec SE: Volker Braun, SVP Head of Global Investor Relations & ESG, Phone: +49.(0)40.56081-775, [emailprotected]

SOURCE: Evotec AG

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Evotec and Medical Center Hamburg-Eppendorf Enter Partnership to Develop iPSC-Based Tissue Therapy for Heart Failure - GuruFocus.com

Researchers curb local immune response in horses receiving stem cell injury therapy – Horsetalk

Cultures with treated stem cells had a 50% higher stem cell survival rate than untreated cultures. Image by carolem41

Treating equine donor stem cells with a growth factor called TGF-2 may allow them to avoid tripping the immune response in recipients, according to new research.

The work carried out at North Carolina State University could simplify the stem cell treatment process for ligament and tendon injuries in horses, and may also have implications for human stem cell therapies.

Mesenchymal stem cell therapy is a promising avenue for treating musculoskeletal injuries, particularly tendon and ligament injuries, in horses.

Mesenchymal stem cells are adult stem cells found in bone marrow that act as repair directors, producing secretions that recruit healing-related paracrine factors to the site of injury.

Just as blood cells have types, depending upon which antigens are on the blood cells surface, mesenchymal stem cells have differing sets of major histocompatibility complex molecules, or MHCs, on their surfaces.

If the MHCs of donor and recipient arent a match, the donors stem cells cause an immune response. In organ transplants, MHCs are carefully matched to prevent rejection.

These treatments arent like a bone marrow transplant or an organ transplant, says Lauren Schnabel, associate professor of equine orthopedic surgery at the university and corresponding author of the study, reported in the journal Frontiers in Cell and Developmental Biology.

Since the mesenchymal stem cells are being used temporarily to treat localized injury, researchers once thought that they didnt need to be matched that they wouldnt cause an immune response. Unfortunately, that isnt the case.

Schnabel and Alix Berglund, a research scholar at the university and lead author of the paper, wanted to find a way to use mesenchymal stem cell therapy without the time, effort and additional cost of donor/recipient matching.

Since these cells dont have to be in the body as long as an organ does, hiding them from the immune system long enough for them to secrete their paracrine factors could be a way around donor/recipient matching, Berglund says. Downregulating expression of the MHC molecules could be one way to do this.

The researchers cultured stem cells and lymphocytes, or T cells, from eight horses, cross-pairing them in vitro so that the stem cells and lymphocytes had differing MHC haplotypes.

In one group, stem cells had been treated with transforming growth factor beta (TGF-2) prior to being added to the lymphocytes in the culture media; the other group was untreated. TGF-2 is a cell-signaling molecule produced by white blood cells that blocks immune responses.

Cultures with treated stem cells had a 50% higher stem cell survival rate than untreated cultures.

We use mesenchymal stem cells to treat musculoskeletal injuries particularly tendon injuries in horses very effectively, Schnabel says.

And while you can extract the secretions from the stem cells, you get better results with the cells themselves. Stem cells arent just a reservoir of secretions, theyre a communications hub that tells other cells what they should be doing. So finding a way to utilize these cells without stimulating immune response gives us better treatment options.

This is a promising pilot study, Berglund says. Our next steps will be to further explore the immune response in vivo, and to look at human cells in vitro, as this work has excellent potential to help humans with these injuries as well.

The research was supported by the National Institutes of Health and the Morris Animal Foundation. Research specialist Julie Long and statistician James Robertson, both with the university, also contributed to the work.

TGF-b2 Reduces the Cell-Mediated Immunogenicity of Equine MHC-Mismatched Bone Marrow-Derived Mesenchymal Stem Cells Without Altering Immunomodulatory Properties Alix K. Berglund, Julie M. Long, James B. Robertson, Lauren V. Schnabel Cell Dev. Biol., 04 February 2021 https://doi.org/10.3389/fcell.2021.628382

The study, published under a Creative Commons License, can be read here.

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Researchers curb local immune response in horses receiving stem cell injury therapy - Horsetalk

Biobanking Market Report Research and Global Outlook 2021 to 2025 KSU | The Sentinel Newspaper – KSU | The Sentinel Newspaper

A New Research report Biobanking Market has been recently added to the Market Insights Reports database. The report offers definitive information pertaining to the commercialization aspects, revenue estimation, and market size of the industry. The report defines the status of key players in the competitive landscape including their portfolio and geographical expansion pursuits. This report also focuses on Biobanking Market Trend, volume, and value at the global level, regional level, and company level.

According to this study, over the next five years the Biobanking market will register a 6.0% CAGR in terms of revenue, the global market size will reach $ 3381 million by 2025, from $ 2676.4 million in 2019.

The report presents the market competitive landscape and a corresponding detailed analysis of the major vendor/key players in the market.Top Companiesin the Global Biobanking Market:Beckman Coulter, Tecan Group, Thermo Fisher, Sigma-Aldrich, SOL Group, Panasonic, Brooks Life Science, Promega, QIAGEN, BD, Askion, Cryo Bio System, Biolife Solutions, Lifeline Scientific, DNA Genotek, LVL Technologies, Micronic, So-Low, BioRep and Others.

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Market Overview:

The major factors for the growth of the global biobanks market include the innovations in regenerative medicine, the growing incidence of chronic diseases, advances in drug discovery and development, and R&D funding and investments by government and non-governmental organizations. These factors are expected to a boost the growth of the market over the forecast period.

Regenerative medicine through stem cell technology is one of the important treatments for diseases, such as Alzheimers, diabetes, cancers, and rare genetic diseases. In order to benefit from the existing therapies, umbilical cord cells and other stem cells are preserved.

Stem cell practices are on the rise, globally, and are contributing to the development of new solutions for various diseases. Boston-based biotech start-up, Orig3n, is looking to build the largest and most diverse biobank, harnessing the power of induced pluripotent stem cell technology to accelerate regenerative medicine. Treatments for diseases, like muscular degeneration, using adult stem cells are now going into Phase 3 clinical trials in Japan. These successes are driving both the government and the private sector organizations into investing in more stem cell banks.

With the increase in awareness about stem cell therapies, there have been larger number of parents who are choosing umbilical cord banks for their children. There are a number of donor banks that are coming up as well. Biobanks not only aid in the therapies for genetic diseases, but also in medical research on rare genetic disorders. Increasing awareness about stem cell therapies and innovation in the field of regenerative medicine are driving the growth of the global biobank market.

