Articles tagged with Drug Resistance
Researchers identify detailed structure of protein complex used by bacteria to detect environmental changes and adapt to them. This discovery sheds light on how bacteria develop resistance to antibiotics.
A combination of a PARP inhibitor and a kinase inhibitor showed significant tumor shrinkage in 36% of patients with platinum-resistant ovarian cancer, a surprising improvement over solo PARP inhibitor treatment. The treatment was well-tolerated, with four patients discontinuing due to toxicity.
Scientists at Liverpool School of Tropical Medicine have created a new way to screen potential treatments for Tuberculosis (TB), which may reduce treatment duration from six months to weeks.
Researchers at Mass General Hospital identified novel resistance mechanisms in patients with liver tumors receiving FGFR inhibitor treatment. The study found that different mutations within individual patients and across multiple samples could confer resistance, highlighting the need for more effective treatments.
Trichomonosis is a common infectious cause of large bowel diarrhea in cats, characterized by 'cow pie' consistency and mucus/blood in faeces. The infection is caused by the protozoan Tritrichomonas foetus, which can be transmitted from cat to cat via the faecal-oral route.
Scientists have found that two immune system molecules, interleukin 1 beta (IL1β) and tumor necrosis factor alpha (TNFα), may drive drug resistance in estrogen-driven breast cancers by modifying the shape of the estrogen receptor. This finding could lead to novel therapeutic approaches.
Researchers identified a secondary pathway to reactivate EthA enzyme in resistant TB strains, boosting treatment efficacy. The combination of SMARt-420 and ethionamide effectively treated resistant TB strains, reducing bacterial load in mouse lungs.
Researchers at Cardiff University have devised a new way of creating the leading anti-malarial drug artemisinin, which could reduce market fluctuations in the supply chain and help study resistance to the drug. The new method bypasses several key steps in the production process, achieving the desired outcome in just four steps.
Researchers have created a precise atomic map of the frontline antimalarial drug mefloquine, showing how its structure could be changed to make it more effective. The study provides a route to develop new treatments with fewer resources and potentially reduced side effects.
Researchers have created a detailed atomic map of the frontline antimalarial drug mefloquine, showing how its structure could be tweaked to increase effectiveness. The study aims to create a more targeted and safer treatment by redesigning the drug's molecular machinery.
Researchers at Mayo Clinic have identified a specific protein implicated in drug resistance, as well as a possible therapeutic tool. By engineering a peptide that blocks the activity of another protein ERK, the team found that it can prevent chemotherapy resistance and tumor growth.
Research reveals that expression levels of ABCB1 and ABCG2 transporters significantly affect cell resistance to Dasatinib. Lower transporter expression levels mediate lower resistance, implying a potential breakthrough for targeted cancer treatment.
Research reveals that only one in five patients with resistant hypertension are taking all their prescribed medications, while 20% are not taking any. The study found that adherence to medication greatly affects the ability to assess the value of another treatment, and patients can take steps to prevent high blood pressure from remaini...
Researchers at Ohio State University Comprehensive Cancer Center have identified a mechanism by which cancer cells develop resistance to FGFR inhibitors. By inhibiting the regulatory protein Akt, they found that cell proliferation, migration, and invasion could be slowed in lung and bladder cancer cells.
Scientists at The Wistar Institute have identified an anti-aging gene that inhibits a protein involved in metastatic progression and resistance to targeted therapies. Activating this gene with an anti-diabetic drug may provide a promising adjuvant therapy for older melanoma patients.
Scientists have detected an artemisinin-resistant malaria parasite originating from West Africa for the first time in Africa, posing a significant threat to malaria control efforts. The finding confirms that the parasite carries a new mutation in the Kelch13 gene, which is the primary driver of resistance in Southeast Asia.
Researchers aim to develop novel treatments and preventative medicines to assist with malaria eradication and elimination, replacing ineffective current drugs that are losing efficacy.
A new mathematical analysis provides guidance for treating infections and tumors with drug resistance, suggesting that containment may extend effective life and improve patient outcomes in some cases. The study identifies two main factors influencing the choice between containment and aggressive treatment.
Researchers discovered that malaria parasites produce HMBPP, which stimulates red blood cells to release carbon dioxide and volatile compounds attracting malaria mosquitoes. The parasite uses this system to transfer from one host to another, making it harder to control the spread of malaria.
Researchers identify factors determining when containment or aggressive treatment is best, providing new guidance for physicians and patients. Containment strategies can prolong treatment life and improve outcomes in certain situations.
