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Antisense oligonucleotides against Il6ra ameliorate cancer cachexia in mice
Author Correction: Nanopore-enabled time-resolved monitoring of catecholamine-related phenylalanine metabolism
Nature Nanotechnology, Published online: 09 September 2026; doi:10.1038/s41565-026-02294-y
Author Correction: Nanopore-enabled time-resolved monitoring of catecholamine-related phenylalanine metabolismGenerative AI for Analysts
LipoAgent: Coordinating Fine-Tuned LLM Agents for Safer Lipid Design
Integrative Multi-Omics Analysis Identifies FTO as a Genetic and Epigenetic Link Between Metabolic Susceptibility and Staphylococcus aureus-Induced Airway Remodeling in Chronic Rhinosinusitis
Chem Biol Drug Des. 2026 Apr;107(4):e70297. doi: 10.1111/cbdd.70297.
ABSTRACT
This study identifies fat mass and obesity-associated protein (FTO) as a pivotal link between metabolic predisposition and pathogenesis associated with Staphylococcus aureus in chronic rhinosinusitis (CRS). These findings were established through the application of an integrative multi-omics framework. We demonstrate that S. aureus upregulates FTO, which functions as an m6A demethylase to stabilize the Metastasis Associated Lung Adenocarcinoma Transcript 1 (MALAT1). This molecular axis suppresses GSK-3β and promotes β-catenin nuclear translocation, thereby driving epithelial-mesenchymal transition (EMT) and pathological mucosal remodeling. By mapping the FTO-MALAT1-GSK-3β/β-catenin signaling network, this research elucidates how metabolic susceptibility facilitates infection-triggered epithelial reprogramming. These findings establish FTO as a promising biomarker and potential therapeutic target, providing a systemic foundation for personalized CRS treatment strategies.
PMID:41973807 | DOI:10.1111/cbdd.70297