This report segments the Global Biobanking Market on the basis ofTypesare:

Equipment Consumable

On the basis ofApplication,the Global Biobanking Market is segmented into:

Virtual Biobanks Tissue Biobanks Population Biobanks

Top Line Market Forecast:

Both Regional and Global sectors are included in the Outlook, with special breakouts for the NAM, European, MENA, and Asia-Pacific regions. The data covered is from 2015 to 2019 historically and from 2021 to 2025 forecast, it also includes the impact of Covid-19 both on the short- and long-term prospects of the industry.

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Detailed overview of Market Changing market dynamics of the industry In-depth market segmentation by Type, Application etc. Historical, current and projected market size in terms of volume and value Recent industry trends and developments Competitive landscape of Biobanking Market Strategies of key players and product offerings Potential and niche segments/regions exhibiting promising growth

The research includes historic data from 2015 to 2021 and forecasts until 2025 which makes the report an invaluable resource for industry executives, marketing, sales and product managers, consultants, analysts and stakeholders looking for key industry data in readily accessible documents with clearly presented tables and graphs.

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MarketInsightsReportsprovides syndicated market research on industry verticals includingHealthcare, Information and Communication Technology (ICT), Technology and Media, Chemicals, Materials, Energy, Heavy Industry, etc.MarketInsightsReportsprovides global and regional market intelligence coverage, a 360-degree market view which includes statistical forecasts, competitive landscape, detailed segmentation, key trends, and strategic recommendations.

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Biobanking Market Report Research and Global Outlook 2021 to 2025 KSU | The Sentinel Newspaper - KSU | The Sentinel Newspaper

Animal Stem Cell Therapy Market By Product Type (Dogs, Horses) And By End-Users/Application (Veterinary Hospitals, Research Organizations) Market…

COVID-19 can affect the global economy in three main ways: by directly affecting production and demand, by creating supply chain and market disruption, and by its financial impact on firms and financial markets. Animal Stem Cell Therapy Market size has covered and analyzed the potential of Worldwide market Industry and provides statistics and information on market dynamics, market analysis, growth factors, key challenges, major drivers & restraints, opportunities and forecast. This report presents a comprehensive overview, market shares, and growth opportunities of market 2028 by product type, application, key manufacturers and key regions and countries.

The recently released report byResearch N Reportstitled as Animal Stem Cell Therapy Market is a detailed analogy that gives the reader an insight into the intricacies of the various elements like the growth rate, and impact of the socio-economic conditions that affect the market space. An in-depth study of these numerous components is essential as all these aspects need to blend-in seamlessly for businesses to achieve success in this industry.

The report includes profiles of leading companies in the Animal Stem Cell Therapy market. Some of the key players profiled include:

The following manufacturers are covered in this report: Aratana Therapeutics Cell Therapy Sciences VETSTEM BIOPHARMA Magellan Stem Cells U.S. Stem Cell VetCell Therapeutics J-ARM Animal Care Stem ANIMAL CELL THERAPIES Cells Power Japan MediVet Biologic Animacel Celavet

Animal Stem Cell Therapy Market Segmentation: The report offers in-depth analysis of the Animal Stem Cell Therapy market based on various segments such as type, application and end-use industry. The Animal Stem Cell Therapy market is segmented as follows:

Animal Stem Cell Therapy Market, by Type:

Animal Stem Cell Therapy Market, by Application:

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The research report includes company Competitors top sellers profiles, their data, deals income, revenue share, deal volume, and purchaser volume are equally specified. The conclusions provided in this report are of great value for the leading industry players. Every organization partaking in the global production of the Animal Stem Cell Therapy products have been mentioned in this report, in order to study the insights on cost-effective manufacturing methods, competitive landscape, and new avenues for applications. The report is molded by tracking market performance since 2015 and is one of the most detailed reports.

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This research study examines the current market trends related to the demand, supply, and sales, in addition to the recent developments. Major drivers, restraints, and opportunities have been covered to provide an exhaustive picture of the market. The analysis presents in-depth information regarding the development, trends, and industry policies and regulations implemented in each of the geographical regions. Further, the overall regulatory framework of the market has been exhaustively covered to offer stakeholders a better understanding of the key factors affecting the overall market environment.

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Animal Stem Cell Therapy Market By Product Type (Dogs, Horses) And By End-Users/Application (Veterinary Hospitals, Research Organizations) Market...

Stem Cell Assay Market Share, Demand, Manufacturers and Forecast till 2027 | Merck & Co., Thermo Fisher Scientific, GE Healthcare, Agilent…

The Report Titled on Stem Cell Assay Market which provides COVID19 Impact analysis on Market Size (Production, Capacity, Value, Values & Consumption), Regional and Country-Level Market Size, Segmentation Market Growth, Market Share, Competitive Landscape, Sales Analysis, Impact of Domestic and Market Players. Stem Cell Assay Market detailed study of historical and present/future market data. Economic growth, GDP (Gross Domestic Product), and inflation are some of the elements included in this report to offer crystal clear picture of the Stem Cell Assay industry at global level.

Stem Cell Assay Market competitive landscapes provides details by topmost manufactures like (Merck & Co., Thermo Fisher Scientific, GE Healthcare, Agilent Technologies, Bio-Rad Laboratories, Promega Corporation, Cell Biolabs, PerkinElmer, Miltenyi Biotec, HemoGenix, Bio-Techne Corporation, STEMCELL Technologies, and Cellular Dynamics International.), including Capacity, Production, Price, Revenue, Cost, Gross, Gross Margin, Growth Rate, Import, Export, Market Share and Technological Developments.

