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4l, Supplementary Data 5a), we confirmed that rapamycin inhibited mTOR-MYC signaling/targets as well as downregulated all major metabolic pathways (OXPHOS, glycolysis and fatty acid metabolism) and T cell activation/effector pathways (IL-2-STAT5, IL-6-JAK-STAT3, allogenic activity, and interferon response)

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(4) The researchers reported, On days 6, 10, and 13, tripeptide-copper complex-treated wounds contained significantly lower concentrations of TNF-alpha and MMP-2 and MMP-9 than control wounds. Tumor necrosis factor-alpha (TNF-alpha), a cytokine involved in systemic inflammation, along with matrix metalloproteinase-2 (MMP-2) and matrix metalloproteinase-9 (MMP-9) enzymes that break down extracellular matrix proteins might potentially influence both the inflammatory processes and the remodeling of tissues

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