Articles tagged with Drug Targets
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A new study demonstrates the effectiveness of antisense drugs in targeting a wide range of tissues and organs, including liver, kidney, lung, muscle, and peripheral nerves. The findings suggest that antisense therapeutics have broad therapeutic potential for various disease indications.
Scientists have identified a key metabolic enzyme used by Plasmodium species at each stage of infection, paving the way for more effective drugs and potentially eradicating malaria. The discovery could lead to radical cures and prevent infections, blocking transmission back to mosquitoes.
A new study by Columbia University researchers has found a single overactive enzyme that worsens both impaired insulin sensitivity and overproduction of glucose in obese individuals, suggesting a potential target for treating type 2 diabetes. The enzyme MK2 can be inhibited with metformin, leading to additive benefits when combined.
A targeted effort to improve adherence to drug regimens in high-risk heart failure patients showed promise but had limited impact on reducing hospital readmission rates. Patients who received coaching from nurses were four times more likely to adhere to their medication regimens, but readmissions remained unchanged.
Medical researchers at the University of Alberta have discovered a potential drug target for a rare genetic disease, paving the way for an alternative treatment. The discovery links specific defects in the enzyme to specific symptoms and could lead to the development of drugs to treat less severe forms of the disease.
A WSU-led study finds that modifying a drug to target specific human proteins could lead to new treatments for cancers and immune-related diseases. Researchers discovered that simple modifications to the drug furamidine have a major impact on its ability to affect genes.
Researchers at University College London have developed a new method for building membrane-crossing pores using Lego-like DNA building blocks. This approach provides a simple and low-cost tool for synthetic biology and has potential applications in diagnostic devices and drug discovery. The technique uses two large anchors to embed the...
Researchers found that tumors may switch dependence from VEGF-A to related growth factors like VEGF-C, VEGF-D, and placental growth factor when targeted by bevacizumab. This change allows colorectal cancer to continue growing despite the blockage of VEGF-A.
Researchers at Linköping University have identified six proteins in spinal fluid that can be used as markers for the illness, offering a potential step towards early diagnosis. The study found that these proteins are associated with the breakdown of brain cells and toxic accumulations of beta amyloid protein.
Researchers at WashU Medicine found that chronic itching incorporates more neurons than normal itch signals and co-opts pain neurons to intensify the sensation. This discovery may lead to more effective treatments targeting activity in both pain and itch neurons.
Researchers created a massive online database that matches thousands of genes linked to cancer and other diseases with drugs that target those genes. The database includes over 14,000 drug-gene interactions and is publicly available for research purposes.
A massive DNA study has uncovered 157 genetic changes that alter cholesterol and blood fat levels, potentially leading to new medications. Triglycerides play a larger role in heart disease risk than previously thought, and the research provides strong foundation for further investigation.
IU researchers and collaborators found two new targets, Rac GTPase and Pak, that can be inhibited to kill leukemia cells. The study aims to improve treatment options for patients with mast cell leukemia and acute myeloid leukemia.
Stem cells can be engineered as targeted drug factories to deliver anti-inflammatory molecules to sites of inflammation, reducing swelling. The approach uses modified messenger RNA to stimulate cell production and secretion, overcoming previous limitations such as rapid clearance.
Researchers at Rutgers University have identified chemical agents that block the ability of flu viruses to replicate in cells. The compounds show promise for a new class of antiviral medicines to fight pandemic influenza outbreaks, such as H5N1 and H7N9.
Researchers found that activating serotonin 5-HT2A receptors potently blocks TNF-alpha induced inflammation, offering a potential breakthrough in treating inflammatory diseases. The findings have the potential to lead to new oral medications for atherosclerosis and IBS.
A study published in Cancer Cell identified a previously unknown vulnerability in triple-negative breast cancers, which can be effectively treated with an FDA-approved drug. The researcher found that targeting the cystine transporter xCT significantly inhibited tumor growth in mice and cell culture.
A $5.9 million Department of Defense grant enables the development of drugs that target androgen receptors as a driver of breast cancer. The treatment shows promising results in preclinical work and may offer new options for patients with previously limited therapy.
Researchers at Scripps Research Institute discovered that an essential protein evolved chiefly by changing its movement, rather than structure. This finding has implications for designing more effective antibiotics and drugs targeting the protein dihydrofolate reductase.
Researchers found that essential proteins evolve chiefly by changing how they move, rather than their molecular structure. This discovery has significant implications for the design of antibiotics and other drugs targeting dihydrofolate reductase.