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Market Segmentation & Coverage:

This research report categorizes the Stem Cell Assay to forecast the revenues and analyze the trends in each of the following sub-markets:

By Product Type-InstrumentsReagents & KitsBy Cell Type Adult Stem CellsInduced Pluripotent Stem CellsMesenchymal Stem CellsNeural Stem CellsHematopoietic Stem CellsUmbilical Cord Stem CellsHuman Embryonic Stem CellsBy Process Cell CultureEngineeringDifferentiationCharacterizationOthersBy Application -ResearchDrug Discovery & DevelopmentRegenerative Medicine

Based on Geography, the Stem Cell Assay Market studied across Americas, Asia-Pacific, and Europe, Middle East & Africa. The Americas region surveyed across Argentina, Brazil, Canada, Mexico, and United States. The Asia-Pacific region surveyed across Australia, China, India, Indonesia, Japan, Malaysia, Philippines, South Korea, and Thailand. The Europe, Middle East & Africa region surveyed across France, Germany, Italy, Netherlands, Qatar, Russia, Saudi Arabia, South Africa, Spain, United Arab Emirates, and United Kingdom.

Impact of COVID-19 on this Market:

The pandemic of COVID-19 continues to expand and impact over 175 countries and territories. Although the outbreak appears to have slowed in China, COVID-19 has impacted globally. The pandemic could affect three main aspects of the global economy: production, supply chain, and firms and financial markets. National governments have announced largely uncoordinated, country-specific responses to the virus. As authorities encourage social distancing and consumers stay indoors, several businesses are hit. However, coherent, coordinated, and credible policy responses are expected to offer the best chance at limiting the economic fallout.

We, at Coherent Market Insights, understand the economic impact on various sectors and markets. Using our holistic market research methodology, we are focused on aiding your business sustain and grow during COVID-19 pandemics. With deep expertise across various industries-no matter how large or small- and with a team of highly experienced and dedicated analysts, Coherent Market Insights will offer you an impact analysis of coronavirus outbreak across industries to help you prepare for the future.

The Stem Cell Assay Market on the basis of Business Strategy (Business Growth, Industry Coverage, Financial Viability, and Channel Support) and Product Satisfaction (Value for Money, Ease of Use, Product Features, and Customer Support) that aids businesses in better decision making and understanding the competitive landscape.

Competitive Strategic Window:

Competitive Strategic Window analyses the competitive landscape in terms of markets, applications, and geographies. Competitive Strategic Window helps the vendor define an alignment or fit between their capabilities and opportunities for future growth prospects. During a forecast period, it defines the optimal or favorable fit for the vendors to adopt successive merger and acquisition strategies, geography expansion, research & development, and new product introduction strategies to execute further business expansion and growth.

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The report provides insights on the following pointers:

Market Penetration: Provides comprehensive information on the market offered by the key players

Market Development: Provides in-depth information about lucrative emerging markets and analyzes the markets

Market Diversification: Provides detailed information about new product launches, untapped geographies, recent developments, and investments

Competitive Assessment & Intelligence: Provides an exhaustive assessment of market shares, strategies, products, and manufacturing capabilities of the leading players

Product Development & Innovation: Provides intelligent insights on future technologies, R&D activities, and new product developments

The report answers questions such as:

What is the market size and forecast of the Global Stem Cell Assay Market?

What are the inhibiting factors and impact of COVID-19 shaping the Global Stem Cell Assay Market during the forecast period?

Which are the products/segments/applications/areas to invest in over the forecast period in the Global Stem Cell Assay Market?

What is the competitive strategic window for opportunities in the Global Stem Cell Assay Market?

What are the technology trends and regulatory frameworks in the Global Stem Cell Assay Market?

What are the modes and strategic moves considered suitable for entering the Global Stem Cell Assay Market?

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Stem Cell Assay Market Share, Demand, Manufacturers and Forecast till 2027 | Merck & Co., Thermo Fisher Scientific, GE Healthcare, Agilent...

Global Apoptosis Assays Market Set To Grow At Healthy CAGR Of 11.10% By 2027||Abcam plc, Research And Diagnostic Systems, Inc., Sartorius AG, Biotium,…

Apoptosis Assays market report provides the best research offerings and the required critical information when it is about looking for new product trends or competitive analysis of an existing or emerging market. With this business report companies can hone their competitive edge again and again. The report comprises of expert insights on global industries, products, company profiles, and market trends. Users can gain unlimited, company-wide access to a comprehensive catalog of industry-specific market research from this industry analysis report. The global Apoptosis Assays marketing document examines industries at a much higher level than a market study.

Apoptosis assays marketis expected to gain market growth in the forecast period of 2020 to 2027. Data Bridge Market Research analyses that the market is growing with a CAGR of 11.10% in the forecast period of 2020 to 2027 and is expected to reach USD 8.80 billion by 2027.

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The major players covered in the apoptosis assays market report are Merck Group, Thermo Fisher Scientific, Inc., BD, Bio-Rad Laboratories, Promega, Abcam plc, Research And Diagnostic Systems, Inc., Sartorius AG, Biotium, Inc., Creative Bioarray, GE Healthcare, Danaher Corporation, Geno Technology Inc, GeneCopoeia, Inc, Bio-Techne, PerkinElmer, Promega, General Electric and BioTek among other domestic and global players.

Segmentation:Global Apoptosis Assays Market

Apoptosis Assays MarketBy Product

(Assay Kits, Reagents, Microplates, Instruments),

Apoptosis Assays Market By Technology

(Flow Cytometry, Cell Imaging & Analysis Systems, Spectrophotometry, Other Detection Technologies),

Apoptosis Assays Market By End User

(Pharmaceutical and Biotechnology Companies, Hospital and Diagnostic Laboratories, Academic and Research Institutes),

Apoptosis Assays Market By Application

(Drug Discovery & Development, Clinical & Diagnostic Applications, Basic Research, Stem Cell Research),

Apoptosis Assays MarketBy Country

(U.S., Canada, Mexico, Germany, Italy, U.K., France, Spain, Netherland, Belgium, Switzerland, Turkey, Russia, Rest of Europe, Japan, China, India, South Korea, Australia, Singapore, Malaysia, Thailand, Indonesia, Philippines, Rest of Asia-Pacific, Brazil, Argentina, Rest of South America, South Africa, Saudi Arabia, UAE, Egypt, Israel, Rest of Middle East & Africa)

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Global Apoptosis Assays Market Drivers & Restraints:

The increasing cell-based research will help in escalating the growth of the apoptosis assays market.

The increasing incidence and prevalence of chronic and infectious diseases, development of apoptosis-modulating drugs, rising funding for cancer research, growing population suffering from chronic and autoimmune diseases are some of the factors expected to drive the growth of the apoptosis assays market in the forecast period of 2020 to 2027.