Researchers are studying the effectiveness of two treatment options for children with Kawasaki disease who resist initial therapy. The study aims to compare the impact of IVIG and infliximab on preventing heart damage in these patients.
Mass drug administration programmes have significantly increased treatment for bilharzia, killing an estimated 280,000 people annually. Praziquantel MDA programmes are effective but long-term effects and resistance to the drug are largely unknown.
Dr. Timothy Anderson received a 5-year, $4.6 million MERIT Award to study drug resistance in malaria parasites and develop effective treatment strategies. The award supports his efforts to understand the genetic determinants of resistance and apply powerful gene editing technologies.
A new approach to treating tuberculosis could significantly reduce treatment time and improve patient outcomes. Researchers identified an effective four-drug regimen that kills TB bacteria in the lungs and cures mice up to four times faster than current treatments.
A study published in The New England Journal of Medicine found that extensively drug-resistant tuberculosis (XDR TB) is spread through person-to-person contact in the KwaZulu-Natal province, South Africa. This epidemic highlights the need for effective infection control and treatment measures to prevent further spread.
Researchers found a wide variety of CRE species and genetic traits enabling resistance, with traits transferring easily among species. The findings suggest that CRE may be transmitting from person to person asymptomatically, highlighting the need for increased genomic surveillance.
Researchers have solved the atomic structure of HIV's intasome, a key piece of machinery that integrates virus into human DNA. The discovery provides structural clues informing the development of new HIV drugs and sheds light on mechanisms of viral resistance.
Researchers found that tumors shed between seven and 18 mutations in neoantigen-coding genes after developing resistance to immunotherapy drugs. This phenomenon could lead to new ways to improve current cancer immunotherapies.
A new study reveals that cancer cells can develop resistance to proteasome inhibitors by suppressing the expression of proteasome subunits, leading to a broadly altered cell state with unique vulnerabilities. This finding may expose opportunities for targeted therapies that can be effective against diverse cancers.
Researchers identified gene mutations associated with steroid resistance in pediatric T-cell acute lymphoblastic leukemia, leading to poor clinical outcomes. A new therapeutic approach targeting individual signaling proteins restored steroid sensitivity in leukemic cells from patients.
Researchers at IRB Barcelona have discovered 10 new drug combinations that show high synergy in treating breast cancer, outperforming individual treatments. These combinations aim to overcome treatment resistance by attacking tumour cells from multiple angles.
A study published in Cell Reports found that glioblastoma cells with different resistance levels to therapy and radiation are linked to disease outcomes. Researchers identified a continuum of cells with varying resistance levels, which may enable the development of targeted therapies.
Researchers have developed a rapid test to monitor drug resistance in hookworms, which can cause disease and stunted growth. The new test uses short nucleotide polymorphisms to detect drug-resistant mutations in as little as 1% of a sample, taking only 60 minutes.
Researchers at the Weizmann Institute of Science have identified a promising new combination therapy for triple negative breast cancer, which inhibits tumor growth and survival while preventing drug resistance. The therapy targets EGFR and PYK2 molecules, leading to a more potent therapeutic effect than inhibiting either molecule alone.
Researchers found that blocking tumor interferon pathway with a JAK inhibitor improves checkpoint inhibitor drugs and bypasses the need for combinations, which often come with serious side effects. The study suggests a new approach to addressing cancer immunotherapies' limitations.
Researchers at the University of Southampton have characterised the molecular mechanisms behind idelalisib's effectiveness in treating chronic lymphocytic leukaemia. The study found that the drug disrupts survival signals and prevents tumour cell communication, leading to cancer cell death.
A study investigated infectious disease mortality trends in the US from 1980 to 2014, revealing overall and infectious disease mortality decreased until 1995, then leveled off. The introduction of antiretroviral therapy for HIV/AIDS led to a decline in overall and HIV/AIDS mortality rates.
Researchers investigated resistance to antiangiogenic therapies using animal models, finding inconsistent definitions of treatment failure. The study emphasizes the need for improved methodology to accurately predict alternative strategies that benefit patients.
Scientists have identified two genetic markers associated with piperaquine resistance in malaria parasites, allowing for early detection and alternative treatment options. The markers are linked to increased production of plasmepsin enzymes, which the parasite uses to digest human blood.
A newly identified protein, NTR2, has been discovered that activates drugs like delamanid against leishmaniasis. This finding holds promise for developing more effective treatments for the disease.
Scientists discovered genetic markers linked with piperaquine resistance in Plasmodium parasites, allowing health officials to monitor the spread of resistance and guide treatment decisions. The emergence of piperaquine resistance in Cambodia threatens global efforts to eliminate malaria.
