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Cancer-associated adipocytes exhibit phenotypic changes including secretion of the lipids, inflammatory cytokines, and an imbalance in adipokine signaling pathways, such as the upregulation of leptin and downregulation of adiponectin, which promote tumor proliferation and invasion (123)

While the general principles of N-terminal acetylation and C-terminal amidation are well established in peptide chemistry, their specific effects on the AEDG sequences biological activity, pharmacokinetics in research models, and pathway engagement have not been formally evaluated in peer-reviewed literature (8)