J Cell Biol 1987
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Acting as incretin mimetics, they enhance glucose-dependent insulin secretion, suppress glucagon release, delay gastric emptying, and promote satiety, addressing several core abnormalities in T2DM pathophysiology ( Since the approval of exenatide in 2005, the GLP-1 RA class has expanded to include liraglutide, semaglutide, dulaglutide, and lixisenatide, each differing in half-life, route of administration, and molecular structure ( Pancreatic cancer has drawn particular scrutiny due to its high fatality rate and some early observational reports suggesting elevated risk with incretin-based therapies ( Given the expanding use of GLP-1 RAs in populations already at elevated risk for gastrointestinal malignancies, there is a clear need for a comprehensive synthesis of high-quality evidence ( 2 Materials and methods 2.1 Search strategy and data sources The systematic review and meta-analysis were conducted in accordance with the PRISMA 2020 guidelines (Supplementary Table S1

Nevertheless, there exists a limited selection of thermally sensitive materials, and certain materials fall outside the parameters of biological systems or cannot be adjusted to an alternative temperature
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