On the other hand, the growing adoption of apoptosis assays in developing markets will create several opportunities that will lead to the growth of the apoptosis assays market in the above mentioned period.

Lack of skilled personnel for research and development of apoptosis assays will likely to hamper growth of the apoptosis assays market in the above mentioned period.

Table of Contents:

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Key points for analysis

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Global Apoptosis Assays Market Set To Grow At Healthy CAGR Of 11.10% By 2027||Abcam plc, Research And Diagnostic Systems, Inc., Sartorius AG, Biotium,...

Jill Biden signals White House resolve on cancer research: This is the fight of our lives – The Cancer Letter

Ned Sharpless: I want to begin by thanking Dr. Biden for joining us today. Its great to have the first lady visit the NCI.

We all need this morale boost: 2020 has been a pretty rough year. This global tragedy of the public health has been hard on an agency whose mission is devoted to advancing the public health, so we really appreciate your interest and I want to express our heartfelt thanks.

Despite the challenges of the last year, it has been a remarkably productive time for cancer research and a remarkably productive time at the NCI. We are seeing progress against cancer at a faster rate than at any time in human history:

Lots of new great scientific advances that translate into new ways to diagnose, prevent, and treat cancer,

Important advances in cancer screening and prevention, and improvements in how we do clinical trials,

Record numbers of FDA approvals for new drugs and devices for cancer, and, importantly,

A steadily dropping annual cancer mortality.

Cancer mortality in the U.S. has been declining since the early 1990s, but in the last few years the pace of that progress has sharply accelerated, with the largest year-over-year declines in cancer mortality in the history of our statistics occurring in the last two years in a row!

As you know, Feb. 4 is World Cancer Day, which focuses on Intl Progress Against Cancer. NCI is proud to work with many international partners throughout the world to address cancer on a global scale and that work is coordinated by our outstanding Center for Global Health.

In 2021, the National Cancer Institute is partnering with others across the community to commemorate the 50th anniversary of the National Cancer Act, legislation that established some of the programs that form the backbone of todays cancer research enterprise. So, its really a good time to reflect on whats been accomplished and how much work remains.

Its all too clear that despite this progress I mentioned, this has not been good enough. We still have too many Americans dying of cancer, and we have too little progress against certain types of cancer like pancreatic cancer and glioblastoma. And even when we have treatments for these cancers that are able to cure some of these patients, often these treatments are really toxic and leave patients with lifelong survivorship challenges.

And now we have this new problem against that backdrop of the pandemics effect on cancer diagnosis and cancer care. The pandemic has closed hospitals and clinics throughout the country. And because of this, there have been many delays in screenings, diagnosis, and treatments, and we believe these delays incurred may translate into worse outcomes for people with cancer over the next decade.

So, a main challenge right now for the NCI is to get over the disruption caused by the pandemic and to get back on that great pace of progress in cancer research. We will face this challenge and declare together that nothing will stop us, nothing will stop us in our work on behalf of people with cancer.

And I know that Dr. Biden is very much with us in this challenge. The first lady, as everyone knows, has been a longtime advocate for cancer research and for people with cancer. Her interest in the topic began in the 1990s when friends were diagnosed with breast cancer. And I think we are all aware of Beau Bidens battle with glioblastoma, succumbing to that disease in 2015 and the impact this has had on the president and first lady.

In fact, I think it was this private tragedy of the Biden family that led to a really great public act, the Beau Biden Cancer Moonshot, which came about under the leadership of then-Vice President Biden. The NCI staff here today, took that vision and ran with it, bringing together stakeholders across the research community to work towards the goals he set for us.

To date, this has led to the launching of more than 240 exciting new programs and initiatives aimed at the laudable goal of rapidly accelerating cancer progress. It includes things like expanding our ability to treat cancer by awakening the immune system.

The Moonshot has worked on new approaches to fight childhood cancer. And there are Moonshot initiatives aimed at improving cancer care and underserved populations so that all patients can benefit from cancer progress and this is really just scratching the surface. There are many more great programs in the Moonshot. It is our fervent hope and belief at the NCI that this remarkable effort to improve the lives of all people with cancer will live up to Beaus memory. So Dr. Biden, thank you again for coming today and we were so eager to hear your remarks.

Jill Biden: Thank you, Dr. Sharpless, and your remarks are so heartwarming to me. Ned, were so grateful to have an accomplished researcher, academic inventor, physician, and author at the head of our nations premier cancer research institution. So, thank you for your leadership.

And Dr. Collins, thank you for joining us today as well and for your years of service at NIH in three administrations now. On behalf of both the president and me, I also want to thank you and the NIH for helping to create the vaccines and the treatments that are going to save so many lives and help our nation recover. And were just so lucky to have you.

So, its a pleasure to visit the National Cancer Institute virtually today. And Im grateful to be coming to you from the White House today as your first lady. Its the honor of a lifetime, but I know that even more than that, its a responsibility to serve the American people.

And from coast to coast, we face so many diverse and complicated challenges and yet when I was second lady and in my travels across the country over the last few years, Ive seen again and again, that there is one challenge that unites us all, one thread of pain that runs through every community, North and South, rich and poor, in the best of times, the depths of this pandemicand thats cancer.

The first time I heard the diagnosis for someone I loved, I was in my early 40s and the year it happened, not one, but actually four of my friends found out that they had breast cancer. And cancer took the life of both my parents. My sister had to have an auto-stem cell transplant and then, there was our son, Beau, as you referred to. Cancer touches us all and because of that, your work touches us all.

Youve brought the Cancer Moonshot to where it is today. Youve dedicated years to studying our immune systems and supporting clinical trials. Youve lifted up community-based clinics and treatment research. Youve led breakthroughs and discovered new ways to test.

And though this last year has been so difficult, NCI has risen to meet the challenge, uncovering how this pandemic has affected rates and figuring out how to continue this work, your work, because cancer doesnt stop for COVID. For more than 50 years, this organization, your organization has pioneered this frontier. Thanks to you, countless lives have been saved, countless families are whole, and there is more hope than ever for every person who is touched by this disease.

So, on behalf of the president and me, thank you, on behalf of every family who has faced cancer and a very grateful nation, thank you. We are so proud of everything that youre doing here, and now Im more excited to learn about the work that youre doing, so let me pass it back to Ned.

