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Funding This work was supported by grants from the National Natural Science Foundation of China (NSFC Numbers 81672800, 81603009, 81673020, 81802632, and 82173830), Natural Science Foundation of Shaanxi (2020JQ-445), and the Key Research and Development Program of Shaanxi Province (2021SF-207, 2021SF-223, and 2022ZDLSF05-19)
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In this context, the functional mimicry of GLP-1 should be considered worthwhile if the designed agonist can act as a biased agonist of GLP-1R, selectively triggering anti-inflammatory signaling pathways that can aid in reducing the growth and differentiation of certain types of neuroendocrine tumors
J Mol Neurosci 68:389396
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