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Hepatic hormone FGF21 and its analogues in clinical trials

Fibroblast growth factor 21 (FGF21) is a fasting or stress inducible metabolic hormone produced mainly in the liver. It plays important roles in regulating both glucose and lipid homeostasis via interacting with a heterodimeric receptor complex comprising FGF receptor 1 (FGFR1) and β‐klotho (KLB). F...

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Detalles Bibliográficos
Autores principales: Shao, Weijuan, Jin, Tianru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9126297/
https://www.ncbi.nlm.nih.gov/pubmed/35620160
http://dx.doi.org/10.1016/j.cdtm.2021.08.005
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author Shao, Weijuan
Jin, Tianru
author_facet Shao, Weijuan
Jin, Tianru
author_sort Shao, Weijuan
collection PubMed
description Fibroblast growth factor 21 (FGF21) is a fasting or stress inducible metabolic hormone produced mainly in the liver. It plays important roles in regulating both glucose and lipid homeostasis via interacting with a heterodimeric receptor complex comprising FGF receptor 1 (FGFR1) and β‐klotho (KLB). For the past decade, great effort has been made on developing FGF21 derivatives or specific FGF21 receptor agonists into therapeutic agents for various metabolic disorders including type 2 diabetes (T2D), obesity, and more importantly, nonalcoholic fatty liver disease (NAFLD). Here we have reviewed FGF21 gene and protein structures, its expression pattern, cellular signaling cascades that mediate FGF21 production and function. We have then summarized the six clinical trials utilizing four FGF21 analogues. Finally, two recent literatures on the development of GLP‐1 and FGF21 dual agonists were presented briefly.
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spelling pubmed-91262972022-05-25 Hepatic hormone FGF21 and its analogues in clinical trials Shao, Weijuan Jin, Tianru Chronic Dis Transl Med Reviews Fibroblast growth factor 21 (FGF21) is a fasting or stress inducible metabolic hormone produced mainly in the liver. It plays important roles in regulating both glucose and lipid homeostasis via interacting with a heterodimeric receptor complex comprising FGF receptor 1 (FGFR1) and β‐klotho (KLB). For the past decade, great effort has been made on developing FGF21 derivatives or specific FGF21 receptor agonists into therapeutic agents for various metabolic disorders including type 2 diabetes (T2D), obesity, and more importantly, nonalcoholic fatty liver disease (NAFLD). Here we have reviewed FGF21 gene and protein structures, its expression pattern, cellular signaling cascades that mediate FGF21 production and function. We have then summarized the six clinical trials utilizing four FGF21 analogues. Finally, two recent literatures on the development of GLP‐1 and FGF21 dual agonists were presented briefly. John Wiley and Sons Inc. 2022-02-23 /pmc/articles/PMC9126297/ /pubmed/35620160 http://dx.doi.org/10.1016/j.cdtm.2021.08.005 Text en © 2022 The Authors. Chronic Diseases and Translational Medicine published by John Wiley & Sons, Ltd on behalf of Chinese Medical Association https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Reviews
Shao, Weijuan
Jin, Tianru
Hepatic hormone FGF21 and its analogues in clinical trials
title Hepatic hormone FGF21 and its analogues in clinical trials
title_full Hepatic hormone FGF21 and its analogues in clinical trials
title_fullStr Hepatic hormone FGF21 and its analogues in clinical trials
title_full_unstemmed Hepatic hormone FGF21 and its analogues in clinical trials
title_short Hepatic hormone FGF21 and its analogues in clinical trials
title_sort hepatic hormone fgf21 and its analogues in clinical trials
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9126297/
https://www.ncbi.nlm.nih.gov/pubmed/35620160
http://dx.doi.org/10.1016/j.cdtm.2021.08.005
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