Researchers at MUSC Hollings Cancer Center discover a mechanism conferring resistance to AML drugs and develop a ceramide-based therapeutic that reactivates mitophagy, killing drug-resistant cancer cells. The treatment has clinical appeal due to its specificity towards cancer cells.
Researchers found no differences in HIV drug resistance between women using dapivirine and placebo rings in the ASPIRE trial. The dapivirine ring was safe and helped protect against HIV, with an overall risk reduction of 27%.
A MGH team found that treating metastatic colorectal cancer with antiangiogenic drugs increases extracellular matrix components and stiffness, contributing to treatment resistance. Antiangiogenic therapy also attracts suppressor immune cells, reducing the immune response against tumors.
Scientists at Harvard's Wyss Institute have developed a way to analyze the effect of mechanical stiffness on chemotherapy treatment. The new method uses alginate hydrogels to mimic tumor and normal tissue environments, revealing that softer matrix conditions lead to increased resistance.
Researchers developed a new image analysis technique to distinguish between epithelial and mesenchymal cells in tumors. The algorithm achieved over 92% accuracy in categorizing individual cells, revealing potential insights into cancer drug resistance and treatment.
A mathematical model suggests that alternating between erlotinib and evofosfamide could help prevent drug resistance in non-small cell lung cancer patients. This treatment schedule is more effective than using either drug alone, according to a study published in PLOS Computational Biology.
Researchers have identified a potential antifungal mechanism by targeting mitochondrial respiration in pathogenic fungi, which could enable combination therapy with fluconazole and prevent drug resistance. The approach has shown promise in treating severe invasive fungal infections, including those caused by Candida albicans.
A study led by Case Western Reserve University researchers has identified a gene, S100P, that may help tumors evade trastuzumab, a common breast cancer treatment. By blocking S100P, tumor cells became sensitive to the drug again.
Researchers found that inactivating mutations in STAG2 or STAG3 can reactivate the MAPK cell-growth pathway, leading to treatment resistance. Knockdown of these proteins reduced sensitivity to BRAF inhibition, while increasing their expression increased treatment effectiveness.
Australian researchers have developed a new test that can predict patients' long-term response to treatment for chronic myeloid leukemia. The test assesses the levels of P-glycoprotein in patient cells and identifies those at risk of developing resistance, allowing doctors to adjust treatment strategies.
Researchers found that replication fork protection is a major mechanism of drug resistance in BRCA1/2-mutant breast and ovarian cancers. Proteins such as PTIP, CHD4, and PARP1 promote destabilization of replication forks, making cells chemoresistant.
Researchers have discovered how new HIV drugs work by locking the immature form of the virus in place, preventing it from maturing and infecting other cells. The study provides insights into the workings of these drugs and their resistance to mutations.
Scientists developed a novel algorithm to predict synergistic antifungal drug combinations for treating drug-resistant fungal infections. The algorithm, NLLSS, integrates various information types and experimentally validated 7 out of 13 predicted combinations for Candida albicans, providing new treatment options.
A global trial of midostaurin reveals that the drug can produce partial or complete resolution of organ damage in 60% of patients with advanced systemic mastocytosis. Patients treated with midostaurin experienced improved liver function, fewer signs of malabsorption, and increased survival rates.
A new study by bioengineers at Brigham and Women's Hospital demonstrates the effectiveness of combination therapies in eliminating cancer cells. By pairing chemotherapy drug docetaxel with a targeted PI3K inhibitor, researchers achieved greater tumor inhibition and eliminated evidence of resistance.
Researchers at Johns Hopkins have found that emetine, an old drug once used to treat amebiasis, can also halt the replication of cytomegalovirus (CMV), a herpesvirus causing serious disease in immunocompromised individuals. Lower concentrations and less frequent doses of emetine may be effective for CMV inhibition.
A study on Plasmodium vivax reveals rapid evolution of drug resistance in response to widely-used antimalarial drugs. The genomic data sets will guide effective malaria control and elimination strategies, supporting local public health efforts.
The global mapping of artemisinin resistance, led by Institut Pasteur researchers, has confirmed that resistance to the main malaria drug is confined to Southeast Asia. The study identified 70 new mutations, including those in Cambodia and Vietnam-Laos, which were not associated with resistance.
Researchers develop a revolutionary approach to cancer treatment that activates two drugs within the same cell at the same time, preventing resistance in aggressive cancers. By tracking cellular signals and molecular pathways, they discovered vulnerabilities to small molecule PI3K/AKT kinase inhibitors.