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Proglucagon-Derived Peptides as Therapeutics

Journal

FRONTIERS IN ENDOCRINOLOGY
Volume 12, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fendo.2021.689678

Keywords

proglucagon; glucagon; GLP-1; GLP-2; oxyntomodulin; diabetes; obesity; multi-agonist

Funding

  1. Diabetes UK
  2. European Foundation for the Study of Diabetes
  3. Diabetes Research and Wellness Foundation
  4. Invest Northern Ireland
  5. Invest Northern Ireland, Northern Ireland Department for Education, and Ulster University Strategic Fund

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Originally discovered as an impurity in insulin preparations, glucagon has evolved significantly in our understanding over the years. The family of PGDP peptides, including GLP-1, GLP-2, OXM, glicentin, and GRPP, exert unique physiological effects on metabolism and energy regulation, with some of them being utilized as long-acting, enzymatically resistant analogues for various pathologies. The therapeutic applications of these peptides have expanded to include rescue of hypoglycemia, management of short bowel syndrome, and treatment of Type 2 diabetes mellitus, with newer benefits being uncovered in areas such as cardioprotection, bone health, and cognitive function.
Initially discovered as an impurity in insulin preparations, our understanding of the hyperglycaemic hormone glucagon has evolved markedly over subsequent decades. With description of the precursor proglucagon, we now appreciate that glucagon was just the first proglucagon-derived peptide (PGDP) to be characterised. Other bioactive members of the PGDP family include glucagon-like peptides -1 and -2 (GLP-1 and GLP-2), oxyntomodulin (OXM), glicentin and glicentin-related pancreatic peptide (GRPP), with these being produced via tissue-specific processing of proglucagon by the prohormone convertase (PC) enzymes, PC1/3 and PC2. PGDP peptides exert unique physiological effects that influence metabolism and energy regulation, which has witnessed several of them exploited in the form of long-acting, enzymatically resistant analogues for treatment of various pathologies. As such, intramuscular glucagon is well established in rescue of hypoglycaemia, while GLP-2 analogues are indicated in the management of short bowel syndrome. Furthermore, since approval of the first GLP-1 mimetic for the management of Type 2 diabetes mellitus (T2DM) in 2005, GLP-1 therapeutics have become a mainstay of T2DM management due to multifaceted and sustainable improvements in glycaemia, appetite control and weight loss. More recently, longer-acting PGDP therapeutics have been developed, while newfound benefits on cardioprotection, bone health, renal and liver function and cognition have been uncovered. In the present article, we discuss the physiology of PGDP peptides and their therapeutic applications, with a focus on successful design of analogues including dual and triple PGDP receptor agonists currently in clinical development.

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