Articles tagged with Drug Targets
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The discovery of CRISPR-Cas9 systems has revolutionized pharmaceutical research by allowing for industrial-scale gene editing and functional genomic screening. This enables the identification of new biological targets for precision medicines and the exploration of mechanisms of drug resistance and sensitivity ahead of clinical trials.
The Kong group will investigate how neurons and muscle cells communicate, with the goal of understanding how to reactivate neurons in injured muscle. They will also develop a drug delivery system to target tau proteins responsible for Alzheimer's disease.
The new guidelines, if implemented, would lead to a substantial financial burden on health systems due to the high cost of PCSK9 inhibitors. Around 50% of patients with a recent heart attack would be eligible for these expensive drugs, which could increase treatment costs by over 4,500 euros annually.
A team of NUS researchers identified a novel protein S1P2 that can protect nerve cells from damage and pain when activated with a drug-like compound. This discovery holds promise for the prevention and treatment of chemotherapy-induced neuropathy, as well as other forms of neuropathy.
Target-based ecological compensation provides a framework for linking compensatory requirements to biodiversity targets, ensuring no net loss of species habitats. This approach resolves uncertainty and promotes better outcomes for the planet and people.
A novel injectable drug, NOV004, is being developed by Novosteo Inc. to heal broken bones faster and strengthen weak bones. The treatment concentrates at the fracture site while reducing exposure to the rest of the body, potentially reducing mortality rates among older adults.
Researchers discovered EphA2 protein plays a crucial role in cerebral malaria by disrupting blood-brain barrier, leading to leaky brain and deadly symptoms. Blocking EphA2 with drugs may prevent disease in humans, offering hope for alleviating this condition.
Scientists have made an important discovery that could lead to more effective treatments for people living with multiple sclerosis (MS). The study found that drugs targeting the IL-17 molecule may not need to get across the blood-brain-barrier to be effective in treating MS.
A recent study published in Blood Advances eliminates BCL-W as a potential therapeutic target for B cell lymphomas. The research team used gene editing technology and demonstrated that human B cell lymphoma cell lines can survive without BCL-W, contradicting earlier speculation about its role in cancer survival.
A newly identified compound, C1, is a covalent gamma-secretase inhibitor that blocks the production of amyloids by inhibiting the enzyme's activity on the amyloid precursor protein. This approach avoids traditional enzyme inhibitors' severe side effects and shows promise for treating Alzheimer's disease.
A research team has discovered a possible target for new sleeping sickness drugs using an X-ray laser. The scientists decoded the structure of a key enzyme in the parasite Trypanosoma brucei, which could lead to a specific drug that kills the parasite.
A collaboration between Rutgers University and Scripps Research has led to the discovery of a small molecule that reduces α-synuclein protein levels, potentially slowing or stopping Parkinson's disease progression. This finding offers hope for early-stage patients and may be applicable to other neurodegenerative diseases like Alzheimer's.
A comprehensive roadmap has been established to evaluate and implement ivermectin as a complementary vector control tool against malaria. The roadmap aims to decrease malaria transmission by targeting the vector population, bypassing challenges of insecticide resistance and residual transmission.
Scientists have shed light on the structure and functioning mechanism of CysLT receptors, regulating inflammatory responses associated with allergic disorders. The study identified critical ligand-binding determinants, enabling better understanding of receptor-ligand complexes and potential drug targets.
A new study reveals that certain enzymes, known as cathepsins, not only promote diseases like cancer but also cannibalize and deactivate each other. By modeling these interactions, researchers hope to develop more effective inhibitors with fewer side effects.
Researchers mapped protein-drug interactions in rat organs and blood, revealing potential drug targets. The study represents a significant advancement for translational research, allowing direct monitoring of biological changes in an organ.
Researchers scanned the brains of young adults with ADHD while taking methylphenidate to study its effect on the brain's reward system. The results showed that methylphenidate increased activity in the ventral striatum in response to rewards, suggesting a possible mechanism for improving focus and behavior in individuals with ADHD.
Researchers at UC Riverside are targeting cancer-causing genes Mcl-1 and Bfl-1 for novel therapies in melanoma and lung cancers. They aim to develop potent agents that can help tackle chemotherapy-resistant cancers.
Researchers found an average increase in stem cell count of 68% with minimal side effects, reducing 'stressed' cells and improving conditions for pregnancy. The treatment aims to prevent miscarriage by normalizing the womb lining.
Australian researchers have identified a new drug target for preventing the deadliest malaria parasite from spreading infection. The breakthrough involves blocking the export of gametocyte proteins, essential for malaria transmission, using small molecule inhibitors developed at the Walter and Eliza Hall Institute.