Sharpless: Thank you. To give you a flavor of some of the great work that goes on at the NCI, we have three of our researchers here to tell you about their areas of cancer investigation.

The first is Dr. Worta McCaskill-Stevens. Worta is a medical oncologist and chief of our Community Oncology and Prevention Trials Research Group. And then well hear from Dr. Stephanie Goff, who is a surgical oncologist at the National Cancer Institute. And then finally, from Dr. Ligia Pinto, whos a scientist at NCIs Frederick National Lab.

I thought wed start by hearing about patient outreach and engagement, and this is getting patients from underserved populations into clinical trials. For example, as you can imagine, a big problem in cancer research is translating these exciting new advances in cancer therapy and cancer prevention into real-world progress for all patients. This means reaching cancer patients in rural communities and underserved populations. And its really critical that we figure out how to do this.

And so, Ive asked Dr. McCaskill-Stevens here to come to tell you about the NCORP Network. Worta, will you take it over?

Worta McCaskill-Stevens: Thank you, Dr. Biden and welcome to the National Cancer Institute. Thank you, Ned.

Clinical trials provide the scientific pathway to treatment. However, clinical trials are much more than science. They are about science helping people. Through clinical trials, our aim is to enable the advances in cancer research and to make sure that theyre applied as broadly as possible. We wont have done our job if the outstanding research that we conduct is only enjoyed by a few.

But it all begins by improving access and diligently seeking ways in which we can increase participation in clinical trials. One way that we do this is to take the trials where the people are, and this brings me to the NCI Community Oncology Research Program, which provides access to clinical trials in communities where adults and children with cancer and those who are at risk of cancer live.

The NCI NCORP program is an academic and community partnership in which clinical trials related to the management of symptoms, prevention, screening, the delivery of care, quality of life and disparities and treatment are conducted.

NCORP has 46 community sites, 14 of these sites are focused in areas throughout the country that have large areas of rural patients and racial and ethnic minorities. Over 4,000 physicians participate in this network at over 1,000 sites that reflect very diverse oncology practices.

Enrollment into NCORP traverses over 43 states and includes Puerto Rico in Guam. Enrollment from the NCORP is almost one half of the enrollment in the NCI National Clinical Trials Network, which enrolls over 20,000 patients per year. Enrollment at the local NCORP sites allows those sites to be up-to-date on research tools and for their staff to contribute to the progress against cancer.

Weve learned a lot from the community sites. This has led us to great insights about the importance, for example, of understanding chronic diseases, diabetes, and hypertension, which is so prevalent in underserved communities. Also, to appreciate interactions of socioeconomic factors of social injustice when enrolling, and to have us consider these factors in our trial designs. Allow me to share with you an example of a recent trial that has been practice-changing.

This is the TAILORx trial. This is the trial that assigned individualized options for treatment. This was the first and the largest of NCIs precision cancer trials. It enrolled over 2,000 woman, 16% of which were minors and most of these women came from rural areas and community settings. This trial showed us that only about 20% of the women with early-stage breast cancer benefited from chemotherapy after surgery. These data affect and apply to 50% of breast cancer in the United States.

This trial, due to its size, the duration, and the fact that it had hypothesis testing, the fact that women may receive less therapy, could only have been conducted within the NCI. We now know using a molecular test that we can identify those women who only need endocrine therapy to reduce their risks of recurrence. These women now dont have to have chemotherapy side effects such as nausea, fatigue, risk of infection, or hair loss. These women can be cured and go back to their families and to their work.

So, that woman in rural America doesnt have to drive many miles to have the chemotherapy. Access to this and other very important clinical trials, we think, is a very important step in the direction of health in cancer therapy. Thank you.

Biden: Thanks. Can you tell me, how do people find out about your trials? Is it through their oncologists and how do you get the word to all the oncologists across this nation?

McCaskill-Stevens: Well, this is actually a network and one of the unique things about the NCORP is that they really connect with their communities. When they come in they bring the specific demographics and understand their patients. They have connections within the community so that the referral patterns come to them.

The NCI also does a great job of providing information to the public about clinical trials. Information comes from our societal meetings, and because its an academic-community partnership, much information is shared at those meetings and those direct contacts with those individuals, those organizations.

Biden: Well, Ive seen a lot of the need for the information to get out to the rural communities as Ive traveled around this country. And really one of the major places that I actually saw a need forlike youre saying, the chemotherapy clinicwas the Navajo nation and how they had no chemotherapy center. And they were traveling two hours to go get chemotherapy and then to travel home.

So, I think we just have to do a better job disseminating information out to communities about whats available to help people, because I think people are desperate for information on people who have cancer. Thank you for all that youre doing. I really appreciate it.

Sharpless: The dissemination of information about clinical trials is a real challenge because its often hard to match patients to the right trial and its something weve really worked on very hard. And having the ability to enroll patients at 1,100 sites nationally has, I think, made that somewhat easier, but theres still challenges that exist. Thanks, Worta.

Next, Id like to have you hear about some really exciting NCI intramural science on how to treat cancer. This involves this topic of cellular immunotherapy, which sounds like science fiction, but the idea is you use a patients own T cells to sweep them up, in a way, and give them back to the patients, reinfuse them to treat their cancer and this technology really was pioneered at the National Cancer Institute. And so Id like to invite Dr. Stephanie Goff to tell you about her exciting work in this area, Stephanie?

Stephanie Goff: Thank you, Dr. Sharpless, and thank you, Dr. Biden. As the daughter of a teacher, its a real honor for me to be able to present my work to you, and a virtual welcome to building 10. Dr. Collins refers to the NIH as the National Institutes of Hope and every place like that needs a house and so this is the house of hope here in Bethesda, where were able to take care of the patients that enroll in all of the clinical trials, across the institutes and centers.

We practice the medicine of tomorrow here and we take that responsibility very seriously. There are approximately 1,600 different clinical trials happening at the clinical center right now. And even in this challenging pandemic year that we just finished, 45 new clinical trials were started by investigators in the NCI and we were able to see over 1,500 new patients from all 50 states and territories.

And the work that we do here is the work that we refer to as first-in-human. So, its really after those long hours and nights in the lab, its when those moments that a theory becomes a reality when youre able to see it work for the first time in a patient and those moments are magical.

