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FIGURE 3 4.2 KRAS mutation in PDAC metabolic reprogramming KRAS mutation could accelerate PDAC progression depending on, not only the activation of signaling pathways, but also the induction of metabolic reprogramming ( KRAS mutation could regulate glucose, amino acid, and lipid metabolism in PDAC cancer cells ( 4.2.1 Glucose Pancreatic cancer cells facilitate glycolysis under adequate oxygen conditions

these showed that increased cellular GSSG accumulation, rather than GSH reduction, rendered hepatocytes susceptible to TNF-induced cytotoxicity

Screening for lipid-metabolism-related genes and identifying the diagnostic potential of ANGPTL6 for HBV-related early-stage hepatocellular carcinoma

Bromocoumarinplatin, targeting simultaneously mitochondria and nuclei with p53 apoptosis pathway to overcome cisplatin resistance

Ionizing radiation decomposes water molecules, which in turn results in the formation of secondary radicals