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doi: 10.1136/gutjnl-2023-330291 Summary Keywords colorectal cancer (CRC), metabolic reprogramming, tumor microenvironment, immune evasion, gut microbiota, metabolism-targeted therapy Citation Hu S, Heng H, Yang F, Wang M, Liu G, Xiang Y and Miao H (2025) The metabolism-immune axis in colorectal cancer: remodeling the tumor microenvironment through metabolite signaling

Neural Plast 2021:7174287 Cao LR, 2016 #5988}, Chen R, Xu J et al (2009) Vitamin E inhibits activated chaperone-mediated autophagy in rats with status epilepticus [J]

This is a sign that the antioxidant is doing its job at a systemic level

The majority of co-culture models are engineered to replicate the spatial organization of cells within the epithelial-mesenchymal trophic unit (EMTU), which includes a reduced fibroblast sheath within an ECM produced by large stellate interwoven fibroblasts that are near a reticular beneath membrane and aid in lung epithelium adhesion