Researchers at Karolinska Institutet have developed a new tool that provides more reliable and precise results in identifying protein targets for cancer drugs. The tool uses a database of experimentally determined data to analyze the effects of different drugs on various types of cancer cells.
A new analysis confirms human genomic data can predict success in clinical trials, with genetically supported drug targets twice as likely to be approved. Historically, drugs targeting proteins with amino acid sequence changes linked to the disease have the best chance of approval.
A study published in EMBO Molecular Medicine suggests that blocking the protease MT1-MMP could protect the vasculature in the inflamed gut and reduce severity of colitis. The research found that inhibiting this protease could have potential clinical implications, including identifying biomarkers for mild IBD.
A new study found that Class I drug treatment showed increased rates of AFib reoccurrence in obese patients compared to non-obese patients. The study suggests that obesity hinders the effectiveness of these medications, which could impact ethnic minority populations who are more likely to experience obesity and have poorer outcomes.
Researchers have identified 111,582 gene fusions in eight species, including humans, mice, and cattle. The ChiTaRS database provides a list of over 800 druggable fusions useful for personalized therapy in complex diseases like cancers and Alzheimer's.
Researchers at Cold Spring Harbor Laboratory have developed a new therapy that extends the survival of mice with acute myeloid leukemia by blocking the Salt-Inducible Kinase 3 (SIK3) pathway. The treatment, YKL-05-099, is a first in demonstrating anti-cancer effects of SIK3 inhibition using pharmacological blockade.
Researchers discovered that cells with extra chromosome 21 in DS mice activated a biological circuit that detects stress and tamps down protein production, leading to cognitive impairments. By targeting this stress response, scientists were able to reverse learning and memory deficits in the mouse model.
A Scottish government-funded social prescribing initiative failed to improve patients' health-related quality of life. In a subgroup analysis, those who visited the practitioner three or more times showed improved quality of life, but many non-users did not fully utilize the program.
A research team found that Dasatinib, a leukemia treatment, suppressed glial cell activity and pro-inflammatory cytokine expression, inhibiting encephalitis reactions. The study revealed the efficacy of drug repositioning to treat degenerative brain diseases like Alzheimer's.
Researchers used ultrashort X-ray pulses to study Photosystem I, a large biomolecular system converting sunlight into chemical energy. This breakthrough paves the way for time-resolved studies on electron transfer in photosynthesis, with potential applications in medicine and next-generation solar energy storage.
Researchers identify a potential target for eliminating leukemia stem cells using vitamin K3, which stabilizes the DYRK2 enzyme. This approach could lead to treatment-free remissions and improved patient outcomes.
A new poll finds that half of older Americans have taken leftover antibiotics without guidance, while one in five expect doctors to prescribe them for colds. Despite widespread awareness of antibiotic resistance, many older adults engage in risky practices, highlighting opportunities for education and improved prescribing.
A new healthcare framework aims to improve diagnosis and treatment of age-related diseases by classifying and staging severity. The framework, developed by an international team of experts, includes a comprehensive classification system for aging-related diseases in all organs.
A comprehensive genome sequencing study reveals rare CFTR mutations in Puerto Rican and Dominican patients, driving the disease's progression. This finding underscores the need for diverse clinical trials to develop personalized therapies, as transformative new drugs may not benefit minority populations.
Researchers solved the three-dimensional structure of potassium chloride cotransporter 1 (KCC1) using cryo-electron microscopy. The study's findings provide new insights into the protein's role in regulating cell volume, particularly in the kidneys and brain, and shed light on potential treatments for hereditary epilepsy.
Researchers have identified a new mechanism by which cancer cells become resistant to ferroptosis, a type of cell death. A molecule called FSP1 acts as a lipid antioxidant, rescuing cancer cells from ferroptosis even when they are starved of GPX4.
Researchers at the University of Dundee have discovered an enzyme that could prevent Group A Streptococcus infections by inhibiting a carbohydrate coating on the bacterium's surface. The discovery offers new opportunities for developing antimicrobial drugs with minimal off-target effects.
Researchers found that suppressing neural overactivity extends life span in humans, while excessive activity is linked to shorter life spans. The study suggests a role for the protein REST in modulating neural activity and activating a longevity pathway.
A modern chemotherapy drug is more effective against advanced prostate cancer than a second targeted hormone therapy, with cabazitaxel extending men's lives by an average of 3 months. The study suggests that cancer's lethal ability to develop drug resistance affects treatment response across precision medicines.
A phase III trial found that olaparib significantly delayed disease progression by about four months compared to enzalutamide and abiraterone, resulting in a 66 per cent greater delay. The study highlighted the importance of genomic testing in prostate cancer patients.