I was fortunate enough to train here and now have been able to come back and work side-by-side with my mentor, Dr. Steven Rosenberg, who has been pursuing this concept of immunotherapy quite literally my entire life. And what hes been pursuing is, can we get the immune cells of our body to learn how to see cancer? And because of the pandemic, so many people now understand a little bit about how T cells see things, particularly viruses.

We have a lot of amateur immunologists blooming these days, but can we get T cells to see a patients cancer? And if they can do that, can they make it go away? His career has been one built on bench-to-bedside. That cycle of learning that we all do. When we take something from the lab, we try it in patients once its safe. And then we see if we can get it to work. We learn from the successes, we learn from the failures, and then we go back and we try again.

He started that work in patients with metastatic melanoma, a very rare disease, but a very deadly one. And he learned that by stimulating all the T cells in the body with a drug called interleukin-2, which was one of the first immunotherapies to be approved, that he could make peoples tumors go away.

And it wasnt just away for a little while, it was away forever. There was a small portion of patients, maybe 4-5%, but they would live the rest of their lives cancer-free, normal lives, no more chemotherapy, no more additional drugs.

And so, as our tools got better, as Dr. Collins and the work that he did on the human genome became possible, we became able to see tumors much more clearly in a way that we couldnt do before, because the problem is that our immune systems are actually designed to ignore our bodies. We dont want them attacking all the tissues that we have, not to attack our breast or our thigh or our pancreas.

But when that tissue starts to go bad, when it becomes a cancer, what is it that makes it switch? How can we get the immune system to engage? And it turns out when you look down at the very, very fundamental level, at the DNA, when that change is enough to make that cell no longer look like the person that it lives in, thats when the immune system can kick in.

So, if we can find those cells, what can we learn from them? And how can we give them back to patients? Because if we can harness that, then we can just set the body on top of itself. The Achilles heel of that cancer is that it has changed and made itself visible.

I was teaching a course in basic immunology and cancer immunology to a group of breast cancer advocates, when a woman who was suffering from widespread metastatic cancer caught me and said that she wanted to join us as a patient volunteer.

And we did some stuff first to make sure that we werent going to be wasting her time, because time is such a valuable and precious commodity. And once it became clear that she was eligible, I took her to the operating room, I took a small tumor off her chest wall, and we were able to study that tumor in a number of ways.

We were able to look at the DNA changes in her tumor and we were able to test the T cells that lived there. And it turns out that takes us some time and her cancer was worsening, she was having to increase her pain medication, the lymph nodes in her armpit had started to press on her nerves, such that she couldnt use her arm.

And we finally had the cells ready. She came to us in Bethesda, she was here with us for about three weeks and she was convinced the treatment was working even while she was here. Now, Im a little bit more suspect than that and I wanted to watch and wait and see, but it turns out she was right.

Five years later, shes disease-free. She has taken up ocean kayaking. So shes using that arm with no problems and she hasnt had to have another single treatment for her cancer since then. She teases me though that I wont say that shes cured. Ill continue to say though, that she has no evidence of disease.

I could tell you a handful of stories like that, but the reality is there are far more families, as you well know, that dont have happy endings. And I, and so many of us carry those stories with us during the late nights and weekends in the lab and on the ward, because the NCI gives us the space and time to create tomorrows medicine and thats really what were all here for. So, thank you for paying attention to the work thats going on at the NCI. And on behalf of all my colleagues here in Bethesda, welcome.

Biden: Having lived through cancer with so many members of my family and Beau, its just amazing what youre doing and the hope that youre giving to families. Because I know with Beaus cancer, I mean, we tried everything and its just, like youre saying, youre trying all different things and youre giving families hope, and you have no idea how much that means. Thanks.

Sharpless: Thank you, Stephanie. That was terrific. I thought next Id like you to hear, Dr. Biden, a little bit about our work were doing related to SARS-CoV-2, to the coronavirus pandemic. It may not be obvious why the National Cancer Institute would work on coronavirus, but about 30% of cancers worldwide are caused by viruses. And so, theres been a long interest in virology at the NCI.

HIV, the virus that causes AIDS was co-discovered at the National Cancer Institute as was the first effective therapeutic for HIV. And then, John Schiller and Doug Lowy, who are still quite active NCI researchers invented the vaccine against Human Papillomavirus, which shows the significant expertise of the NCI in vaccinology.

Importantly, relevant to SARS-CoV-2, we have this really great serology lab, which studies antibody levels in the blood, run by Dr. Pinto at Frederick National Lab, which had been working on HPV serology with the WHO. Frederick International Lab is the largest federal biomedical research facility, run by the NCI.

And so, when the pandemic began, it was relatively straightforward for the NCI to pivot that serology lab on HPV to SARS-CoV-2 and this is how I think we played a crucial role in the fight against COVID. So, let me get Ligia to tell you about what her team has been doing as part of the coronavirus research effort.

Ligia Pinto: Thank you, Dr. Sharpless, Dr. Biden. Id like to share with you some of the key highlights of the exciting work on COVID-19 serology that we have been doing at the Frederick National Laboratory and the NCI. Frederick National Lab is a Federally Funded Research and Development Center with the infrastructure and the expertise to rapidly respond to public health crisis, such as the COVID-19 pandemic.

First, Id like to tell you a little bit about myself. Im originally from Portugal and I came to the NCI to do my PhD in immunology almost 30 years ago. My initial plan was to return to Portugal, but I decided to stay because of the incredible research opportunities at the NCI and in the United States in general. Our group works on serology. Let me tell you why we think its important and why this work is being done by cancer researchers.

Serology is the measurement of antibodies in blood predicting response to infection or vaccination. For COVID-19, serology tests are a critical public health tool for identifying individuals who were previously infected with SARS-CoV-2 or were vaccinated, and therefore maybe protected against the new infection. In order to inform public health decisions, antibody tests need to be reliable and highly accurate.

My laboratory at the Frederick National Lab has leveraged our expertise in studying immune responses to Human Papillomavirus infection and cervical cancer vaccines to develop serology tests and standards that are relevant to understanding SARS-CoV-2 infection and immune responses to the virus.

