Amidst the ever-evolving landscape of biomedical research, G-quadruplex (G4) structures have emerged as captivating therapeutic targets, holding immense promise for precision medicine and molecular diagnostics. These intricate DNA or RNA formations play crucial roles in regulating gene expression and are implicated in the pathogenesis of various diseases, including cancer and neurological disorders. The interaction between G4s and ligands derived from medicinal plants offers a compelling avenue for therapeutic intervention and diagnostic applications. G4-interacting ligands have demonstrated remarkable potential as therapeutic agents, selectively targeting G4 structures and modulating their biological functions. However, the effective delivery of these ligands into living cells remains a formidable challenge. Existing physical and biochemical methods are often limited to settings due to concerns regarding toxicity and nonspecific binding. Overcoming this delivery hurdle is paramount for translating G4-targeting therapies into clinically viable treatments. The development of novel G4 ligands with enhanced affinity and selectivity is essential for realizing the full therapeutic potential of G4-targeting strategies. Understanding the shared structural features of G4 ligands, such as the presence of an aromatic core for π-π stacking interactions and positive moieties for interactions with DNA or RNA backbones, provides valuable insights into ligand design. G4/ligand interactions hold immense promise for molecular diagnostics. By exploiting the specific recognition and binding capabilities of G4 ligands, researchers can develop biosensors and bioimaging tools for the detection and diagnosis of G4-related diseases. These diagnostic tools have the potential to revolutionize disease management by enabling early detection, personalized treatment plans, and improved patient outcomes.Communicated by Ramaswamy H. Sarma.
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http://dx.doi.org/10.1080/07391102.2024.2306498 | DOI Listing |
Neurology
February 2025
Department of Advanced Biomedical Sciences, University "Federico II," Naples, Italy.
Background And Objectives: Although multiple sclerosis (MS) can be conceptualized as a network disorder, brain network analyses typically require advanced MRI sequences not commonly acquired in clinical practice. Using conventional MRI, we assessed cross-sectional and longitudinal structural disconnection and morphometric similarity networks in people with MS (pwMS), along with their relationship with clinical disability.
Methods: In this longitudinal monocentric study, 3T structural MRI of pwMS and healthy controls (HC) was retrospectively analyzed.
Environ Health Perspect
January 2025
Division of Experimental Medicine, Department of Medicine, McGill University, Montréal, Canada.
Background: Millions worldwide are exposed to elevated levels of arsenic that significantly increase their risk of developing atherosclerosis, a pathology primarily driven by immune cells. While the impact of arsenic on immune cell populations in atherosclerotic plaques has been broadly characterized, cellular heterogeneity is a substantial barrier to in-depth examinations of the cellular dynamics for varying immune cell populations.
Objectives: This study aimed to conduct single-cell multi-omics profiling of atherosclerotic plaques in apolipoprotein E knockout () mice to elucidate transcriptomic and epigenetic changes in immune cells induced by arsenic exposure.
Science
January 2025
Center for Pulmonary Vascular Biology and Medicine, Pittsburgh, Heart, Lung, and Blood Vascular Medicine Institute, University of Pittsburgh, Pittsburgh, PA, USA.
Vascular inflammation regulates endothelial pathophenotypes, particularly in pulmonary arterial hypertension (PAH). Dysregulated lysosomal activity and cholesterol metabolism activate pathogenic inflammation, but their relevance to PAH is unclear. Nuclear receptor coactivator 7 () deficiency in endothelium produced an oxysterol and bile acid signature through lysosomal dysregulation, promoting endothelial pathophenotypes.
View Article and Find Full Text PDFPLoS One
January 2025
Cancer Center, Kagoshima University Hospital, Kagoshima, Japan.
Kinase-related gene fusion and point mutations play pivotal roles as drivers in cancer, necessitating optimized, targeted therapy against these alterations. The efficacy of molecularly targeted therapeutics varies depending on the specific alteration, with great success reported for such therapeutics in the treatment of cancer with kinase fusion proteins. However, the involvement of actionable alterations in solid tumors, especially regarding kinase fusions, remains unclear.
View Article and Find Full Text PDFPLoS Negl Trop Dis
January 2025
Center for Infection and Molecular Medicine, Amsterdam UMC location University of Amsterdam, Amsterdam, the Netherlands.
The global priorities in the field of infectious diseases are constantly changing. While emerging viral infections have regularly dominated public health attention, which has only intensified after the COVID-19 pandemic, numerous bacterial diseases have previously caused, and continue to cause, significant morbidity and mortality-deserving equal attention. Three potentially life-threatening endemic bacterial diseases (leptospirosis, melioidosis, and rickettsioses) are a huge public health concern especially in low- and middle-income countries.
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