Researchers at University of Eastern Finland developed a new approach to improve brain drug delivery by utilizing LAT1. The study showed that prodrugs can be converted into active drugs that utilize LAT1 for cell entry, achieving higher concentrations in target cells.
Researchers use CRISPR gene editing and MICS to identify genes that can be targeted by drugs in cancer and regenerative medicine, revealing promising targets for cancer treatment. The technology also enables faster harvesting of desired cell types for therapy.
Researchers identified links between genetic variants and early activation of memory T cells, suggesting problems with regulating this process could lead to immune diseases. The study's findings could help narrow down the search for molecular pathways involved in immune diseases.
A new study found that combining a G12C KRAS inhibitor with two other compounds can significantly shrink lung tumours in mice and human cancer cells. This combination block the mTOR and IGF1R pathways, making it a promising avenue for treating lung adenocarcinomas with the deadly G12C KRAS mutation.
A study of people who use illicit opioids found that 27% prefer drugs with fentanyl, and these users are more likely to be younger, white, and daily users. The study suggests that harm-reduction strategies should target users who fit this profile, particularly those using portable drug-checking technologies.
Researchers compared three frontline breast cancer drugs and found significant differences in their biological activity. Abemaciclib was shown to be more effective than other drugs at high doses, affecting proteins beyond CDK4/6, suggesting it may work differently for patients who don't respond to other treatments.
A breakthrough in monkey malaria research by University of Otago scientists could help diagnose and treat a relapsing form of human malaria. The team has developed an in vitro culture method for the vivax malaria parasite, which is closely related to the relapsing parasite.
Researchers developed a fruit fly strain that builds up uric acid when triggered by high-purine diet, revealing the insulin-like signaling pathway's role in regulating uric acid levels. This model could help identify new drugs for diseases linked to uric acid accumulation.
Research in flies reveals potential drug targets for gout, metabolic syndrome, diabetes, and kidney stones by manipulating insulin-like signaling pathway. Elevated uric acid levels increase risk of these diseases, emphasizing the importance of routine screenings in humans.
Researchers at NUST MISIS have identified a mechanism for removing magnetic nanoparticles through the kidneys, allowing for safer drug delivery. The study used a combination of techniques to track nanoparticle transport, revealing that they can be excreted directly into the renal tubule, reducing the risk of liver accumulation.
Researchers developed a new method to analyze nanoparticles' movements in real-time, finding that targeting nanostars rotate faster and move across larger areas than non-targeting counterparts. This technology holds promise for reducing side effects of cancer treatments by delivering drugs directly to diseased cells.
Researchers have identified propranolol's molecular target for its ability to treat vascular diseases, including hemangiomas and hypotrichosis-lymphedema-telangiectasia. The study suggests that a specific component of the drug may be responsible for its therapeutic effects.
A study by University of Notre Dame researcher Siyuan Zhang and collaborators identified a gene that makes triple-negative breast cancer (TNBC) cells vulnerable to existing therapies. The discovery suggests that a targeted drug therapy may be effective for this aggressive type of breast cancer.
A new study using a cryo-electron microscope provides critical information for developing anti-nausea drugs that are effective against cancer patients' vomiting side effects. The high-resolution images reveal the attachment site of widely-used setron drugs on serotonin receptors, offering insights into how their design might be improved.
Researchers found ivacaftor significantly reduces P. aeruginosa, Staphylococcus aureus and Aspergillus spp. infections in CF patients, with a 32% reduction in P. aeruginosa and 15% reduction in Staphylococcus aureus.
Serial femtosecond X-ray crystallography (SFX) allows researchers to analyze the tertiary structure of proteins previously inaccessible. This method uses powerful X-ray free-electron lasers to generate diffraction patterns before destroying the sample, enabling faster and cheaper drug design.
A stealthy new drug-delivery system has been developed that disguises chemotherapeutics as fat, allowing it to penetrate and destroy tumors while minimizing side effects. The system uses a long-chain fatty acid with two binding sites to attach to drugs, which are then carried by human serum albumin throughout the body.
Researchers found a human gene present in 75% of the population affects treatment response in Alzheimer's patients. The study suggests that different mechanisms work in different patients, requiring personalized treatments to improve outcomes.
Rutgers researchers created a portable device that combines artificial intelligence and biosensors to detect live cancer cells after treatment, providing rapid results for personalized interventions. The device achieves 95.9% accuracy in counting live cancer cells without staining, enabling further molecular analysis and instant detect...
A new class of drug lead derived from N-arylpyrrole exhibits potent anesthetic activity with minimal blood pressure suppression, suggesting a safer alternative to traditional anesthetics. The compound shows promise in tadpoles and rats, providing hope for improved patient safety.