Researchers found that tempol, an anti-oxidant drug, reduces weight gain in mice fed a high-fat diet. The drug targets the gut microbiome, specifically reducing Lactobacillus levels and increasing tauro-beta-muricholic acid, which inhibits FXR and regulates metabolism.
Researchers found that a class of proteins affecting visual system development also appears to affect vulnerability to Alzheimer's disease in the aging brain. The proteins, such as LilrB2 and PirB, physically partner with beta-amyloid, triggering a harmful chain reaction in brain cells.
Scientists at EMBL and Regensburg University identify DGKi as a potential drug target for cystic fibrosis, which regulates ENaC activity and reduces mucus thickness in patients' airways. The discovery uses large-scale screening to uncover genes not previously linked to the disease.
Scientists at the University of Notre Dame have identified a protein called SIK1 that can help regulate the body's internal clock. By blocking its activity, researchers found that mice adjusted faster to changes in their environment, suggesting that SIK1 could be a target for treating jet lag and shift work disorders.
Researchers have identified a potential new angle for drug development in preventing thrombosis, a dangerous blood clot that can lead to stroke and heart attack. The study uncovered a key platelet protein that could be exploited to develop drugs that keep platelets from forming pathological clots.
Researchers identified a mechanism that limits the body clock's ability to adjust to changes in light patterns, slowing down recovery from jet-lag. Blocking this gene in mice allowed them to recover faster.
Researchers have identified five enzymes essential to the survival of a parasitic worm infecting livestock worldwide, including two already studied as potential drug targets against other pathogens. The genome of Haemonchus contortus provides valuable insights into how treatments work and reveals new drug and vaccine targets.
The study showed that the Ebola VP40 protein exists as a dimer and rearranges its structure to assemble filaments for the virus shell or bind RNA, controlling various steps of the life cycle with multiple functions.
Vinculin plays a critical role in enabling cell movement by interacting with the actin cytoskeleton. Disrupting this interaction can lead to chaotic cell movement, impacting organ development and cancer progression.
A targeted cancer drug has shown dramatic responses in patients with specific gene mutations, raising questions about the need for expensive Phase III trials. The author argues that a lower bar for approval could streamline the process and bring effective treatments to patients sooner.
Researchers found that full activation of a crucial brain-signaling molecule requires coordinated motion of its segments. The study may reveal additional drug-binding sites on the receptor, aiding the development of drugs for conditions like epilepsy and Parkinson's disease.
Researchers have discovered that two receptors of leukotriene B4 play opposing roles in inflammation, with BLT1 promoting and BLT2 weakening inflammation during an allergic reaction. This finding suggests new approaches to developing anti-asthma and anti-COPD drugs.
A laboratory study shows that a nanotechnology drug called SapC-DOPS crosses the blood-brain barrier and targets brain-tumor cells, retarding growth of tumor blood vessels. The agent also sensitizes hypoxic cells to killing, supporting further development as a novel treatment for glioblastoma.
Researchers developed statistical models to predict which drug is best for a specific individual with a specific disease, considering pharmacokinetics, pharmacodynamics, and genetic factors. The framework will help doctors and pharmacists simulate variables like protein-protein interactions and predict treatment effectiveness.
A study led by the University of Exeter found that 27% of over-70s with type 2 diabetes achieved better glycaemic control through individualized care alone. Researchers introduced a 'one-size-fits-all' approach for older patients, which proved ineffective due to multiple complications.
A recent study published in Nature reveals that septins play a crucial role in activating the calcium channel on T cell surfaces, allowing them to fight disease. This discovery provides new insights into the intricate pathways involved in turning on T cells and could lead to the development of more targeted drugs.
Researchers have discovered a crucial signaling network between EGFR and MCM7 proteins, which plays a key role in DNA replication and cell growth. In breast cancer patients, high expression of Lyn and MCM7 is associated with reduced survival rates, highlighting a potential new target for cancer therapy.
Researchers used nanosensors and advanced imaging techniques to track the spread of pancreatic tumors and monitor the effectiveness of drugs. The study reveals promising results for combination therapies that can enhance drug delivery and improve clinical outcomes.
The new ProteomicsDB contains over 11,000 datasets from human cancer cell lines and tissues, enabling real-time analysis of large data sets. The database provides instant value for researchers to test analytical hypotheses and develop new drugs with reduced side effects.
A protein complex called Mediator, specifically enzyme CDK8, plays a crucial role in tumor cell survival under hypoxic conditions. Inhibiting CDK8 could provide a potential target for cancer-fighting drugs, particularly those targeting HIF1A transcription factor.
