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Lancet 2016;387:67990.ArticlePubMed 80

This mechanism is distinct from growth hormone secretagogues, incretin mimetics, or direct receptor agonistsmeaning AHK-Cu doesn't compete for the same binding sites as GLP-1 analogs, growth hormone releasing peptides, or melanocortin receptor targets

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157 Besides, the ZIP7 mRNA level was increased in both GC tissues and cell lines, which boosted cell proliferation and migration, while inhibiting apoptosis in GC