jason fung glp-1 As good as Ozempic? Tools for Managing Hunger How GLP-1 Receptor Agonists Evolved

Use of incretin-based drugs and risk of cholangiocarcinoma: scandinavian cohort study

IGF1 indirectly increases DNA repair by 50% through increasing the p53 dependence in the p21, while inhibition IGF1R by siRNA in human prostate cancer cells enhances the sensitivity of ionizing radiation to SSBs and DSBs (Turney et al., 2012)

It belongs to a novel class of agents known as triple receptor agonists, meaning it is designed to simultaneously activate three distinct hormone receptors: the glucagon-like peptide-1 (GLP-1) receptor, the glucose-dependent insulinotropic polypeptide (GIP) receptor, and the glucagon receptor

PMID: 32132921