Because of this expertise at the beginning of the pandemic in April, when many serology tests were being developed, the FDA asked us to assist in evaluation of commercially available antibody tests for SARS-CoV-2, leading to evaluating more than 100 of these tests for the FDA. We have been able to do this thanks to a fantastic trans-governmental collaboration.

It has included several government agencies and academic medical centers. The FDA has used our performance evaluation data along with the other information to address some of these tests and reject others. Other critical tools for serology testing are standards. It enables comparison of antibody responses between different vaccines and other antibody studies.

In the spirit of the World Cancer Day, we had already developed standard reagents for our work on HPV and cervical cancer vaccines in cooperation with the National Institutes for Biological Standards and Control and the World Health Organization. And now, we have developed a serology standard for SARS-CoV-2. We are making it available to anyone in the scientific community.

Lastly, we have rapidly implemented a new initiative called Serological Sciences Network, SeroNet. This is one of the largest coordinated efforts across 25 of the nations top biomedical research institutions, where we have organized work collaboratively to study immune responses to SARS-CoV-2.

We believe that this collaborative network is an outstanding resource for tackling the emerging challenges associated with new viral variance, and understanding their potential impact on antibody testing and vaccine efficacy.

Two lessons that we have learned in all these efforts are that collaboration and sharing are key to making rapid advances. Thank you so much, Dr. Biden.

Biden: Thank you.

Sharpless: Well, so thats a sort of brief couple of snapshots of whats going on at the National Cancer Institute. Theres so much more work in both our intramural funded program and our extramural funded portfolio that wed love to tell you about, and we hope we get a chance to have you back sometime to talk more, but we really, really, really appreciate your doing this. It means so much to the National Cancer Institute to have you come and visit, and its so exciting for everyone at the NCI and we very much appreciate it.

Biden: Oh gosh. Thank you, Ned. And thank you to everyone who shared their stories today and what youve been doing. Its just incredible and I have to agree that you are the Institute of Hope, because so many people in this country are patients of cancer or have someone they love thats dealing with cancer, and Joe and I have worked in this space for a long time. I have personally worked with families and caregivers.

One thing I think that we found in the Obama-Biden administration was the benefit of collaboration and how much that meant, whether it was through all the agencies of the government just working together.

And so, I hope that you know of our commitmentof Joes commitment and my commitmentto carry on that work and to really be a partner with you and everybody at NIH, NCI, because weve got to work to fight cancer as we know it. I mean, we have to, because its not a red issue, a blue issue. Its a human issue, it affects all Americans.

So, I want to thank you just really, for all that youre doing. And as you said, Im a teacher and Im a professor of English and writing. So, I want to end with a little poetry today, something beautiful, because, obviously, what youre doing is so beautiful.

So, the poet, Gwendolyn Brooks, another life lost to cancer, wrote:

We are each others harvest:

We are each others business:

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Jill Biden signals White House resolve on cancer research: This is the fight of our lives - The Cancer Letter

Tiny sensor technique reveals cellular forces involved in tissue generation – Brown University

PROVIDENCE, R.I. [Brown University] A new technique developed by Brown University researchers reveals the forces involved at the cellular level during biological tissue formation and growth processes. The technique could be useful in better understanding how these processes work, and in studying how they may respond to environmental toxins or drug therapies.

As described in the journal Biomaterials, the technique makes use of cell-sized spheres made from a highly compliant polymer material, which can be placed in laboratory cultures of tissue-forming cells. As the tissue-formation process unfolds, microscope imaging of the spheres, which are stained with fluorescent dye, reveals the extent to which they are deformed by the pressure of surrounding cells. A computational algorithm then uses that deformation to calculate the forces at work in that cellular microenvironment.

We know that mechanical forces are important stimuli in tissue formation and development, but actually measuring those forces is pretty difficult, said Eric Darling, an associate professor of medical science, engineering and orthopedics at Brown. These spheres that weve developed give us an extremely sensitive technique for measuring those forces over time in the same sample. And we can do this with multiple samples at a time on a 96-well plate, so its a high-throughput method as well.

The research was a collaboration between Darlings lab and the lab of Haneesh Kesari, an assistant professor of engineering at Brown and an expert in solid mechanics. Darling and graduate student Robert Gutierrez developed the spheres and performed cell culture experiments with them, while Kesari and graduate student Wenqiang Fang developed the computational algorithm to calculate the forces.

The spheres are made from a polymer called polyacrylamide. The spheres have no apparent effect on the behavior of the newly forming tissues, Darling said, and the polyacrylamide material has mechanical properties that are highly consistent and tunable, which made it possible to make spheres soft enough to deform measurably when exposed to cellular forces.

The key to this is having a highly controlled material, with a very precise shape as well as finely tuned and uniform mechanical stiffness, Kesari said. If we know the properties of the spheres, then we can take pictures of how their shapes change and back out the forces necessary to make those changes.

As a proof of concept, the researchers performed a series of experiments to measure forces involved in mesenchymal condensation a process in which stem cells cluster together and eventually differentiate into tissue-specific cell types. The process is central to the formation of teeth, bones, cartilage and other tissue.

In one experiment, the team included the force-sensing spheres in cultures of cells were coming together to form multicellular balls. Microscope images of the cultures were taken every hour for 14 hours, enabling the team to track changes in the forces involved in each culture over time. The experiments showed that the forces involved in mesenchymal condensation were highly variable for the first 5 or so hours of the process, before settling down into a much steadier force profile. This was the first time such force dynamics had ever been measured, the researchers say.

To help verify that the spheres were truly sensitive to cellular forces, the team repeated the experiment using cultures treated with a cytoskeletal inhibitor, a drug that weakens the tiny contractile motors inside a cell. As expected, the spheres detected markedly weaker forces in the cultures treated with the drug.

In another set of experiments, the researchers added the sensor spheres to preformed cellular masses to observe how the spheres were taken up into the mass. Some of the spheres had been treated with a collagen coating, which enables cells to bind with the sensors, while others were uncoated.

We were able to see differences in the force profiles between the coated and uncoated spheres, Darling said. Overall there was a large compressive force, but with the coated cells we could see the cells interacting with the spheres directly, pulling on them and exerting a tensile force as well.

Darling says hes hopeful the technique could reveal fundamental details about how tissue-forming processes work. In the future, it may also be used screen drugs aimed at modulating these processes, or to test the effects of environmental toxins. It could also be useful in tissue engineering.

