Results 231 to 240 of about 58,740 (306)
Heat Shock Proteins in Cancer: Mechanisms and Therapeutic Targeting
This review illustrates heat shock proteins (HSPs) as central regulators of cancer metabolic reprogramming. By stabilizing key metabolic enzymes and coordinating glycolysis, oxidative phosphorylation, redox homeostasis, and stress adaptation, HSPs support tumor growth, metastasis, and therapeutic resistance. Targeting HSP networks may therefore provide
Sheng Ma +5 more
wiley +1 more source
Twist Family BHLH Transcription Factor 1 orchestrates hypoxia-lactate crosstalk to bridge glycolytic flux and tubular maladaptation in fibrotic kidneys. [PDF]
Yu Z +9 more
europepmc +1 more source
Microbial signals from gut and tumor‐resident bacteria, fungi, viruses, and bacteriophages reshape immune and metabolic networks within the tumor microenvironment, thereby influencing cancer progression, treatment response. Therapeutic modulations, including dietary interventions, probiotics, antibiotics, fecal microbiota transplantation, engineered ...
Juan Lu +8 more
wiley +1 more source
HKDC1-mediated polyamine rewiring drives lenvatinib resistance and immune escape in hepatocellular carcinoma. [PDF]
Chen S +13 more
europepmc +1 more source
Among 23,882 PCI patients, metabolic phenotypes were classified as MHN, MHO, MUN, and MUO. During the 3‐year follow‐up, MUN was independently associated with higher cardiovascular risk compared with MHN (HR 1.27, 95% CI 1.07–1.52), mainly driven by MI and stroke. Metabolic phenotype stratification may improve risk assessment after PCI. ABSTRACT Obesity
Bowen Li +6 more
wiley +1 more source
SLC Transporter-Mediated Functional Imaging in Cancer Diagnosis. [PDF]
Zhang L, He J.
europepmc +1 more source
Findings from this study suggest that aging is accompanied by altered skeletal muscle mitochondrial redox regulation and exercise responsiveness, with decreased mtDNA copy number, increased mtDNA mutation deletion frequency, and selective redox remodeling of key mitochondrial proteins representing potential contributors to these changes. ABSTRACT Redox
Bradley A. Ruple +11 more
wiley +1 more source
Resveratrol Inhibits Macrophage Glucose Metabolism Reprogramming and Inflammatory Activation to Delay COPD Progression Through the TLR4/HK2 Pathway. [PDF]
Li Z +6 more
europepmc +1 more source
Benzothiazephane‐based curcuminoids are more potent than curcumin to inhibit liver cancer outgrowth in a Caco‐2/HepG2 coculture model, depending on methylation and heterocyclic substituent pattern. This may be the result of altered absorption, metabolism, and mitochondrial function, which are relevant targets for drug design.
Fuhua Li +7 more
wiley +1 more source