A Singapore research team has identified a protein enzyme, MNK kinase, as a key player in the progression of chronic myeloid leukemia (CML) to its deadly terminal stage. The researchers found that targeting this enzyme could help prevent cancer stem cells from developing drug resistance and improve patient survival.
Researchers have discovered a new oncogene, RET rearrangement, which is present in 15.7% of lung adenocarcinoma patients and may be targeted with existing tyrosine-kinase inhibitors. This finding presents a promising treatment option for patients with this specific mutation.
Researchers developed a novel approach to make ovarian cancer cells susceptible to an antitumor drug, potentially improving treatment outcomes. The strategy targets telomeres and shows promise in treating other epithelial cancers.
Two genetic mutations, PDGFRB and NOTCH3, have been identified as potential therapeutic targets for infantile myofibromatosis (IM), a rare and debilitating disorder. Current treatment options involve repeated surgical removal of tumors, which can be invasive and disfiguring.
Researchers successfully targeted doxorubicin to mitochondria, killing cancer cells even those with developed pumps. The study suggests this approach could work with other nucleus-targeting anti-cancer drugs.
Researchers have identified Dkk1 as a key player in the development of atherosclerosis, a condition that causes arteries to become stiff and narrow, leading to impaired blood flow. Targeting Dkk1 signaling may help limit arteriosclerotic disease, according to a new study.
A new osteoporosis treatment combination of denosumab and teriparatide was found to be more effective than individual therapies, increasing bone density in women with osteoporosis. The study showed significant improvements in BMD at the spine, hip, and femoral neck in women treated with the combination therapy.
Researchers at Scripps Research Institute discovered how to control natural gene silencing processes, leading to a powerful new class of drugs against viral infections, cancers and diseases. The study found that guide RNAs can be designed to destabilize or stabilize the miRNA-Argonaute complex.
Scientists from the University of Pennsylvania define a novel mechanism of tumor hypoxia induced by the longitudinal gradient of residual oxygen along tumor vessels as they transverse the tumor. The researchers found large regions of moderate hypoxia that were not easily explained by existing concepts, suggesting a new scale for unders...
Researchers have discovered a previously unknown link between over-stimulation and brain tissue destruction, pointing to a potential drug target. The study identified NOS1AP as the key protein that links nitric oxide production to cell damage.
Researchers have developed a new technique to improve the use of nanoparticles as a drug delivery system. The study found that smaller particles degrade faster in the body than predicted by in vitro measurements. By understanding this degradation, a mathematical model can be developed to optimize nanoparticle-based therapeutic systems.
Researchers used computer simulations to investigate the energy landscape of ion channels, identifying a critical amino acid that regulates their function. The study provides new insights into ion channel mechanisms, which are essential for developing targeted therapies.
A recent study reveals that a protein in our cells, responsible for transporting vital substances, also enables bacterial cells to develop resistance to antibiotics. This mechanism is linked to the development of antibiotic resistance and cancer drug resistance, highlighting the need for new therapeutic strategies.
Researchers at Duke Medicine found a biomarker produced by mast cells can predict severe dengue cases. Asthma drugs targeting mast cells also showed effectiveness in limiting vascular leakage associated with dengue infections.
BIND-014, a targeted docetaxel Accurin candidate, demonstrated encouraging anti-tumor activity and was well-tolerated in 28 heavily-pretreated patients with advanced or metastatic solid tumors. The Phase 1 results established the maximum tolerated dose of 60 mg/m2 and showed signs of stable disease lasting at least four cycles.
BIND-014, a PSMA-targeted nanoparticle containing docetaxel, demonstrated anti-tumor activity in 28 patients with advanced or metastatic solid tumors. The Phase 1 trial showed encouraging signs of effectiveness, including one complete response and five patients with stable disease.
Children with fragile X syndrome showed significant improvements in general behavior, anxiety, and mood-related behaviors after three months of minocycline treatment. The study provides evidence for the efficacy of minocycline as a targeted treatment for fragile X syndrome.
Researchers have mapped tapeworm genomes to identify potential drug targets using existing drugs, which could lead to faster and more effective treatments. The discovery has significant implications for the development of urgently needed therapies for these devastating diseases.
A new study published in Biological Psychiatry found that antipsychotics with high binding affinity of alpha2 adrenergic and M1 muscarinic receptors are associated with a greater risk of stroke in elderly patients. The study also suggests that stroke risk is highest in the initial weeks of treatment and for those with higher daily doses.
A phase IIa study suggests that ORM-12741, a new add-on drug, improves memory scores by 4% in individuals with moderate Alzheimer's disease, while worsening it by 33% in those receiving a placebo. The study found significant benefits in improving brain functions under stressful conditions.