If we want to grow cartilage, it might be helpful to know that the types of forces that these cells are exerting on each other because we might be able to apply an external force that matches or complements that force profile, Darling said. So in addition to fundamental discovery, I think there is some translational potential for this down the road.

The work was funded by the National Institutes of Health (R01 AR063642), National Science Foundation (2018260690) and a Brown University Research Seed Award.

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Tiny sensor technique reveals cellular forces involved in tissue generation - Brown University

Leukemia in children: Symptoms, causes, treatment, outlook, and more – Medical News Today

Leukemia is a type of cancer that affects the blood. The two most common types in children are acute lymphoblastic leukemia and acute myelogenous leukemia.

In a person with leukemia, blood cells are released into the bloodstream before they are fully formed, so there are fewer healthy blood cells in the body.

Below, we describe the types of childhood leukemia, the symptoms, and the treatments. We then look at when to contact a doctor, what questions to ask, and where to find support.

Childhood leukemia is the most common form of cancer in children. It affects up to 3,800 children under the age of 15 in the United States each year.

Leukemia occurs when bone marrow releases new blood cells into the bloodstream before they are fully mature.

These immature blood cells do not function as they should, and eventually, the number of immature cells overtakes the number of healthy ones.

Leukemia can affect red and white blood cells and platelets.

The bone marrow produces stem cells. A blood stem cell can become a myeloid stem cell or a lymphoid stem cell.

Lymphoid stem cells become white blood cells. Myeloid stem cells can become:

Leukemia is typically acute or chronic, and chronic types are rare in children. They can include chronic myeloid leukemia or chronic lymphocytic leukemia.

Most childhood leukemias are acute, meaning that they progress quickly and need treatment as soon as possible.

Acute lymphoblastic leukemia (ALL) is the most common type in children, accounting for 75% of childhood leukemia cases.

It affects cells called lymphocytes, a type of white blood cell.

In a person with ALL, the bone marrow releases a large number of underdeveloped white blood cells called blast cells. As the number of these increases, the number of red blood cells and platelets decreases.

There are two subtypes of ALL: B-cell and T-cell.

In most childhood cases of ALL, the cancer develops in the early forms of B-cells. The other type, T-cell ALL, typically affects older children.

Research from 2020 reports that the majority of people diagnosed with ALL are under 18 and typically between 2 and 10 years old.

The American Cancer Society report that children under 5 years old have the highest risk of developing ALL and that this risk slowly declines until a person reaches their mid-20s.

The outlook for ALL depends on the subtype, the persons age, and factors specific to each person.

Myeloid leukemias account for approximately 20% of childhood leukemia cases, and most myeloid leukemias are acute.

Acute myelogenous leukemia (AML) affects white blood cells other than the lymphocytes. It may also affect red blood cells and platelets.

AML can begin in:

Juvenile myelomonocytic leukemia (JMML) accounts for approximately 12% of leukemia cases in children.

This rare type is neither acute nor chronic. JMML begins in the myeloid cells, and it typically affects children younger than 2 years.

Symptoms can include:

The symptoms of leukemia may be nonspecific similar to those of other common childhood illnesses.

A doctor will ask how long the child has been experiencing the symptoms, which can include:

Children may experience specific symptoms depending on the type of blood cell that the leukemia is affecting.

A low number of red blood cells can cause:

A low number of healthy white blood cells can cause infections or a fever with no other sign of an infection.

A low platelet count can cause:

Various factors can increase a childs risk of leukemia, and most are not preventable.

The following genetic conditions can increase the risk of leukemia:

Also, having a sibling with leukemia may increase the risk of developing it.

These can include exposure to:

If a child has symptoms that might indicate leukemia, a doctor may perform or request:

A bone marrow aspiration involves using a syringe to take a liquid sample of bone marrow cells. The doctor may give the child a drug that allows them to sleep through this test.

During the diagnostic process, a person might ask:

The doctor may recommend a variety of treatments for childhood leukemia, and the best option depends on a range of factors specific to each person.

The treatment usually consists of two phases. The first aims to kill the leukemia cells in the childs bone marrow, and the second aims to prevent the cancer from coming back.

The child may need:

Before or during treatment, a person might ask the doctor:

Questions to ask after the treatment might include:

Children who have undergone leukemia treatments require follow-up care, as the treatments often cause late effects.

These can develop in anyone who has received treatment for cancer, and they may not arise for months or years after the treatment has ended.

Treatments that can cause late effects include:

These complications may affect:

The late effects that may come can also depend on the type of treatment and the form of leukemia.

Because many leukemia symptoms can also indicate other issues, it can be hard to know when to contact a doctor.

Overall, it is best to seek medical advice if a child shows symptoms or behaviors that are not normal for them.

If a child has received a leukemia diagnosis, the effects can extend to parents, other family members, caregivers, and friends.

A person can find support and additional resources from:

The following organizations based in the United Kingdom also provide support and guidance:

Childhood leukemia can affect mental health, as well as physical health.

Learn more about mental health resources here.

According to the American Cancer Society, most children with leukemia have no known risk factors. There is no way to prevent leukemia from developing.

Because there are very few lifestyle-related or environmental causes of childhood leukemia, it is very unlikely that a caregiver can do anything to help prevent the disease.

A childs outlook depends on the type of leukemia. It is important to keep in mind that current estimates do not take into account recent advances in technology and medicine.

For example, the most recent 5-year survival rate estimates reflect the experiences of children who received their diagnoses and treatments more than 5 years ago.

The American Cancer Society report that the 5-year survival rate for children with ALL is 90%. The same rate for children with AML is 6570%.

Childhood leukemia is typically acute, which means that it develops quickly. As a result, a person should contact a doctor if they notice any of the symptoms.

The most common type of childhood leukemia is ALL, representing 3 out of 4 leukemia cases in children.

Treatment may include a combination of chemotherapy, targeted drugs, immunotherapy, stem cell transplants, surgery, and radiation.

The prognosis depends on the type of leukemia and the childs age.

This diagnosis can affect mental as well as physical health, and the effects can extend to caregivers, family members, and friends. Many different resources are available for support.

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Leukemia in children: Symptoms, causes, treatment, outlook, and more - Medical News Today